US20090143470A1 - Invisible Antimicrobial Glove and Hand Antiseptic - Google Patents

Invisible Antimicrobial Glove and Hand Antiseptic Download PDF

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US20090143470A1
US20090143470A1 US12/273,905 US27390508A US2009143470A1 US 20090143470 A1 US20090143470 A1 US 20090143470A1 US 27390508 A US27390508 A US 27390508A US 2009143470 A1 US2009143470 A1 US 2009143470A1
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composition
skin
surgical scrub
microbial
weight percent
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US12/273,905
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Minh Quang Hoang
Donald Edward Hunt
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Becton Dickinson and Co
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Becton Dickinson and Co
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Priority to US12/273,905 priority Critical patent/US20090143470A1/en
Publication of US20090143470A1 publication Critical patent/US20090143470A1/en
Priority to US14/955,396 priority patent/US20160081894A1/en
Assigned to BECTON, DICKINSON AND COMPANY reassignment BECTON, DICKINSON AND COMPANY ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: HOANG, MINH QUANG, HUNT, DONALD EDWARD
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    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/33Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
    • A61K8/34Alcohols
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/33Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
    • A61K8/34Alcohols
    • A61K8/342Alcohols having more than seven atoms in an unbroken chain
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/33Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
    • A61K8/37Esters of carboxylic acids
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/40Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing nitrogen
    • A61K8/41Amines
    • A61K8/416Quaternary ammonium compounds
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/40Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing nitrogen
    • A61K8/43Guanidines
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/46Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing sulfur
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/72Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
    • A61K8/73Polysaccharides
    • A61K8/731Cellulose; Quaternized cellulose derivatives
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/72Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
    • A61K8/81Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds obtained by reactions involving only carbon-to-carbon unsaturated bonds
    • A61K8/817Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a single or double bond to nitrogen or by a heterocyclic ring containing nitrogen; Compositions or derivatives of such polymers, e.g. vinylimidazol, vinylcaprolactame, allylamines (Polyquaternium 6)
    • A61K8/8176Homopolymers of N-vinyl-pyrrolidones. Compositions of derivatives of such polymers
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/72Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
    • A61K8/84Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds obtained by reactions otherwise than those involving only carbon-carbon unsaturated bonds
    • A61K8/86Polyethers
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/92Oils, fats or waxes; Derivatives thereof, e.g. hydrogenation products thereof
    • A61K8/922Oils, fats or waxes; Derivatives thereof, e.g. hydrogenation products thereof of vegetable origin
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61QSPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q17/00Barrier preparations; Preparations brought into direct contact with the skin for affording protection against external influences, e.g. sunlight, X-rays or other harmful rays, corrosive materials, bacteria or insect stings
    • A61Q17/005Antimicrobial preparations
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61QSPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q19/00Preparations for care of the skin
    • A61Q19/10Washing or bathing preparations
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B08CLEANING
    • B08BCLEANING IN GENERAL; PREVENTION OF FOULING IN GENERAL
    • B08B3/00Cleaning by methods involving the use or presence of liquid or steam
    • B08B3/04Cleaning involving contact with liquid
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K2800/00Properties of cosmetic compositions or active ingredients thereof or formulation aids used therein and process related aspects
    • A61K2800/20Chemical, physico-chemical or functional or structural properties of the composition as a whole
    • A61K2800/28Rubbing or scrubbing compositions; Peeling or abrasive compositions; Containing exfoliants
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K2800/00Properties of cosmetic compositions or active ingredients thereof or formulation aids used therein and process related aspects
    • A61K2800/40Chemical, physico-chemical or functional or structural properties of particular ingredients
    • A61K2800/54Polymers characterized by specific structures/properties
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K2800/00Properties of cosmetic compositions or active ingredients thereof or formulation aids used therein and process related aspects
    • A61K2800/40Chemical, physico-chemical or functional or structural properties of particular ingredients
    • A61K2800/54Polymers characterized by specific structures/properties
    • A61K2800/542Polymers characterized by specific structures/properties characterized by the charge
    • A61K2800/5426Polymers characterized by specific structures/properties characterized by the charge cationic
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K2800/00Properties of cosmetic compositions or active ingredients thereof or formulation aids used therein and process related aspects
    • A61K2800/40Chemical, physico-chemical or functional or structural properties of particular ingredients
    • A61K2800/59Mixtures
    • A61K2800/592Mixtures of compounds complementing their respective functions
    • A61K2800/5922At least two compounds being classified in the same subclass of A61K8/18

