WO2013009782A2 - Communication system with enhanced partial power source and method of manufacturing same - Google Patents

Communication system with enhanced partial power source and method of manufacturing same Download PDF

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Publication number
WO2013009782A2
WO2013009782A2 PCT/US2012/046120 US2012046120W WO2013009782A2 WO 2013009782 A2 WO2013009782 A2 WO 2013009782A2 US 2012046120 W US2012046120 W US 2012046120W WO 2013009782 A2 WO2013009782 A2 WO 2013009782A2
Authority
WO
WIPO (PCT)
Prior art keywords
layer
depositing
adhesion
support structure
power source
Prior art date
Application number
PCT/US2012/046120
Other languages
French (fr)
Other versions
WO2013009782A3 (en
Inventor
Jeremy Frank
Peter Bjeletich
Hooman Hafezi
Robert Azevedo
Robert Duck
Iliya Pesic
Benedict Costello
Eric Snyder
Original Assignee
Proteus Biomedical, Inc.
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Priority to RU2014104692/14A priority Critical patent/RU2014104692A/en
Priority to CA2841830A priority patent/CA2841830A1/en
Application filed by Proteus Biomedical, Inc. filed Critical Proteus Biomedical, Inc.
Priority to UAA201401331A priority patent/UA116434C2/en
Priority to MX2014000484A priority patent/MX337131B/en
Priority to KR1020147003475A priority patent/KR20140051298A/en
Priority to JP2014520264A priority patent/JP6259395B2/en
Priority to AU2012282777A priority patent/AU2012282777A1/en
Priority to BR112014000641A priority patent/BR112014000641A2/en
Priority to CN201280043578.4A priority patent/CN103957773A/en
Priority to EP12811820.5A priority patent/EP2731489A4/en
Publication of WO2013009782A2 publication Critical patent/WO2013009782A2/en
Publication of WO2013009782A3 publication Critical patent/WO2013009782A3/en
Priority to IL230388A priority patent/IL230388B/en
Priority to ZA2014/00337A priority patent/ZA201400337B/en
Priority to HK14111828.9A priority patent/HK1198283A1/en
Priority to IL26412119A priority patent/IL264121B/en

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Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61BDIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B5/00Measuring for diagnostic purposes; Identification of persons
    • A61B5/07Endoradiosondes
    • A61B5/073Intestinal transmitters
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61BDIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B5/00Measuring for diagnostic purposes; Identification of persons
    • A61B5/0002Remote monitoring of patients using telemetry, e.g. transmission of vital signals via a communication network
    • A61B5/0031Implanted circuitry
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61BDIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B5/00Measuring for diagnostic purposes; Identification of persons
    • A61B5/01Measuring temperature of body parts ; Diagnostic temperature sensing, e.g. for malignant or inflamed tissue
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61BDIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B5/00Measuring for diagnostic purposes; Identification of persons
    • A61B5/145Measuring characteristics of blood in vivo, e.g. gas concentration, pH value; Measuring characteristics of body fluids or tissues, e.g. interstitial fluid, cerebral tissue
    • A61B5/14539Measuring characteristics of blood in vivo, e.g. gas concentration, pH value; Measuring characteristics of body fluids or tissues, e.g. interstitial fluid, cerebral tissue for measuring pH
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61BDIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B5/00Measuring for diagnostic purposes; Identification of persons
    • A61B5/68Arrangements of detecting, measuring or recording means, e.g. sensors, in relation to patient
    • A61B5/6846Arrangements of detecting, measuring or recording means, e.g. sensors, in relation to patient specially adapted to be brought in contact with an internal body part, i.e. invasive
    • A61B5/6847Arrangements of detecting, measuring or recording means, e.g. sensors, in relation to patient specially adapted to be brought in contact with an internal body part, i.e. invasive mounted on an invasive device
    • A61B5/6861Capsules, e.g. for swallowing or implanting
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61JCONTAINERS SPECIALLY ADAPTED FOR MEDICAL OR PHARMACEUTICAL PURPOSES; DEVICES OR METHODS SPECIALLY ADAPTED FOR BRINGING PHARMACEUTICAL PRODUCTS INTO PARTICULAR PHYSICAL OR ADMINISTERING FORMS; DEVICES FOR ADMINISTERING FOOD OR MEDICINES ORALLY; BABY COMFORTERS; DEVICES FOR RECEIVING SPITTLE
    • A61J3/00Devices or methods specially adapted for bringing pharmaceutical products into particular physical or administering forms
    • A61J3/007Marking tablets or the like
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01MPROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M4/00Electrodes
    • H01M4/02Electrodes composed of, or comprising, active material
    • H01M4/04Processes of manufacture in general
    • H01M4/0402Methods of deposition of the material
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01MPROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M4/00Electrodes
    • H01M4/02Electrodes composed of, or comprising, active material
    • H01M4/06Electrodes for primary cells
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01MPROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M4/00Electrodes
    • H01M4/02Electrodes composed of, or comprising, active material
    • H01M4/06Electrodes for primary cells
    • H01M4/08Processes of manufacture
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01MPROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M4/00Electrodes
    • H01M4/02Electrodes composed of, or comprising, active material
    • H01M4/36Selection of substances as active materials, active masses, active liquids
    • H01M4/38Selection of substances as active materials, active masses, active liquids of elements or alloys
    • H01M4/381Alkaline or alkaline earth metals elements
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01MPROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M4/00Electrodes
    • H01M4/02Electrodes composed of, or comprising, active material
    • H01M4/36Selection of substances as active materials, active masses, active liquids
    • H01M4/58Selection of substances as active materials, active masses, active liquids of inorganic compounds other than oxides or hydroxides, e.g. sulfides, selenides, tellurides, halogenides or LiCoFy; of polyanionic structures, e.g. phosphates, silicates or borates
    • H01M4/582Halogenides
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01MPROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M6/00Primary cells; Manufacture thereof
    • H01M6/30Deferred-action cells
    • H01M6/32Deferred-action cells activated through external addition of electrolyte or of electrolyte components
    • H01M6/34Immersion cells, e.g. sea-water cells
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01QANTENNAS, i.e. RADIO AERIALS
    • H01Q1/00Details of, or arrangements associated with, antennas
    • H01Q1/27Adaptation for use in or on movable bodies
    • H01Q1/273Adaptation for carrying or wearing by persons or animals
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61BDIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B2560/00Constructional details of operational features of apparatus; Accessories for medical measuring apparatus
    • A61B2560/02Operational features
    • A61B2560/0204Operational features of power management
    • A61B2560/0214Operational features of power management of power generation or supply
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61BDIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B2562/00Details of sensors; Constructional details of sensor housings or probes; Accessories for sensors
    • A61B2562/12Manufacturing methods specially adapted for producing sensors for in-vivo measurements
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61BDIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B2562/00Details of sensors; Constructional details of sensor housings or probes; Accessories for sensors
    • A61B2562/12Manufacturing methods specially adapted for producing sensors for in-vivo measurements
    • A61B2562/125Manufacturing methods specially adapted for producing sensors for in-vivo measurements characterised by the manufacture of electrodes
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61BDIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B2562/00Details of sensors; Constructional details of sensor housings or probes; Accessories for sensors
    • A61B2562/16Details of sensor housings or probes; Details of structural supports for sensors
    • A61B2562/162Capsule shaped sensor housings, e.g. for swallowing or implantation
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61BDIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B5/00Measuring for diagnostic purposes; Identification of persons
    • A61B5/0002Remote monitoring of patients using telemetry, e.g. transmission of vital signals via a communication network
    • A61B5/0026Remote monitoring of patients using telemetry, e.g. transmission of vital signals via a communication network characterised by the transmission medium
    • A61B5/0028Body tissue as transmission medium, i.e. transmission systems where the medium is the human body
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61BDIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B5/00Measuring for diagnostic purposes; Identification of persons
    • A61B5/48Other medical applications
    • A61B5/4836Diagnosis combined with treatment in closed-loop systems or methods
    • A61B5/4839Diagnosis combined with treatment in closed-loop systems or methods combined with drug delivery
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01MPROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M2220/00Batteries for particular applications
    • H01M2220/30Batteries in portable systems, e.g. mobile phone, laptop
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01MPROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M4/00Electrodes
    • H01M4/02Electrodes composed of, or comprising, active material
    • H01M4/36Selection of substances as active materials, active masses, active liquids
    • H01M4/362Composites
    • H01M4/366Composites as layered products
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01MPROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M4/00Electrodes
    • H01M4/02Electrodes composed of, or comprising, active material
    • H01M4/64Carriers or collectors
    • H01M4/66Selection of materials
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T156/00Adhesive bonding and miscellaneous chemical manufacture
    • Y10T156/10Methods of surface bonding and/or assembly therefor
    • Y10T156/1052Methods of surface bonding and/or assembly therefor with cutting, punching, tearing or severing
    • Y10T156/1056Perforating lamina
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T29/00Metal working
    • Y10T29/49Method of mechanical manufacture
    • Y10T29/49002Electrical device making
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T29/00Metal working
    • Y10T29/49Method of mechanical manufacture
    • Y10T29/49002Electrical device making
    • Y10T29/49117Conductor or circuit manufacturing

Definitions

  • the present invention is related to communication systems for detection of an event. More specifically, the present disclosure includes a system that includes a device with various power sources and communication schemes.
  • Ingestible devices that include electronic circuitry have been proposed for use in a variety of different medical applications, including both diagnostic and therapeutic applications. These devices typically require an internal power supply for operation.
  • ingestible devices are ingestible electronic capsules which collect data as they pass through the body, and transmit the data to an external receiver system.
  • An example of this type of electronic capsule is an in-vivo video camera.
  • the swallowable capsule includes a camera system and an optical system for imaging an area of interest onto the camera system.
  • the transmitter transmits the video output of the camera system and the reception system receives the transmitted video output.
  • Other examples include an ingestible imaging device, which has an internal and self-contained power source, which obtains images from within body lumens or cavities.
  • the electronic circuit components of the device are enclosed by an inert indigestible housing (e.g. glass housing) that passes through the body internally.
  • an ingestible data recorder capsule medical device e.g. sensor, recorder, battery etc.
  • the electronic circuits of the disclosed device e.g. sensor, recorder, battery etc.
  • the electronic circuits of the disclosed device are housed in a capsule made of inert materials.
  • fragile radio frequency identification (RFID) tags are used in drug ingestion monitoring applications. In order for the RFID tags to be operational, each requires an internal power supply.
  • the RFID tags are antenna structures that are configured to transmit a radio-frequency signal through the body.
  • the present disclosure includes a system for producing a unique signature that indicates the occurrence of an event.
  • the system includes circuitry and components that can be placed within certain environments that include a conducting fluid.
  • a conducting fluid such as a sealed bag with a solution, which includes an IV bag.
  • Another example is within the body of a living organism, such as an animal or a human.
  • the systems are ingestible and/or digestible or partially digestible.
  • the system includes dissimilar materials positioned on the framework such that when a conducting fluid comes into contact with the dissimilar materials, a voltage potential difference is created. The voltage potential difference, and hence the voltage, is used to power up control logic that is positioned within the framework. Ions or current flows from the first dissimilar material to the second dissimilar material via the control logic and then through the conducting fluid to complete a circuit.
  • the control logic controls the conductance between the two dissimilar materials and, hence, controls or modulates the conductance.
  • the ingestible circuitry is made up of ingestible, and even digestible, components, the ingestible circuitry results in little, if any, unwanted side effects, even when employed in chronic situations.
  • Examples of the range of components that may be included are: logic and/or memory elements; effectors; a signal transmission element; and a passive element, such as a resistor or inductor.
  • the one or more components on the surface of the support may be laid out in any convenient configuration. Where two or more components are present on the surface of the solid support, interconnects may be provided. All of the components and the support of the ingestible circuitry are ingestible, and in certain instances digestible or partially digestible. Furthemore, the circuitry is manufactured according to a process to enhance adhesion of the materials.
  • Fig. 1 shows a pharmaceutical product with an event indicator system according to the teaching of the present invention, wherein the product and the event indicator system combination are within the body.
  • Fig. 2A shows the pharmaceutical product of Fig. 1 with the event indicator system on the exterior of the pharmaceutical product.
  • Fig. 2B shows the pharmaceutical product of Fig. 1 with the event indicator system positioned inside the pharmaceutical product.
  • Fig. 3 is a block diagram representation of one aspect of the event indicator system with dissimilar metals positioned on opposite ends.
  • Fig. 4 is a block diagram representation of another aspect of the event indicator system with dissimilar metals positioned on the same end and separated by a non-conducting material.
  • Fig. 5 shows ionic transfer or the current path through a conducting fluid when the event indicator system of Fig. 3 is in contact with conducting liquid and in an active state.
  • Fig. 5A shows an exploded view of the surface of dissimilar materials of Fig. 5.
  • Fig. 5B shows the event indicator system of Fig. 5 with a pH sensor unit.
  • Fig. 5C shows the event indicator system in accordance with another aspect of the present invention.
  • Fig. 6 is a block diagram illustration of one aspect of the control device used in the system of Figs. 3 and 4.
  • Fig. 7 shows a cross sectional side view of the event indicator system in accordance with the present invention.
  • Fig. 8 is an exploded view of two components of the event indicator system of Fig. 7 in accordance with the present invention.
  • Fig. 9 is an assembly process of a portion of the event indicator system of Fig. 7 in accordance with the present invention.
  • Fig. 10 shows a wafer with multiple event indicator systems in accordance with the present invention.
  • Fig. 1 1 shows a non-conducting membrane sheet with holes for receiving a device forming part of the event indicator system of Fig. 7 in accordance with the present invention.
  • FIG. 12 is a functional block diagram of a demodulation circuit that performs coherent demodulation that may be present in a receiver, according to one aspect.
  • FIG. 13 illustrates a functional block diagram for a beacon module within a receiver, according to one aspect.
  • FIG. 14 is a block diagram of the different functional modules that may be present in a receiver, according to one aspect.
  • FIG. 15 is a block diagram of a receiver, according to one aspect.
  • FIG. 16 provides a block diagram of a high frequency signal chain in a receiver, according to one aspect.
  • FIG. 17 provides a diagram of how a system that includes a signal receiver and an ingestible event marker may be employed, according to one aspect..
  • the present disclosure includes multiple aspects for indicating the occurrence of an event.
  • a system of the present invention is used with a conducting fluid to indicate the event marked by contact between the conducting fluid and the system.
  • the system of the present disclosure may be used with pharmaceutical product and the event that is indicated is when the product is taken or ingested.
  • the term "ingested” or “ingest” or “ingesting” is understood to mean any introduction of the system internal to the body.
  • ingesting includes simply placing the system in the mouth all the way to the descending colon.
  • the term ingesting refers to any instant in time when the system is introduced to an environment that contains a conducting fluid.
  • Another example would be a situation when a non-conducting fluid is mixed with a conducting fluid. In such a situation the system would be present in the non- conduction fluid and when the two fluids are mixed, the system comes into contact with the conducting fluid and the system is activated. Yet another example would be the situation when the presence of certain conducting fluids needed to be detected. In such instances, the presence of the system, which would be activated, within the conducting fluid could be detected and, hence, the presence of the respective fluid would be detected.
