US3607097A - Analyzer for liquid samples - Google Patents

Abstract

An apparatus for automatically transporting a plurality of liquid samples, such as blood through a series of programmed steps for colorimetric analysis of the samples. A first conveyor belt carries the samples to be analyzed, an adjacent belt carries working tubes in which the tests occur, and a third belt carries substances to be added to the samples during the tests. Needles and tubes are provided between the containers of substances on the three belts for piercing container walls and then transferring liquids between the containers.

Description

United States Patent [72] Inventors MichelAuphan dOrleans-Neuilly;

Jean Perilhou, Arnoux-Bourg la Reine,

XXXMM 33U 55 22 3 2 33 22 2 a m ml m "8 0 d u" w "a w .me fluh t th S m.l. p.l Hmu WHSA 0 6770 6667 9999 a 1111 00 2 I. m a X 8896 E 957.7 ,52 W 6760 a 6909 m n 3333 P n o u a r O p 0 e 1 m a 695r 9 4 LM & 1 h r! mw w b7ASU 0. de N 00 Mm I. d- Wm M Ahm-A 2 .1 n 2247 Assistant Examiner -R. E. Serwin New York, NY. Aug. 9, 1967 France Attorney- Frank R. Trifari [32] Priority [54] ANALYZER FOR LIQUID SAMPLES plurality of liquid samples, such as blood through a series of 0 I I i 1Claims 3 Drawing Figs programmed steps for colorimetric analysis of the samples. A

2 /2 first conveyor belt carries the samples to be analyzed, an adjacent belt carries working tubes in which the tests occur, and

a third belt carries substances to be added to the samples during the tests. Needles and tubes are provided between the containers of substances on the three belts for piercing container walls and then transferring liquids between the containers.

PATENTED SEP21 |97| INVENTORS MIG-IE1. AUPHAN JEAN PERILHOU BY ANALYZER FOR LIQUID SAMPLES This invention relates to US. Pat. No. 3,490,876 in which an automatic analyzer for liquid samples is described, in which colorimetry is used in the liquid phase or in the flame. Such an apparatus is particularly suitable for the automatic quantitive analysis of the main chemical constituents of blood (urea, glucose, cholesterol, sodium, potassium, etc., by means of a minimum number of operations on a large number of samples to be subjected to the same analysis.

In the apparatus described a sequence of tubes having flexible walls and filled with the liquid samples to be analyzed (termed herein working tubes) are arranged parallel to each other on a belt which is adapted to run around drums carrying out predetermined movements, means being provided for carrying out the treatments required for the analysis in a given order of succession of the sample in each tube, for instance, injection of auxiliary liquids, mixtures and so on.

For this purpose the apparatus comprises rows of thrust feet arranged parallel to the tubes, each row cooperating with'a single stationary member associated with a row, the number of rows being at least equal to the number of auxiliary liquids to be introduced into the samples. A programming device controls the thrust feet, each of which can be pressed against the wall of the opposite tube so that the liquid is displaced against the wall of the length of the tube and the predetermined treatment can be carried out. Each working tube comprises in its interior filters for performing the number of required filtrations during the analysis.

The invention has for its object to provide further mechanization of the apparatus, and accordingly the invention there is provided a second belt having parallel tubes for the auxiliary liquids consisting of flexible material and being displaceable by actuating at least one pushbutton into a position near the working tube, each auxiliary liquid tube having an injection needle for injecting the auxiliary liquid into the working tube.

The invention will be described more fully with reference to the accompanying drawing, in which:

FIG. 1 shows schematically an elevation of the various belts provided with tubes in an apparatus according to the invention,

H6. 2 is a sectional view of an auxiliary liquid tube comprising two chambers, and

FIG. 3 is a schematic elevation of a detail of the cooperating tubes connected with thrust feet.

The improvement provided by the invention relates particularly to the quantitative analysis of one or more constituents of the blood of a large number of patients. The analysis of glucose described before is chosen by way of example. For the blood analysis of a patient all treatments are carried out within asingle working tube 2 of small diameter, for example, of a synthetic resin resistant to the chemical reagents. Theworking tubes 2 are arranged parallel to each other on a belt 1, termed the working belt. The belt is adapted to move along two drums, one of which is shown at 31in the spaces 4 between every twotubes 2 the working belt is provided with the patients data and the coded analysis in the form of perforations.

In the example described each working tube has at one end ahollow needle 5 for taking in the blood serum, which will be described more fully hereinafter. The working belt is associated with a number of rows of thrust feet (not shown in FIG. l), the number of rows being at least equal to the number of reagents or auxiliary liquids to be introduced during the same analysis into the sample to be analyzed.

