US3068855A

US3068855A - Disposable blood-gas analyzer

Info

Publication number: US3068855A
Application number: US854214A
Authority: US
Inventors: Jr Norman B Furlong
Original assignee: Individual
Current assignee: Individual
Priority date: 1957-04-29
Filing date: 1959-11-19
Publication date: 1962-12-18
Anticipated expiration: 1979-12-18

Description

Dec. 18, 1962 N. B. FURLONG, JR

DISPOSABLE BLOOD-GAS ANALYZER Original Filed April 29, 1957 s a M a a a a a IN V EN TOR.

4 0 EMF 8. (held/V6 4 Claims. (Cl. 1282) (Granted under Title 35, US. Code (1952), sec. 266) The invention described herein may be manufactured and used by or for the United States Government for governmental purposes without payment to me of any royalty thereon.

This invention relates to a device for providing a roughly accurate quantitative analysis of the carbon monoxide content in blood.

As a background for understanding the present invention reference is made to Handbook of Poisons by Robert H. Dreisbach, published in 1955 by Lange Medical Publications, University Medical Publishers, Los Altos, California. This application is a division of the Norman B. Furlong application, Serial Number 655,922 filed April 29, 1957, that is copending herewith and now issued as Patent No. 2,940,448.

A brief summary of the invention follows indicating its nature and substance together with a statement of the object of the invention commensurate and consistent with the invention as claimed and also setting out the exact nature, the operation and the essence of the invention complete with proportions and techniques that are necessary for its use. The purpose of the invention also is stipulated. The presentation is adequate for any person who is skilled in the art and science to which the invention pertains, to use it without involving extensive experimentation. The best mode of carrying out the invention is presented by the citing of a specific operative example, inclusive of the preparation and the use of at least one example of the invention.

I The object of this invention is to provide a self-contained, inexpensive, disposable device which may be rapidly used by an untrained person with simple manipulation in the making of a reasonably close approximation of a quantitative determination of the carboxy-haemoglobin in a blood sample under standard conditions, after which the device is discarded.

The device does not replace an exact quantitative determination of carbon monoxide absorption into the blood stream, but it is adequate for providing a quick estimate in the hands of a person without skill beyond observation and judgment in the comparison of shades of color. The device contemplated hereby includes in one unit the factors of sterilization, vein puncture, blood sampling, chemical reaction reagents to release carbon monoxide from the carboxy-haemoglobin molecule and means for making a quantitative colorimetric close determination of the carbon monoxide released from the blood sample taken from the patient.

In the accompanying drawing:

FIG. 1 is a plan view, partly in section, of a hypodermic syringe reaction chamber and a protective covering, which embody the present invention;

FIG. 2 is an enlarged sectional view of the hypodermic needle protecting and sterilizing cap shown in FIG. 1;

:FIG. 3 is an elevational view of the open end of the cap shown in FIG. 2;

FIG. 4 is an enlarged sectional view of the hypodermic syringe shown in FIG. 1;

FIG. 5 is a sectional view taken along the line 5-5 of FIG. 4;

FIG. 6 is a plan view, partly in section, of a commer- 3,068,855 Patented Dec. 18, 1962 cially available colorimetric analyzing equipment, as applied to the assembly shown in FIG. 4; and

FIG. 7 is a quantitative carbon monoxide colorimetric chart, usable with the color band of the colorimetric tube shown in FIG. 6.

The syringe illustrated in FIG. 1 of the accompanying drawing consists of a hollow steel hypodermic needle 1 with its distal or unattached end 2 sharpened for skin and vein penetration and a reaction chamber 3 hand grasp support for the needle. The proximal or the attached end of the hollow needle 1 is mounted in sealing engagement with and is supported by the extreme end of the flexible neck portion of the tough, flexible plastic reaction chamber 3. The opening through the hypodermic needle 1 is in arrested or blocked communication with the interior of the reaction chamber 3. The thin neck of an evacuated capsule 6 makes a close, axial, sealing slip fit into the neck of the reaction chamber 3 and a loose, spaced penetration into the base of the needle 1.