  • the device comes into contact with the conducting liquid of the body.
  • the system of the present invention comes into contact with the body fluid, a voltage potential is created and the system is activated.
  • a portion of the power source is provided by the device, while another portion of the power source is provided by the conducting fluid, which is discussed in detail below.
  • an ingestible product 14 that includes a system of the present invention is shown inside the body.
  • the product 14 is configured as an orally ingestible pharmaceutical formulation in the form of a pill or capsule.
  • the pill moves to the stomach.
  • stomach fluid 18 Upon reaching the stomach, the product 14 is in contact with stomach fluid 18 and undergoes a chemical reaction with the various materials in the stomach fluid 18, such as hydrochloric acid and other digestive agents.
  • the system of the present invention is discussed in reference to a pharmaceutical environment. However, the scope of the present invention is not limited thereby.
  • the present invention can be used in any environment where a conducting fluid is present or becomes present through mixing of two or more components that result in a conducting liquid.
  • a pharmaceutical product 10 similar to the product 14 of Fig. 1 , is shown with a system 12, such as an ingestible event marker or an ionic emission module.
  • a system 12 such as an ingestible event marker or an ionic emission module.
  • the product 10 can be a capsule, a time-release oral dosage, a tablet, a gel cap, a sub-lingual tablet, or any oral dosage product that can be combined with the system 12.
  • the product 10 has the system 12 secured to the exterior using known methods of securing micro-devices to the exterior of pharmaceutical products.
  • Example of methods for securing the micro-device to the product is disclosed in US Provisional Application No. 61 /142,849 filed on Jan 1 , 2009 and entitled “HIGH-THROUGHPUT PRODUCTION OF INGESTIBLE EVENT MARKERS” as well as US Provisional Application No. 61/177,61 1 filed on May 12, 2009 and entitled “INGESTIBLE EVENT MARKERS COMPRISING AN IDENTIFIER AND AN INGESTIBLE COMPONENT", the entire disclosure of each is incorporated herein by reference.
  • the system 12 comes into contact with body liquids and the system 12 is activated.
  • the system 12 uses the voltage potential difference to power up and thereafter modulates conductance to create a unique and identifiable current signature.
  • the system 12 controls the conductance and, hence, current flow to produce the current signature.
  • the system 12 may be coated with a shielding material or protective layer. The layer is dissolved over a period of time, thereby allowing the system 12 to be activated when the product 10 has reached a target location.
  • a pharmaceutical product 20 similar to the product 14 of Fig. 1 , is shown with a system 22, such as an ingestible event marker or an identifiable emission module.
  • a system 22 such as an ingestible event marker or an identifiable emission module.
  • the scope of the present invention is not limited by the environment to which the system 22 is introduced.
  • the system 22 can be enclosed in a capsule that is taken in addition to/independently from the pharmaceutical product.
  • the capsule may be simply a carrier for the system 22 and may not contain any product.
  • the scope of the present invention is not limited by the shape or type of product 20.
  • the product 20 can be a capsule, a time-release oral dosage, a tablet, a gel capsule, a sub-lingual tablet, or any oral dosage product.
  • the product 20 has the system 22 positioned inside or secured to the interior of the product 20.
  • the system 22 is secured to the interior wall of the product 20.
  • the content of the gel capsule is a non-conducting gel-liquid.
  • the system 22 is coated with a protective cover to prevent unwanted activation by the gel capsule content.
  • the system 22 is positioned or placed within the capsule. If the product 20 is a tablet or hard pill, then the system 22 is held in place inside the tablet. Once ingested, the product 20 containing the system 22 is dissolved. The system 22 comes into contact with body liquids and the system 22 is activated. Depending on the product 20, the system 22 may be positioned in either a near-central or near-perimeter position depending on the desired activation delay between the time of initial ingestion and activation of the system 22. For example, a central position for the system 22 means that it will take longer for the system 22 to be in contact with the conducting liquid and, hence, it will take longer for the system 22 to be activated. Therefore, it will take longer for the occurrence of the event to be detected.
  • system 30 in one aspect, the systems 12 and 22 of Figs. 2A and 2B, respectively, are shown in more detail as system 30.
  • the system 30 can be used in association with any pharmaceutical product, as mentioned above, to determine when a patient takes the pharmaceutical product.
  • the scope of the present invention is not limited by the environment and the product that is used with the system 30.
  • the system 30 may be placed within a capsule and the capsule is placed within the conducting liquid. The capsule would then dissolve over a period of time and release the system 30 into the conducting liquid.
  • the capsule would contain the system 30 and no product.
  • Such a capsule may then be used in any environment where a conducting liquid is present and with any product.
  • the capsule may be dropped into a container filled with jet fuel, salt water, tomato sauce, motor oil, or any similar product.
  • the capsule containing the system 30 may be ingested at the same time that any pharmaceutical product is ingested in order to record the occurrence of the event, such as when the product was taken.
  • the system 30 includes a framework 32.
  • the framework 32 is a chassis for the system 30 and multiple components are attached to, deposited upon, or secured to the framework 32.
  • a digestible material 34 is physically associated with the framework 32.
  • the material 34 may be chemically deposited on, evaporated onto, secured to, or built-up on the framework all of which may be referred to herein as "deposit" with respect to the framework 32.
  • the material 34 is deposited on one side of the framework 32.
  • the materials of interest that can be used as material 34 include, but are not limited to: Cu or Cul.
  • the material 34 is deposited by physical vapor deposition, electrodeposition, or plasma deposition, among other protocols.
  • the material 34 may be from about 0.05 to about 500 ⁇ thick, such as from about 5 to about 100 ⁇ thick.
  • the shape is controlled by shadow mask deposition, or photolithography and etching. Additionally, even though only one region is shown for depositing the material, each system 30 may contain two or more electrically unique regions where the material 34 may be deposited, as desired.
  • the various methods for depositing the materials onto the framework 32 are discussed in greater detail with respect to Figs. 7-9 below.
  • Another digestible material 36 is deposited, such that materials 34 and 36 are dissimilar.
  • the different side selected may be the side next to the side selected for the material 34.
  • the scope of the present invention is not limited by the side selected and the term "different side" can mean any of the multiple sides that are different from the first selected side.
  • the shape of the system is shown as a square, the shape maybe any geometrically suitable shape.
  • Material 34 and 36 are selected such that they produce a voltage potential difference when the system 30 is in contact with conducting liquid, such as body fluids.
  • the materials of interest for material 36 include, but are not limited to: Mg, Zn, or other electronegative metals.
  • the material 36 may be chemically deposited on, evaporated onto, secured to, or built-up on the framework. Also, an adhesion layer may be necessary to help the material 36 (as well as material 34 when needed) to adhere to the framework 32. Typical adhesion layers for the material 36 are Ti, TiW, Cr or similar material. Anode material and the adhesion layer may be deposited by physical vapor deposition, electrodeposition or plasma deposition. The material 36 may be from about 0.05 to about 500 ⁇ thick, such as from about 5 to about 100 ⁇ thick. However, the scope of the present invention is not limited by the thickness of any of the materials nor by the type of process used to deposit or secure the materials to the framework 32.
  • the materials 34 and 36 can be any pair of materials with different electrochemical potentials. Additionally, in the aspects wherein the system 30 is used in-vivo, the materials 34 and 36 may be vitamins that can be absorbed. More specifically, the materials 34 and 36 can be made of any two materials appropriate for the environment in which the system 30 will be operating. For example, when used with an ingestible product, the materials 34 and 36 are any pair of materials with different electrochemical potentials that are ingestible. An illustrative example includes the instance when the system 30 is in contact with an ionic solution, such as stomach acids.
  • Suitable materials are not restricted to metals, and in certain aspects the paired materials are chosen from metals and non-metals, e.g., a pair made up of a metal (such as Mg) and a salt (such as CuCI or Cul).
  • a metal such as Mg
  • a salt such as CuCI or Cul
  • any pairing of substances - metals, salts, or intercalation compounds - with suitably different electrochemical potentials (voltage) and low interfacial resistance are suitable.
  • Materials and pairings of interest include, but are not limited to, those reported in Table 1 below.
  • one or both of the metals may be doped with a non-metal, e.g., to enhance the voltage potential created between the materials as they come into contact with a conducting liquid.
  • Non-metals that may be used as doping agents in certain aspects include, but are not limited to: sulfur, iodine and the like.
  • the materials are copper iodine (Cul) as the anode and magnesium (Mg) as the cathode.
  • Electrodes of the present invention use electrode materials that are not harmful to the human body.
  • a current path is formed through the conducting liquid between material 34 and 36.
  • a control device 38 is secured to the framework 32 and electrically coupled to the materials 34 and 36.
  • the control device 38 includes electronic circuitry, for example control logic that is capable of controlling and altering the conductance between the materials 34 and 36.
  • the voltage potential created between the materials 34 and 36 provides the power for operating the system as well as produces the current flow through the conducting fluid and the system.
  • the system operates in direct current mode.
  • the system controls the direction of the current so that the direction of current is reversed in a cyclic manner, similar to alternating current.
  • a receiver not shown, can detect the presence of the current and recognize that the system 30 has been activate and the desired event is occurring or has occurred.
  • Illustrative examples of receivers are shown in Figs. 12 to 17, as described hereinafter.
  • the two materials 34 and 36 are similar in function to the two electrodes needed for a direct current power source, such as a battery.
  • the conducting liquid acts as the electrolyte needed to complete the power source.
  • the completed power source described is defined by the electrochemical reaction between the materials 34 and 36 of the system 30 and enabled by the fluids of the body.
  • the completed power source may be viewed as a power source that exploits electrochemical conduction in an ionic or a conducting solution such as gastric fluid, blood, or other bodily fluids and some tissues.
  • the environment may be something other than a body and the liquid may be any conducting liquid.
  • the conducting fluid may be salt water or a metallic based paint.
  • these two materials are shielded from the surrounding environment by an additional layer of material. Accordingly, when the shield is dissolved and the two dissimilar materials are exposed to the target site, a voltage potential is generated.
  • the complete power source or supply is one that is made up of active electrode materials, electrolytes, and inactive materials, such as current collectors, packaging, etc.
  • the active materials are any pair of materials with different electrochemical potentials. Suitable materials are not restricted to metals, and in certain aspects the paired materials are chosen from metals and non-metals, e.g., a pair made up of a metal (such as Mg) and a salt (such as Cul).
  • a metal such as Mg
  • a salt such as Cul
  • any pairing of substances - metals, salts, or intercalation compounds - with suitably different electrochemical potentials (voltage) and low interfacial resistance are suitable.
  • a variety of different materials may be employed as the materials that form the electrodes.
  • electrode materials are chosen to provide for a voltage upon contact with the target physiological site, e.g., the stomach, sufficient to drive the system of the identifier.
  • the voltage provided by the electrode materials upon contact of the metals of the power source with the target physiological site is 0.001 V or higher, including 0.01 V or higher, such as 0.1 V or higher, e.g., 0.3 V or higher, including 0.5 volts or higher, and including 1 .0 volts or higher, where in certain aspects, the voltage ranges from about 0.001 to about 10 volts, such as from about 0.01 to about 10 V.
  • the materials 34 and 36 provide the voltage potential to activate the control device 38.
  • the control device 38 can alter conductance between the materials 34 and 36 in a unique manner.
  • the control device 38 is capable of controlling the magnitude of the current through the conducting liquid that surrounds the system 30. This produces a unique current signature that can be detected and measured by a receiver (not shown), which can be positioned internal or external to the body. Illustrative examples of receivers are shown in Figs. 12 to 17, as described hereinafter.
  • non-conducting materials, membrane, or “skirt” are used to increase the "length" of the current path and, hence, act to boost the conductance path, as disclosed in the U.S. Patent Application Serial No. 12/238,345 entitled, "In-Body Device with Virtual Dipole Signal Amplification” filed September 25, 2008, the entire content of which is incorporated herein by reference.
  • nonconducting material “membrane”, and “skirt” are used interchangeably with the term “current path extender” without impacting the scope or the present aspects and the claims herein.
  • the skirt shown in portion at 35 and 37, respectively, may be associated with, e.g., secured to, the framework 32.
  • Various shapes and configurations for the skirt are contemplated as within the scope of the present invention.
  • the system 30 may be surrounded entirely or partially by the skirt and the skirt maybe positioned along a central axis of the system 30 or off- center relative to a central axis.
  • the scope of the present invention as claimed herein is not limited by the shape or size of the skirt.
  • the materials 34 and 36 may be separated by one skirt that is positioned in any defined region between the materials 34 and 36.
  • the system 40 includes a framework 42.
  • the framework 42 is similar to the framework 32 of Fig. 3.
  • a digestible or dissolvable material 44 is deposited on a portion of one side of the framework 42.
  • another digestible material 46 is deposited, such that materials 44 and 46 are dissimilar. More specifically, material 44 and 46 are selected such that they form a voltage potential difference when in contact with a conducting liquid, such as body fluids.
  • a current path is formed through the conducting liquid between material 44 and 46.
  • a control device 48 is secured to the framework 42 and electrically coupled to the materials 44 and 46.
  • the control device 48 includes electronic circuitry that is capable of controlling part of the conductance path between the materials 44 and 46.
  • the materials 44 and 46 are separated by a non-conducting skirt 49.
  • Various examples of the skirt 49 are disclosed in US Provisional Application No. 61 /173,51 1 filed on April 28, 2009 and entitled "HIGHLY RELIABLE INGESTIBLE EVENT MARKERS AND METHODS OF USING SAME" and US Provisional Application No.
  • control device 48 can alter conductance between the materials 44 and 46.
  • the control device 48 is capable of controlling the magnitude of the current through the conducting liquid that surrounds the system 40.
  • a unique current signature that is associated with the system 40 can be detected by a receiver (not shown) to mark the activation of the system 40. Illustrative examples of receivers are shown in Figs. 12 to 17, as described hereinafter.
  • FIG. 5 the system 30 of Fig. 3 is shown in an activated state and in contact with conducting liquid.
  • the system 30 is grounded through ground contact 52.
  • the conducting fluid provides the ground.
  • the system 30 also includes a sensor module 74, which is described in greater detail with respect to Fig. 6.
  • Ion or current paths 50 extend between material 34 to material 36 and flow through the conducting fluid in contact with the system 30.
  • the voltage potential created between the material 34 and 36 is created through chemical reactions between materials 34/36 and the conducting fluid.
  • the unit 75 sends a signal to the control device 38 to alter the conductance between the materials 34 and 36 to allow for communication using the current signature of the system 30.
  • the system 30 can be activated again.
  • Fig. 5A shows an exploded view of the surface of the material 34.
  • the surface of the material 34 is not planar, but rather an irregular surface.
  • the irregular surface increases the surface area of the material and, hence, the area that comes in contact with the conducting fluid.
  • there is an electrochemical reaction between the material 34 and the surrounding conducting fluid such that mass is exchanged with the conducting fluid.
  • masses as used here includes any ionic or non-ionic species that may be added or removed from the conductive fluid as part of the electrochemical reactions occurring on material 34.