Att'ultliltg In tlultivcnliml there is added to the working belt I asecond belt 7. which can bemoved by adrum 8 and which is provided withtubes 9 of flexible synthetic resin containing the substances to be added during the analysis. Thebelt 7 has a given thickness so that thetubes 9, arranged parallel to each other, can be fixed in openings in the direction of thickness of thebelt 7. Thetubes 9 can be pressed out of the openings by means of athrust pin 10 and be moved to the area above aworking tube 2 on the belt 1. Eachtube 9 has aneedle 11, which is capable of piercing the wall ofaworking tube 2.

Some reagents may be stored for a long time in a sealed glass ampulla. In this case atube 9 contains the glass ampulla sealed by a pigtail, which can be broken across the tube, for example, by means of a thrust pin. However, if the reagent cannot be kept for sufficient time not even in sealed ampullae, and if it has to be freshly produced, thetube 9 may be shaped in the form shown in FIG. 2. This tube comprises twoseparate chambers 91 and 92, communicating with each other throughopenings 96, thechamber 91 being divided intoseparate spaces 93, separated from each other byclosed partitions 94. Each space contains a constituent of the reagent, for example, in the sealedampullae 95. Eachseparate space 93 communicates with thechamber 92 via ahollow needle 96. For producing the reagent pigtails are broken by exerting pressure across the synthetic resin wall so that the liquids flow into the spaces concerned. Thrust members (not shown) permit of introducing into thechamber 92 the desired quantities of the constituents which form the final reagent by mixing, if necessary with the supply of heat. Thechamber 92 has ahollow needle 11.

In the example chosen and in particular for the analysis of blood the apparatus comprises athird belt 12, termed herein take-in belt, adapted to be moved between twodrums 13 and supportingparallel tubes 14, each of which contains blood of a patient. Thetubes 14 are provided at one end with alancet 15 and the blood can be taken in, for example, from the patients ear lobe manually or automatically by means of an apparatus independent of the analyzer into which thebelt 12 has to be introduced subsequently. Thetubes 14 are fixed on thebelt 12 in rigid supports by means ofa spring (not shown) arranged on stv Thefree space 16 between twotubes 14 contains all data relating to the patient and the desired analysis in the form of coded perforations which data can be transferred to the belt 1 by means of a photoelectric cell. The take-intubes 14 with the blood are first centrifuged before thebelt 12 is inserted into the analyzerso that serum and corpuscles are separated from each other.

The operation of the analyzer will now be described briefly with reference to the assessment of the glucose content of blood. Thedrum 13 and the take-in belt 12 are moved so that invariable atube 14 is located opposite a workingtube 2. The belt 1 with theworking tubes 2 is arranged so that the needle ofaworking tube 2 can penetrate into the take-intube 14 just above the portion filled with corpuscles, after which the desired quantity of serum can be sucked into theworking tube 2. At the same time the associated coded information of thebelt 12 is read and punched in the belt 1. A programming device receiving the punched information of thebelt 12 will control the course of the three belts l, 7 and l2.

All desired analyses can be carried out in order of succession. After the serum of the tube concerned is taken in, thebelt 12 moves on by one step so that thetube 14 of a further patient occupies the emptied space opposite a next-followingworking tube 2, which has arrived at the area of the preceding tube due to the propagation of thebelt 17 The serum of the next patient is taken in and the coded indications of thebelt 12 are transferred to the belt 1.

dle ll piercing the wall. When all analyses are of the same nature, thebelt 7 comprises a number oftubes 9 containing reagents corresponding with the number of patients.

With the glucose analysis and with the aid of reduction of I ferric cyanide it is necessary to introduce the following three reagents in a given order of succession of the desired instant and at the desired area ofthe working tube 2:

Reagent A (for expelling protein) copper sulfate 5 H,0 0.31 g. sodium tungstcnate 2H,!) [.22 gs. barium chloride 2H 0.26 g. distilled water [00 cc.

Reagent B (ferric-ferrous cyanide) pure potassium ferro-cyanidc 0.006 g. pure potassium ferri-cyanide 0.033 g. pure dry sodium carbonate 0.4 g.

distilled water 100 cc.

Reagent C (ferric phosphate) pure potassium fcrri-cyanide 0.04 g. SS'k-ic phosphoric acid 4.7 gs. distilled water I00 cc.

Since the first reagent having a pH value exceeding 8 can be kept in good condition, it may be provided in the ready state in a glass ampulla in atube 9 and the sealing tip of the ampulla can be broken at the exact instant.

Thetube 9 is then moved to above the belt 1 with the workingtubes 2, where thetube 9 stands still until the termination of the glucose analysis. The hollow needle of thetube 9 can penetrate by pressure into the workingtube 2 by means of thrust feet. This is shown in detail in FIG. 3. Thetube 9 with the filledchamber 92 is located above the workingtube 2 and theneedle 11 has pierced the wall. Thethrust feet 17 press the workingtube 2 flat against themember 18 and after the return movement of the feet thetube 2 sucks in a quantity of reagent. By pressing the correct number offeet 17 against the member 18 a quantity of uL. is urged 20 times in order of succession forwardly in the tube portion serving for the analysis and for taking in serum.