The reaction chamber 3 is closed and is sealed at its end remote from the needle 1 by being cemented to a cap 4, which is provided with a thin-section tear seal 5 or the like. The hollow glass capsule 6, which is exhausted to a desired degree of vacuum, has a thin-walled, shear end positioned within and supported by the base of the needle 1 in the neck of the reaction chamber 3. Reagent containing, additional sealed, thin glass capsules, such as the capsule 7, may also be positioned within the chamber 3. Where desired, the capsules may be secured in place by stainless steel rings, such as the spring steel ring 8 or the like, within the chamber 3. The ring 8 is shown as a continuous wire with spaced ends. The wire is bent to a circular shape with a loop midway between its ends to receive the necked portion of the reagent containing capsule 7 within the loop. The stainless steel ring 8 is adapted for being depressed somewhat, in which state its unattached ends approach each other. The partly depressed, capsule supporting ring 8 is then inserted within the interior of the reaction chamber 3 to a desired position and then released so that the legs of the ring 8 bear outwardly against the inner surface of the reaction chamber 3 and retain the capsule 7 in position. The ring 8 serves the purpose of restricting the undesirable freedom of motion of the capsule it supports so that the capsule is out of contact with other occupants of the interior of the reaction chamber 3. The contents and the number of reagent containers, of which the capsule 7 may be taken as being illustrative, positioned within the reaction chamber 3 may be modified in conformity with requirements, within the contemplation of the present invention.

The capsules 6, 7, etc. within the reaction chamber 3 are made of sutficiently thin-walled glass, or similar material, so that they may be fractured or crushed by finger pressure without puncturing the walls of the reaction chamber 3. Illustratively, one of the thin-walled glass capsules may contain mg. of powdered dry potassium ferricyanide or a corresponding water solution thereof. A; second capsule (not shown) may contain a buffer solution such as 50 mg. of citric acid and 50 mg. of sodium citrate, 10 mg. of powdered saponin, 3 drops of caprylic alcohol and illustratively 1 /2 to 2 cc. of water. Where desired, the caprylic alcohol may be contained within the evacuated capsule 6, where it minimizes foaming of blood drawn into the capsule 6. The water, or a stable solution, may be left free in the reaction chamber 3 to minimize damage by freezing. Illustratively, the water may be outside of the capsule 7 and the above dry reagents may be positioned within the capsule 7, within the reaction chamber 3.

A hypodermic needle protecting and sterilizing chamher providing cap or sheath consists of a plastic cylinder or conical member, closed at one end and with its opposite end open and fitting tightly over the needle supporting neck end of the reaction chamber shown in FIG. 1, in sealing relation therewith. The cap or sheath 10 preferably is stiffened against lateral deformation with externally positioned longitudinally extending ribs as indicated in FIG. 3, or the like.

The sheath or cap 10 preferably contains a swab 11 and an antiseptic solution, of which denatured alcohol may be taken as being representative. The hypodermic needle 1 is maintained sterilized by the antiseptic, by which the swab 11 may be saturated. In FIG. 1 of the accompanying drawing, the hypodermic needle, with its antiseptic protective sheath 10, which engages the neck of the reaction chamber 3 in sealing contact therewith, shows the assembly in its sealed condition and suitable for handling and for storage.

Preparatory to the use of the assembly shown in FIG. 1 of the drawing the cap or sheath 10 is withdrawn from its sealing engagement with the neck of the reaction chamber 3 and the cap 10 is tapped against the hand for causing the swab 11 to be removed therefrom. The swab 11 may then be applied along the hypodermic needle 1, for assuring the sterilization thereof. The swab 11 may then be applied to the skin overlying the vein at the inner portion of the elbow bend, which is positioned midway between the extremities of the human arm, or elsewhere, preparatory to causing the penetration of the sharpened tip 2 of the hypodermic needle 1 into the vein for the withdrawal of a blood sample therefrom.

With the tip 2 of the hypodermic needle 1 within the blood-filled vein, the flexible neck of the reaction chamber 3 is deflected by the thumb, as the fingers extend around the reaction chamber 3 of the device. The thumb deflection of the flexible neck of the reaction chamber 3 is sufiicient to rupture the thin-walled seal end of the vacuum capsule 6, thereby opening communication between the interior of the vacuum capsule 6 and the blood filled vein thereby causing the capsule 6 to be filled with a, predetermined amount of blood. The hypodermic needle 1 is then withdrawn from the patient and the swab 11 is again used to sterilize the skin wound resulting therefrom. Where desired, the protective cap 10 may be replaced in sealing engagement with the neck of the reaction chamber 3, thereby increasing the air pressure upon the blood remaining within the hypodermic needle 1 and urging the blood toward the, reaction chamber 3 or, if preferred, the sharp tip 2 of the hypodermic needle 1 may be caused to penetrate a rubber or cork stopper or the like, to minimize any blood loss of the sample as taken.