  • One example includes the instant where the material is CuCI and when in contact with the conducting fluid, CuCI is converted to Cu metal (solid) and CI- is released into the solution.
  • the flow of positive ions into the conducting fluid is depicted by the current path 50.
  • Negative ions flow in the opposite direction.
  • the release of negative ions at the material 34 and release of positive ions by the material 36 are related to each other through the current flow that is controlled by the control device 38.
  • the rate of reaction and hence the ionic emission rate or current is controlled by the control device 38.
  • the control device 38 can increase or decrease the rate of ion flow by altering its internal conductance, which alters the impedance, and therefore the current flow and reaction rates at the materials 34 and 36.
  • the system 30 can encode information in the ionic flow.
  • the system 30 encodes information using ionic emission or flow.
  • the control device 38 can vary the duration of ionic flow or current while keeping the current or ionic flow magnitude near constant, similar to when the frequency is modulated and the amplitude is constant. Also, the control device 38 can vary the level of the ionic flow rate or the magnitude of the current flow while keeping the duration near constant. Thus, using various combinations of changes in duration and altering the rate or magnitude, the control device 38 encodes information in the current or the ionic flow. For example, the control device 38 may use, but is not limited to any of the following techniques, including Binary Phase- Shift Keying (PSK), Frequency modulation, Amplitude modulation, on-off keying, and PSK with on-off keying.
  • PSK Binary Phase- Shift Keying
  • the various aspects disclosed herein include electronic components as part of the control device 38 or the control device 48.
  • Components that may be present include but are not limited to: logic and/or memory elements, an integrated circuit, an inductor, a resistor, and sensors for measuring various parameters.
  • Each component may be secured to the framework and/or to another component.
  • the components on the surface of the support may be laid out in any convenient configuration. Where two or more components are present on the surface of the solid support, interconnects may be provided.
  • the system such as control devices 30 and 40, control the conductance between the dissimilar materials and, hence, the rate of ionic flow or current.
  • the system is capable of encoding information in the ionic flow and the current signature.
  • the ionic flow or the current signature is used to uniquely identify the specific system.
  • the systems 30 and 40 are capable of producing various different unique patterns or signatures and, thus, provide additional information.
  • a second current signature based on a second conductance alteration pattern may be used to provide additional information, which information may be related to the physical environment.
  • a first current signature may be a very low current state that maintains an oscillator on the chip and a second current signature may be a current state at least a factor of ten higher than the current state associated with the first current signature.
  • the device 30 includes a control module 62, a counter or clock 64, and a memory 66. Additionally, the control device 38 is shown to include a sensor module 72 as well as the sensor module 74, which was referenced in Fig. 5.
  • the control module 62 has an input 68 electrically coupled to the material 34 and an output 70 electrically coupled to the material 36.
  • the control module 62, the clock 64, the memory 66, and the sensor modules 72/74 also have power inputs (some not shown). The power for each of these components is supplied by the voltage potential produced by the chemical reaction between materials 34 and 36 and the conducting fluid, when the system 30 is in contact with the conducting fluid.
  • the control module 62 controls the conductance through logic that alters the overall impedance of the system 30.
  • the control module 62 is electrically coupled to the clock 64.
  • the clock 64 provides a clock cycle to the control module 62. Based upon the programmed characteristics of the control module 62, when a set number of clock cycles have passed, the control module 62 alters the conductance characteristics between materials 34 and 36. This cycle is repeated and thereby the control device 38 produces a unique current signature characteristic.
  • the control module 62 is also electrically coupled to the memory 66. Both the clock 64 and the memory 66 are powered by the voltage potential created between the materials 34 and 36.
  • the control module 62 is also electrically coupled to and in communication with the sensor modules 72 and 74.
  • the sensor module 72 is part of the control device 38 and the sensor module 74 is a separate component.
  • either one of the sensor modules 72 and 74 can be used without the other and the scope of the present invention is not limited by the structural or functional location of the sensor modules 72 or 74.
  • any component of the system 30 may be functionally or structurally moved, combined, or repositioned without limiting the scope of the present invention as claimed.
  • the sensor modules 72 or 74 can include any of the following sensors: temperature, pressure, pH level, and conductivity.
  • the sensor modules 72 or 74 gather information from the environment and communicate the analog information to the control module 62.
  • the control module then converts the analog information to digital information and the digital information is encoded in the current flow or the rate of the transfer of mass that produces the ionic flow.
  • the sensor modules 72 or 74 gather information from the environment and convert the analog information to digital information and then communicate the digital information to control module 62.
  • the sensor modules 74 is shown as being electrically coupled to the material 34 and 36 as well as the control device 38.
  • the sensor module 74 is electrically coupled to the control device 38 at connection 78.
  • the connection 78 acts as both a source for power supply to the sensor module 74 and a communication channel between the sensor module 74 and the control device 38.
  • the system 30 includes a pH sensor module 76 connected to a material 39, which is selected in accordance with the specific type of sensing function being performed.
  • the pH sensor module 76 is also connected to the control device 38.
  • the material 39 is electrically isolated from the material 34 by a non-conductive barrier 55.
  • the material 39 is platinum.
  • the pH sensor module 76 uses the voltage potential difference between the materials 34/36.
  • the pH sensor module 76 measures the voltage potential difference between the material 34 and the material 39 and records that value for later comparison.
  • the pH sensor module 76 also measures the voltage potential difference between the material 39 and the material 36 and records that value for later comparison.
  • the pH sensor module 76 calculates the pH level of the surrounding environment using the voltage potential values.
  • the pH sensor module 76 provides that information to the control device 38.
  • the control device 38 varies the rate of the transfer of mass that produces the ionic transfer and the current flow to encode the information relevant to the pH level in the ionic transfer, which can be detected by a receiver (not shown). Illustrative examples of receivers are shown in Figs.12 to 17 as described hereinafter.
  • the system 30 can determine and provide the information related to the pH level to a source external to the environment.
  • control device 38 can be programmed in advance to output a pre-defined current signature.
  • system can include a receiver system that can receive programming information when the system is activated. Illustrative examples of receivers are shown in Figs. 12 to 17, as described hereinafter.
  • the switch 64 and the memory 66 can be combined into one device.
  • the system 30 may also include one or other electronic components.
  • Electrical components of interest include, but are not limited to: additional logic and/or memory elements, e.g., in the form of an integrated circuit; a power regulation device, e.g., battery, fuel cell or capacitor; a sensor, a stimulator, etc. ; a signal transmission element, e.g., in the form of an antenna, electrode, coil, etc. ; a passive element, e.g., an inductor, resistor, etc.
  • the system 30 is shown with the skirt portions 35 and 37 secured to the framework 32, as discussed in detail below.
  • the material 34 and the material 36 extend beyond the framework 32 onto the skirt portions 35 and 37.
  • the materials 34 and 36 can extend to the edge of the skirt portions 35 and 37. The increase in the area of the materials 34 and 36 results in an increase in the power supplied.
  • the first material region 34a includes an adhering material 86.
  • the adhering material 86 can be any material selected to adhere and hold onto a first material region 88, which material region 88 is made of CuCI in accordance with one aspect of the present invention as discussed above with respect to the first material 34.
  • the second material region 36a includes a transition metal 96 that is made of any transition metal, for example titanium in accordance with one aspect of the present invention.
  • the second material region 36a also includes a second material region 98, which is made of magnesium (Mg) in accordance with one aspect of the present invention as discussed above with respect to the second material 36.
  • Mg magnesium
  • the material 86 is made of a non-reactive and conducting material, for example gold. To enhance the adhesion properties of the material 86 to the material region 88, the material 86 has an unfinished or rough surface.
  • the material 86 is deposited onto the framework 32. Additionally, according to one aspect of the present invention, the material 86 defines a plurality of holes 87 spaced a distance DD from the edge of the framework 32 corresponding to the edge of the material 86.
  • the distance DD is the minimum distance that is needed to separate the holes 87 from the edge of the material 86 and allow all the of the holes 87 to fall within a boundary 89 so that the edge of the material region 88 is not positioned over any hole; this design enhances the adhesion property and characteristics of the material 86 to the material region 88.
  • a process of securing the metal 96 to the framework 32 is shown. Initially the metal 96 is deposited onto the framework 32. Then the metal 86 with the framework 32 is heated. Then the surface of the metal 96 is cleaned using, for example, an ion gun cleaner. Then the magnesium is deposited onto the cleaned surface of the metal 86 to form the material region 98.
  • a plurality of frameworks 32 are built on a wafer 100, as shown in the top view illustration of Fig. 10.
  • the wafer 100 can include any number of frameworks 32.
  • each complete framework 32 is cut from the wafer 100 and inserted or press fitted or placed into an opening 1 12 of Fig. 1 1 of a sheet 1 10 to produce the system 12, 22, 30, or 40 as shown and discussed about in accordance with the various aspects of the present invention.
  • the opening 1 12 is matingly cut to the shape of the framework 32.
  • the sheet 1 10 is then passed through a punch press (not shown) that punches out each of systems 12, 22, 30, or 40 as noted.
  • the ingestible circuitry includes a coating layer.
  • the protective coating may be applied to the wafer 100 using a spinning process prior to removal of the framework 32 from the wafer 100 of Fig. 10.
  • the protective coating may be applied to the system, for example the system 30, after being punched out or cut out from the sheet 1 10 of Fig. 1 1 .
  • the purpose of this coating layer can vary, e.g., to protect the circuitry, the chip and/or the battery, or any components during processing, during storage, or even during ingestion. In such instances, a coating on top of the circuitry may be included.
  • coatings that are designed to protect the ingestible circuitry during storage, but dissolve immediately during use.
  • coatings that dissolve upon contact with an aqueous fluid, e.g. stomach fluid, or the conducting fluid as referenced above.
  • protective processing coatings that are employed to allow the use of processing steps that would otherwise damage certain components of the device. For example, in aspects where a chip with dissimilar material deposited on the top and bottom is produced, the product needs to be diced. However, the dicing process can scratch off the dissimilar material, and also there might be liquid involved which would cause the dissimilar materials to discharge or dissolve. In such instances, a protective coating on the materials prevents mechanical or liquid contact with the component during processing can be employed.
  • Another purpose of the dissolvable coatings may be to delay activation of the device.
  • the coating that sits on the dissimilar material and takes a certain period of time, e.g., five minutes, to dissolve upon contact with stomach fluid may be employed.
  • the coating can also be an environmentally sensitive coating, e.g., a temperature or pH sensitive coating, or other chemically sensitive coating that provides for dissolution in a controlled fashion and allows one to activate the device when desired.
  • Coatings that survive the stomach but dissolve in the intestine are also of interest, e.g., where one desires to delay activation until the device leaves the stomach.
  • An example of such a coating is a polymer that is insoluble at low pH, but becomes soluble at a higher pH.
  • pharmaceutical formulation protective coatings e.g., a gel cap liquid protective coating that prevents the circuit from being activated by liquid of the gel cap.
  • Identifiers of interest include two dissimilar electrochemical materials, which act similar to the electrodes (e.g., anode and cathode) of a power source.
  • the reference to an electrode or anode or cathode are used here merely as illustrative examples.
  • the scope of the present invention is not limited by the label used and includes the aspect wherein the voltage potential is created between two dissimilar materials.
  • reference is made to an electrode, anode, or cathode it is intended as a reference to a voltage potential created between two dissimilar materials.
  • a potential difference that is, a voltage
  • the electrodes As a result of the respective oxidation and reduction reactions incurred to the two electrode materials.
  • a voltaic cell, or battery can thereby be produced.
  • such power supplies are configured such that when the two dissimilar materials are exposed to the target site, e.g., the stomach, the digestive tract, etc., a voltage is generated.
  • one or both of the metals may be doped with a non-metal, e.g., to enhance the voltage output of the battery.
  • Non-metals that may be used as doping agents in certain aspects include, but are not limited to: sulfur, iodine and the like.
  • FIG. 12 provides a functional block diagram of how a receiver may implement a coherent demodulation protocol, according to one aspect of the invention. It should be noted that only a portion of the receiver is shown in FIG. 12.
  • FIG. 12 illustrates the process of mixing the signal down to baseband once the carrier frequency (and carrier signal mixed down to carrier offset) is determined.
  • a carrier signal 2221 is mixed with a second carrier signal 2222 at mixer 2223.
  • a narrow low-pass filter 2220 is applied of appropriate bandwidth to reduce the effect of out-of-bound noise.
  • Demodulation occurs at functional blocks 2225 in accordance with the coherent demodulation scheme of the present invention.
  • the unwrapped phase 2230 of the complex signal is determined.
  • An optional third mixer stage, in which the phase evolution is used to estimate the frequency differential between the calculated and real carrier frequency can be applied.
  • the structure of the packet is then leveraged to determine the beginning of the coding region of the BPSK signal at block 2240. Mainly, the presence of the sync header, which appears as an FM porch in the amplitude signal of the complex demodulated signal is used to determine the starting bounds of the packet.
  • the transbody communication module may include a forward error correction module, which module provides additional gain to combat interference from other unwanted signals and noise.
  • Forward error correction functional modules of interest include those described in PCT Application Serial No. PCT/US2007/024225 and published as WO 2008/063626, the disclosure of which is herein incorporated by reference.
  • the forward error correction module may employ any convenient protocol, such as Reed-Solomon, Golay, Hamming, BCH, and Turbo protocols to identify and correct (within bounds) decoding errors.
  • the receiver includes a beacon module as shown in the functional block diagram of FIG. 13.
  • the scheme outlined in FIG. 13 outlines one technique for identifying a valid beacon.
  • the incoming signal 2360 represents the signals received by electrodes, bandpass filtered (such as from 10 KHz to 34 KHz) by a high frequency signaling chain (which encompasses the carrier frequency), and converted from analog to digital.
  • the signal 2360 is then decimated at block 2361 and mixed at the nominal drive frequency (such as, 12.5 KHz, 20 KHz, etc.) at mixer 2362.
  • the resulting signal is decimated at block 2364 and low-pass filtered (such as 5 KHz BW) at block 2365 to produce the carrier signal mixed down to carrier offset- signal 2369.
  • Signal 2369 is further processed by blocks 2367 (fast Fourier transform and then detection of two strongest peaks) to provide the true carrier frequency signal 2368. This protocol allows for accurate determination of the carrier frequency of the transmitted beacon.
  • FIG. 14 provides a block functional diagram of an integrated circuit component of a signal receiver according to an aspect of the invention.
  • receiver 2700 includes electrode input 2710. Electrically coupled to the electrode input 2710 are transbody conductive communication module 2720 and physiological sensing module 2730.
  • transbody conductive communication module 2720 is implemented as a high frequency (HF) signal chain and physiological sensing module 2730 is implemented as a low frequency (LF) signal chain.
  • CMOS temperature sensing module 2740 for detecting ambient temperature
  • Receiver 2700 also includes a processing engine 2760 (for example, a microcontroller and digital signal processor), non-volatile memory 2770 (for data storage) and wireless communication module 2780 (for data transmission to another device, for example in a data upload action).
  • processing engine 2760 for example, a microcontroller and digital signal processor
  • non-volatile memory 2770 for data storage
  • wireless communication module 2780 for data transmission to another device, for example in a data upload action.