The serum is taken in the same manner by means of theneedle 5. In order to cause this needle to penetrate into the centrifuged take-intubes 14, the latter are pressed against the needle by a thrust foot. The needles are adjusted so that they penetrate just above the blood clot so that no serum gets lost.

After the serum is taken into the workingtube 2, It is mixed with the reagent by the alternate displacement of the evennumbered and odd-numberedthrust feet 17. The mixture is then filtered by a hard-glass filter 6 in the interior of the workingtube 2. By the action of the thrust feet the liquid is injected under pressure through the walls of the filter. Then the workingtube 2 is displaced by one step, after which the same cycle is repeated for the analysis of the glucose content of a further patient and so on until the doses to be analyzed are exhausted or thetube 9 is empty.

The second treatment of the filtrate consists in the introduction of the ferri-ferro-cyanide, the glucose reduction of which is measured. This reagent has to be produced separately, Thetube 9 has in this case two chambers, one of which is divided into threeseparate spaces 93 which contain the previously weighed quantities of ferrous cyanide, ferric cyanide and a solution of sodium carbonate in a glass ampulla. By a technique similar to the preceding technique a quantity of, for example, cc. accurately determined by means of thrust pins can be readily supplied from the ampulla containing sodium carbonate under gas pressure. This quantity of the solution is then inserted into theother chamber 92 and mixed therein with the ferrous cyanide and the ferric cyanide.

After these treatments thetube 9 is moved near the workingtube 2 for the injection of the reagent. For each workingtube 2 the process is then as follows: In an accurately determined portion of thetube 2 L. of the filtrate of the first treatment is absorbed, after which this quantity is shifted upwards.

In the same tube portion is then absorbed a quantity of 4X30 ,uL. of the ferrLferro-cyanide. The filtrate is mixed as before with the reagent and the same treatment is carried out on all tubes.

The reaction is completed by heating at near the boiling point of the liquid for one quarter of an hour, for example, in a bath, which may be a circulating heating bath. Each tube is passed through the bath for the same period of time. After the bath a quantity of ,u.L. of ferric phosphide is introduced in the same way as described above. For color stabilization the belt is held for about 15 minutes at 20 C. in a drying furnace. Thetubes 2 are then subjected to colorimetric analysis.

When several sequences of analyses have to be performed (glucose, urea etc.), thebelt 12 is moved back to its initial position after termination of the first sequence of analyses and a new sequence oftubes 2 is applied to the belt 1, each of which can take in a new quantity of serum. At the same time thebelt 7 with the reagents is moved so that thetubes 9 are disposed in accordance with the new sequence of analyses. By the supply of fresh tubes with the reagents to above the workingtubes 2, the tubes employed for the preceding analysis are conducted away and rejected. For the invention it is not essential whether the disposition of the belts in this example, the shape of the tubes containing the reagents and the displacing members are different.

What is claimed is:

1. Apparatus for automatic analysis of liquid samples obtained from a plurality of containers, comprising:

a. a housing,

b. a plurality offlexible working tubes,

c. first means for carrying the working tubes between different positions along a path,

d. means for selectively compressing and releasing each working tube which is subsequently expandable to develop suction therein,

e. second means for carrying the containers of liquid samples along a second path, whereby each container is disposed adjacent one working tube, first duct means for communicating the sample liquid from each container to a working tube, with said liquid being drawable into the working tube by said suction therein,

. a plurality of auxiliary containers, each containing at least one reagent,

h. third means for carrying auxiliary containers along a third path and for disposing each to be closely adjacent a working tube, and

. second duct means for communicating each reagent from its auxiliary container to a working tube, the reagent being drawable onto the working tube by said suction therein, whereby each sample is mixed within a working tube at least one reagent subsequent analysis.

2. Apparatus according to claim 1 wherein at least one of the auxiliary liquid containers comprises a first chamber separated into two spaces, each adapted to house an ampulla containing a constituent of a reagent, and a second chamber communicating with said spaces for receiving and mixing said constituents and for discharging the mixed constituents into the working tube.

3. Apparatus according toclaim 2 further comprising means for breaking open the ampullae in said spaces of the first chamber and for urging the constituents into the second chamber.

4. Apparatus according to claim 1 wherein said means for compressing and releasing each working tube comprises a plurality of thrust feet, each movable between an inactive position, an an active position in pressure contact with a working tube for compressing same.

5. Apparatus according to claim 4 wherein said thrust feet are selectively movable into pressure contact with each working tube to mix the liquid sample and reagent therein and subsequently to discharge the mixed fluid from the working tube.