The previously evacuated tube or vacuum capsule 6,

Within the reaction chamber 3, is then crushed by finger pressure to release all entrapped blood within the interior of the reaction chamber 3. The capsule 7, and any other capsules which may be contained within the reaction chamber 3, in a similar manner may be ruptured and preferably reduced in particle size by the fingers to release completely their contents into the interior of the reaction chamber 3 and to assure that their contents will be mixed thoroughly with the blood sample within the reaction chamber 3.

The contents of the reaction chamber 3 are then mixed thoroughly by shaking or the like, to release substantially all of the blood carried gas as a vapor, of which carbon monoxide released from carboxy-haemoglobin is taken herein as being representative, within the interior of the reaction chamber 3. At this stage of the development, substantially all of the gas carrying blood sample is positioned within the reaction chamber 3 and is thor oughly mixed with those reagents which are to act upon the blood sample in releasing its gaseous content therefrom. Within the shaken reaction chamber 3, the

cracked glass, by a mechanical scrubbing action, assists in promoting the reaction between the blood and the reagents present, in accomplishing the complete extraction of gas from the blood samples. The crushable vacuum capsule 6 has a precision small volume, which illustratively may be /2 cc., which is maintained within a tolerance of about 5% The equipment shown in FIG. 6 and the chart shown The equipment with a carbon monoxide synthetic yellow reagent colorimetric band 16 intermediate its ends and a slow filling squeeze bulb 17. The squeeze bulb 17. is provided with a resilient tube 18 within the free end of which the less filled end of the tube 15 may be inserted in sealing engagement therewith. The colorimetric tube 15 contains white silica jel plugged in place on the opposite sides of the color band 16. The colorimetric tube 15 has a,

sturdy mid-section, which is drawn at its opposite ends to glass of sufiiciently thinner sections to be frangible, with out causing splitting up in the mid-portion of the tube.

In use, both ends of the colorimetric tube 15 are broken open, the less filled end is inserted into the open end of the resilient tube 18 and the opposite end of the tube 15 is caused to penetrate the tear seal 5 of the closure cap 4, in sealing engagement therewith also. The resilience of the wall of the squeeze bulb 17 causes it to dilate against the ambient atmosphere which, upon the removal of the hypodermic needle protecting cap 10, or the removal of the hypodermic needle from a rubber or cork stopper or the like, permits the ambient atmosphere to enter the needle tip 2, to pass along the channel of the needle 1 and to displace any blood within the needle 1 and cause it to flow into the reaction chamber 3 where it is reacted with by the reagents present in causing the liberation of the carbon monoxide gas therefrom.

The continued slow dilation of the squeeze bulb 17 draws the vapor content within the reaction chamber 3 through the colorimetric tube 15, thereby replacing the vapor within the reaction chamber 3 with ambient air which enters the reaction chamber 3 through the channel of the hypodermic needle 1.

The original color of the yellow colorimetric band 16 of the colorimetric tube 15 matches the yellow color of the patch 20, of a patch series numbered 20 to 25, inclusive, shown in FIG. 7. Thepatch series 20 to 25, inclusive, is shaded from the yellow patch 20 through

greens

21, 22, 23 and 24 of increasing blue content, to the blue patch 25.

band 16 of the colorimetric tube 15 in the presence with in the reaction chamber 3 of suflicient quantities of car'- bon monoxide in air, in registration with the individual patches and appearing in line 26 thereabove,-.to cover the range from .005 to .l'percentage of carbon monoxide I11 air.

rows and columns of patient exposure effects from carbon monoxide in air. In the first column all of the squares bear the legend no efiects. 'In the second column, in order from the bottom, there are ,no appreciable effects until the patient has been exposed 8 hours to a concentration of .00 5 carbon monoxide in air, at which time the.

effects are just perceptible. In the third column, in order from bottom for carbon monoxide concentrations in air of .0l%, the patient experiences no appreciable effects from exposure from one to three hours, inclusive.

The yellow patch 20, as indicated in line 26 thereabove, indicates zero percentage of carbon monoxide in air. The other color patches 21 to 25, inclusive, are color shades assumed by the colorimetric I Above the row 26 in FIG. 7 of the drawingappears v he is exposed for four hours the patient experiences headaches and nausea and the patient exposed to 0.02% carbon monoxide in air for eight hours is in a dangerous condition. In the fifth column a patient exposed to 0.04% carbon carbon monoxide in air for one hour experiences appreciable effects; for two hours he experiences headaches and nausea; and he is in dangerous condition when he is exposed from three to eight hours to 0.04% carbon monoxide in air. A patient exposed to 0.1% carbon monoxide in air for one hour experiences headaches and nausea; when he is exposed for two hours he is in a dangerous condition; and death results from exposure to 0.1% carbon monoxide in air for three hours and beyond.