  • FIG. 15 provides a more detailed block diagram of a circuit configured to implement the block functional diagram of the receiver depicted in FIG. 14, according to one aspect of the invention.
  • receiver 2800 includes electrodes e1 , e2 and e3 (281 1 , 2812 and 2813) which, for example, receive the conductively transmitted signals by an I EM and/or sense physiological parameters or biomarkers of interest.
  • the signals received by the electrodes 281 1 , 2812, and 2813 are multiplexed by multiplexer 2820 which is electrically coupled to the electrodes.
  • Multiplexer 2820 is electrically coupled to both high band pass filter 2830 and low band pass filter 2840.
  • the high and low frequency signal chains provide for programmable gain to cover the desired level or range.
  • high band pass filter 2830 passes frequencies in the 10 KHz to 34 KHz band while filtering out noise from out-of-band frequencies. This high frequency band may vary, and may include, for example, a range of 3 KHz to 300 KHz.
  • the passing frequencies are then amplified by amplifier 2832 before being converted into a digital signal by converter 2834 for input into high power processor 2880 (shown as a DSP) which is electrically coupled to the high frequency signal chain.
  • DSP digital signal processor
  • Low band pass filter 2840 is shown passing lower frequencies in the range of 0.5 Hz to 150 Hz while filtering out out-of-band frequencies.
  • the frequency band may vary, and may include, for example, frequencies less than 300 Hz, such as less than 200 Hz, including less than 150 Hz.
  • the passing frequency signals are amplified by amplifier 2842.
  • accelerometer 2850 electrically coupled to second multiplexer 2860.
  • Multiplexer 2860 multiplexes the signals from the accelerometer with the amplified signals from amplifier 2842.
  • the multiplexed signals are then converted to digital signals by converter 2864 which is also electrically coupled to low power processor 2870.
  • a digital accelerometer (such as one manufactured by Analog Devices), may be implemented in place of accelerometer 2850.
  • Various advantages may be achieved by using a digital accelerometer. For example, because the signals the digital accelerometer would produce signals already in digital format, the digital accelerometer could bypass converter 2864 and electrically couple to the low power microcontroller 2870-in which case multiplexer 2860 would no longer be required.
  • the digital signal may be configured to turn itself on when detecting motion, further conserving power.
  • continuous step counting may be implemented.
  • the digital accelerometer may include a FIFO buffer to help control the flow of data sent to the low power processor 2870. For instance, data may be buffered in the FIFO until full, at which time the processor may be triggered to turn awaken from an idle state and receive the data.
  • Low power processor 2870 may be, for example, an MSP430 microcontroller from Texas Instruments. Low power processor 2870 of receiver 2800 maintains the idle state, which as stated earlier, requires minimal current draw--e.g., 10 .mu.A or less, or 1 .mu.A or less.
  • High power processor 2880 may be, for example, a VC5509 digital signal process from Texas Instruments.
  • the high power processor 2880 performs the signal processing actions during the active state. These actions, as stated earlier, require larger amounts of current than the idle state ⁇ e.g., currents of 30 .mu.A or more, such as 50 .mu.A or more--and may include, for example, actions such as scanning for conductively transmitted signals, processing conductively transmitted signals when received, obtaining and/or processing physiological data, etc.
  • flash memory 2890 electrically coupled to high power processor 2880.
  • flash memory 2890 may be electrically coupled to low power processor 2870, which may provide for better power efficiency.
  • Wireless communication element 2895 is shown electrically coupled to high power processor 2880 and may include, for example, a BLUETOOTH. TM. wireless communication transceiver. In one aspect, wireless communication element 2895 is electrically coupled to high power processor 2880. In another aspect, wireless communication element 2895 is electrically coupled to high power processor 2880 and low power processor 2870. Furthermore, wireless communication element 2895 may be implemented to have its own power supply so that it may be turned on and off independently from other components of the receiver ⁇ e.g., by a microprocessor. [085] With, for example, an idle state in mind, the following paragraphs provide example configurations of receiver components shown in FIG. 15 during various states of the receiver, according to one aspect of the invention. It should be understood that alternative configurations may be implemented depending on the desired application.
  • Receiver 2800 is configured such that low power processor 2870 is in an inactive state (such as idle state) and high power processor 2880 is in an inactive state (such as idle state), and circuit blocks related to peripheral circuitry and their power supplies required during various active states remain off (for example, wireless communication module 2895 and the analog front end).
  • the low power processor may have a 32 KHz oscillator active and may consume a few .mu.A current or less, including 0.5 .mu.A or less.
  • the low power processor 2870 may, for example, wait for a signal to transfer to an active state.
  • the signal might be external such as an interrupt or internally generated by one of the device's peripherals, such as a timer.
  • the high power processor may, for example, be running off a 32 KHz watch crystal.
  • the high power processor may, for example, wait for a signal to transfer to active state.
  • the beacon signal module may implement various types of sniff signals to achieve low power efficiency.
  • a higher power demodulate and decode state may be entered.
  • low power processor 2870 is in an active state and high power processor 2880 is in an active state.
  • High power processor 2880 may, for example, be running from a 12 MHz or near crystal oscillator with a PLL-based clock multiplier giving the device a 108 MHz clock speed.
  • the low power processor 2870 may, for example, run off an internal R-C oscillator in the range of 1 MHz to 20 MHz and consume power in the range of 250 to 300 uA per MHz clock speed during active states.
  • the active state allows for processing and any transmissions that may follow. Required transmissions may trigger the wireless communication module to cycle from off to on.
  • the high power processor 2880 is in an in idle state during collection, and in an active state (for example, running from a 12 MHz or near crystal oscillator with a PLL-based clock multiplier giving the device a 108 MHz clock speed) during processing and transmission.
  • the low power processor 2870 is in an active state during this state and may run off an internal R-C oscillator in the range of 1 MHz to 20 MHz and consume power in the range of 250 to 300 uA per MHz clock speed.
  • the low power processor e.g., MSP shown in FIG. 13
  • high power processor e.g., DSP shown in FIG. 13
  • SPI bus serial peripheral interface bus
  • FIG. 16 provides a view of a block diagram of hardware in a receiver according to an aspect of the invention related to the high frequency signal chain.
  • receiver 2900 includes receiver probes (for example in the form of electrodes 291 1 , 2912 and 2913) electrically coupled to multiplexer 2920. Also shown are high pass filter 2930 and low pass filter 2940 to provide for a band pass filter which eliminates any out-of-band frequencies. In the aspect shown, a band pass of 10 KHz to 34 KHz is provided to pass carrier signals falling within the frequency band. Example carrier frequencies may include, but are not limited to, 12.5 KHz and 20 KHz. One or more carriers may be present.
  • receiver 2900 includes analog to digital converter 2950 ⁇ for example, sampling at 500 KHz.
  • the digital signal can thereafter be processed by the DSP.
  • Shown in this aspect is DMA to DSP unit 2960 which sends the digital signal to dedicated memory for the DSP.
  • the direct memory access provides the benefit of allowing the rest of the DSP to remain in a low power mode.
  • system 3500 includes a pharmaceutical composition 3510 that comprises an ingestible device such as an ingestible event marker, " I EM.” Also present in system 3500 is signal receiver 3520. Signal receiver 3520 is configured to detect a signal emitted from the identifier of the I EM 3510. Signal receiver 3520 also includes physiologic sensing capability, such as ECG and movement sensing capability. Signal receiver 3520 is configured to transmit data to a patient's an external device or PDA 3530 (such as a smart phone or other wireless communication enabled device), which in turn transmits the data to a server 3540.
  • PDA 3530 such as a smart phone or other wireless communication enabled device
  • Server 3540 may be configured as desired, e.g., to provide for patient directed permissions.
  • server 3540 may be configured to allow a family caregiver 3550 to participate in the patient's therapeutic regimen, e.g., via an interface (such as a web interface) that allows the family caregiver 3550 to monitor alerts and trends generated by the server 3540, and provide support back to the patient, as indicated by arrow 3560.
  • the server 3540 may also be configured to provide responses directly to the patient, e.g., in the form of patient alerts, patient incentives, etc., as indicated by arrow 3565 which are relayed to the patient via PDA 3530.
  • Server 3540 may also interact with a health care professional (e.g., RN, physician) 3555, which can use data processing algorithms to obtain measures of patient health and compliance, e.g., wellness index summaries, alerts, cross-patient benchmarks, etc., and provide informed clinical communication and support back to the patient, as indicated by arrow 3580.
  • a health care professional e.g., RN, physician
  • measures of patient health and compliance e.g., wellness index summaries, alerts, cross-patient benchmarks, etc.
  • a method of manufacturing a communication device including a partial power source comprising the steps of:
  • each partial power source device is prepared according to a process that includes the step of depositing a layer of transition metal on an opposite surface of the support structure from a surface having an adhesion material.
  • step of depositing a layer of non-reactive material further comprises the step of defining a group of holes, wherein each group of holes is contained within one boundary selected from the plurality of boundaries, such that the position of each hole within the group of holes is within the corresponding boundary.
  • a device comprising a partial power source for communication, obtainable according to the method of any of the preceding clauses, preferably wherein the device is prepared by a process comprising the steps of:

Abstract

The system of the present invention includes a conductive element, an electronic component, and a partial power source in the form of dissimilar materials. Upon contact with a conducting fluid, a voltage potential is created and the power source is completed, which activates the system. The electronic component controls the conductance between the dissimilar materials to produce a unique current signature. The system can also measure the conditions of the environment surrounding the system.

Description

COMMUNICATION SYSTEM WITH ENHANCED PARTIAL POWER SOURCE AND METHOD OF MANUFACTURING SAME
CROSS-REFERENCE TO RELATED APPLICATIONS
[001] This application is a continuation-in-part of U.S. Patent Application No. 13/180,525 filed on July 1 1 , 201 1 and entitled "Communication System with Enhanced Partial Power Source and Method of Manufacturing the Same," which application is a continuation-in-part of U.S. Patent Application No. 12/564,017, filed on Sept 21 , 2009 and entitled "Communication System with Partial Power Source", published on April 1 , 2010 as U.S. Publication No. US2010-0081894A1 , which is a continuation-in-part application of U.S. Patent Application No. 1 1 /912,475 filed June 23, 2008 and entitled "Pharma-lnformatics System", published on November 20, 2008 as U.S. Publication No. 2008-0284599A1 which application is a 371 application of PCT Application No. PCT/US06/16370 filed April 28, 2006 and entitled "Pharma- lnformatics System"; published as WO Application No. WO 2006/1 16718, which application pursuant to 35 U.S.C. § 1 19 (e), claims priority to the filing dates of: United States Provisional Patent Application Serial No. 60/676,145 filed April 28, 2005 and entitled "Pharma-lnformatics System"; United States Provisional Patent Application Serial No. 60/694,078, filed June 24, 2005, and entitled "Pharma- lnformatics System"; United States Provisional Patent Application Serial No. 60/713,680 filed September 1 , 2005 and entitled "Medical Diagnostic And Treatment Platform Using Near-Field Wireless Communication Of Information Within A Patient's Body"; and United States Provisional Patent Application Serial No. 60/790,335 filed April 7, 2006 and entitled "Pharma-lnformatics System"; the disclosures of which are herein incorporated by reference.
[002] This application is related to the following US Applications filed on July 1 1 , 201 1 , the disclosures of which are incorporated herein by reference: US Application Serial No. 13/180,516, filed July 1 1 , 201 1 entitled COMMUNICATION SYSTEM WITH REMOTE ACTIVATION; US Application Serial No. 13/180,498, filed July 1 1 , 201 1 , entitled COMMUNICATION SYSTEM WITH MULTIPLE TYPES OF POWER; US Application Serial No. 13/180,539, filed July 1 1 , 201 1 , entitled COMMUNICATION SYSTEM USING AN IMPLANTABLE DEVICE; US Application Serial No. 13/180,538, filed July 1 1 , 201 1 , entitled COMMUNICATION SYSTEM USING POLYPHARMACY CO-PACKAGED MEDICATION DOSING UNIT; and US Application Serial No. 13/180,507, filed July 1 1 , 201 1 , entitled COMMUNICATION
SYSTEM INCORPORATED IN AN INGESTIBLE PRODUCT.
FIELD
[003] The present invention is related to communication systems for detection of an event. More specifically, the present disclosure includes a system that includes a device with various power sources and communication schemes.
INTRODUCTION
[004] Ingestible devices that include electronic circuitry have been proposed for use in a variety of different medical applications, including both diagnostic and therapeutic applications. These devices typically require an internal power supply for operation. Examples of such ingestible devices are ingestible electronic capsules which collect data as they pass through the body, and transmit the data to an external receiver system. An example of this type of electronic capsule is an in-vivo video camera. The swallowable capsule includes a camera system and an optical system for imaging an area of interest onto the camera system. The transmitter transmits the video output of the camera system and the reception system receives the transmitted video output. Other examples include an ingestible imaging device, which has an internal and self-contained power source, which obtains images from within body lumens or cavities. The electronic circuit components of the device are enclosed by an inert indigestible housing (e.g. glass housing) that passes through the body internally. Other examples include an ingestible data recorder capsule medical device. The electronic circuits of the disclosed device (e.g. sensor, recorder, battery etc.) are housed in a capsule made of inert materials. [005] In other examples, fragile radio frequency identification (RFID) tags are used in drug ingestion monitoring applications. In order for the RFID tags to be operational, each requires an internal power supply. The RFID tags are antenna structures that are configured to transmit a radio-frequency signal through the body.
[006] The problem these existing devices pose is that the power source is internal to device and such power sources are costly to produce and potentially harmful to the surrounding environment if the power source leaks or is damaged. Additionally, having antennas extending from the device is a concern as related to the antennas getting damaged or causing a problem when the device is used in-vivo. Therefore, what is needed is suitable system with circuitry that eliminates the need for an internal power source and antennas.
SUMMARY
[007] The present disclosure includes a system for producing a unique signature that indicates the occurrence of an event. The system includes circuitry and components that can be placed within certain environments that include a conducting fluid. One example of such an environment is inside a container that houses the conducting fluid, such as a sealed bag with a solution, which includes an IV bag. Another example is within the body of a living organism, such as an animal or a human. The systems are ingestible and/or digestible or partially digestible. The system includes dissimilar materials positioned on the framework such that when a conducting fluid comes into contact with the dissimilar materials, a voltage potential difference is created. The voltage potential difference, and hence the voltage, is used to power up control logic that is positioned within the framework. Ions or current flows from the first dissimilar material to the second dissimilar material via the control logic and then through the conducting fluid to complete a circuit. The control logic controls the conductance between the two dissimilar materials and, hence, controls or modulates the conductance.
[008] As the ingestible circuitry is made up of ingestible, and even digestible, components, the ingestible circuitry results in little, if any, unwanted side effects, even when employed in chronic situations. Examples of the range of components that may be included are: logic and/or memory elements; effectors; a signal transmission element; and a passive element, such as a resistor or inductor. The one or more components on the surface of the support may be laid out in any convenient configuration. Where two or more components are present on the surface of the solid support, interconnects may be provided. All of the components and the support of the ingestible circuitry are ingestible, and in certain instances digestible or partially digestible. Furthemore, the circuitry is manufactured according to a process to enhance adhesion of the materials.
