|Publication number||US3607097 A|
|Publication date||Sep 21, 1971|
|Filing date||Aug 6, 1968|
|Priority date||Aug 9, 1967|
|Publication number||US 3607097 A, US 3607097A, US-A-3607097, US3607097 A, US3607097A|
|Inventors||Michel Auphan, Jean Perilhou|
|Original Assignee||Philips Corp|
|Export Citation||BiBTeX, EndNote, RefMan|
|Patent Citations (4), Referenced by (73), Classifications (25)|
|External Links: USPTO, USPTO Assignment, Espacenet|
United States Patent  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 695 r 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  Priority  ANALYZER FOR LIQUID SAMPLES plurality of liquid samples, such as blood through a series of 0 I I i 1 Claims 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 a single working tube 2 of small diameter, for example, of a synthetic resin resistant to the chemical reagents. The working 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 two tubes 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 a hollow 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 a second belt 7. which can bemoved by a drum 8 and which is provided with tubes 9 of flexible synthetic resin containing the substances to be added during the analysis. The belt 7 has a given thickness so that the tubes 9, arranged parallel to each other, can be fixed in openings in the direction of thickness of the belt 7. The tubes 9 can be pressed out of the openings by means of a thrust pin 10 and be moved to the area above a working tube 2 on the belt 1. Each tube 9 has a needle 11, which is capable of piercing the wall ofa working tube 2.
Some reagents may be stored for a long time in a sealed glass ampulla. In this case a tube 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, the tube 9 may be shaped in the form shown in FIG. 2. This tube comprises two separate chambers 91 and 92, communicating with each other through openings 96, the chamber 91 being divided into separate spaces 93, separated from each other by closed partitions 94. Each space contains a constituent of the reagent, for example, in the sealed ampullae 95. Each separate space 93 communicates with the chamber 92 via a hollow 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 the chamber 92 the desired quantities of the constituents which form the final reagent by mixing, if necessary with the supply of heat. The chamber 92 has a hollow needle 11.
In the example chosen and in particular for the analysis of blood the apparatus comprises a third belt 12, termed herein take-in belt, adapted to be moved between two drums 13 and supporting parallel tubes 14, each of which contains blood of a patient. The tubes 14 are provided at one end with a lancet 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 the belt 12 has to be introduced subsequently. The tubes 14 are fixed on the belt 12 in rigid supports by means ofa spring (not shown) arranged on stv The free space 16 between two tubes 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-in tubes 14 with the blood are first centrifuged before the belt 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. The drum 13 and the take-in belt 12 are moved so that invariable a tube 14 is located opposite a working tube 2. The belt 1 with the working tubes 2 is arranged so that the needle ofa working tube 2 can penetrate into the take-in tube 14 just above the portion filled with corpuscles, after which the desired quantity of serum can be sucked into the working tube 2. At the same time the associated coded information of the belt 12 is read and punched in the belt 1. A programming device receiving the punched information of the belt 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, the belt 12 moves on by one step so that the tube 14 of a further patient occupies the emptied space opposite a next-following working tube 2, which has arrived at the area of the preceding tube due to the propagation of the belt 17 The serum of the next patient is taken in and the coded indications of the belt 12 are transferred to the belt 1.
dle ll piercing the wall. When all analyses are of the same nature, the belt 7 comprises a number of tubes 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 a tube 9 and the sealing tip of the ampulla can be broken at the exact instant.
The tube 9 is then moved to above the belt 1 with the working tubes 2, where the tube 9 stands still until the termination of the glucose analysis. The hollow needle of the tube 9 can penetrate by pressure into the working tube 2 by means of thrust feet. This is shown in detail in FIG. 3. The tube 9 with the filled chamber 92 is located above the working tube 2 and the needle 11 has pierced the wall. The thrust feet 17 press the working tube 2 flat against the member 18 and after the return movement of the feet the tube 2 sucks in a quantity of reagent. By pressing the correct number of feet 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 the needle 5. In order to cause this needle to penetrate into the centrifuged take-in tubes 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 working tube 2, It is mixed with the reagent by the alternate displacement of the evennumbered and odd-numbered thrust feet 17. The mixture is then filtered by a hard-glass filter 6 in the interior of the working tube 2. By the action of the thrust feet the liquid is injected under pressure through the walls of the filter. Then the working tube 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 the tube 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, The tube 9 has in this case two chambers, one of which is divided into three separate 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 the other chamber 92 and mixed therein with the ferrous cyanide and the ferric cyanide.