The data chart represented in FIG. 7 is derived from the Bureau of Standards, as connected with the equipment shown in FIG. 6. The squeeze bulb 17 has a content of about 60 cc. Within the reaction chamber 3, the cracked glass permeated by bubbling air passing through the blood sample in the presence of the described reagents, provides a scrubbing action which assists in the substantially complete extraction of carbon monoxide from the blood sample. The mixing of the blood sample with the reagents within the reaction chamber 3 is continued for a prescribed period of time, of which 30 seconds may be taken as being illustrative, to insure the complete release of carbon monoxide from the blood. The equipment and the procedures disclosed herein may be used for quantitative determinations of materials other than the described procedure, within the conception of the present invention.

It will be understood that modifications may be made in the equipment disclosed, in the reagents cited and in the manipulations described and in departures from the standard conditions of temperature and pressure contemplated hereby, for particular adaptations and uses without departing from the spirit and the scope of the present invention.

I claim:

1. The method for accomplishing the separation of carbon monoxide from a sample of blood which comprises drawing a predetermined blood sample into an evacuated frangible first capsule within a reaction chamber that is provided with a flexible wall and the reaction chamber containing a second frangible capsule that contains reagents, crushing said first frangible capsule and causing blood from the first capsule to be released into the reaction chamber, crushing within the reaction chamber said reagent-containing second capsule and thereby releasing within the reaction chamber reagents that liberate carbon monoxide from the blood within the reaction chamber, mixing the blood with the reagents for releasing the carbon monoxide from the blood in the reaction chamber, and passing air through the blood and reagent mixture within the reaction chamber for separating the carbon monoxide from the blood.

2. The method of separating gaseous carbon monoxide from fluid blood containing carboxy-haemoglobin which comprises drawing a predetermined blood sample into an evacuated frangible capsule mounted within a reaction chamber with a deformable wall and containing reagents in a second frangible capsule, fracturing said first frangible blood filled formerly evacuated capsule within the reaction chamber and thereby releasing the blood sample into the reaction chamber, fracturing the reagent containing capsule by deformation of the reaction chamber wall for reacting the blood sample with the reagent in releasing gaseous carbon monoxide from the carboxyhaemoglobin, and withdrawing the gaseous carbon monoxide from the reaction chamber for determining quantitatively the carbon monoxide content of the blood sample.

3. The method for making a quantitative determination of carbon monoxide in a blood sample by injecting a hollow needle into a blood source while gripping the needle handle that is a hollow reaction chamber provided with a deformable wall and containing a frangible evacuated first capsule having a portion outside the reaction chamber and attached to the hollow needle and the reaction chamber also containing a frangible reagent containing second capsule, manipulating the deformable wall of the reaction chamber sufliciently to rupture the portion of the first capsule outside the reaction chamber and to place the interior of the first capsule into communication with the interior of the needle and drawing a predetermined quantity of blood sample from the blood source into the interior of the first capsule, manipulating the deformable wall of the reaction chamber in crushing the portion of the first capsule which is within the reaction chamber and releasing the blood that it contains into the interior of the reaction chamber, manipulating the deformable wall of the reaction chamber in crushing the second capsule and releasing into the interior of the reaction chamber the reagents milligrams of potassium ferricyanide and 50 milligrams of citric acid and 50 milligrams of sodium citrate and .10 milligrams of saponin and 3 drops of caprylic alcohol and from /2 to 2 cubic centimeters of water, mixing the released reagents with the blood sample within the reaction chamber for releasing the gas content of the blood sample, and determining colorimetrically and quantitatively the carbon monoxide content of the blood sample.

4. The process in the quantitative determination of carbon monoxide in carboxy-haemoglobin of a blood sample of releasing the carbon monoxide from the carboxy-haemoglobin confined within a reaction chamber by scrubbing the blood sample with fragmented glass and a mixture of 100 milligrams of potassium ferricyanide, 50 milligrams of citric acid, 50 milligrams of sodium citrate, 10 milligrams of saponin, 3 drops of caprylic alcohol and about 2 centimeters of water.

References Cited in the file of this patent UNITED STATES PATENTS 2,054,885 Schroter Sept. 22, 1936 2,103,136 Bangert Dec. 21, 1937 2,799,660 Nicholls July 16, 1957 2,940,448 Furlong June 14, 1960

Claims

1. THE METHOD FOR ACCOMPLISHING THE SEPARATION OF CARBON MONOXIDE FROM A SAMPLE OF BLOOD WHICH COMPRISES