Definitions

  • the present invention relates to an alcohol-based antiseptic surgical scrub, which leaves an anti-microbial invisible film or “glove” on the hands, following alcohol evaporation.
  • Diligent hand washing and the wearing of gloves by healthcare professionals are essential components of effective infection control in the healthcare environment.
  • Healthcare professionals regularly wash their hands and wear gloves to control the spread of bacteria and infection from patient to patient, and to themselves.
  • Hand washing procedures are performed in several ways and include products such as an ordinary anti-microbial bar soap, skin disinfecting or pre-operative agents or rubbing alcohol. Such procedures and products contain anti-microbial agents such as alcohol, iodine, chlorhexidine digluconate, chloroxylenol, triclosan and hexachlorophenes. Gloving by the healthcare workers is a normal practice in the hospital setting to create a barrier that protects themselves and the patient from transmitted bacteria.
  • Alcohols in general, are recognized for their disinfection properties. Rubbing alcohol, containing 70% ethyl alcohol (Formula 23-H) and 30% water, and isopropyl rubbing alcohol, containing 70% isopropyl alcohol and 30% water, are commonly used disinfectants. Alcohol is a potent anti-microbial agent, and, if used with surgical scrub, will cause significant mean log reduction of bacterial counts on the hands of healthcare workers. However, the use of alcohols for surgical scrubs has never become popular in the United States of America, even though the compound has very good properties for immediate reduction of microbial flora on the hands. This may be due to the fact that alcohol is a defatting agent. When applied to the human skin, it can make the skin very dry, often leading to chapped and cracked skin. These characteristics thus often result in difficult and painful sensitivity for the users.
  • U.S. Pat. No. 4,678,606 discloses a personal liquid cleaning composition having a primary surfactant selected from the group of anionic, cationic, zwitterionic, amphoteric and semipolar surfactants, an auxiliary surfactant selected from certain ethoxylated aliphatic alcohols and a water-soluble polymeric thickening agent.
  • U.S. Pat. No. 4,374,126 discloses an alcohol insoluble antimicrobial topical lotion including a lower acrylate interpolymer.
  • U.S. Pat. No. 5,512,199 discloses an antimicrobial hand wipe which includes an alcohol.
  • U.S. Pat. No. 6,180,584 is directed to a film forming antimicrobial composition. Notably, this composition is an alcohol-free anti-microbial skin sanitizing composition.
  • the present invention is an alcohol based hand surgical scrub, which includes dual anti-microbial agent preservatives, cationic polymer film-forming agents and provides a long term residual, anti-microbial “invisible glove” on the skin.
  • the composition desirably comprises an alcohol, anti-microbial agent which prevents the growth of bacteria and a polymer system to form a barrier on the skin.
  • the polymer system creates an invisible film on the skin following solvent evaporation. This invisible film provides a lasting anti-microbial barrier on the skin.
  • the composition desirably includes an alcohol, a positive charged anti-microbial agent, skin emollients and lubricants and a film-forming polymer system.
  • the composition may also include one or both of methyl and propyl parabens and silicone.
  • the anti-microbial agents prevent bacteria from growing back to the baseline of the normal skin flora population.
  • the surgical scrub composition contains chemical ingredients to remove extraneous matter and organisms from the hands. Skin emollients and lubricants are also provided to prevent the defatting effect of the alcohol, thereby eliminating the dry, chapped feeling on the skin. Additional or complimentary anti-microbial agents are preferably included to serve as preservative and persistent active agents.
  • the polymer system is included to create an invisible film after the solvent is evaporated.
  • This invisible film acts as a physical anti-microbial barrier or “glove” to protect the healthcare worker's hands.
  • This film has an anti-microbial effect at least for six hours to prevent and kill the bacteria on the healthcare worker's hands.
  • FIG. 1 is a graphical presentation of the log 10 reductions from baseline for the preferred formula and BD E-Z ScrubTM [BD Catalog #371073] plus the most preferred embodiment.
  • the surgical scrub composition of the present invention includes alcohol, a positive-charged anti-microbial agent, skin emollients and lubricants, and a cationic polymer film-forming thickening agent.
  • Alcohols which may be used in the present composition include isopropyl alcohol, ethanol, and n-propanol. In the most preferred embodiment, ethyl alcohol is used. Preferably, alcohol is present in the surgical scrub composition in an amount from about 60 to about 95 weight percent, and most preferably, at about 71 weight percent.
  • Emollients are utilized in the surgical scrub composition of the present invention to lessen the drying effect of the alcohol on the skin.
  • a preferred emollient is isopropyl palmitate, which is an ester emollient available from Amerchol Corporation of Edison, N.J. When used on the skin, isopropyl palmitate leaves a soft, non-sticky feel to the skin.
  • Isopropyl palmitate is a lipophillic emollient, an oily, fatty substance which is water insoluble.
  • Lanolin and its derivatives are a large group of fatty materials with active emollient properties that can be utilized as emulsifiers or lubricants in the composition.
  • the preferred embodiment includes glycerin as a hydrophilic emollient and a humectant to maintain the water in equilibrium.
  • Glycerin is available from Spectrum Quality products.
  • Glycerin is a water and alcohol soluble emollient that provides skin conditioning properties to the composition.
  • propylene glycol may be substituted for glycerin.
  • glycerin is present in the surgical scrub composition, by weight percent of the entire composition, in an amount of from about 0.1% to about 5%, and most preferably, about 1.4%.
  • the surgical scrub composition further includes a silicone fluid.
  • the silicone fluid is dimethicone copolyol, cyclomethicone and dimethicone. Most preferably, dimethicone is utilized. Dimethicone 350 is commercially available from General Electric Corporation. Silicone fluids provide good lubricating, aesthetic and occlusive action on the skin. Silicone fluids not only lubricate the skin surface, they also act as a gas barrier to reduce water vapor transmission. Silicone fluids are water and gas insoluble.
  • the silicone fluid is present in the surgical scrub composition, by weight percent of the entire composition, in an amount from 0 to about 5%, and most preferably, about 0.03%.
  • hydrocarbons are derived from petrolatum crude by a fractional distillation process. Such hydrocarbons function as emollients due to their ability to lubricate and hold water at the skin surface due to their relative occlusivity.
  • Mineral oil and isopropyl palmitate are included in the most preferred embodiment. Despite its lack of aesthetic properties, petrolatum may be utilized. Alternatively or additionally, lanolin derivatives may be included.
  • mineral oil is present in the surgical scrub composition, by weight percent of the entire composition, in an amount from 0 to about 5%, and most preferably, about 0.2%.
  • isopropyl palmitate is present in the surgical scrub composition, by weight percent of the entire composition, in an amount from about 0.1% to about 5%, and most preferably about 0.4%.
  • the surgical scrub composition includes about 0.1% to about 5% of an emollient or emollients.
  • An anti-microbial agent is included in the surgical scrub composition to kill microorganisms and prevent or inhibit their growth and reproduction. In the absence of an antimicrobial agent, microbial flora will grow on the skin following alcohol evaporation.
  • the antimicrobial agents present in the surgical scrub composition are selected to be compatible with the chemical and physical properties of the skin. In addition, the antimicrobial agent should be non-toxic and environmentally friendly.
  • the alcohol component of the surgical scrub composition is an excellent antimicrobial agent. It also acts as a preservative. However, following application of the surgical scrub composition, the alcohol will evaporate from the skin over time. In the most preferred embodiment, the residue remaining on the skin following alcohol evaporation will include an amount of an antimicrobial agent which also acts as a preservative.
  • Suitable antimicrobial agents which act as preservatives may be selected from the class of phenols including para-chloro-meta-xylenol, bis-biguanides such as chlorhexidine digluconate, chlorhexidine diacetate or quaterium class such as benzethonium chloride, benzalkonium chloride.
  • Chloroxylenol, triclosan, hexachlorophenes, octenidine and quarternary compounds may be included.
  • Hexetidine, germaben II, kathon CG, triclosan are other antimicrobial agents may also be suitable as preservatives.
  • Benzethonium chloride and benalkonium chloride are available from Lonza Inc.
  • chlorhexidine digluconate is available from Xttrium Laboratories
  • gennaben II is available from Sutton Laboratories.
  • benzethonium chloride, chlorhexidine digluconate (20%) and benzelkonium chloride (80%) are present.
  • benzethonium chloride is present in the scrub composition, by weight percent of the entire composition, in an amount from about 0.05% to about 5%, and most preferably, about 0.09%.
  • chlorhexidine digluconate (20%) is present in the surgical scrub composition, by weight percent of the entire composition, in an amount from about 0.05% to about 5%, and most preferably about 0.45%.
  • benzalkonium chloride (80%) is present in the surgical scrub composition, by weight percent of the entire composition, in an amount from 0 to about 5%, and most preferably, about 0.09%.
  • the composition includes about 0% to about 5% of an anti-microbial agent.
  • Methylparaben and propylparaben are desirably included in the surgical scrub composition as preservatives. These are further desired for their moisturizing and film forming characteristics.
  • methylparaben is contained in the surgical scrub composition, by weight percent of the entire composition, in an amount from about 0 to about 5%, and most preferably about 0.03%.
  • propylparaben is present in the surgical scrub, by weight percent of the entire composition, in an amount from about 0 to about 5%, and most preferably, about 0.03%.
  • One or both of these compositions are preferably included in the amount of about 0% to about 5% of the surgical scrub composition.
  • cationic polymer thickening agents are employed. Thickening agents must be soluble in the alcohol and compatible with cationic ingredients.
  • the cationic polymer thickening agents are preferably present in the surgical scrub composition, by weight percent of the entire composition, in the amount of about 0.1% to about 5%.
  • Incroquat behenyl TMS is most preferably used as a cationic polymer. It is a strong conditioning agent and an outstanding cationic emulsifier. This composition bonds to the skin due to the skin's negative charge.
  • Incroquat behenyl TMS is a compound of 25% active solution of behenyl trimonium methosulfate in cetearyl alcohol and is available in flaked/pastel form and supplied by Croda Inc.
  • Incroquat CR concentrate is preferably used as an additional cationic polymer. Incroquat CR concentrate is available from Croda me. and is comprised of cetearyl alcohol, castor oil and stearalkonium chloride. This composition is a one-part formulating aid.
  • incroquat behenyl TMS and incroquat CR concentrate provides a smooth feel to the skin and neutralizes the static charge of the human skin.
  • incroquat BTMS is present in the surgical scrub composition, by weight percent of the entire composition, in an amount from about 0.1% to about 5%, and most preferably about 0.4%.
  • incroquat CR is present in the surgical scrub composition, by weight percent of the entire composition, in an amount from 0 to about 5%, and most preferably about 0.1%.
  • Alternative or additional polymers include cellulose, polyvinylpyrolidone and waxes.
  • the most preferred embodiment includes the additional components 1-Docosanol as a moisturizer and film forming substance, PEG-10 behenyl ether as a moisturizer, fragrance and water.
  • 1-Docosanol is present in the surgical scrub composition, by weight percent of the entire composition, in an amount from about 0.1% to about 5%, and most preferably about 1%.
  • PEG-10 behenyl ether is present in the surgical scrub composition, by weight percent of the entire composition, in an amount from about 0.1% to about 5%, and most preferably about 1.5%.
  • purified water is present in the surgical scrub composition, in an amount from about 1% to about 35%, and most preferably about 23%.
  • the surgical scrub composition does not cause skin irritation or sensitization. Additional advantages of the composition include its compatibility with positive-charged anti-microbial agents such as chlorhexidine digluconate, thus ensuring the effectiveness of the anti-microbial agent or agents.
  • the included skin emollients and lubricants eliminate skin drying or chapping. These compositions counteract the defatting effect of the alcohol.
  • the surgical scrub composition includes anti-microbial agents, which act as both persistent active agents and suitable preservatives. This composition permits a very small amount of an anti-microbial agent to improve anti-microbial activities and provide long-term residual activity for the skin.
  • An improved method may be to apply water to the skin, perform hand scrubbing at the beginning of the day using a scrub brush and anti-microbial scrub solution, rinsing the anti-microbial scrub solution with water, and then utilization of the composition of the present invention prior to subsequent surgical procedures.
  • a high level of hand antisepsis can be achieved via this method without abrasive scrubbing multiple times a day.
  • Standard testing of the most preferred embodiment demonstrates its effectiveness as an antiseptic to provide an immediate reduction of microbes and then to prevent microbial growth back to baseline within a 6-hour period.
  • the immediate log reduction was 2.65 on day 1, 2.92 on day 2 and 3.04 on day 3.
  • the residual effect was a log reduction six hours after hand cleaning of 1.45 on day 1, 1.79 on day 2 and 2. 18 on day 3.
  • the residual anti-microbial activity is facilitated by the containment of the anti-microbial agent in the polymer film that is formed.
  • the film forms an invisible “glove” containing an anti-microbial agent.
  • the anti-microbial agent remains on the skin in the film and continues to be bactericidal over extended periods of time.
  • the invisible glove prevents microbes that may be present on the hands of the healthcare worker from infecting a patient and the glove also provides a barrier for microbes infecting the healthcare worker from the patient.
  • the critical indices for this study were an immediate one (1) log 10 reduction in microorganisms on Day 1; an immediate two (2) log 10 reduction in microorganisms on Day 2; an immediate three (3) log 10 reduction in microorganisms on Day 5; and that microorganism populations from the approximately three (3) hour to three (3) hour and thirty (30) minute AND approximately six (6) hour to six (6) hour and thirty (30) minute samples not return to baseline level.
  • the critical indices for this study were an immediate one (1) log 10 reduction in microorganisms on Day 1; an immediate two (2) log 10 reduction in microorganisms on Day 2; an immediate three (3) log 10 reduction in microorganisms on Day 5; and that microorganism populations from the approximately three (3) hour to three (3) hour and thirty (30) minute AND approximately six (6) hour to six (6) hour and thirty (30) minute samples not return to baseline level.
  • the most preferred embodiment was also tested in conjunction with a standard hand scrub utilizing a brush impregnated with an anti-microbial agent.
  • the composition was applied to the hands of the test subject one-half hour following the standard scrub.
  • Test results showed an increased log reduction of microbes when the scrubbing and the preferred composition were used together.
  • Log reductions of microbes were 3.66 for Day 1, 3.98 for Day 2, and 3.70 for Day 3.
  • Use of the preferred composition in conjunction with a standard scrub exceeded industry standards for anti-microbial compositions. Refer to Table II and FIG. 1 .

Abstract

An alcohol based hand surgical scrub, which includes cationic anti-microbial agent preservatives, cationic polymer film-forming agents and a skin emollient, and provides a long term residual, anti-microbial “invisible glove” on the skin. The composition provides an immediate reduction in bacterial microbes. The polymer system creates an invisible film on the skin following solvent evaporation. This invisible film provides a lasting anti-microbial barrier on the skin which acts to prevent microbial growth.