After these treatments the tube 9 is moved near the working tube 2 for the injection of the reagent. For each working tube 2 the process is then as follows: In an accurately determined portion of the tube 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. The tubes 2 are then subjected to colorimetric analysis.
When several sequences of analyses have to be performed (glucose, urea etc.), the belt 12 is moved back to its initial position after termination of the first sequence of analyses and a new sequence of tubes 2 is applied to the belt 1, each of which can take in a new quantity of serum. At the same time the belt 7 with the reagents is moved so that the tubes 9 are disposed in accordance with the new sequence of analyses. By the supply of fresh tubes with the reagents to above the working tubes 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 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.
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 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.
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.
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.
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
|Cited Patent||Filing date||Publication date||Applicant||Title|
|US3266298 *||Jul 30, 1963||Aug 16, 1966||Technicon Instr||Means and method for the identification of samples for blood typing|
|US3297558 *||Mar 12, 1965||Jan 10, 1967||Instrumentation Labor Inc||Fluid control apparatus|
|US3306229 *||Apr 5, 1965||Feb 28, 1967||Technicon Instr||Pump apparatus and method of operation thereof|
|US3490876 *||Mar 29, 1967||Jan 20, 1970||Philips Corp||Analysing devices for fluid samples|
|Citing Patent||Filing date||Publication date||Applicant||Title|
|US3713771 *||May 13, 1971||Jan 30, 1973||H Divelbiss||Method for organized assay and bendable test tube rack therefor|
|US3812597 *||Jun 1, 1973||May 28, 1974||Philips Corp||Oven|
|US3869252 *||Apr 20, 1973||Mar 4, 1975||Haug Hans||Dose distribution means|
|US3883305 *||Mar 14, 1973||May 13, 1975||Coulter Electronics||Automatic chemical analysis apparatus|
|US3902852 *||Jul 13, 1973||Sep 2, 1975||Univ Sherbrooke||Apparatus for multiple sample application|
|US3918913 *||Dec 2, 1974||Nov 11, 1975||Lilly Co Eli||Sampler-injector for liquid chromatography|
|US3948606 *||Jan 26, 1973||Apr 6, 1976||Johnson Derrold D||Programmed test tube rack for manually performing medical diagnostic assays|
|US4106911 *||Jun 29, 1977||Aug 15, 1978||Societe Francaise Pour Le Developpement De L'automatisme En Biologie||Device for examining a plurality of microdoses of liquids|
|US4120662 *||Jan 18, 1978||Oct 17, 1978||Cortex Research Corporation||Specimen sampling apparatus|
|US4311484 *||Apr 9, 1980||Jan 19, 1982||Cortex Research Corporation||Specimen sampling apparatus|
|US4872353 *||Feb 19, 1988||Oct 10, 1989||Micromeritics Instrument Corp.||Automatic sample feeder for suspended samples|
|US4937049 *||Feb 23, 1988||Jun 26, 1990||Ibg Systems Limited||Sample transfer device|
|US4960566 *||Aug 19, 1987||Oct 2, 1990||Mochida Pharmaceutical Co., Ltd.||Chemical reaction apparatus|
|US5988947 *||Nov 4, 1997||Nov 23, 1999||Bruso; Bruce L.||Multi-section soil remediation device|
|US6318191||Jun 23, 1999||Nov 20, 2001||Chen & Chen, Llc||Fluid sample testing system|