BRIEF DESCRIPTION OF THE FIGURES
[009] Fig. 1 shows a pharmaceutical product with an event indicator system according to the teaching of the present invention, wherein the product and the event indicator system combination are within the body.
[010] Fig. 2A shows the pharmaceutical product of Fig. 1 with the event indicator system on the exterior of the pharmaceutical product.
[011] Fig. 2B shows the pharmaceutical product of Fig. 1 with the event indicator system positioned inside the pharmaceutical product.
[012] Fig. 3 is a block diagram representation of one aspect of the event indicator system with dissimilar metals positioned on opposite ends.
[013] Fig. 4 is a block diagram representation of another aspect of the event indicator system with dissimilar metals positioned on the same end and separated by a non-conducting material.
[014] Fig. 5 shows ionic transfer or the current path through a conducting fluid when the event indicator system of Fig. 3 is in contact with conducting liquid and in an active state.
[015] Fig. 5A shows an exploded view of the surface of dissimilar materials of Fig. 5.
[016] Fig. 5B shows the event indicator system of Fig. 5 with a pH sensor unit.
[017] Fig. 5C shows the event indicator system in accordance with another aspect of the present invention. [018] Fig. 6 is a block diagram illustration of one aspect of the control device used in the system of Figs. 3 and 4.
[019] Fig. 7 shows a cross sectional side view of the event indicator system in accordance with the present invention.
[020] Fig. 8 is an exploded view of two components of the event indicator system of Fig. 7 in accordance with the present invention.
[021 ] Fig. 9 is an assembly process of a portion of the event indicator system of Fig. 7 in accordance with the present invention.
[022] Fig. 10 shows a wafer with multiple event indicator systems in accordance with the present invention.
[023] Fig. 1 1 shows a non-conducting membrane sheet with holes for receiving a device forming part of the event indicator system of Fig. 7 in accordance with the present invention.
[024] FIG. 12 is a functional block diagram of a demodulation circuit that performs coherent demodulation that may be present in a receiver, according to one aspect.
[025] FIG. 13 illustrates a functional block diagram for a beacon module within a receiver, according to one aspect.
[026] FIG. 14 is a block diagram of the different functional modules that may be present in a receiver, according to one aspect.
[027] FIG. 15 is a block diagram of a receiver, according to one aspect.
[028] FIG. 16 provides a block diagram of a high frequency signal chain in a receiver, according to one aspect.
[029] FIG. 17 provides a diagram of how a system that includes a signal receiver and an ingestible event marker may be employed, according to one aspect..
DETAILED DESCRIPTION
[030] The present disclosure includes multiple aspects for indicating the occurrence of an event. As described in more detail below, a system of the present invention is used with a conducting fluid to indicate the event marked by contact between the conducting fluid and the system. For example, the system of the present disclosure may be used with pharmaceutical product and the event that is indicated is when the product is taken or ingested. The term "ingested" or "ingest" or "ingesting" is understood to mean any introduction of the system internal to the body. For example, ingesting includes simply placing the system in the mouth all the way to the descending colon. Thus, the term ingesting refers to any instant in time when the system is introduced to an environment that contains a conducting fluid. Another example would be a situation when a non-conducting fluid is mixed with a conducting fluid. In such a situation the system would be present in the non- conduction fluid and when the two fluids are mixed, the system comes into contact with the conducting fluid and the system is activated. Yet another example would be the situation when the presence of certain conducting fluids needed to be detected. In such instances, the presence of the system, which would be activated, within the conducting fluid could be detected and, hence, the presence of the respective fluid would be detected.
[031] Referring again to the instance where the system is used with the product that is ingested by the living organism, when the product that includes the system is taken or ingested, the device comes into contact with the conducting liquid of the body. When the system of the present invention comes into contact with the body fluid, a voltage potential is created and the system is activated. A portion of the power source is provided by the device, while another portion of the power source is provided by the conducting fluid, which is discussed in detail below.
[032] Referring now to Fig. 1 , an ingestible product 14 that includes a system of the present invention is shown inside the body. The product 14 is configured as an orally ingestible pharmaceutical formulation in the form of a pill or capsule. Upon ingestion, the pill moves to the stomach. Upon reaching the stomach, the product 14 is in contact with stomach fluid 18 and undergoes a chemical reaction with the various materials in the stomach fluid 18, such as hydrochloric acid and other digestive agents. The system of the present invention is discussed in reference to a pharmaceutical environment. However, the scope of the present invention is not limited thereby. The present invention can be used in any environment where a conducting fluid is present or becomes present through mixing of two or more components that result in a conducting liquid. [033] Referring now to Fig. 2A, a pharmaceutical product 10, similar to the product 14 of Fig. 1 , is shown with a system 12, such as an ingestible event marker or an ionic emission module. The scope of the present invention is not limited by the shape or type of the product 10. For example, it will be clear to one skilled in the art that the product 10 can be a capsule, a time-release oral dosage, a tablet, a gel cap, a sub-lingual tablet, or any oral dosage product that can be combined with the system 12. In the referenced aspect, the product 10 has the system 12 secured to the exterior using known methods of securing micro-devices to the exterior of pharmaceutical products. Example of methods for securing the micro-device to the product is disclosed in US Provisional Application No. 61 /142,849 filed on Jan 1 , 2009 and entitled "HIGH-THROUGHPUT PRODUCTION OF INGESTIBLE EVENT MARKERS" as well as US Provisional Application No. 61/177,61 1 filed on May 12, 2009 and entitled "INGESTIBLE EVENT MARKERS COMPRISING AN IDENTIFIER AND AN INGESTIBLE COMPONENT", the entire disclosure of each is incorporated herein by reference. Once ingested, the system 12 comes into contact with body liquids and the system 12 is activated. The system 12 uses the voltage potential difference to power up and thereafter modulates conductance to create a unique and identifiable current signature. Upon activation, the system 12 controls the conductance and, hence, current flow to produce the current signature.
[034] There are various reasons for delaying the activation of the system 12. In order to delay the activation of the system 12, the system 12 may be coated with a shielding material or protective layer. The layer is dissolved over a period of time, thereby allowing the system 12 to be activated when the product 10 has reached a target location.
[035] Referring now to Fig. 2B, a pharmaceutical product 20, similar to the product 14 of Fig. 1 , is shown with a system 22, such as an ingestible event marker or an identifiable emission module. The scope of the present invention is not limited by the environment to which the system 22 is introduced. For example, the system 22 can be enclosed in a capsule that is taken in addition to/independently from the pharmaceutical product. The capsule may be simply a carrier for the system 22 and may not contain any product. Furthermore, the scope of the present invention is not limited by the shape or type of product 20. For example, it will be clear to one skilled in the art that the product 20 can be a capsule, a time-release oral dosage, a tablet, a gel capsule, a sub-lingual tablet, or any oral dosage product. In the referenced aspect, the product 20 has the system 22 positioned inside or secured to the interior of the product 20. In one aspect, the system 22 is secured to the interior wall of the product 20. When the system 22 is positioned inside a gel capsule, then the content of the gel capsule is a non-conducting gel-liquid. On the other hand, if the content of the gel capsule is a conducting gel-liquid, then in an alternative aspect, the system 22 is coated with a protective cover to prevent unwanted activation by the gel capsule content. If the content of the capsule is a dry powder or microspheres, then the system 22 is positioned or placed within the capsule. If the product 20 is a tablet or hard pill, then the system 22 is held in place inside the tablet. Once ingested, the product 20 containing the system 22 is dissolved. The system 22 comes into contact with body liquids and the system 22 is activated. Depending on the product 20, the system 22 may be positioned in either a near-central or near-perimeter position depending on the desired activation delay between the time of initial ingestion and activation of the system 22. For example, a central position for the system 22 means that it will take longer for the system 22 to be in contact with the conducting liquid and, hence, it will take longer for the system 22 to be activated. Therefore, it will take longer for the occurrence of the event to be detected.
[036] Referring now to Fig. 3, in one aspect, the systems 12 and 22 of Figs. 2A and 2B, respectively, are shown in more detail as system 30. The system 30 can be used in association with any pharmaceutical product, as mentioned above, to determine when a patient takes the pharmaceutical product. As indicated above, the scope of the present invention is not limited by the environment and the product that is used with the system 30. For example, the system 30 may be placed within a capsule and the capsule is placed within the conducting liquid. The capsule would then dissolve over a period of time and release the system 30 into the conducting liquid. Thus, in one aspect, the capsule would contain the system 30 and no product. Such a capsule may then be used in any environment where a conducting liquid is present and with any product. For example, the capsule may be dropped into a container filled with jet fuel, salt water, tomato sauce, motor oil, or any similar product. Additionally, the capsule containing the system 30 may be ingested at the same time that any pharmaceutical product is ingested in order to record the occurrence of the event, such as when the product was taken.
[037] In the specific example of the system 30 combined with the pharmaceutical product, as the product or pill is ingested, the system 30 is activated. The system 30 controls conductance to produce a unique current signature that is detected, thereby signifying that the pharmaceutical product has been taken. The system 30 includes a framework 32. The framework 32 is a chassis for the system 30 and multiple components are attached to, deposited upon, or secured to the framework 32. In this aspect of the system 30, a digestible material 34 is physically associated with the framework 32. The material 34 may be chemically deposited on, evaporated onto, secured to, or built-up on the framework all of which may be referred to herein as "deposit" with respect to the framework 32. The material 34 is deposited on one side of the framework 32. The materials of interest that can be used as material 34 include, but are not limited to: Cu or Cul. The material 34 is deposited by physical vapor deposition, electrodeposition, or plasma deposition, among other protocols. The material 34 may be from about 0.05 to about 500 μιτι thick, such as from about 5 to about 100 μιτι thick. The shape is controlled by shadow mask deposition, or photolithography and etching. Additionally, even though only one region is shown for depositing the material, each system 30 may contain two or more electrically unique regions where the material 34 may be deposited, as desired. The various methods for depositing the materials onto the framework 32 are discussed in greater detail with respect to Figs. 7-9 below.
[038] At a different side, which is the opposite side as shown in Fig. 3, another digestible material 36 is deposited, such that materials 34 and 36 are dissimilar. Although not shown, the different side selected may be the side next to the side selected for the material 34. The scope of the present invention is not limited by the side selected and the term "different side" can mean any of the multiple sides that are different from the first selected side. Furthermore, even though the shape of the system is shown as a square, the shape maybe any geometrically suitable shape. Material 34 and 36 are selected such that they produce a voltage potential difference when the system 30 is in contact with conducting liquid, such as body fluids. The materials of interest for material 36 include, but are not limited to: Mg, Zn, or other electronegative metals. As indicated above with respect to the material 34, the material 36 may be chemically deposited on, evaporated onto, secured to, or built-up on the framework. Also, an adhesion layer may be necessary to help the material 36 (as well as material 34 when needed) to adhere to the framework 32. Typical adhesion layers for the material 36 are Ti, TiW, Cr or similar material. Anode material and the adhesion layer may be deposited by physical vapor deposition, electrodeposition or plasma deposition. The material 36 may be from about 0.05 to about 500 μιτι thick, such as from about 5 to about 100 μιτι thick. However, the scope of the present invention is not limited by the thickness of any of the materials nor by the type of process used to deposit or secure the materials to the framework 32.
[039] According to the disclosure set forth, the materials 34 and 36 can be any pair of materials with different electrochemical potentials. Additionally, in the aspects wherein the system 30 is used in-vivo, the materials 34 and 36 may be vitamins that can be absorbed. More specifically, the materials 34 and 36 can be made of any two materials appropriate for the environment in which the system 30 will be operating. For example, when used with an ingestible product, the materials 34 and 36 are any pair of materials with different electrochemical potentials that are ingestible. An illustrative example includes the instance when the system 30 is in contact with an ionic solution, such as stomach acids. Suitable materials are not restricted to metals, and in certain aspects the paired materials are chosen from metals and non-metals, e.g., a pair made up of a metal (such as Mg) and a salt (such as CuCI or Cul). With respect to the active electrode materials, any pairing of substances - metals, salts, or intercalation compounds - with suitably different electrochemical potentials (voltage) and low interfacial resistance are suitable.
[040] Materials and pairings of interest include, but are not limited to, those reported in Table 1 below. In one aspect, one or both of the metals may be doped with a non-metal, e.g., to enhance the voltage potential created between the materials as they come into contact with a conducting liquid. Non-metals that may be used as doping agents in certain aspects include, but are not limited to: sulfur, iodine and the like. In another aspect, the materials are copper iodine (Cul) as the anode and magnesium (Mg) as the cathode. Aspects of the present invention use electrode materials that are not harmful to the human body.
Figure imgf000013_0001
[041] Thus, when the system 30 is in contact with the conducting liquid, a current path, an example is shown in Fig. 5, is formed through the conducting liquid between material 34 and 36. A control device 38 is secured to the framework 32 and electrically coupled to the materials 34 and 36. The control device 38 includes electronic circuitry, for example control logic that is capable of controlling and altering the conductance between the materials 34 and 36.
[042] The voltage potential created between the materials 34 and 36 provides the power for operating the system as well as produces the current flow through the conducting fluid and the system. In one aspect, the system operates in direct current mode. In an alternative aspect, the system controls the direction of the current so that the direction of current is reversed in a cyclic manner, similar to alternating current. As the system reaches the conducting fluid or the electrolyte, where the fluid or electrolyte component is provided by a physiological fluid, e.g., stomach acid, the path for current flow between the materials 34 and 36 is completed external to the system 30; the current path through the system 30 is controlled by the control device 38. Completion of the current path allows for the current to flow and in turn a receiver, not shown, can detect the presence of the current and recognize that the system 30 has been activate and the desired event is occurring or has occurred. Illustrative examples of receivers are shown in Figs. 12 to 17, as described hereinafter.
[043] In one aspect, the two materials 34 and 36 are similar in function to the two electrodes needed for a direct current power source, such as a battery. The conducting liquid acts as the electrolyte needed to complete the power source. The completed power source described is defined by the electrochemical reaction between the materials 34 and 36 of the system 30 and enabled by the fluids of the body. The completed power source may be viewed as a power source that exploits electrochemical conduction in an ionic or a conducting solution such as gastric fluid, blood, or other bodily fluids and some tissues. Additionally, the environment may be something other than a body and the liquid may be any conducting liquid. For example, the conducting fluid may be salt water or a metallic based paint.
[044] In certain aspects, these two materials are shielded from the surrounding environment by an additional layer of material. Accordingly, when the shield is dissolved and the two dissimilar materials are exposed to the target site, a voltage potential is generated.