Description

    CROSS REFERENCE TO RELATED APPLICATIONS
  • This application is a continuation application of U.S. patent application Ser. No. 10/550,184, filed Jul. 24, 2006, which is a national phase of PCT/US04/009009, filed Mar. 24, 2004, which claims priority from U.S. Provisional Application No. 60/457,054, filed Mar. 24, 2003.
  • BACKGROUND OF THE INVENTION
  • 1. Field of the Invention
  • The present invention relates to an alcohol-based antiseptic surgical scrub, which leaves an anti-microbial invisible film or “glove” on the hands, following alcohol evaporation.
  • 2. Description of Related Art
  • Diligent hand washing and the wearing of gloves by healthcare professionals are essential components of effective infection control in the healthcare environment. Healthcare professionals regularly wash their hands and wear gloves to control the spread of bacteria and infection from patient to patient, and to themselves.
  • Hand washing procedures are performed in several ways and include products such as an ordinary anti-microbial bar soap, skin disinfecting or pre-operative agents or rubbing alcohol. Such procedures and products contain anti-microbial agents such as alcohol, iodine, chlorhexidine digluconate, chloroxylenol, triclosan and hexachlorophenes. Gloving by the healthcare workers is a normal practice in the hospital setting to create a barrier that protects themselves and the patient from transmitted bacteria.
  • Healthcare workers commonly use scrub brushes impregnated with anti-microbial agents for antiseptic hand washing prior to surgical procedures and other invasive patient care procedures. These impregnated scrub brushes have proven to be an effective method of reducing the spread of infection in the healthcare setting. Anti-microbial solutions are specially designed for use in the scrub brush where the mechanical action of scrubbing with the brush creates a foam or lather. Before performing a surgical procedure, the surgical team uses surgical scrubs to disinfect their hands with such a standardized scrub procedure, usually lasting 5 to 10 minutes, then don sterile gloves before initializing the surgical procedure.
  • Alcohols, in general, are recognized for their disinfection properties. Rubbing alcohol, containing 70% ethyl alcohol (Formula 23-H) and 30% water, and isopropyl rubbing alcohol, containing 70% isopropyl alcohol and 30% water, are commonly used disinfectants. Alcohol is a potent anti-microbial agent, and, if used with surgical scrub, will cause significant mean log reduction of bacterial counts on the hands of healthcare workers. However, the use of alcohols for surgical scrubs has never become popular in the United States of America, even though the compound has very good properties for immediate reduction of microbial flora on the hands. This may be due to the fact that alcohol is a defatting agent. When applied to the human skin, it can make the skin very dry, often leading to chapped and cracked skin. These characteristics thus often result in difficult and painful sensitivity for the users.
  • The prior art includes many examples of varying antiseptic skin cleaners and wipes, some of which include alcohol. U.S. Pat. No. 4,678,606 discloses a personal liquid cleaning composition having a primary surfactant selected from the group of anionic, cationic, zwitterionic, amphoteric and semipolar surfactants, an auxiliary surfactant selected from certain ethoxylated aliphatic alcohols and a water-soluble polymeric thickening agent. U.S. Pat. No. 4,374,126 discloses an alcohol insoluble antimicrobial topical lotion including a lower acrylate interpolymer. U.S. Pat. No. 5,512,199 discloses an antimicrobial hand wipe which includes an alcohol. U.S. Pat. No. 6,180,584 is directed to a film forming antimicrobial composition. Notably, this composition is an alcohol-free anti-microbial skin sanitizing composition.
  • However, none of these prior art products provide the benefits of the presently disclosed surgical scrub composition, which not only includes alcohol, but also provides the desired invisible, anti-microbial long-lasting film on the hands following solvent evaporation.
  • SUMMARY OF THE INVENTION
  • The present invention is an alcohol based hand surgical scrub, which includes dual anti-microbial agent preservatives, cationic polymer film-forming agents and provides a long term residual, anti-microbial “invisible glove” on the skin. The composition desirably comprises an alcohol, anti-microbial agent which prevents the growth of bacteria and a polymer system to form a barrier on the skin. The polymer system creates an invisible film on the skin following solvent evaporation. This invisible film provides a lasting anti-microbial barrier on the skin.
  • The composition desirably includes an alcohol, a positive charged anti-microbial agent, skin emollients and lubricants and a film-forming polymer system. The composition may also include one or both of methyl and propyl parabens and silicone. The anti-microbial agents prevent bacteria from growing back to the baseline of the normal skin flora population. The surgical scrub composition contains chemical ingredients to remove extraneous matter and organisms from the hands. Skin emollients and lubricants are also provided to prevent the defatting effect of the alcohol, thereby eliminating the dry, chapped feeling on the skin. Additional or complimentary anti-microbial agents are preferably included to serve as preservative and persistent active agents. These anti-microbial agents in the composition will improve the anti-microbial characteristics of the formulation and provide a long-term residual activity for the skin. As previously noted, the polymer system is included to create an invisible film after the solvent is evaporated. This invisible film acts as a physical anti-microbial barrier or “glove” to protect the healthcare worker's hands. This film has an anti-microbial effect at least for six hours to prevent and kill the bacteria on the healthcare worker's hands.
  • BRIEF DESCRIPTION OF THE DRAWING
  • FIG. 1 is a graphical presentation of the log10 reductions from baseline for the preferred formula and BD E-Z Scrub™ [BD Catalog #371073] plus the most preferred embodiment.
  • DESCRIPTION OF THE PREFERRED EMBODIMENTS
  • This invention may be satisfied by embodiments in many different forms, and is not limited to any specific or preferred embodiments of the invention, which are merely exemplary of the principles of the invention. Various other modifications will be apparent to and readily made by those skilled in the art without departing from the scope and spirit of the invention. The scope of the invention will be measured by the appended claims and their equivalents.
  • The surgical scrub composition of the present invention includes alcohol, a positive-charged anti-microbial agent, skin emollients and lubricants, and a cationic polymer film-forming thickening agent.
  • One or more alcohols are utilized in the surgical scrub composition due to alcohol's well known germicidal properties. Alcohols which may be used in the present composition include isopropyl alcohol, ethanol, and n-propanol. In the most preferred embodiment, ethyl alcohol is used. Preferably, alcohol is present in the surgical scrub composition in an amount from about 60 to about 95 weight percent, and most preferably, at about 71 weight percent.
  • Emollients are utilized in the surgical scrub composition of the present invention to lessen the drying effect of the alcohol on the skin. A preferred emollient is isopropyl palmitate, which is an ester emollient available from Amerchol Corporation of Edison, N.J. When used on the skin, isopropyl palmitate leaves a soft, non-sticky feel to the skin. Isopropyl palmitate is a lipophillic emollient, an oily, fatty substance which is water insoluble. Lanolin and its derivatives are a large group of fatty materials with active emollient properties that can be utilized as emulsifiers or lubricants in the composition.
  • The preferred embodiment includes glycerin as a hydrophilic emollient and a humectant to maintain the water in equilibrium. Glycerin is available from Spectrum Quality products. Glycerin is a water and alcohol soluble emollient that provides skin conditioning properties to the composition. In another embodiment, propylene glycol may be substituted for glycerin. Preferably, glycerin is present in the surgical scrub composition, by weight percent of the entire composition, in an amount of from about 0.1% to about 5%, and most preferably, about 1.4%.
  • The surgical scrub composition further includes a silicone fluid. Preferably, the silicone fluid is dimethicone copolyol, cyclomethicone and dimethicone. Most preferably, dimethicone is utilized. Dimethicone 350 is commercially available from General Electric Corporation. Silicone fluids provide good lubricating, aesthetic and occlusive action on the skin. Silicone fluids not only lubricate the skin surface, they also act as a gas barrier to reduce water vapor transmission. Silicone fluids are water and gas insoluble. Preferably, the silicone fluid is present in the surgical scrub composition, by weight percent of the entire composition, in an amount from 0 to about 5%, and most preferably, about 0.03%.
  • Most hydrocarbons are derived from petrolatum crude by a fractional distillation process. Such hydrocarbons function as emollients due to their ability to lubricate and hold water at the skin surface due to their relative occlusivity. Mineral oil and isopropyl palmitate are included in the most preferred embodiment. Despite its lack of aesthetic properties, petrolatum may be utilized. Alternatively or additionally, lanolin derivatives may be included. Preferably, mineral oil is present in the surgical scrub composition, by weight percent of the entire composition, in an amount from 0 to about 5%, and most preferably, about 0.2%. Preferably, isopropyl palmitate is present in the surgical scrub composition, by weight percent of the entire composition, in an amount from about 0.1% to about 5%, and most preferably about 0.4%.
  • Preferably, the surgical scrub composition includes about 0.1% to about 5% of an emollient or emollients.
  • An anti-microbial agent is included in the surgical scrub composition to kill microorganisms and prevent or inhibit their growth and reproduction. In the absence of an antimicrobial agent, microbial flora will grow on the skin following alcohol evaporation. The antimicrobial agents present in the surgical scrub composition are selected to be compatible with the chemical and physical properties of the skin. In addition, the antimicrobial agent should be non-toxic and environmentally friendly.