|US6748332||Jul 20, 2001||Jun 8, 2004||Chen & Chen, Llc||Fluid sample testing system|
|US7337072||Jun 8, 2004||Feb 26, 2008||Chen & Chen, Llc||Fluid sample testing system|
|US7799521||Sep 21, 2010||Chen & Chen, Llc||Thermal cycling|
|US7833489||Nov 16, 2010||Chen & Chen, Llc||Fluid sample testing system|
|US8496601||Apr 16, 2007||Jul 30, 2013||Sanofi-Aventis Deutschland Gmbh||Methods and apparatus for lancet actuation|
|US8556829||Jan 27, 2009||Oct 15, 2013||Sanofi-Aventis Deutschland Gmbh||Method and apparatus for penetrating tissue|
|US8562545||Dec 16, 2008||Oct 22, 2013||Sanofi-Aventis Deutschland Gmbh||Tissue penetration device|
|US8574168||Mar 26, 2007||Nov 5, 2013||Sanofi-Aventis Deutschland Gmbh||Method and apparatus for a multi-use body fluid sampling device with analyte sensing|
|US8574895||Dec 30, 2003||Nov 5, 2013||Sanofi-Aventis Deutschland Gmbh||Method and apparatus using optical techniques to measure analyte levels|
|US8579831||Oct 6, 2006||Nov 12, 2013||Sanofi-Aventis Deutschland Gmbh||Method and apparatus for penetrating tissue|
|US8622930||Jul 18, 2011||Jan 7, 2014||Sanofi-Aventis Deutschland Gmbh||Tissue penetration device|
|US8636673||Dec 1, 2008||Jan 28, 2014||Sanofi-Aventis Deutschland Gmbh||Tissue penetration device|
|US8641643||Apr 27, 2006||Feb 4, 2014||Sanofi-Aventis Deutschland Gmbh||Sampling module device and method|
|US8641644||Apr 23, 2008||Feb 4, 2014||Sanofi-Aventis Deutschland Gmbh||Blood testing apparatus having a rotatable cartridge with multiple lancing elements and testing means|
|US8652831||Mar 26, 2008||Feb 18, 2014||Sanofi-Aventis Deutschland Gmbh||Method and apparatus for analyte measurement test time|
|US8668656||Dec 31, 2004||Mar 11, 2014||Sanofi-Aventis Deutschland Gmbh||Method and apparatus for improving fluidic flow and sample capture|
|US8679033 *||Jun 16, 2011||Mar 25, 2014||Sanofi-Aventis Deutschland Gmbh||Tissue penetration device|
|US8690796||Sep 29, 2006||Apr 8, 2014||Sanofi-Aventis Deutschland Gmbh||Method and apparatus for penetrating tissue|
|US8702624||Jan 29, 2010||Apr 22, 2014||Sanofi-Aventis Deutschland Gmbh||Analyte measurement device with a single shot actuator|
|US8721671||Jul 6, 2005||May 13, 2014||Sanofi-Aventis Deutschland Gmbh||Electric lancet actuator|
|US8784335||Jul 25, 2008||Jul 22, 2014||Sanofi-Aventis Deutschland Gmbh||Body fluid sampling device with a capacitive sensor|
|US8808201||Jan 15, 2008||Aug 19, 2014||Sanofi-Aventis Deutschland Gmbh||Methods and apparatus for penetrating tissue|
|US8828203||May 20, 2005||Sep 9, 2014||Sanofi-Aventis Deutschland Gmbh||Printable hydrogels for biosensors|
|US8845549||Dec 2, 2008||Sep 30, 2014||Sanofi-Aventis Deutschland Gmbh||Method for penetrating tissue|
|US8845550||Dec 3, 2012||Sep 30, 2014||Sanofi-Aventis Deutschland Gmbh||Tissue penetration device|
|US8905945||Mar 29, 2012||Dec 9, 2014||Dominique M. Freeman||Method and apparatus for penetrating tissue|
|US8936933||May 18, 2010||Jan 20, 2015||IQumm, Inc.||Sample processing methods|
|US8945910||Jun 19, 2012||Feb 3, 2015||Sanofi-Aventis Deutschland Gmbh||Method and apparatus for an improved sample capture device|
|US8965476||Apr 18, 2011||Feb 24, 2015||Sanofi-Aventis Deutschland Gmbh||Tissue penetration device|
|US9005551||Feb 7, 2011||Apr 14, 2015||Roche Molecular Systems, Inc.||Sample vessels|