6. Apparatus according toclaim 2 wherein said first, second, and third means for carrying respectively said working tubes, sample containers, and auxiliary containers and belts movable about drums.

7. Apparatus according toclaim 6 wherein said tubes and containers are disposed in parallel and oriented transverse to the direction of their respective belt movement.

8. Apparatus comprising a device according toclaim 6, further comprising means for programming said belts to move in phased relationship, for phased interrelationship between said tubes and containers.

9. Apparatus according to claim 1 further comprising in each working tube a filter for filtering the sample after it is mixed with the reagent.

10. Apparatus for automatic colorimetric analysis of liquid fluid samples obtained from a plurality of containers, comprising:

a. a frame,

b. a plurality of flexible working tubes, each having an external hollow needle communicating with the tubess interior,

c. first belt for carrying the working tubes between different positions along a first path,

d. a plurality of thrust feet, each movable between an inactive position, an an active position in pressure contact with a working tube for selectively 'compressing same, the tube being subsequently expanded to develop suction therein when each thrust foot is returned to its inactive position,

. means for moving said feet between said active and inacg. a plurality of auxiliary containers, each having a discharge needle and containing at least one reagent,

h. third belt for carrying the auxiliary containers and for disposing each to be closely adjacent a working tube and for then urging the needle of each auxiliarfcontainer to penetrate a working tube, the reagent then being drawable into the working tube by said suction therein, whereby each blood sample is mixed within a working tube with at least one reagent for subsequent colorimetric analysis.

P049; UNITED STATES PATENT OFFICE CERTIFICATE OF CORRECTION Patent No. V Dated September 21 I MICHEL AUPHAN and JEAN PERILHOU It is certified that error appears in the above-identified patent and that said Letters Patent are hereby corrected as shown below:

Col.l,line 8, after "etc." delete and insert Col. 1, line 25 and 26. cancel "against the wall of the" and insert in the direction of- Col. 6, line 1, "an" (first occurrence) should be -andline 3, "expanded" should be expandable- Signed and sealed this 26th day of December 1972 (SEAL) A ies:

EDWARD M.FLELCHER,JR. ROBERJ. GOI'TSCHALK Arm-acting Officer Commissioner of Patents

Claims (9)

1. 2. Apparatus according to claim 1 wherein at least one of the auxiliary liquid containers comprises a first chamber separated into two spaces, each adapted to house an ampulla containing a constituent of a reagent, and a second chamber communicating with said spaces for receiving and mixing said constituents and for discharging the mixed constituents into the working tube.
2. 3. Apparatus according to claim 2 further comprising means for breaking open the ampullae in said spaces of the first chamber and for urging the constituents into the second chamber.
3. 4. Apparatus according to claim 1 wherein said means for compressing and releasing each working tube comprises a plurality of thrust feet, each movable between an inactive position, an an active position in pressure contact with a working tube for compressing same.
4. 5. Apparatus according to claim 4 wherein said thrust feet are selectively movable into pressure contact with each working tube to mix the liquid sample and reagent therein and subsequently to discharge the mixed fluid from the working tube.
5. 6. Apparatus according to claim 2 wherein said first, second, and third means for carrying respectively said working tubes, sample containers, and auxiliary containers and belts movable about drums.
6. 7. Apparatus according to claim 6 wherein said tubes and containers are disposed in parallel and oriented transverse to the direction of their respective belt movement.
7. 8. Apparatus comprising a device according to claim 6, further comprising means for programming said belts to move in phased relationship, for phased interrelationship between said tubes and containers.
8. 9. Apparatus according to claim 1 further comprising in each working tube a filter for filtering the sample after it is mixed with the reagent.
9. 10. Apparatus for automatic colorimetric analysis of liquid fluid samples obtained from a plurality of containers, comprising: a. a frame, b. a plurality of flexible working tubes, each having an external hollow needle communicating with the tubes''s interior, c. first belt for carrying the working tubes between different positions along a first path, d. a plurality of thrust feet, each movable between an inactive position, an an active position in pressure contact with a working tube for selectively compressing same, the tube being subsequently expanded to develop suction therein when each thrust foot is returned to its inactive position, e. means for moving said feet between said active and inactive positions, f. second belt for carrying the containers of liquid samples along a second path, whereby each container is disposed adjacent one working tube, and for urging the needle of the working tube to penetrate a container, with said liquid sample then being drawable from the container into the working tube by said suction therein, g. a plurality of auxiliary containers, each having a discharge needle and containing at least one reagent, h. third belt for carrying the auxiliary containers and for disposing each to be closely adjacent a working tube and for then urging the needle of each auxiliary container to penetrate a working tube, the reagent then being drawable into the working tube by said suction therein, whereby each blood sample is mixed within a working tube with at least one reagent for subsequent colorimetric analysis.

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