  • As previously noted, the alcohol component of the surgical scrub composition is an excellent antimicrobial agent. It also acts as a preservative. However, following application of the surgical scrub composition, the alcohol will evaporate from the skin over time. In the most preferred embodiment, the residue remaining on the skin following alcohol evaporation will include an amount of an antimicrobial agent which also acts as a preservative. Suitable antimicrobial agents which act as preservatives may be selected from the class of phenols including para-chloro-meta-xylenol, bis-biguanides such as chlorhexidine digluconate, chlorhexidine diacetate or quaterium class such as benzethonium chloride, benzalkonium chloride. Chloroxylenol, triclosan, hexachlorophenes, octenidine and quarternary compounds may be included. Hexetidine, germaben II, kathon CG, triclosan are other antimicrobial agents may also be suitable as preservatives. Benzethonium chloride and benalkonium chloride (as hyamine 3500) are available from Lonza Inc., chlorhexidine digluconate is available from Xttrium Laboratories, gennaben II is available from Sutton Laboratories. In a most preferred embodiment, benzethonium chloride, chlorhexidine digluconate (20%) and benzelkonium chloride (80%) are present. Preferably, benzethonium chloride is present in the scrub composition, by weight percent of the entire composition, in an amount from about 0.05% to about 5%, and most preferably, about 0.09%. Preferably, chlorhexidine digluconate (20%) is present in the surgical scrub composition, by weight percent of the entire composition, in an amount from about 0.05% to about 5%, and most preferably about 0.45%. Preferably, benzalkonium chloride (80%) is present in the surgical scrub composition, by weight percent of the entire composition, in an amount from 0 to about 5%, and most preferably, about 0.09%. Preferably, the composition includes about 0% to about 5% of an anti-microbial agent.
  • Methylparaben and propylparaben (both available from Mallinckrodt Chemical Company) are desirably included in the surgical scrub composition as preservatives. These are further desired for their moisturizing and film forming characteristics. Preferably, methylparaben is contained in the surgical scrub composition, by weight percent of the entire composition, in an amount from about 0 to about 5%, and most preferably about 0.03%. Preferably, propylparaben is present in the surgical scrub, by weight percent of the entire composition, in an amount from about 0 to about 5%, and most preferably, about 0.03%. One or both of these compositions are preferably included in the amount of about 0% to about 5% of the surgical scrub composition.
  • To create the desired residual film of the surgical scrub composition, cationic polymer thickening agents are employed. Thickening agents must be soluble in the alcohol and compatible with cationic ingredients. The cationic polymer thickening agents are preferably present in the surgical scrub composition, by weight percent of the entire composition, in the amount of about 0.1% to about 5%.
  • Incroquat behenyl TMS is most preferably used as a cationic polymer. It is a strong conditioning agent and an outstanding cationic emulsifier. This composition bonds to the skin due to the skin's negative charge. Incroquat behenyl TMS is a compound of 25% active solution of behenyl trimonium methosulfate in cetearyl alcohol and is available in flaked/pastel form and supplied by Croda Inc. Incroquat CR concentrate is preferably used as an additional cationic polymer. Incroquat CR concentrate is available from Croda me. and is comprised of cetearyl alcohol, castor oil and stearalkonium chloride. This composition is a one-part formulating aid. It is a conditioner and self-emulsifier. The desired combination of the incroquat behenyl TMS and incroquat CR concentrate provides a smooth feel to the skin and neutralizes the static charge of the human skin. Preferably, incroquat BTMS is present in the surgical scrub composition, by weight percent of the entire composition, in an amount from about 0.1% to about 5%, and most preferably about 0.4%. Preferably, incroquat CR is present in the surgical scrub composition, by weight percent of the entire composition, in an amount from 0 to about 5%, and most preferably about 0.1%.
  • Alternative or additional polymers include cellulose, polyvinylpyrolidone and waxes.
  • The most preferred embodiment of the surgical scrub composition is as follows:
  • % of Total (w/w)
    1-Docosanol 1.00%
    Benzethonium Chloride 0.09%
    Chlorhexidine Digluconate, (20%) 0.45%
    Dimethicone 0.03%
    Ethyl Alcohol 71.00%
    Glycerin 1.40%
    Benzalkonium Chloride 0.09%
    Incroquat BTMS 0.40%
    Incroquat CR 0.10%
    Isopropyl Palmitate 0.40%
    Mineral Oil 0.20%
    Methylparaben 0.03%
    PEG-10 Behenyl Ether 1.50%
    Propylparaben 0.03%
    Purified Water 23.28%
  • The most preferred embodiment includes the additional components 1-Docosanol as a moisturizer and film forming substance, PEG-10 behenyl ether as a moisturizer, fragrance and water. Preferably, 1-Docosanol is present in the surgical scrub composition, by weight percent of the entire composition, in an amount from about 0.1% to about 5%, and most preferably about 1%. Preferably, PEG-10 behenyl ether is present in the surgical scrub composition, by weight percent of the entire composition, in an amount from about 0.1% to about 5%, and most preferably about 1.5%. Preferably, purified water is present in the surgical scrub composition, in an amount from about 1% to about 35%, and most preferably about 23%.
  • The surgical scrub composition does not cause skin irritation or sensitization. Additional advantages of the composition include its compatibility with positive-charged anti-microbial agents such as chlorhexidine digluconate, thus ensuring the effectiveness of the anti-microbial agent or agents. The included skin emollients and lubricants eliminate skin drying or chapping. These compositions counteract the defatting effect of the alcohol.
  • The surgical scrub composition includes anti-microbial agents, which act as both persistent active agents and suitable preservatives. This composition permits a very small amount of an anti-microbial agent to improve anti-microbial activities and provide long-term residual activity for the skin.
  • Traditionally, healthcare workers have scrubbed prior to every surgical procedure. An improved method may be to apply water to the skin, perform hand scrubbing at the beginning of the day using a scrub brush and anti-microbial scrub solution, rinsing the anti-microbial scrub solution with water, and then utilization of the composition of the present invention prior to subsequent surgical procedures. A high level of hand antisepsis can be achieved via this method without abrasive scrubbing multiple times a day.
  • EXAMPLES
  • The following examples are not intended to limit the scope of the invention, but are only intended to be exemplary in nature.
  • Standard testing of the most preferred embodiment demonstrates its effectiveness as an antiseptic to provide an immediate reduction of microbes and then to prevent microbial growth back to baseline within a 6-hour period. The immediate log reduction was 2.65 on day 1, 2.92 on day 2 and 3.04 on day 3. The residual effect was a log reduction six hours after hand cleaning of 1.45 on day 1, 1.79 on day 2 and 2. 18 on day 3. The residual anti-microbial activity is facilitated by the containment of the anti-microbial agent in the polymer film that is formed. The film forms an invisible “glove” containing an anti-microbial agent. The anti-microbial agent remains on the skin in the film and continues to be bactericidal over extended periods of time. The invisible glove prevents microbes that may be present on the hands of the healthcare worker from infecting a patient and the glove also provides a barrier for microbes infecting the healthcare worker from the patient.
  • Through testing, the composition has been shown to exceed industry standards. The critical indices for this study were an immediate one (1) log10 reduction in microorganisms on Day 1; an immediate two (2) log10 reduction in microorganisms on Day 2; an immediate three (3) log10 reduction in microorganisms on Day 5; and that microorganism populations from the approximately three (3) hour to three (3) hour and thirty (30) minute AND approximately six (6) hour to six (6) hour and thirty (30) minute samples not return to baseline level. Refer to Table I.
  • TABLE I
    Statistical Summary of the Log10 Recovery
    Values of Most Preferred Embodiment
    Stan- Log10 TFM (1994)
    Sam- dard 95% Reduction Required
    ple Devi- Confidence from Log10
    Sample Size Mean ation Interval Baseline Reduction
    Baseline 36 6.01 0.40 5.88 to N/A
    6.15
    Day 1, 12 3.36 0.68 2.93 to 2.65 1
    Immediate 3.79
    Day 1, 3 12 4.08 0.99 3.45 to 1.93 No return to
    Hour 4.71 baseline
    Day
    1, 6 12 4.56 0.68 4.13 to 1.45 No return to
    Hour 4.99 baseline
    Day
    2, 11 3.09 0.53 2.74 to 2.92 2
    Immediate 3.45
    Day 2, 3 11 3.73 0.90 3.12 to 2.28 No return to
    Hour 4.34 baseline
    Day
    2, 6 12 4.22 0.81 3.70 to 1.79 No return to
    Hour 4.73 baseline
    Day
    5, 10 2.97 0.47 2.63 to 3.04 3
    Immediate 3.31
    Day 5, 3 11 3.50 0.61 3.09 to 2.51 No return to
    Hour 3.91 baseline
    Day
    5, 6 11 3.83 1.01 3.15 to 2.18 No return to
    Hour 4.51 baseline
  • The most preferred embodiment was also tested in conjunction with a standard hand scrub utilizing a brush impregnated with an anti-microbial agent. The composition was applied to the hands of the test subject one-half hour following the standard scrub. Test results showed an increased log reduction of microbes when the scrubbing and the preferred composition were used together. Log reductions of microbes were 3.66 for Day 1, 3.98 for Day 2, and 3.70 for Day 3. Use of the preferred composition in conjunction with a standard scrub exceeded industry standards for anti-microbial compositions. Refer to Table II and FIG. 1.
  • TABLE II
    Statistical Summary of the Log10 Recovery Values Using BD E-Z Scrub
    Catalog #371073 Plus Most Preferred Embodiment Sample
    Stan- Log10 TFM (1994)
    Sam- dard 95% Reduction Required
    ple Devi- Confidence from Log10
    Sample Size Mean ation Interval Baseline Reduction
    Baseline 38 6.10 0.38 5.97 to N/A
    6.22
    Day 1, 12 2.88 0.46 2.15 to 3.66 1
    Immediate 2.73
    Day 1, 3 13 3.13 0.79 2.65 to 2.97 No return
    Hour 3.60 baseline
    Day
    1, 6 13 3.79 0.88 3.26 to 2.31
    Hour 4.32
    Day 2, 12 2.12 0.35 1.90 to 3.98 2
    Immediate 2.34
    Day 2, 3 12 2.58 0.93 1.99 to 3.52 No return
    Hour 3.17 baseline
    Day
    2, 6 12 2.58 0.66 2.16 to 3.52
    Hour 3.00
    Day 5, 10 2.29 0.37 2.02 to 3.81 3
    Immediate 2.55
    Day 5, 3 10 2.28 0.32 2.05 to 3.82 No return
    Hour 2.51 baseline
    Day
    5, 6 12 2.40 0.49 2.09 to 3.70
    Hour 2.71