|US9034639||Jun 26, 2012||May 19, 2015||Sanofi-Aventis Deutschland Gmbh||Method and apparatus using optical techniques to measure analyte levels|
|US9072842||Jul 31, 2013||Jul 7, 2015||Sanofi-Aventis Deutschland Gmbh||Method and apparatus for penetrating tissue|
|US9089294||Jan 16, 2014||Jul 28, 2015||Sanofi-Aventis Deutschland Gmbh||Analyte measurement device with a single shot actuator|
|US9089678||May 21, 2012||Jul 28, 2015||Sanofi-Aventis Deutschland Gmbh||Method and apparatus for penetrating tissue|
|US9144401||Dec 12, 2005||Sep 29, 2015||Sanofi-Aventis Deutschland Gmbh||Low pain penetrating member|
|US9186468||Jan 14, 2014||Nov 17, 2015||Sanofi-Aventis Deutschland Gmbh||Method and apparatus for penetrating tissue|
|US9226699||Nov 9, 2010||Jan 5, 2016||Sanofi-Aventis Deutschland Gmbh||Body fluid sampling module with a continuous compression tissue interface surface|
|US9248267||Jul 18, 2013||Feb 2, 2016||Sanofi-Aventis Deustchland Gmbh||Tissue penetration device|
|US9261476||Apr 1, 2014||Feb 16, 2016||Sanofi Sa||Printable hydrogel for biosensors|
|US9314194||Jan 11, 2007||Apr 19, 2016||Sanofi-Aventis Deutschland Gmbh||Tissue penetration device|
|US9339612||Dec 16, 2008||May 17, 2016||Sanofi-Aventis Deutschland Gmbh||Tissue penetration device|
|US20030049833 *||Sep 11, 2002||Mar 13, 2003||Shuqi Chen||Sample vessels|
|US20070123802 *||Sep 25, 2006||May 31, 2007||Freeman Dominique M||Methods and apparatus for an analyte detecting device|
|US20070219463 *||Apr 16, 2007||Sep 20, 2007||Barry Briggs||Methods and apparatus for lancet actuation|
|US20080021491 *||Jul 9, 2007||Jan 24, 2008||Freeman Dominique M||Method and apparatus for penetrating tissue|
|US20080027385 *||Oct 6, 2006||Jan 31, 2008||Freeman Dominique M||Method and apparatus for penetrating tissue|
|US20080038813 *||Apr 26, 2007||Feb 14, 2008||Shuqi Chen||Sample vessels|
|US20090131964 *||Dec 16, 2008||May 21, 2009||Dominique Freeman||Tissue penetration device|
|US20090192410 *||Jul 30, 2009||Dominique Freeman||Universal diagnostic system|
|US20090194422 *||Jan 29, 2009||Aug 6, 2009||George Koltse||Method and apparatus for plating metal parts|
|US20110034829 *||Sep 25, 2006||Feb 10, 2011||Freeman Dominique M||Methods and apparatus for an analyte detecting device|
|US20110064613 *||Nov 16, 2010||Mar 17, 2011||Chen & Chen, Llc||Fluid sample testing system|
|US20110143968 *||Jun 16, 2011||Iquum, Inc.||Sample vessels|
|US20120149999 *||Jun 16, 2011||Jun 14, 2012||Dominique Freeman||Tissue penetration device|
|US20130040830 *||Feb 14, 2013||Chen & Chen, Llc||Fluid Sample Testing System|
|DE2901345A1 *||Jan 15, 1979||Jul 19, 1979||Cortex Res Corp||Geraet zum entnehmen von proben aus blutspezimens o.dgl.|
|EP0254246A2 *||Jul 18, 1987||Jan 27, 1988||Personal Diagnostics, Inc.||Improved cuvette|
|WO1999067646A1 *||Jun 23, 1999||Dec 29, 1999||Chen & Chen, Llc||Fluid sample testing system|
|U.S. Classification||422/66, 422/65, 422/67, 356/39, 422/915|
|International Classification||B01L3/00, G01N35/10, G01N35/04, G01N21/03, G01N35/02|
|Cooperative Classification||B01L3/505, B01L3/0293, G01N35/1002, G01N21/03, G01N35/04, G01N35/1079, G01N2035/0434, G01N35/02, G01N2035/0408|
|European Classification||B01L3/505, B01L3/02H2, G01N35/02, G01N35/04, G01N21/03, G01N35/10A|