[045] In certain aspects, the complete power source or supply is one that is made up of active electrode materials, electrolytes, and inactive materials, such as current collectors, packaging, etc. The active materials are any pair of materials with different electrochemical potentials. Suitable materials are not restricted to metals, and in certain aspects the paired materials are chosen from metals and non-metals, e.g., a pair made up of a metal (such as Mg) and a salt (such as Cul). With respect to the active electrode materials, any pairing of substances - metals, salts, or intercalation compounds - with suitably different electrochemical potentials (voltage) and low interfacial resistance are suitable. [046] A variety of different materials may be employed as the materials that form the electrodes. In certain aspects, electrode materials are chosen to provide for a voltage upon contact with the target physiological site, e.g., the stomach, sufficient to drive the system of the identifier. In certain aspects, the voltage provided by the electrode materials upon contact of the metals of the power source with the target physiological site is 0.001 V or higher, including 0.01 V or higher, such as 0.1 V or higher, e.g., 0.3 V or higher, including 0.5 volts or higher, and including 1 .0 volts or higher, where in certain aspects, the voltage ranges from about 0.001 to about 10 volts, such as from about 0.01 to about 10 V.
[047] Referring again to Fig. 3, the materials 34 and 36 provide the voltage potential to activate the control device 38. Once the control device 38 is activated or powered up, the control device 38 can alter conductance between the materials 34 and 36 in a unique manner. By altering the conductance between materials 34 and 36, the control device 38 is capable of controlling the magnitude of the current through the conducting liquid that surrounds the system 30. This produces a unique current signature that can be detected and measured by a receiver (not shown), which can be positioned internal or external to the body. Illustrative examples of receivers are shown in Figs. 12 to 17, as described hereinafter. In addition to controlling the magnitude of the current path between the materials, non-conducting materials, membrane, or "skirt" are used to increase the "length" of the current path and, hence, act to boost the conductance path, as disclosed in the U.S. Patent Application Serial No. 12/238,345 entitled, "In-Body Device with Virtual Dipole Signal Amplification" filed September 25, 2008, the entire content of which is incorporated herein by reference. Alternatively, throughout the disclosure herein, the terms "nonconducting material", "membrane", and "skirt" are used interchangeably with the term "current path extender" without impacting the scope or the present aspects and the claims herein. The skirt, shown in portion at 35 and 37, respectively, may be associated with, e.g., secured to, the framework 32. Various shapes and configurations for the skirt are contemplated as within the scope of the present invention. For example, the system 30 may be surrounded entirely or partially by the skirt and the skirt maybe positioned along a central axis of the system 30 or off- center relative to a central axis. Thus, the scope of the present invention as claimed herein is not limited by the shape or size of the skirt. Furthermore, in other aspects, the materials 34 and 36 may be separated by one skirt that is positioned in any defined region between the materials 34 and 36.
[048] Referring now to Fig. 4, in another aspect, the systems 12 and 22 of Figs. 2A and 2B, respectively, are shown in more detail as system 40. The system 40 includes a framework 42. The framework 42 is similar to the framework 32 of Fig. 3. In this aspect of the system 40, a digestible or dissolvable material 44 is deposited on a portion of one side of the framework 42. At a different portion of the same side of the framework 42, another digestible material 46 is deposited, such that materials 44 and 46 are dissimilar. More specifically, material 44 and 46 are selected such that they form a voltage potential difference when in contact with a conducting liquid, such as body fluids. Thus, when the system 40 is in contact with and/or partially in contact with the conducting liquid, then a current path, an example is shown in Fig. 5, is formed through the conducting liquid between material 44 and 46. A control device 48 is secured to the framework 42 and electrically coupled to the materials 44 and 46. The control device 48 includes electronic circuitry that is capable of controlling part of the conductance path between the materials 44 and 46. The materials 44 and 46 are separated by a non-conducting skirt 49. Various examples of the skirt 49 are disclosed in US Provisional Application No. 61 /173,51 1 filed on April 28, 2009 and entitled "HIGHLY RELIABLE INGESTIBLE EVENT MARKERS AND METHODS OF USING SAME" and US Provisional Application No. 61 /173,564 filed on April 28, 2009 and entitled "INGESTIBLE EVENT MARKERS HAVING SIGNAL AMPLIFIERS THAT COMPRISE AN ACTIVE AGENT"; as well as U.S. Application No. 12/238,345 filed September 25, 2008 and entitled "IN-BODY DEVICE WITH VIRTUAL DIPOLE SIGNAL AMPLIFICATION"; the entire disclosure of each is incorporated herein by reference.
[049] Once the control device 48 is activated or powered up, the control device 48 can alter conductance between the materials 44 and 46. Thus, the control device 48 is capable of controlling the magnitude of the current through the conducting liquid that surrounds the system 40. As indicated above with respect to system 30, a unique current signature that is associated with the system 40 can be detected by a receiver (not shown) to mark the activation of the system 40. Illustrative examples of receivers are shown in Figs. 12 to 17, as described hereinafter.
[050] In order to increase the "length" of the current path the size of the skirt 49 is altered. The longer the current path, the easier it may be for the receiver to detect the current.
[051] Referring now to Fig. 5, the system 30 of Fig. 3 is shown in an activated state and in contact with conducting liquid. The system 30 is grounded through ground contact 52. For example, when the system 30 is in contact with a conducting fluid, the conducting fluid provides the ground. The system 30 also includes a sensor module 74, which is described in greater detail with respect to Fig. 6. Ion or current paths 50 extend between material 34 to material 36 and flow through the conducting fluid in contact with the system 30. The voltage potential created between the material 34 and 36 is created through chemical reactions between materials 34/36 and the conducting fluid.
[052] If the conditions of the environment change to become favorable to communication, as determined by the measurements of the environment, then the unit 75 sends a signal to the control device 38 to alter the conductance between the materials 34 and 36 to allow for communication using the current signature of the system 30. Thus, if the system 30 has been deactivated and the impedance of the environment is suitable for communication, then the system 30 can be activated again.
[053] Referring now to Fig. 5A, this shows an exploded view of the surface of the material 34. In one aspect, the surface of the material 34 is not planar, but rather an irregular surface. The irregular surface increases the surface area of the material and, hence, the area that comes in contact with the conducting fluid. In one aspect, at the surface of the material 34, there is an electrochemical reaction between the material 34 and the surrounding conducting fluid such that mass is exchanged with the conducting fluid. The term "mass" as used here includes any ionic or non-ionic species that may be added or removed from the conductive fluid as part of the electrochemical reactions occurring on material 34. One example includes the instant where the material is CuCI and when in contact with the conducting fluid, CuCI is converted to Cu metal (solid) and CI- is released into the solution. The flow of positive ions into the conducting fluid is depicted by the current path 50. Negative ions flow in the opposite direction. In a similar manner, there is an electrochemical reaction involving the material 36 that results in ions released or removed from the conducting fluid. In this example, the release of negative ions at the material 34 and release of positive ions by the material 36 are related to each other through the current flow that is controlled by the control device 38. The rate of reaction and hence the ionic emission rate or current, is controlled by the control device 38. The control device 38 can increase or decrease the rate of ion flow by altering its internal conductance, which alters the impedance, and therefore the current flow and reaction rates at the materials 34 and 36. Through controlling the reaction rates, the system 30 can encode information in the ionic flow. Thus, the system 30 encodes information using ionic emission or flow.
[054] The control device 38 can vary the duration of ionic flow or current while keeping the current or ionic flow magnitude near constant, similar to when the frequency is modulated and the amplitude is constant. Also, the control device 38 can vary the level of the ionic flow rate or the magnitude of the current flow while keeping the duration near constant. Thus, using various combinations of changes in duration and altering the rate or magnitude, the control device 38 encodes information in the current or the ionic flow. For example, the control device 38 may use, but is not limited to any of the following techniques, including Binary Phase- Shift Keying (PSK), Frequency modulation, Amplitude modulation, on-off keying, and PSK with on-off keying.
[055] As indicated above, the various aspects disclosed herein, such as systems 30 and 40 of Figs. 3 and 4, respectively, include electronic components as part of the control device 38 or the control device 48. Components that may be present include but are not limited to: logic and/or memory elements, an integrated circuit, an inductor, a resistor, and sensors for measuring various parameters. Each component may be secured to the framework and/or to another component. The components on the surface of the support may be laid out in any convenient configuration. Where two or more components are present on the surface of the solid support, interconnects may be provided.
[056] As indicated above, the system, such as control devices 30 and 40, control the conductance between the dissimilar materials and, hence, the rate of ionic flow or current. Through altering the conductance in a specific manner the system is capable of encoding information in the ionic flow and the current signature. The ionic flow or the current signature is used to uniquely identify the specific system. Additionally, the systems 30 and 40 are capable of producing various different unique patterns or signatures and, thus, provide additional information. For example, a second current signature based on a second conductance alteration pattern may be used to provide additional information, which information may be related to the physical environment. To further illustrate, a first current signature may be a very low current state that maintains an oscillator on the chip and a second current signature may be a current state at least a factor of ten higher than the current state associated with the first current signature.
[057] Referring now to Fig. 6, a block diagram representation of the control device 38 is shown. The device 30 includes a control module 62, a counter or clock 64, and a memory 66. Additionally, the control device 38 is shown to include a sensor module 72 as well as the sensor module 74, which was referenced in Fig. 5. The control module 62 has an input 68 electrically coupled to the material 34 and an output 70 electrically coupled to the material 36. The control module 62, the clock 64, the memory 66, and the sensor modules 72/74 also have power inputs (some not shown). The power for each of these components is supplied by the voltage potential produced by the chemical reaction between materials 34 and 36 and the conducting fluid, when the system 30 is in contact with the conducting fluid. The control module 62 controls the conductance through logic that alters the overall impedance of the system 30. The control module 62 is electrically coupled to the clock 64. The clock 64 provides a clock cycle to the control module 62. Based upon the programmed characteristics of the control module 62, when a set number of clock cycles have passed, the control module 62 alters the conductance characteristics between materials 34 and 36. This cycle is repeated and thereby the control device 38 produces a unique current signature characteristic. The control module 62 is also electrically coupled to the memory 66. Both the clock 64 and the memory 66 are powered by the voltage potential created between the materials 34 and 36.
[058] The control module 62 is also electrically coupled to and in communication with the sensor modules 72 and 74. In the aspect shown, the sensor module 72 is part of the control device 38 and the sensor module 74 is a separate component. In alternative aspects, either one of the sensor modules 72 and 74 can be used without the other and the scope of the present invention is not limited by the structural or functional location of the sensor modules 72 or 74. Additionally, any component of the system 30 may be functionally or structurally moved, combined, or repositioned without limiting the scope of the present invention as claimed. Thus, it is possible to have one single structure, for example a processor, which is designed to perform the functions of all of the following modules: the control module 62, the clock 64, the memory 66, and the sensor module 72 or 74. On the other hand, it is also within the scope of the present invention to have each of these functional components located in independent structures that are linked electrically and able to communicate.
[059] Referring again to Fig. 6, the sensor modules 72 or 74 can include any of the following sensors: temperature, pressure, pH level, and conductivity. In one aspect, the sensor modules 72 or 74 gather information from the environment and communicate the analog information to the control module 62. The control module then converts the analog information to digital information and the digital information is encoded in the current flow or the rate of the transfer of mass that produces the ionic flow. In another aspect, the sensor modules 72 or 74 gather information from the environment and convert the analog information to digital information and then communicate the digital information to control module 62. In the aspect shown in Figs. 5, the sensor modules 74 is shown as being electrically coupled to the material 34 and 36 as well as the control device 38. In another aspect, as shown in Fig. 6, the sensor module 74 is electrically coupled to the control device 38 at connection 78. The connection 78 acts as both a source for power supply to the sensor module 74 and a communication channel between the sensor module 74 and the control device 38.
[060] Referring now to Fig. 5B, the system 30 includes a pH sensor module 76 connected to a material 39, which is selected in accordance with the specific type of sensing function being performed. The pH sensor module 76 is also connected to the control device 38. The material 39 is electrically isolated from the material 34 by a non-conductive barrier 55. In one aspect, the material 39 is platinum. In operation, the pH sensor module 76 uses the voltage potential difference between the materials 34/36. The pH sensor module 76 measures the voltage potential difference between the material 34 and the material 39 and records that value for later comparison. The pH sensor module 76 also measures the voltage potential difference between the material 39 and the material 36 and records that value for later comparison. The pH sensor module 76 calculates the pH level of the surrounding environment using the voltage potential values. The pH sensor module 76 provides that information to the control device 38. The control device 38 varies the rate of the transfer of mass that produces the ionic transfer and the current flow to encode the information relevant to the pH level in the ionic transfer, which can be detected by a receiver (not shown). Illustrative examples of receivers are shown in Figs.12 to 17 as described hereinafter. Thus, the system 30 can determine and provide the information related to the pH level to a source external to the environment.
[061] As indicated above, the control device 38 can be programmed in advance to output a pre-defined current signature. In another aspect, the system can include a receiver system that can receive programming information when the system is activated. Illustrative examples of receivers are shown in Figs. 12 to 17, as described hereinafter. In another aspect, not shown, the switch 64 and the memory 66 can be combined into one device.
[062] In addition to the above components, the system 30 may also include one or other electronic components. Electrical components of interest include, but are not limited to: additional logic and/or memory elements, e.g., in the form of an integrated circuit; a power regulation device, e.g., battery, fuel cell or capacitor; a sensor, a stimulator, etc. ; a signal transmission element, e.g., in the form of an antenna, electrode, coil, etc. ; a passive element, e.g., an inductor, resistor, etc.
[063] Referring now to Fig. 5C, the system 30 is shown with the skirt portions 35 and 37 secured to the framework 32, as discussed in detail below. In accordance with one aspect of the present invention, the material 34 and the material 36 extend beyond the framework 32 onto the skirt portions 35 and 37. In another example in accordance with the present invention, the materials 34 and 36 can extend to the edge of the skirt portions 35 and 37. The increase in the area of the materials 34 and 36 results in an increase in the power supplied.
[064] Referring now to Fig. 7, a cross-sectional view is shown of the system 30 with a first material region 34a and a second material region 36a on the framework 32. The first material region 34a includes an adhering material 86. The adhering material 86 can be any material selected to adhere and hold onto a first material region 88, which material region 88 is made of CuCI in accordance with one aspect of the present invention as discussed above with respect to the first material 34. The second material region 36a includes a transition metal 96 that is made of any transition metal, for example titanium in accordance with one aspect of the present invention. The second material region 36a also includes a second material region 98, which is made of magnesium (Mg) in accordance with one aspect of the present invention as discussed above with respect to the second material 36.
[065] Referring now to Fig. 8, an exploded view of the material 86 and the material region 88 is shown. The material 86 is made of a non-reactive and conducting material, for example gold. To enhance the adhesion properties of the material 86 to the material region 88, the material 86 has an unfinished or rough surface. The material 86 is deposited onto the framework 32. Additionally, according to one aspect of the present invention, the material 86 defines a plurality of holes 87 spaced a distance DD from the edge of the framework 32 corresponding to the edge of the material 86. The distance DD is the minimum distance that is needed to separate the holes 87 from the edge of the material 86 and allow all the of the holes 87 to fall within a boundary 89 so that the edge of the material region 88 is not positioned over any hole; this design enhances the adhesion property and characteristics of the material 86 to the material region 88.
[066] Referring now to Fig. 9, a process of securing the metal 96 to the framework 32 is shown. Initially the metal 96 is deposited onto the framework 32. Then the metal 86 with the framework 32 is heated. Then the surface of the metal 96 is cleaned using, for example, an ion gun cleaner. Then the magnesium is deposited onto the cleaned surface of the metal 86 to form the material region 98.