Claims (19)

1. A surgical scrub composition comprising:
(a) an alcohol;
(b) a cationic anti-microbial agent;
(c) a skin emollient; and
(d) a film-forming cationic polymer system.
2. The surgical scrub composition of claim 1, further comprising a silicone.
3. The surgical scrub composition of claim 2, wherein the silicone includes one or more of the group of dimethicone copolyol, cyclomethicone and dimethicone.
4. The surgical scrub composition of claim 1, further comprising one or more of the group of methylparaben and propylparaben.
5. The surgical scrub composition of claim 1, wherein the anti-microbial agent is one or more of the group including chlorhexidine digluconate, chloroxylenol, parachloro-meta-xylenol, chlorhexidine diacetate, benzethonium chloride, benzalkonium chloride, hexetidine, germaben II, kathon CG, triclosan, hexachlorophenes, octenidine, and quaternary compounds.
6. The anti-microbial composition of claim 1, wherein the polymer system includes one or more of the group including incroquat behenyl TMS, incroquat CR concentrate, cellulose, polyvinylpyrolidone and waxes.
7. A method of disinfecting the skin comprising:
(a) applying prior to surgical procedures an effective amount of a surgical scrub composition including:
i. an alcohol;
ii. a cationic anti-microbial agent;
iii. a skin emollient;
iv. a film-forming cationic polymer system; and
(b) rubbing the skin with the composition until the alcohol has evaporated.
8. A method of using a surgical scrub composition for hand antisepsis comprising:
(a) applying a cleansing liquid to skin;
(b) scrubbing the skin with an anti-microbial scrub solution;
(c) rinsing the anti-microbial scrub solution from the skin; and
(d) applying an effective amount of a surgical scrub composition according to claim 1.
9. The method of claim 8, wherein the surgical scrub composition includes:
the alcohol in an amount from about 60 to about 95 weight percent of the total composition;
the cationic anti-microbial agent in an amount from about 0.1 to about 5 weight percent of the total composition;
the skin emollient in an amount from about 0.1 to about 5 weight percent of the total composition; and
the film-forming cationic polymer system in amount from about 0.1 to about 5 weight percent of the total composition.
10. The method of claim 9, wherein the surgical scrub composition includes a silicone in an amount from about 0.1 to about 5 weight percent of the total composition.
11. The method of claim 8, wherein the film-forming polymer system includes one or more of the group including incroquat behenyl TMS, incroquat CR concentrate, cellulose, polyvinylpyrolidone and waxes.
12. The method of claim 8, wherein the effective amount is 20 cc.
13. A surgical scrub composition comprising:
(a) one or more alcohols in an amount from about 60 to about 95 weight percent of the total composition;
(b) one or more film-forming cationic polymers in an amount from about 0.1 to about 5 weight percent of the total composition;
(c) one or more cationic anti-microbial agents in an amount from about 0.1 to about 5 weight percent of the total composition; and
(d) one or more skin emollients in an amount from about 0.1 to about 5 weight percent of the total composition.
14. The surgical scrub composition of claim 13, further comprising from about 0.01 to about 5 weight percent of a silicone.
15. (canceled)
16. A surgical scrub composition comprising:
(a) a preservative;
(b) chlorhexidine digluconate;
(c) a film-forming system including at least one of the group containing glycerin, methylparaben or propylparaben;
(d) alcohol; and
(e) water.
17. A surgical scrub composition comprising:
(a) one or more alcohols selected from the group of ethyl alcohol, isopropyl alcohol, ethanol and n-propanol;
(b) one or more cationic anti-microbial agents selected from the group of chlorhexidine digluconate, chloroxylenol, para-chloro-meta-xylenol, chlorhexidine diacetate, benzethonium chloride, benzalkonium chloride, hexetidine, germaben II, kathon CG, triclosan, hexachlorophenes, octenidine and quaternary compounds;
(c) a skin emollient; and
(d) a film-forming cationic polymer system including one or more selected from the group of incroquat behenyl TMS, incroquat CR concentrate, cellulose, polyvinylpyrolidone, waxes, behenyl trimonium methosulfate containing compounds and stearalkonium chloride containing compounds.
18. The surgical scrub composition of claim 17, further comprising a silicone.
19. The surgical scrub composition of claim 17, further comprising one or more of methylparaben or propylparaben.
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Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20110030726A1 (en) * 2007-04-02 2011-02-10 C. R. Bard, Inc. Insert for a microbial scrubbing device
US20110152925A1 (en) * 2009-12-22 2011-06-23 Schorr Phillip A Skin Preparation That Immobilizes Bacteria
US8065773B2 (en) 2007-04-02 2011-11-29 Bard Access Systems, Inc. Microbial scrub brush
US8069523B2 (en) 2008-10-02 2011-12-06 Bard Access Systems, Inc. Site scrub brush
US8336151B2 (en) 2007-04-02 2012-12-25 C. R. Bard, Inc. Microbial scrubbing device
US8696820B2 (en) 2008-03-31 2014-04-15 Bard Access Systems, Inc. Method of removing a biofilm from a surface
US9192449B2 (en) 2007-04-02 2015-11-24 C. R. Bard, Inc. Medical component scrubbing device with detachable cap

Families Citing this family (55)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US8512718B2 (en) 2000-07-03 2013-08-20 Foamix Ltd. Pharmaceutical composition for topical application
IL152486A0 (en) 2002-10-25 2003-05-29 Meir Eini Alcohol-free cosmetic and pharmaceutical foam carrier
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US7820145B2 (en) 2003-08-04 2010-10-26 Foamix Ltd. Oleaginous pharmaceutical and cosmetic foam
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US7704518B2 (en) 2003-08-04 2010-04-27 Foamix, Ltd. Foamable vehicle and pharmaceutical compositions thereof
US8900554B2 (en) 2002-10-25 2014-12-02 Foamix Pharmaceuticals Ltd. Foamable composition and uses thereof
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US20080138296A1 (en) 2002-10-25 2008-06-12 Foamix Ltd. Foam prepared from nanoemulsions and uses
US8486376B2 (en) 2002-10-25 2013-07-16 Foamix Ltd. Moisturizing foam containing lanolin
US7488757B2 (en) * 2003-03-24 2009-02-10 Becton, Dickinson And Company Invisible antimicrobial glove and hand antiseptic
US7575739B2 (en) 2003-04-28 2009-08-18 Foamix Ltd. Foamable iodine composition
US8486374B2 (en) 2003-08-04 2013-07-16 Foamix Ltd. Hydrophilic, non-aqueous pharmaceutical carriers and compositions and uses
US8795693B2 (en) 2003-08-04 2014-08-05 Foamix Ltd. Compositions with modulating agents
CA2560138A1 (en) * 2006-09-19 2008-03-19 Professional Artists International Inc. Methods for disinfectant and sanitizing cosmetics
KR101129868B1 (en) * 2006-10-04 2012-04-12 화이자 프로덕츠 인코포레이티드 Pyrido[4,3-d]pyrimidin-43h-one derivatives as calcium receptor antagonists
US20080260655A1 (en) 2006-11-14 2008-10-23 Dov Tamarkin Substantially non-aqueous foamable petrolatum based pharmaceutical and cosmetic compositions and their uses
US8636982B2 (en) 2007-08-07 2014-01-28 Foamix Ltd. Wax foamable vehicle and pharmaceutical compositions thereof
US20090068288A1 (en) * 2007-09-07 2009-03-12 Wayne Kruger Topical antiseptic veterinary solution
US9439857B2 (en) 2007-11-30 2016-09-13 Foamix Pharmaceuticals Ltd. Foam containing benzoyl peroxide
WO2010041141A2 (en) 2008-10-07 2010-04-15 Foamix Ltd. Oil-based foamable carriers and formulations
WO2009072007A2 (en) 2007-12-07 2009-06-11 Foamix Ltd. Carriers, formulations, methods for formulating unstable active agents for external application and uses thereof
CA2712120A1 (en) 2008-01-14 2009-07-23 Foamix Ltd. Poloxamer foamable pharmaceutical compositions with active agents and/or therapeutic cells and uses
US9381150B2 (en) 2008-03-07 2016-07-05 Kimberly-Clark Worldwide, Inc. Alcohol antimicrobial skin sanitizing compositions including cationic compatible thickeners
GB0822059D0 (en) * 2008-12-03 2009-01-07 Reckitt & Colman Overseas Germicidal topical compositions
US10314935B2 (en) 2009-01-07 2019-06-11 Entrotech Life Sciences, Inc. Chlorhexidine-containing antimicrobial laminates
WO2010125470A2 (en) 2009-04-28 2010-11-04 Foamix Ltd. Foamable vehicle and pharmaceutical compositions comprising aprotic polar solvents and uses thereof
WO2011013009A2 (en) 2009-07-29 2011-02-03 Foamix Ltd. Non surfactant hydro-alcoholic foamable compositions, breakable foams and their uses
WO2011013008A2 (en) 2009-07-29 2011-02-03 Foamix Ltd. Non surface active agent non polymeric agent hydro-alcoholic foamable compositions, breakable foams and their uses
CN102665734A (en) * 2009-09-25 2012-09-12 法马索尔有限公司 Surface coatings for skin
US9849142B2 (en) 2009-10-02 2017-12-26 Foamix Pharmaceuticals Ltd. Methods for accelerated return of skin integrity and for the treatment of impetigo
WO2011064631A1 (en) 2009-10-02 2011-06-03 Foamix Ltd. Surfactant-free, water-free, foamable compositions and breakable foams and their uses
US8174881B2 (en) 2009-11-24 2012-05-08 Micron Technology, Inc. Techniques for reducing disturbance in a semiconductor device
AU2011342791B2 (en) 2010-12-14 2016-05-26 Ecolab Usa Inc. Wear resistant antimicrobial compositions and methods of use
WO2012104718A2 (en) 2011-02-04 2012-08-09 Fridolin Voegeli "antinfection" protecting healthcare workers to prevent spreading of communicable and nosocomial infections
AU2012273699A1 (en) * 2011-06-20 2013-11-07 Reckitt & Colman (Overseas) Limited Foaming topical antimicrobial cleaning compositions
US8932664B2 (en) * 2011-10-13 2015-01-13 Bradley P Bengtson Surgical finger, hand and arm barrier coating and covering, method and system
US8481480B1 (en) 2012-04-30 2013-07-09 Uyen T. Lam Anti-adherent formulation including a quaternary ammonium compound and a fatty alcohol
US9821066B2 (en) 2013-03-15 2017-11-21 Carefusion 2200, Inc. Tinted antiseptic solutions having improved stability
US11039615B2 (en) 2014-04-18 2021-06-22 Entrotech Life Sciences, Inc. Methods of processing chlorhexidine-containing polymerizable compositions and antimicrobial articles formed thereby
EP2944565B1 (en) 2014-05-13 2017-09-27 Entrotech, Inc. Erosion protective sleeve
US10925281B2 (en) 2014-11-26 2021-02-23 Microban Products Company Surface disinfectant with residual biocidal property
US10834922B2 (en) 2014-11-26 2020-11-17 Microban Products Company Surface disinfectant with residual biocidal property
US11033023B2 (en) 2014-11-26 2021-06-15 Microban Products Company Surface disinfectant with residual biocidal property
US10842147B2 (en) 2014-11-26 2020-11-24 Microban Products Company Surface disinfectant with residual biocidal property
US11503824B2 (en) 2016-05-23 2022-11-22 Microban Products Company Touch screen cleaning and protectant composition
MX2020012139A (en) 2016-09-08 2021-01-29 Vyne Pharmaceuticals Inc Compositions and methods for treating rosacea and acne.
US20220304939A1 (en) * 2019-06-20 2022-09-29 3M Innovative Properties Company Antimicrobial wipes
ES2784275B2 (en) * 2020-04-24 2021-04-15 Univ Madrid Complutense Long-acting antiseptic for hygienic scrubbing and pre-surgical hand washing
GB2587894B (en) * 2020-07-17 2021-12-01 Kaur Matharu Navjeet Topical sanitisation composition

Citations (57)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2005101A (en) * 1934-09-26 1935-06-18 Herberts Machinery Co Ltd Lathe
US4009714A (en) * 1975-07-30 1977-03-01 Johnson & Johnson Intravenous solution filter unit
US4066556A (en) * 1976-10-28 1978-01-03 Johnson & Johnson Fluid filter and method of making same
US4294594A (en) * 1979-10-02 1981-10-13 United States Surgical Corporation Self-contained filter assembly for removing air, particles and bacteria from a solution
US4309992A (en) * 1980-07-11 1982-01-12 Dodak Michael J Microbicidal filter
US4311587A (en) * 1979-12-10 1982-01-19 Japan Foundation For Artificial Organs Filter arrangement denying bacteria entry to peritoneum
US4374126A (en) * 1981-02-23 1983-02-15 Warner-Lambert Company Film forming antimicrobial material
US4416772A (en) * 1980-08-04 1983-11-22 Kuraray Co., Ltd. Apparatus for concentrating and filtering body cavity fluids
US4560382A (en) * 1983-08-15 1985-12-24 Terumo Corporation Medical container
US4568366A (en) * 1983-08-30 1986-02-04 Baxter Laboratories, Inc. In-line filter
US4678606A (en) * 1984-07-03 1987-07-07 The Procter & Gamble Company Liquid cleansing composition
US4695382A (en) * 1985-11-18 1987-09-22 Microgon, Inc. Combined fluid filter and delivery tubing
US4702829A (en) * 1984-12-07 1987-10-27 Fresenius Ag Hemodiafiltration apparatus
US4714556A (en) * 1981-06-29 1987-12-22 Ambrus Clara M Blood purification
US4738668A (en) * 1981-07-29 1988-04-19 Baxter Travenol Laboratories, Inc. Conduit connectors having antiseptic application means
US4787974A (en) * 1981-06-29 1988-11-29 Ambrus Clara M Blood purification
US4861485A (en) * 1988-01-22 1989-08-29 W. R. Grace & Co. Hemodiafiltration device
US4895566A (en) * 1986-07-25 1990-01-23 C. R. Bard, Inc. Coating medical devices with cationic antibiotics
US5053339A (en) * 1988-11-03 1991-10-01 J P Labs Inc. Color changing device for monitoring shelf-life of perishable products
US5093235A (en) * 1989-09-29 1992-03-03 The United States Of America As Represented By The Secretary Of The Navy Immuno-dye reagent and assay for detection of endotoxin
US5217493A (en) * 1992-03-11 1993-06-08 Board Of Regents, The University Of Texas System Antibacterial coated medical implants
US5252222A (en) * 1990-12-03 1993-10-12 Pall Corporation Filter for parenteral systems and method of using thereof
US5312813A (en) * 1991-05-03 1994-05-17 University Technologies International Biofilm reduction method
US5366505A (en) * 1991-12-06 1994-11-22 North Shore University Hospital Research Corporation Method of reducing medical device related infections
US5512199A (en) * 1993-11-02 1996-04-30 Becton Dickinson And Company Hand wipe solution
US5530102A (en) * 1993-01-12 1996-06-25 Gristina; Anthony G. Methods and compositions for the direct concentrated delivery of passive immunity
US5951993A (en) * 1995-06-22 1999-09-14 Minnesota Mining And Manufacturing Company Stable hydroalcoholic compositions
US20020006974A1 (en) * 1996-09-19 2002-01-17 Lucas Patrick J. Stable, foamed caulk and sealant compounds and methods of use thereof
US20020009561A1 (en) * 1998-08-15 2002-01-24 William Joseph Weikel Lubricated elastomeric article
US20020048592A1 (en) * 1997-06-20 2002-04-25 Sabine Eggers Skin-protective composition
US20030152644A1 (en) * 2001-10-23 2003-08-14 Shanta Modak Gentle-acting skin-disinfectants
US20040058878A1 (en) * 2002-01-18 2004-03-25 Walker Edward B. Antimicrobial and sporicidal composition
US20050059731A1 (en) * 2003-09-16 2005-03-17 Ceramoptec Industries, Inc. Erythrosin-based antimicrobial photodynamic therapy compound and its use
US20050085777A1 (en) * 2003-10-15 2005-04-21 Tan Sharon M.L. Medical device having anti-microbial properties and a false lumen and method of making the same
US20050085775A1 (en) * 2002-02-14 2005-04-21 Ishay Ostfeld Indwelling device
US20050090785A1 (en) * 2003-10-22 2005-04-28 Tan Sharon M.L. Catheter with a sidearm for delivery of antimicrobial agents to prevent infection
US20050095351A1 (en) * 2003-05-29 2005-05-05 Jona Zumeris Method, apparatus and system for nanovibration coating and biofilm prevention associated with medical devices
US20050100937A1 (en) * 2003-09-11 2005-05-12 Holmes Elizabeth A. Medical device for analyte monitoring and drug delivery
US20050118239A1 (en) * 2003-08-18 2005-06-02 Subramaniam Sabesan Process for making antimicrobial articles by reacting chitosan with amino-reactive polymer surfaces
US20050124678A1 (en) * 2001-05-04 2005-06-09 Paratek Pharmaceuticals, Inc. Transcription factor modulating compounds and methods of use thereof
US20050131356A1 (en) * 2002-03-14 2005-06-16 Ash Stephen R. Medical devices exhibiting antibacterial properties
US20050131332A1 (en) * 2003-11-05 2005-06-16 Thomas Kelly High convection home hemodialysis/hemofiltration and sorbent system
US20050137536A1 (en) * 2001-09-28 2005-06-23 Gonnelli Robert R. Microneedle with membrane
US20050143286A1 (en) * 2002-04-18 2005-06-30 The University Of Iowa Research Foundation Methods of inhibiting and treating bacterial biofilms by metal chelators
US20050142622A1 (en) * 2002-01-31 2005-06-30 Sanders Mitchell C. Method for detecting microorganisms
US20050154448A1 (en) * 1999-01-22 2005-07-14 Gore Enterprise Holdings, Inc. Biliary stent-graft
US20050158253A1 (en) * 1997-10-16 2005-07-21 Pharmacal Biotechnologies, Llc. Compositions for treating biofilm
US20050161859A1 (en) * 2002-02-08 2005-07-28 Miller Kathleen M. Implantable or insertable medical device resistant to microbial growth and biofilm formation
US20050171501A1 (en) * 2004-02-03 2005-08-04 Thomas Kelly Intravenous solution producing systems and methods
US20050192590A1 (en) * 2004-02-26 2005-09-01 Kristin Feeley Antimicrobial agent delivery system
US20050199245A1 (en) * 2001-11-02 2005-09-15 Brennan H. G. Nose airway for aromatherapy and detecting airborne pathogens
US20050209547A1 (en) * 2002-06-06 2005-09-22 Burbank Jeffrey H Last-chance quality check and/or air/pathogen filter for infusion systems
US20050221072A1 (en) * 2003-04-17 2005-10-06 Nanosys, Inc. Medical device applications of nanostructured surfaces
US20050220837A1 (en) * 2003-09-30 2005-10-06 Disegi John A Antimicrobial hyaluronic acid coatings for orthopedic implants
US20050233950A1 (en) * 2004-04-01 2005-10-20 Srinivasa Madhyastha Synergistic antimicrobial compositions and methods for reducing biofilm formation
US20050256502A1 (en) * 2003-05-13 2005-11-17 Dimatteo Kristian Anti-infective central venous catheter with diffusion barrier layer
US7488757B2 (en) * 2003-03-24 2009-02-10 Becton, Dickinson And Company Invisible antimicrobial glove and hand antiseptic