[067] In accordance with another aspect of the present invention, a plurality of frameworks 32, as shown in Fig. 1 , are built on a wafer 100, as shown in the top view illustration of Fig. 10. The wafer 100 can include any number of frameworks 32. Once the wafer 100 is complete, then each complete framework 32 is cut from the wafer 100 and inserted or press fitted or placed into an opening 1 12 of Fig. 1 1 of a sheet 1 10 to produce the system 12, 22, 30, or 40 as shown and discussed about in accordance with the various aspects of the present invention. The opening 1 12 is matingly cut to the shape of the framework 32. The sheet 1 10 is then passed through a punch press (not shown) that punches out each of systems 12, 22, 30, or 40 as noted.
[068] In certain aspects, the ingestible circuitry includes a coating layer. In accordance with one aspect of the present invention, the protective coating may be applied to the wafer 100 using a spinning process prior to removal of the framework 32 from the wafer 100 of Fig. 10. In accordance with another aspect of the present invention, the protective coating may be applied to the system, for example the system 30, after being punched out or cut out from the sheet 1 10 of Fig. 1 1 . The purpose of this coating layer can vary, e.g., to protect the circuitry, the chip and/or the battery, or any components during processing, during storage, or even during ingestion. In such instances, a coating on top of the circuitry may be included. Also of interest are coatings that are designed to protect the ingestible circuitry during storage, but dissolve immediately during use. For example, coatings that dissolve upon contact with an aqueous fluid, e.g. stomach fluid, or the conducting fluid as referenced above. Also of interest are protective processing coatings that are employed to allow the use of processing steps that would otherwise damage certain components of the device. For example, in aspects where a chip with dissimilar material deposited on the top and bottom is produced, the product needs to be diced. However, the dicing process can scratch off the dissimilar material, and also there might be liquid involved which would cause the dissimilar materials to discharge or dissolve. In such instances, a protective coating on the materials prevents mechanical or liquid contact with the component during processing can be employed.
[069] Another purpose of the dissolvable coatings may be to delay activation of the device. For example, the coating that sits on the dissimilar material and takes a certain period of time, e.g., five minutes, to dissolve upon contact with stomach fluid may be employed. The coating can also be an environmentally sensitive coating, e.g., a temperature or pH sensitive coating, or other chemically sensitive coating that provides for dissolution in a controlled fashion and allows one to activate the device when desired. Coatings that survive the stomach but dissolve in the intestine are also of interest, e.g., where one desires to delay activation until the device leaves the stomach. An example of such a coating is a polymer that is insoluble at low pH, but becomes soluble at a higher pH. Also of interest are pharmaceutical formulation protective coatings, e.g., a gel cap liquid protective coating that prevents the circuit from being activated by liquid of the gel cap.
[070] Identifiers of interest include two dissimilar electrochemical materials, which act similar to the electrodes (e.g., anode and cathode) of a power source. The reference to an electrode or anode or cathode are used here merely as illustrative examples. The scope of the present invention is not limited by the label used and includes the aspect wherein the voltage potential is created between two dissimilar materials. Thus, when reference is made to an electrode, anode, or cathode it is intended as a reference to a voltage potential created between two dissimilar materials.
[071] When the materials are exposed and come into contact with the body fluid, such as stomach acid or other types of fluid (either alone or in combination with a dried conductive medium precursor), a potential difference, that is, a voltage, is generated between the electrodes as a result of the respective oxidation and reduction reactions incurred to the two electrode materials. A voltaic cell, or battery, can thereby be produced. Accordingly, in aspects of the invention, such power supplies are configured such that when the two dissimilar materials are exposed to the target site, e.g., the stomach, the digestive tract, etc., a voltage is generated.
[072] In certain aspects, one or both of the metals may be doped with a non-metal, e.g., to enhance the voltage output of the battery. Non-metals that may be used as doping agents in certain aspects include, but are not limited to: sulfur, iodine and the like.
[073] For purposes of illustration, various receivers may be used with various aspects of the present invention. In one example of a receiver, sometimes referred to herein as a "signal receiver", two or more different demodulation protocols may be employed to decode a given received signal. In some instances, both a coherent demodulation protocol and a differential coherent demodulation protocol may be employed. FIG. 12 provides a functional block diagram of how a receiver may implement a coherent demodulation protocol, according to one aspect of the invention. It should be noted that only a portion of the receiver is shown in FIG. 12. FIG. 12 illustrates the process of mixing the signal down to baseband once the carrier frequency (and carrier signal mixed down to carrier offset) is determined. A carrier signal 2221 is mixed with a second carrier signal 2222 at mixer 2223. A narrow low-pass filter 2220 is applied of appropriate bandwidth to reduce the effect of out-of-bound noise. Demodulation occurs at functional blocks 2225 in accordance with the coherent demodulation scheme of the present invention. The unwrapped phase 2230 of the complex signal is determined. An optional third mixer stage, in which the phase evolution is used to estimate the frequency differential between the calculated and real carrier frequency can be applied. The structure of the packet is then leveraged to determine the beginning of the coding region of the BPSK signal at block 2240. Mainly, the presence of the sync header, which appears as an FM porch in the amplitude signal of the complex demodulated signal is used to determine the starting bounds of the packet. Once the starting point of the packet is determined the signal is rotated at block 2250 on the IQ plane and standard bit identification and eventually decoded at block 2260. [074] In addition to demodulation, the transbody communication module may include a forward error correction module, which module provides additional gain to combat interference from other unwanted signals and noise. Forward error correction functional modules of interest include those described in PCT Application Serial No. PCT/US2007/024225 and published as WO 2008/063626, the disclosure of which is herein incorporated by reference. In some instances, the forward error correction module may employ any convenient protocol, such as Reed-Solomon, Golay, Hamming, BCH, and Turbo protocols to identify and correct (within bounds) decoding errors.
[075] In another example, the receiver includes a beacon module as shown in the functional block diagram of FIG. 13. The scheme outlined in FIG. 13 outlines one technique for identifying a valid beacon. The incoming signal 2360 represents the signals received by electrodes, bandpass filtered (such as from 10 KHz to 34 KHz) by a high frequency signaling chain (which encompasses the carrier frequency), and converted from analog to digital. The signal 2360 is then decimated at block 2361 and mixed at the nominal drive frequency (such as, 12.5 KHz, 20 KHz, etc.) at mixer 2362. The resulting signal is decimated at block 2364 and low-pass filtered (such as 5 KHz BW) at block 2365 to produce the carrier signal mixed down to carrier offset- signal 2369. Signal 2369 is further processed by blocks 2367 (fast Fourier transform and then detection of two strongest peaks) to provide the true carrier frequency signal 2368. This protocol allows for accurate determination of the carrier frequency of the transmitted beacon.
[076] FIG. 14 provides a block functional diagram of an integrated circuit component of a signal receiver according to an aspect of the invention. In FIG. 14, receiver 2700 includes electrode input 2710. Electrically coupled to the electrode input 2710 are transbody conductive communication module 2720 and physiological sensing module 2730. In one aspect, transbody conductive communication module 2720 is implemented as a high frequency (HF) signal chain and physiological sensing module 2730 is implemented as a low frequency (LF) signal chain. Also shown are CMOS temperature sensing module 2740 (for detecting ambient temperature) and a 3-axis accelerometer 2750. Receiver 2700 also includes a processing engine 2760 (for example, a microcontroller and digital signal processor), non-volatile memory 2770 (for data storage) and wireless communication module 2780 (for data transmission to another device, for example in a data upload action).
[077] FIG. 15 provides a more detailed block diagram of a circuit configured to implement the block functional diagram of the receiver depicted in FIG. 14, according to one aspect of the invention. In FIG. 1 5, receiver 2800 includes electrodes e1 , e2 and e3 (281 1 , 2812 and 2813) which, for example, receive the conductively transmitted signals by an I EM and/or sense physiological parameters or biomarkers of interest. The signals received by the electrodes 281 1 , 2812, and 2813 are multiplexed by multiplexer 2820 which is electrically coupled to the electrodes.
[078] Multiplexer 2820 is electrically coupled to both high band pass filter 2830 and low band pass filter 2840. The high and low frequency signal chains provide for programmable gain to cover the desired level or range. In this specific aspect, high band pass filter 2830 passes frequencies in the 10 KHz to 34 KHz band while filtering out noise from out-of-band frequencies. This high frequency band may vary, and may include, for example, a range of 3 KHz to 300 KHz. The passing frequencies are then amplified by amplifier 2832 before being converted into a digital signal by converter 2834 for input into high power processor 2880 (shown as a DSP) which is electrically coupled to the high frequency signal chain.
[079] Low band pass filter 2840 is shown passing lower frequencies in the range of 0.5 Hz to 150 Hz while filtering out out-of-band frequencies. The frequency band may vary, and may include, for example, frequencies less than 300 Hz, such as less than 200 Hz, including less than 150 Hz. The passing frequency signals are amplified by amplifier 2842. Also shown is accelerometer 2850 electrically coupled to second multiplexer 2860. Multiplexer 2860 multiplexes the signals from the accelerometer with the amplified signals from amplifier 2842. The multiplexed signals are then converted to digital signals by converter 2864 which is also electrically coupled to low power processor 2870.
[080] In one aspect, a digital accelerometer (such as one manufactured by Analog Devices), may be implemented in place of accelerometer 2850. Various advantages may be achieved by using a digital accelerometer. For example, because the signals the digital accelerometer would produce signals already in digital format, the digital accelerometer could bypass converter 2864 and electrically couple to the low power microcontroller 2870-in which case multiplexer 2860 would no longer be required. Also, the digital signal may be configured to turn itself on when detecting motion, further conserving power. In addition, continuous step counting may be implemented. The digital accelerometer may include a FIFO buffer to help control the flow of data sent to the low power processor 2870. For instance, data may be buffered in the FIFO until full, at which time the processor may be triggered to turn awaken from an idle state and receive the data.
[081] Low power processor 2870 may be, for example, an MSP430 microcontroller from Texas Instruments. Low power processor 2870 of receiver 2800 maintains the idle state, which as stated earlier, requires minimal current draw--e.g., 10 .mu.A or less, or 1 .mu.A or less.
[082] High power processor 2880 may be, for example, a VC5509 digital signal process from Texas Instruments. The high power processor 2880 performs the signal processing actions during the active state. These actions, as stated earlier, require larger amounts of current than the idle state~e.g., currents of 30 .mu.A or more, such as 50 .mu.A or more--and may include, for example, actions such as scanning for conductively transmitted signals, processing conductively transmitted signals when received, obtaining and/or processing physiological data, etc.
[083] Also shown in FIG. 13 is flash memory 2890 electrically coupled to high power processor 2880. In one aspect, flash memory 2890 may be electrically coupled to low power processor 2870, which may provide for better power efficiency.
[084] Wireless communication element 2895 is shown electrically coupled to high power processor 2880 and may include, for example, a BLUETOOTH. TM. wireless communication transceiver. In one aspect, wireless communication element 2895 is electrically coupled to high power processor 2880. In another aspect, wireless communication element 2895 is electrically coupled to high power processor 2880 and low power processor 2870. Furthermore, wireless communication element 2895 may be implemented to have its own power supply so that it may be turned on and off independently from other components of the receiver~e.g., by a microprocessor. [085] With, for example, an idle state in mind, the following paragraphs provide example configurations of receiver components shown in FIG. 15 during various states of the receiver, according to one aspect of the invention. It should be understood that alternative configurations may be implemented depending on the desired application.
[086] In an idle state, for example, the receiver draws minimal current. Receiver 2800 is configured such that low power processor 2870 is in an inactive state (such as idle state) and high power processor 2880 is in an inactive state (such as idle state), and circuit blocks related to peripheral circuitry and their power supplies required during various active states remain off (for example, wireless communication module 2895 and the analog front end). For example, the low power processor may have a 32 KHz oscillator active and may consume a few .mu.A current or less, including 0.5 .mu.A or less. In the idle state, the low power processor 2870 may, for example, wait for a signal to transfer to an active state. The signal might be external such as an interrupt or internally generated by one of the device's peripherals, such as a timer. During the high power processor's idle state, the high power processor may, for example, be running off a 32 KHz watch crystal. The high power processor may, for example, wait for a signal to transfer to active state.
[087] When the receiver is in the sniff state, low power processor 2870 is in an idle state and high power processor 2880 is in an idle state. In addition, the circuit blocks relating to the analog front end including A/D converter that is needed for the sniff function are on (in other words, the high frequency signal chain). As stated earlier, the beacon signal module may implement various types of sniff signals to achieve low power efficiency.
[088] Upon detection of a transmitted signal, a higher power demodulate and decode state may be entered. When the receiver is in the demodulate and decode state, low power processor 2870 is in an active state and high power processor 2880 is in an active state. High power processor 2880 may, for example, be running from a 12 MHz or near crystal oscillator with a PLL-based clock multiplier giving the device a 108 MHz clock speed. The low power processor 2870 may, for example, run off an internal R-C oscillator in the range of 1 MHz to 20 MHz and consume power in the range of 250 to 300 uA per MHz clock speed during active states. The active state allows for processing and any transmissions that may follow. Required transmissions may trigger the wireless communication module to cycle from off to on.
[089] When the receiver is in collect ECG and accelerometer state, the circuit blocks relating to the accelerometer and/or ECG signal conditioning chain are on. The high power processor 2880 is in an in idle state during collection, and in an active state (for example, running from a 12 MHz or near crystal oscillator with a PLL-based clock multiplier giving the device a 108 MHz clock speed) during processing and transmission. The low power processor 2870 is in an active state during this state and may run off an internal R-C oscillator in the range of 1 MHz to 20 MHz and consume power in the range of 250 to 300 uA per MHz clock speed.
[090] The low power processor (e.g., MSP shown in FIG. 13) and high power processor (e.g., DSP shown in FIG. 13) may communicate with each other using any convenient communication protocol. In some instances, these two elements, when present, communicate with each via a serial peripheral interface bus (hereinafter "SPI bus"). The following description describes the signaling and messaging scheme implemented to allow the high power processor and low power processor to communicate and send messages back and forth along the SPI bus. For the following description of the communication between the processors, "LPP" and "HPP" are used in place of "low power processor" and "high power processor", respectively, to stay consistent with FIG. 13. The discussion, however, may apply to other processors than those shown in FIG. 13.
[091] FIG. 16 provides a view of a block diagram of hardware in a receiver according to an aspect of the invention related to the high frequency signal chain. In FIG. 16, receiver 2900 includes receiver probes (for example in the form of electrodes 291 1 , 2912 and 2913) electrically coupled to multiplexer 2920. Also shown are high pass filter 2930 and low pass filter 2940 to provide for a band pass filter which eliminates any out-of-band frequencies. In the aspect shown, a band pass of 10 KHz to 34 KHz is provided to pass carrier signals falling within the frequency band. Example carrier frequencies may include, but are not limited to, 12.5 KHz and 20 KHz. One or more carriers may be present. In addition, receiver 2900 includes analog to digital converter 2950~for example, sampling at 500 KHz. The digital signal can thereafter be processed by the DSP. Shown in this aspect is DMA to DSP unit 2960 which sends the digital signal to dedicated memory for the DSP. The direct memory access provides the benefit of allowing the rest of the DSP to remain in a low power mode.