Family Cites Families (106)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
BR9206408A (en) 1991-08-23 1994-11-22 Gillette Canada Oral brush, extended release matrix, process for releasing an antimicrobial agent from an oral brush and for releasing an antimicrobial agent in an animal's mouth and an oral wear indicator brush
US5906834A (en) 1992-06-15 1999-05-25 The Gillette Company Color changing matrix as wear indicator
US6048337A (en) 1992-01-07 2000-04-11 Principal Ab Transdermal perfusion of fluids
US6395561B1 (en) 1992-11-13 2002-05-28 Regents Of The University Of California Polymeric assay film for direct colorimetric detection
US6306598B1 (en) 1992-11-13 2001-10-23 Regents Of The University Of California Nucleic acid-coupled colorimetric analyte detectors
US6660484B2 (en) 1992-11-13 2003-12-09 Regents Of The University Of California Colorimetric glycopolythiophene biosensors
US6022748A (en) 1997-08-29 2000-02-08 Sandia Corporation - New Mexico Regents Of The University Of California Sol-gel matrices for direct colorimetric detection of analytes
US6180135B1 (en) 1994-08-11 2001-01-30 The Regents Of The University Of California Three-dimensional colorimetric assay assemblies
EP1258262A3 (en) 1993-10-28 2002-12-18 Medrad, Inc. Total system for contrast delivery
US5788687A (en) 1994-02-01 1998-08-04 Caphco, Inc Compositions and devices for controlled release of active ingredients
US5554147A (en) 1994-02-01 1996-09-10 Caphco, Inc. Compositions and devices for controlled release of active ingredients
JP2691510B2 (en) 1994-06-02 1997-12-17 株式会社バイオセンサー研究所 Enzyme measuring device
US6468649B1 (en) 1995-02-22 2002-10-22 Scimed Life Systems, Inc. Antimicrobial adhesion surface
GB9516658D0 (en) 1995-08-15 1995-10-18 Smiths Industries Plc Medico-surgical devices
US5645824A (en) 1995-10-02 1997-07-08 Lim; Min H. Color changing reagent composition for coating on needles used in medical applications
US5855896A (en) 1995-10-02 1999-01-05 Lim; Min H. Color changing composition and method for coating said composition on acupuncture needles, hypodermic syringes and other needles used in medical applications
US6171496B1 (en) 1995-12-15 2001-01-09 Microban Products Company Antimicrobial filter cartridge
AU705101B2 (en) 1996-02-15 1999-05-13 Interface Biologics Inc. Bioresponsive pharmacologically-active polymers and articles made therefrom
US6132765A (en) 1996-04-12 2000-10-17 Uroteq Inc. Drug delivery via therapeutic hydrogels
WO1997041901A1 (en) 1996-05-03 1997-11-13 Uros Corporation Pentosanpolysulfate coating for medical devices
EP0824921A1 (en) 1996-08-20 1998-02-25 Smiths Industries Public Limited Company Medical filter
US6017334A (en) 1996-10-03 2000-01-25 Board Of Regents, The University Of Texas System Modified surfaces resistant to bacterial colonization
US6153187A (en) * 1997-09-02 2000-11-28 Insight Strategy & Marketing Ltd. Use of glycosaminoglycans degrading enzymes for management of airway associated diseases
US20020037260A1 (en) * 1997-10-16 2002-03-28 Budny John A. Compositions for treating biofilm
JP3138442B2 (en) 1997-12-26 2001-02-26 株式会社ホギメディカル Color sensor using polydiacetylene film
US6022551A (en) * 1998-01-20 2000-02-08 Ethicon, Inc. Antimicrobial composition
DE69940723D1 (en) 1998-02-12 2009-05-28 Surfacine Dev Co DISINFECTION COMPOSITIONS WITH DELAYED BIOCIDAL ACTIVITY RELEASE
US6399853B1 (en) 1998-06-29 2002-06-04 The Proctor & Gamble Company Disposable article having fecal component sensor
US6093869A (en) * 1998-06-29 2000-07-25 The Procter & Gamble Company Disposable article having a responsive system including a feedback control loop
ES2258335T3 (en) 1998-06-29 2006-08-16 Microban Products Company SEMIPERMEABLES ANTIMICROBIAL MEMBRANES.
US8187278B2 (en) * 1998-08-25 2012-05-29 Advanced Photodynamic Technologies, Inc. Photodynamic cellular and acellular organism eradication utilizing a photosensitive material and benzalkonium chloride
US6758971B1 (en) 1998-08-28 2004-07-06 Sorenson Development, Inc. Self-priming dialysis filter
JP2000107286A (en) 1998-10-07 2000-04-18 Akira Sakai Perfusion apparatus for peritoneal dialyzate and perfusion method
US6475434B1 (en) 1998-12-07 2002-11-05 Baylor College Of Medicine Composition and methods for preventing and removing biofilm embedded microorganisms from the surface of medical devices
US6106287A (en) 1998-12-11 2000-08-22 Yates; Davis Filter system for coupling of a dental handpiece
US6605214B1 (en) 1999-03-03 2003-08-12 Prismedical Corporation Devices for preparing hemodialysis solutions
US6274103B1 (en) 1999-03-26 2001-08-14 Prismedical Corporation Apparatus and method for preparation of a peritoneal dialysis solution
US6159007A (en) 1999-03-15 2000-12-12 Sorensen; Jerold R. Autoclaveable dental unit water line and pre-filter
US6224579B1 (en) 1999-03-31 2001-05-01 The Trustees Of Columbia University In The City Of New York Triclosan and silver compound containing medical devices
US6783713B2 (en) 1999-05-03 2004-08-31 The Procter & Gamble Co. Filters for removal of pathogens from liquids
US6107261A (en) 1999-06-23 2000-08-22 The Dial Corporation Compositions containing a high percent saturation concentration of antibacterial agent
US6501002B1 (en) 1999-06-29 2002-12-31 The Proctor & Gamble Company Disposable surface wipe article having a waste contamination sensor
US6479727B1 (en) 1999-06-29 2002-11-12 Donald C. Roe Diagnostic panel
US6562295B1 (en) 1999-06-30 2003-05-13 Ceramoptec Industries, Inc. Bacteria resistant medical devices
US6350253B1 (en) * 1999-07-19 2002-02-26 I-Flow Corporation Catheter for uniform delivery of medication
US6471689B1 (en) 1999-08-16 2002-10-29 Thomas Jefferson University Implantable drug delivery catheter system with capillary interface
IL131623A0 (en) * 1999-08-27 2001-01-28 Dan Weiss Apparatus to couple ultrasonic energy to catheters and other transdermal medical devices
US6282444B1 (en) 1999-08-31 2001-08-28 Pacesetter, Inc. Implantable device with electrical infection control
US6423219B1 (en) 1999-09-14 2002-07-23 James W. Chandler System and method for controlling microorganisms and biofilms
US6259074B1 (en) 1999-10-26 2001-07-10 Sims Level 1, Inc. Apparatus for regulating the temperature of a fluid
US6257265B1 (en) 1999-10-26 2001-07-10 Sims Level 1 Inc. Apparatus for connecting a heat exchanger with a fluid temperature regulation device
US20020015716A1 (en) * 1999-12-13 2002-02-07 Hanuman B. Jampani Novel skin disinfection procedures
US6579539B2 (en) 1999-12-22 2003-06-17 C. R. Bard, Inc. Dual mode antimicrobial compositions
JP2003527167A (en) 1999-12-23 2003-09-16 メムブラーナ ゲゼルシャフト ミット ベシュレンクテル ハフツング Hemodiafiltration system
US20020009436A1 (en) 1999-12-30 2002-01-24 Doyle Ron J. Methods and compositions for inhibiting adhesion by microorganisms
US6350251B1 (en) 2000-01-18 2002-02-26 Biolink Corporation Biocidal locks
US6436885B2 (en) * 2000-01-20 2002-08-20 The Procter & Gamble Company Antimicrobial cleansing compositions containing 2-pyrrolidone-5-carboxylic acid
US20020066702A1 (en) * 2000-02-22 2002-06-06 Jinfang Liu Antibacterial and antibiofilm bonded permanent magnets
ES2420279T3 (en) 2000-03-02 2013-08-23 Microchips, Inc. Microfabricated devices and methods for storage and selective exposure of chemicals
EP1279023B1 (en) * 2000-03-20 2007-02-21 Analytical Biological Services, Inc. Method for detecting an analyte by fluorescence
AUPQ681200A0 (en) * 2000-04-10 2000-05-11 Unisearch Limited Antimicrobial coatings
US6596505B2 (en) 2000-04-17 2003-07-22 University Technologies International, Inc. Apparatus and methods for testing effects of materials and surface coatings on the formation of biofilms
US6599696B2 (en) * 2000-04-17 2003-07-29 University Technologies International, Inc. Effects of materials and surface coatings on encrustation and biofilm formation
JP2003532698A (en) * 2000-05-10 2003-11-05 プリンストン ユニバーシティ Compounds and methods for regulating bacterial growth and pathogenesis
US6719991B2 (en) 2000-06-09 2004-04-13 Baylor College Of Medicine Combination of antimicrobial agents and bacterial interference to coat medical devices
WO2001098214A1 (en) * 2000-06-19 2001-12-27 Novozymes Biotech, Inc. Methods for eliminating the formation of biofilm
EP1301571A2 (en) * 2000-07-17 2003-04-16 President And Fellows of Harvard College Surfaces that resist the adsorption of biological species
WO2002015897A2 (en) * 2000-08-25 2002-02-28 Microbia, Inc. Use of sublethal concentrations of anti-invasin compounds to therapeutically or prophylactically treat fungal infections
US6866859B2 (en) * 2000-08-30 2005-03-15 Biocoat Incorporated Bi-laminar, hyaluronan coatings with silver-based anti-microbial properties
US6391001B1 (en) 2000-09-21 2002-05-21 Jolie Graham Intravenous line flushing device
AU2002227111A1 (en) 2000-10-30 2002-05-15 Nephros, Inc. Dual-stage filtration cartridge
US6814085B2 (en) 2000-12-29 2004-11-09 Steven J. Brattesani Dental floss with usage identification capability
US6835713B2 (en) 2001-02-16 2004-12-28 University Of Pittsburgh Virus derived antimicrobial peptides
EP1399193B1 (en) 2001-02-16 2014-01-08 Piedmont Renal Clinics, P.A. Automated peritoneal dialysis system and process with in-line sterilization of dialysate
US6887847B2 (en) 2001-02-16 2005-05-03 University Of Pittsburgh Virus derived antimicrobial peptides
WO2002085386A2 (en) 2001-04-23 2002-10-31 Nucryst Pharmaceuticals Corp. Medicament containing a metal such as silver, gold, platinum or palladium as an antimicrobial agent and their use to induce apoptosis in cancerous tissue
EP1524974A4 (en) * 2001-05-04 2007-12-05 Paratek Pharm Innc Transcription factor modulating compounds and methods of use thereof
DE10221569A1 (en) * 2001-05-11 2002-11-21 Poly An Ges Zur Herstellung Vo Reducing adsorption of molecules or cells from solution or suspension onto the surface of (in)organic materials comprises modifying the surface by in-situ polymerization of selected monomers
US20050010158A1 (en) * 2001-05-24 2005-01-13 Brugger James M. Drop-in blood treatment cartridge with filter
US20030065292A1 (en) * 2001-06-08 2003-04-03 Darouiche Rabih O. Ozonated medical devices and methods of using ozone to prevent complications from indwelling medical devices
DE60211339D1 (en) 2001-06-22 2006-06-14 Argonide Corp SUBMICRON FILTER
US6844028B2 (en) 2001-06-26 2005-01-18 Accelr8 Technology Corporation Functional surface coating
US6921390B2 (en) 2001-07-23 2005-07-26 Boston Scientific Scimed, Inc. Long-term indwelling medical devices containing slow-releasing antimicrobial agents and having a surfactant surface
US20030134783A1 (en) * 2001-07-31 2003-07-17 Harshey Rasika M. Use of cyclic heptapeptides for the inhibition of biofilm formation
US6699391B2 (en) 2001-09-07 2004-03-02 Advanced Biocatalytics Corporation Biofilm reduction in crossflow filtration systems
WO2003039529A1 (en) * 2001-11-07 2003-05-15 4Sc A.G. Selective antibacterial agents
CN1301751C (en) * 2002-01-22 2007-02-28 法玛西雅厄普约翰美国公司 Infection-resistant medical devices
US7993390B2 (en) * 2002-02-08 2011-08-09 Boston Scientific Scimed, Inc. Implantable or insertable medical device resistant to microbial growth and biofilm formation
US7338969B2 (en) * 2002-03-08 2008-03-04 Quonova, Llc Modulation of pathogenicity
CA2476288A1 (en) * 2002-03-26 2003-10-09 Biosynexus Incorporated Enzyme disruption of bacterial biofilms
US6787108B2 (en) * 2002-04-02 2004-09-07 Cmc Daymark Corporation Plural intrinsic expiration initiation application indicators
US6800200B2 (en) 2002-04-18 2004-10-05 Cuno Incorporated Dual-flow filter cartridge
US7393501B2 (en) * 2002-05-29 2008-07-01 Nano Vibronix Inc Method, apparatus and system for treating biofilms associated with catheters
US6803363B2 (en) 2002-05-31 2004-10-12 Nd Partners, Llc Peritoneal dialysis solution with taurolidine
US7183455B2 (en) * 2002-08-27 2007-02-27 Drdc Limited Adhesive dressing
US7452345B2 (en) * 2002-09-17 2008-11-18 Baylor College Of Medicine Anti-infective endotracheal tube
US7637942B2 (en) * 2002-11-05 2009-12-29 Merit Medical Systems, Inc. Coated stent with geometry determinated functionality and method of making the same
US7597903B2 (en) * 2002-12-02 2009-10-06 Shenkar College Of Engineering And Design Method and composition for producing catheters with antibacterial property
US20040126897A1 (en) * 2002-12-19 2004-07-01 3M Innovative Properties Company Colorimetric sensors constructed of diacetylene materials
US6723689B1 (en) * 2003-01-08 2004-04-20 Becton Dickinson And Company Emollient alcohol skin disinfecting formulation
US20050038498A1 (en) * 2003-04-17 2005-02-17 Nanosys, Inc. Medical device applications of nanostructured surfaces
US7195615B2 (en) * 2003-05-14 2007-03-27 Boston Scientific Scimed, Inc. System for providing a medical device with anti-microbial properties
US20040254545A1 (en) * 2003-06-16 2004-12-16 Rider Dean Loller Method and apparatus for extending feeding tube longevity
US8454566B2 (en) * 2003-07-10 2013-06-04 Medtronic Minimed, Inc. Methods and compositions for the inhibition of biofilms on medical devices
US7314857B2 (en) * 2003-08-25 2008-01-01 Kane Biotech Inc. Synergistic antimicrobial compositions and methods of inhibiting biofilm formation
US7381751B2 (en) * 2003-08-26 2008-06-03 Shantha Sarangapani Antimicrobial composition for medical articles

Patent Citations (57)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2005101A (en) * 1934-09-26 1935-06-18 Herberts Machinery Co Ltd Lathe
US4009714A (en) * 1975-07-30 1977-03-01 Johnson & Johnson Intravenous solution filter unit
US4066556A (en) * 1976-10-28 1978-01-03 Johnson & Johnson Fluid filter and method of making same
US4294594A (en) * 1979-10-02 1981-10-13 United States Surgical Corporation Self-contained filter assembly for removing air, particles and bacteria from a solution
US4311587A (en) * 1979-12-10 1982-01-19 Japan Foundation For Artificial Organs Filter arrangement denying bacteria entry to peritoneum
US4309992A (en) * 1980-07-11 1982-01-12 Dodak Michael J Microbicidal filter
US4416772A (en) * 1980-08-04 1983-11-22 Kuraray Co., Ltd. Apparatus for concentrating and filtering body cavity fluids
US4374126A (en) * 1981-02-23 1983-02-15 Warner-Lambert Company Film forming antimicrobial material
US4714556A (en) * 1981-06-29 1987-12-22 Ambrus Clara M Blood purification
US4787974A (en) * 1981-06-29 1988-11-29 Ambrus Clara M Blood purification
US4738668A (en) * 1981-07-29 1988-04-19 Baxter Travenol Laboratories, Inc. Conduit connectors having antiseptic application means
US4560382A (en) * 1983-08-15 1985-12-24 Terumo Corporation Medical container
US4568366A (en) * 1983-08-30 1986-02-04 Baxter Laboratories, Inc. In-line filter
US4678606A (en) * 1984-07-03 1987-07-07 The Procter & Gamble Company Liquid cleansing composition
US4702829A (en) * 1984-12-07 1987-10-27 Fresenius Ag Hemodiafiltration apparatus
US4695382A (en) * 1985-11-18 1987-09-22 Microgon, Inc. Combined fluid filter and delivery tubing
US4895566A (en) * 1986-07-25 1990-01-23 C. R. Bard, Inc. Coating medical devices with cationic antibiotics
US4861485A (en) * 1988-01-22 1989-08-29 W. R. Grace & Co. Hemodiafiltration device
US5053339A (en) * 1988-11-03 1991-10-01 J P Labs Inc. Color changing device for monitoring shelf-life of perishable products
US5093235A (en) * 1989-09-29 1992-03-03 The United States Of America As Represented By The Secretary Of The Navy Immuno-dye reagent and assay for detection of endotoxin
US5252222A (en) * 1990-12-03 1993-10-12 Pall Corporation Filter for parenteral systems and method of using thereof
US5312813A (en) * 1991-05-03 1994-05-17 University Technologies International Biofilm reduction method
US5366505A (en) * 1991-12-06 1994-11-22 North Shore University Hospital Research Corporation Method of reducing medical device related infections
US5217493A (en) * 1992-03-11 1993-06-08 Board Of Regents, The University Of Texas System Antibacterial coated medical implants
US5530102A (en) * 1993-01-12 1996-06-25 Gristina; Anthony G. Methods and compositions for the direct concentrated delivery of passive immunity
US5512199A (en) * 1993-11-02 1996-04-30 Becton Dickinson And Company Hand wipe solution
US5951993A (en) * 1995-06-22 1999-09-14 Minnesota Mining And Manufacturing Company Stable hydroalcoholic compositions
US20020006974A1 (en) * 1996-09-19 2002-01-17 Lucas Patrick J. Stable, foamed caulk and sealant compounds and methods of use thereof
US20020048592A1 (en) * 1997-06-20 2002-04-25 Sabine Eggers Skin-protective composition
US20050158253A1 (en) * 1997-10-16 2005-07-21 Pharmacal Biotechnologies, Llc. Compositions for treating biofilm
US20020009561A1 (en) * 1998-08-15 2002-01-24 William Joseph Weikel Lubricated elastomeric article
US20050154448A1 (en) * 1999-01-22 2005-07-14 Gore Enterprise Holdings, Inc. Biliary stent-graft
US20050124678A1 (en) * 2001-05-04 2005-06-09 Paratek Pharmaceuticals, Inc. Transcription factor modulating compounds and methods of use thereof
US20050137536A1 (en) * 2001-09-28 2005-06-23 Gonnelli Robert R. Microneedle with membrane
US20030152644A1 (en) * 2001-10-23 2003-08-14 Shanta Modak Gentle-acting skin-disinfectants
US20050199245A1 (en) * 2001-11-02 2005-09-15 Brennan H. G. Nose airway for aromatherapy and detecting airborne pathogens
US20040058878A1 (en) * 2002-01-18 2004-03-25 Walker Edward B. Antimicrobial and sporicidal composition
US20050142622A1 (en) * 2002-01-31 2005-06-30 Sanders Mitchell C. Method for detecting microorganisms
US20050161859A1 (en) * 2002-02-08 2005-07-28 Miller Kathleen M. Implantable or insertable medical device resistant to microbial growth and biofilm formation
US20050085775A1 (en) * 2002-02-14 2005-04-21 Ishay Ostfeld Indwelling device
US20050131356A1 (en) * 2002-03-14 2005-06-16 Ash Stephen R. Medical devices exhibiting antibacterial properties
US20050143286A1 (en) * 2002-04-18 2005-06-30 The University Of Iowa Research Foundation Methods of inhibiting and treating bacterial biofilms by metal chelators
US20050209547A1 (en) * 2002-06-06 2005-09-22 Burbank Jeffrey H Last-chance quality check and/or air/pathogen filter for infusion systems
US7488757B2 (en) * 2003-03-24 2009-02-10 Becton, Dickinson And Company Invisible antimicrobial glove and hand antiseptic
US20050221072A1 (en) * 2003-04-17 2005-10-06 Nanosys, Inc. Medical device applications of nanostructured surfaces
US20050256502A1 (en) * 2003-05-13 2005-11-17 Dimatteo Kristian Anti-infective central venous catheter with diffusion barrier layer
US20050095351A1 (en) * 2003-05-29 2005-05-05 Jona Zumeris Method, apparatus and system for nanovibration coating and biofilm prevention associated with medical devices
US20050118239A1 (en) * 2003-08-18 2005-06-02 Subramaniam Sabesan Process for making antimicrobial articles by reacting chitosan with amino-reactive polymer surfaces
US20050100937A1 (en) * 2003-09-11 2005-05-12 Holmes Elizabeth A. Medical device for analyte monitoring and drug delivery
US20050059731A1 (en) * 2003-09-16 2005-03-17 Ceramoptec Industries, Inc. Erythrosin-based antimicrobial photodynamic therapy compound and its use
US20050220837A1 (en) * 2003-09-30 2005-10-06 Disegi John A Antimicrobial hyaluronic acid coatings for orthopedic implants
US20050085777A1 (en) * 2003-10-15 2005-04-21 Tan Sharon M.L. Medical device having anti-microbial properties and a false lumen and method of making the same
US20050090785A1 (en) * 2003-10-22 2005-04-28 Tan Sharon M.L. Catheter with a sidearm for delivery of antimicrobial agents to prevent infection
US20050131332A1 (en) * 2003-11-05 2005-06-16 Thomas Kelly High convection home hemodialysis/hemofiltration and sorbent system
US20050171501A1 (en) * 2004-02-03 2005-08-04 Thomas Kelly Intravenous solution producing systems and methods
US20050192590A1 (en) * 2004-02-26 2005-09-01 Kristin Feeley Antimicrobial agent delivery system
US20050233950A1 (en) * 2004-04-01 2005-10-20 Srinivasa Madhyastha Synergistic antimicrobial compositions and methods for reducing biofilm formation

Cited By (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20110030726A1 (en) * 2007-04-02 2011-02-10 C. R. Bard, Inc. Insert for a microbial scrubbing device
US8065773B2 (en) 2007-04-02 2011-11-29 Bard Access Systems, Inc. Microbial scrub brush
US8336152B2 (en) 2007-04-02 2012-12-25 C. R. Bard, Inc. Insert for a microbial scrubbing device
US8336151B2 (en) 2007-04-02 2012-12-25 C. R. Bard, Inc. Microbial scrubbing device
US8671496B2 (en) 2007-04-02 2014-03-18 C.R. Bard, Inc. Insert for a microbial scrubbing device
US9186707B2 (en) 2007-04-02 2015-11-17 C. R. Bard, Inc. Insert for a microbial scrubbing device
US9192449B2 (en) 2007-04-02 2015-11-24 C. R. Bard, Inc. Medical component scrubbing device with detachable cap
US9352140B2 (en) 2007-04-02 2016-05-31 C. R. Bard, Inc. Medical component scrubbing device with detachable cap
US8696820B2 (en) 2008-03-31 2014-04-15 Bard Access Systems, Inc. Method of removing a biofilm from a surface
US8069523B2 (en) 2008-10-02 2011-12-06 Bard Access Systems, Inc. Site scrub brush
US20110152925A1 (en) * 2009-12-22 2011-06-23 Schorr Phillip A Skin Preparation That Immobilizes Bacteria
WO2011077281A3 (en) * 2009-12-22 2011-11-17 Kimberly-Clark Worldwide, Inc. Skin preparation that immobilizes bacteria

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WO2004084973A2 (en) 2004-10-07
US7488757B2 (en) 2009-02-10
US20160081894A1 (en) 2016-03-24
US20060263323A1 (en) 2006-11-23

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