[092] An example of a system that includes a receiver is shown in FIG. 17. In FIG. 17, system 3500 includes a pharmaceutical composition 3510 that comprises an ingestible device such as an ingestible event marker, " I EM." Also present in system 3500 is signal receiver 3520. Signal receiver 3520 is configured to detect a signal emitted from the identifier of the I EM 3510. Signal receiver 3520 also includes physiologic sensing capability, such as ECG and movement sensing capability. Signal receiver 3520 is configured to transmit data to a patient's an external device or PDA 3530 (such as a smart phone or other wireless communication enabled device), which in turn transmits the data to a server 3540. Server 3540 may be configured as desired, e.g., to provide for patient directed permissions. For example, server 3540 may be configured to allow a family caregiver 3550 to participate in the patient's therapeutic regimen, e.g., via an interface (such as a web interface) that allows the family caregiver 3550 to monitor alerts and trends generated by the server 3540, and provide support back to the patient, as indicated by arrow 3560. The server 3540 may also be configured to provide responses directly to the patient, e.g., in the form of patient alerts, patient incentives, etc., as indicated by arrow 3565 which are relayed to the patient via PDA 3530. Server 3540 may also interact with a health care professional (e.g., RN, physician) 3555, which can use data processing algorithms to obtain measures of patient health and compliance, e.g., wellness index summaries, alerts, cross-patient benchmarks, etc., and provide informed clinical communication and support back to the patient, as indicated by arrow 3580.
[093] It is to be understood that this invention is not limited to particular embodiments or aspects described and, as such, may vary. It is also to be understood that the terminology used herein is for the purpose of describing particular aspects only, and is not intended to be limiting, since the scope of the present invention will be limited only by the appended claims.
[094] Where a range of values is provided, it is understood that each intervening value, to the tenth of the unit of the lower limit unless the context clearly dictates otherwise, between the upper and lower limit of that range and any other stated or intervening value in that stated range, is encompassed within the invention. The upper and lower limits of these smaller ranges may independently be included in the smaller ranges and are also encompassed within the invention, subject to any specifically excluded limit in the stated range. Where the stated range includes one or both of the limits, ranges excluding either or both of those included limits are also included in the invention.
[095] Unless defined otherwise, all technical and scientific terms used herein have the same meaning as commonly understood by one of ordinary skill in the art to which this invention belongs. Although any methods and materials similar or equivalent to those described herein can also be used in the practice or testing of the present invention, representative illustrative methods and materials are now described.
[096] All publications and patents cited in this specification are herein incorporated by reference as if each individual publication or patent were specifically and individually indicated to be incorporated by reference and are incorporated herein by reference to disclose and describe the methods and/or materials in connection with which the publications are cited. The citation of any publication is for its disclosure prior to the filing date and should not be construed as an admission that the present invention is not entitled to antedate such publication by virtue of prior invention. Further, the dates of publication provided may be different from the actual publication dates which may need to be independently confirmed.
[097] It is noted that, as used herein and in the appended claims, the singular forms "a", "an", and "the" include plural referents unless the context clearly dictates otherwise. It is further noted that the claims may be drafted to exclude any optional element. As such, this statement is intended to serve as antecedent basis for use of such exclusive terminology as "solely," "only" and the like in connection with the recitation of claim elements, or use of a "negative" limitation.
[098] Notwithstanding the claims, the invention is also referred to in the following clauses:
[099] 1 . A method of manufacturing a communication device including a partial power source, the method comprising the steps of:
[0100] depositing a layer of adhesion material onto a first location of a support structure, wherein the layer of adhesion material defines a plurality of holes;
[0101] depositing a first material onto the layer of adhesion material, wherein the first material adheres to the adhesion material;
[0102] depositing a layer of transition material on a second location of the support structure; and
[0103] depositing a second material onto the layer of transition metal, wherein the first material and the second material to represent a voltage potential difference when the first material and the second material come into contact with a conducting fluid.
[0104] 2. The method of clause 1 , wherein the adhesion material is gold.
[0105] 3. The method of clause 2, further comprising the step of roughing the surface of the gold to enhance adhesion property.
[0106] 4. The method according to any of the clauses 1 -3 wherein the support structure is a silicon based material.
[0107] 5. The method according to any of the clauses 1 -4 wherein the step of depositing the first material includes evaporating deposition using electron beams.
[0108] 6. The method according to any of the preceding clauses wherein the adhesion layer is less than 100 microns thick. [0109] 7. The method according to any of the preceding clauses wherein the step of depositing a layer of transition metal includes the steps of:
[0110] depositing the transition metal onto the support structure;
[0111] heating the support structure with the transition metal deposit; and
[0112] cleaning an exposed surface of the transition metal such that the resulting structure is ready to receive the second material.
[0113] 8. The method according to any of the preceding clauses wherein the step of cleaning the exposed surface comprising cleaning with an ion gun.
[0114] 9. The method according to any of the preceding clauses further comprising the step of spinning a polymer onto the device to provide a protective coating, preferably wherein the step of depositing includes spinning the device to evenly distribute the polymer on the surface of the device.
[0115] 10. The method according to any of the preceding clauses further comprising the step of inserting the device into a non-conducting membrane.
[0116] 1 1 . A method of manufacturing a plurality of communication devices, wherein each device includes a non-conducting membrane and a partial power source device, the method comprising the steps of:
[0117] cutting a plurality of openings into a sheet of non-conducting material to produce an assembly membrane sheet, wherein the shape of each opening corresponds to the shape of a framework of the device; and
[0118] inserting one partial power source device selected from the plurality of partial power source devices into each opening of the assembly membrane to produce a loaded membrane sheet, wherein each partial power source device is prepared according to a process that includes the step of depositing a layer of transition metal on an opposite surface of the support structure from a surface having an adhesion material. [0119] 12. The method of clause 1 1 further comprising the steps of:
[0120] depositing a layer of non-reactive material onto the loaded membrane sheet on a side opposite the transition metal to produce an adhesion membrane sheet, wherein the layer of non-reactive material defines a plurality of holes;
[0121] depositing a first material onto the adhesion membrane sheet on the side with the adhesive material, wherein the first material adheres to the non-reactive material;
[0122] depositing a second material onto the layer of transition metal to produce a partial power device sheet, wherein the first material and the second material represent a voltage potential difference.
[0123] 13. The method of clause 1 1 or 12 further comprising the step of defining a plurality of boundaries on the support structure, wherein each boundary corresponds to circuitry of each device.
[0124] 14. The method of clause 12 or 13, wherein the step of depositing a layer of non-reactive material further comprises the step of defining a group of holes, wherein each group of holes is contained within one boundary selected from the plurality of boundaries, such that the position of each hole within the group of holes is within the corresponding boundary.
[0125] 15. The method according to any of the preceding clauses wherein the transitional metal is titanium.
[0126] 16. A device comprising a partial power source for communication, obtainable according to the method of any of the preceding clauses, preferably wherein the device is prepared by a process comprising the steps of:
[0127] depositing a layer of adhesion material onto a first location of a support structure, wherein the layer of adhesion material defines a plurality of holes;
[0128] depositing a first material onto the adhesion layer, wherein the first material adheres to the adhesion material; [0129] depositing a layer of transition material on a second location of the support structure;
[0130] depositing a second material onto the layer of transition metal, wherein the first material and the second material represent a voltage potential difference when the first material and the second material come into contact with a conducting fluid.
[0131] As will be apparent to those of skill in the art upon reading this disclosure, each of the individual aspects described and illustrated herein has discrete components and features which may be readily separated from or combined with the features of any of the other several aspects without departing from the scope or spirit of the present invention. Any recited method can be carried out in the order of events recited or in any other order which is logically possible.
[0132] Although the foregoing invention has been described in some detail by way of illustration and example for purposes of clarity of understanding, it is readily apparent to those of ordinary skill in the art in light of the teachings of this invention that certain changes and modifications may be made thereto without departing from the spirit or scope of the appended claims.
[0133] Accordingly, the preceding merely illustrates the principles of the invention. It will be appreciated that those skilled in the art will be able to devise various arrangements which, although not explicitly described or shown herein, embody the principles of the invention and are included within its spirit and scope. Furthermore, all examples and conditional language recited herein are principally intended to aid the reader in understanding the principles of the invention and the concepts contributed by the inventors to furthering the art, and are to be construed as being without limitation to such specifically recited examples and conditions. Moreover, all statements herein reciting principles, aspects, and aspects of the invention as well as specific examples thereof, are intended to encompass both structural and functional equivalents thereof. Additionally, it is intended that such equivalents include both currently known equivalents and equivalents developed in the future, i.e., any elements developed that perform the same function, regardless of structure. The scope of the present invention, therefore, is not intended to be limited to the exemplary aspects shown and described herein. Rather, the scope and spirit of present invention is embodied by the appended claims.

Claims

What is claimed is:
1 . A method of manufacturing a communication device including a partial power source, the method comprising the steps of:
depositing a layer of adhesion material onto a first location of a support
structure, wherein the layer of adhesion material defines a plurality of holes;
depositing a first material onto the layer of adhesion material, wherein the first material adheres to the layer of adhesion material;
depositing a layer of transition material on a second location of the support structure; and
depositing a second material onto the layer of transition material, wherein the first material and the second material represent a voltage potential difference when the first material and the second material come into contact with a conducting fluid.
2. The method of claim 1 , wherein the layer of adhesion material is gold.
3. The method of claim 1 , further comprising the step of roughing the surface of the gold to enhance adhesion property.
4. The method of claim 1 , wherein the support structure is a silicon based material.
5. The method of claim 1 , wherein the step of depositing the first material includes evaporating deposition using electron beams.
6. The method of claim 2, wherein the layer of adhesion material is less than 100 microns thick.
7. The method of claim 1 , wherein the step of depositing a layer of transition material includes the steps of: depositing the layer of transition material onto the support structure;
heating the support structure with the layer of transition material deposit; and cleaning an exposed surface of the layer of transition material such that the
resulting structure is ready to receive the second material.
8. The method of claim 7, wherein the step of cleaning the exposed surface further comprises cleaning with an ion gun.
9. The method of claim 1 , further comprising the step of spinning a polymer onto the device to provide a protective coating.
10. The method of claim 7, further comprising the step of spinning the device to evenly distribute a polymer on the surface of the device.
1 1 . The method of claim 1 , further comprising the step of inserting the device into a non-conducting membrane.
12. A method of manufacturing a plurality of communication devices, wherein each device includes a non-conducting membrane and a partial power source device, the method comprising the steps of:
cutting a plurality of openings into a sheet of non-conducting material to
produce an assembly membrane sheet, wherein the shape of each opening corresponds to the shape of a framework of the device; and inserting one partial power source device selected from the plurality of partial power source devices into each opening of the assembly membrane to produce a loaded membrane sheet, wherein each partial power source device is prepared according to a process that includes the step of depositing a layer of transition metal on an opposite surface of a support structure from a surface having an adhesion material.
13. The method of claim 12 further comprising the steps of:
depositing a layer of non-reactive material onto the loaded membrane sheet on a side opposite the transition metal to produce an adhesion membrane sheet, wherein the layer of non-reactive material defines a plurality of holes; depositing a first material onto the adhesion membrane sheet on the side with the adhesive material, wherein the first material adheres to the non-reactive material;
depositing a second material onto the layer of transition metal to produce a partial power device sheet, wherein the first material and the second material represent a voltage potential difference.
14. The method claim 13 further comprising the step of defining a plurality of boundaries on the support structure, wherein each boundary corresponds to circuitry of each device.
15. The method of claim 14, wherein the step of depositing a layer of non-reactive material further comprises the step of defining a group of holes, wherein each group of holes is contained within one boundary selected from the plurality of boundaries, such that the position of each hole within the group of holes is within the
corresponding boundary.
16. A device comprising a partial power source for communication, wherein the
device is prepared by a process comprising the steps of:
depositing a layer of adhesion material onto a first location of a support
structure, wherein the layer of adhesion material defines a plurality of holes;
depositing a first material onto the layer of adhesion material, wherein the first material adheres to the layer of adhesion material;
depositing a layer of transition material onto a second location of the support structure; depositing a second material onto the layer of transition material, wherein the first material and the second material represent a voltage potential difference when the first material and the second material come into contact with a conducting fluid.
17. The method of claim 1 , wherein the transitional material is titanium.
18. A device including a partial power source for communication, wherein the device comprises:
a support structure made from a silicon material; and
a CuCI layer deposited on a first location of the support structure using physical vapor deposition.
19. The device of claim 18, wherein the physical vapor deposition is achieved through sputter deposition.
20. The device of claim 18, wherein the physical vapor deposition is achieved through arc deposition.
PCT/US2012/046120 2011-07-11 2012-07-10 Communication system with enhanced partial power source and method of manufacturing same WO2013009782A2 (en)

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CN201280043578.4A CN103957773A (en) 2011-07-11 2012-07-10 Communication system with enhanced partial power source and method of manufacturing same
BR112014000641A BR112014000641A2 (en) 2011-07-11 2012-07-10 communication system with intensified partial energy source and method of manufacture thereof
UAA201401331A UA116434C2 (en) 2011-07-11 2012-07-10 Communication system with enhanced partial power source and method of manufacturing same
CA2841830A CA2841830A1 (en) 2011-07-11 2012-07-10 Communication system with enhanced partial power source and method of manufacturing same
KR1020147003475A KR20140051298A (en) 2011-07-11 2012-07-10 Communication system with enhanced partial power source and method of manufacturing same
JP2014520264A JP6259395B2 (en) 2011-07-11 2012-07-10 Method for manufacturing a plurality of communication devices
EP12811820.5A EP2731489A4 (en) 2011-07-11 2012-07-10 Communication system with enhanced partial power source and method of manufacturing same
RU2014104692/14A RU2014104692A (en) 2011-07-11 2012-07-10 COMMUNICATION SYSTEM USING THE PARTIAL POWER SUPPLY OF THE HIGH POWER AND THE METHOD FOR THEIR MANUFACTURE
MX2014000484A MX337131B (en) 2011-07-11 2012-07-10 Communication system with enhanced partial power source and method of manufacturing same.
AU2012282777A AU2012282777A1 (en) 2011-07-11 2012-07-10 Communication system with enhanced partial power source and method of manufacturing same
IL230388A IL230388B (en) 2011-07-11 2014-01-09 Method of manufacturing a communication device including a partial power source
ZA2014/00337A ZA201400337B (en) 2011-07-11 2014-01-16 Communication system with enhanced partial power source and method of manufacturing same
HK14111828.9A HK1198283A1 (en) 2011-07-11 2014-11-21 Communication system with enhanced partial power source and method of manufacturing same
IL26412119A IL264121B (en) 2011-07-11 2019-01-07 Method of manufacturing a communication device including a partial power source

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US13/180,525 US8802183B2 (en) 2005-04-28 2011-07-11 Communication system with enhanced partial power source and method of manufacturing same
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