|Número de publicación||US3899296 A|
|Tipo de publicación||Concesión|
|Fecha de publicación||12 Ago 1975|
|Fecha de presentación||17 Jul 1974|
|Fecha de prioridad||17 Jul 1974|
|Número de publicación||US 3899296 A, US 3899296A, US-A-3899296, US3899296 A, US3899296A|
|Inventores||Johnson Wayne F, Mailen James C|
|Cesionario original||Us Energy|
|Exportar cita||BiBTeX, EndNote, RefMan|
|Citas de patentes (3), Citada por (57), Clasificaciones (9)|
|Enlaces externos: USPTO, Cesión de USPTO, Espacenet|
United States Patent [191 Mailen et al.
[ Aug. 12, 1975  WHOLE BLOOD ANALYSIS ROTOR FOR A MULTISTATION DYNAMIC PHOTOMETER  Inventors: James C. Mailen, Oak Ridge; Wayne F. Johnson, Loudon, both of Tenn.
 Assignee: The United States of America as represented by the United States Energy Research and Development Administration, Washington, DC.
 Filed: July 17, 1974  Appl. No.: 489,305
 U.S. Cl. 23/259; 233/26; 356/39; 356/246 ] Int. Cl. ..B04B 5/12; GOIN 33/16; GOIN 21/00; 'GOIN H10  Field of Search 23/253 R, 259; 356/39, 356/197, 246; 233/26  References Cited UNITED STATES PATENTS 3,744,974 7/1973 Maddox et al 23/259 7 1973 Mailen ..23 259 3 1974 Mailen ..23/259x Primary ExaminerMorris O. Wolk Assistant ExaminerTim0thy W. Hagan Attorney, Agent, or Firr'r'z Dean E. Carlson; David S. Zachry; Stephen D. Hamel 1 I ABSTRACT A rotor for performing photometric analyses using whole blood samples. Following static loading of a gross blood sample in the rotor the red blood cells in the gross sample are centrifugally separated from the plasma and measured 'subvolumes of plasma distributed to respective sample analysis cuvettes positioned in an annular array about the rotor periphery. Means for adding reagents to the respective cuvettes are also described.
5 Claims, 4 Drawing Figures BACKGROUND OF THE INVENTION The invention described herein relates generally to" photometers and more particularly to an improved whole blood analysis rotor for a multistation dynamic photometer of the rotary cuvette type. It was made in the course of,v or under, a" contract with the U.S. Atomic Energy Commission.
Fast photometric analyzers incorporating multistation rotary cuvette systems are becoming widely used in various laboratories because of their ability to'rapidly and accurately analyze large numbers of samples. Of particular interest areblood tests including glucose, LDl-I, SG'OT, SG PT, BUN,'total protein, alkaline phosphatse, bilirubin, calcium, chloride, sodium, potassium and magnesium. Since such tests are normally performed onblood plasma, blood cells must be removed from whole blood samples prior to analysis; Cuvette rotors designed to accept and automatically process whole blood samples must, therefore, be capable of separating plasma from cellular material. In addition, such rotors 'mustbe designed for receiving a sample in a loading operation, measuring discrete subvolumes of separated plasma for each sample analysis cuve'tte and transferring the subvolumes into the respective cuvettes. I
It is, accordingly, a general object of the invention to provide an improved rotor for a multistation photometr'nixed with suitable rereavnym opencommu riication-with: the'centr'al loading port; and valve containing connectingpassageways extending between the'annulus 'an'd the centrifugal ends of the seeond'and third segments of the third capillarysized passageways Rotors made-according-to the invention accept'whole blood samples, separate plasma from cellular material, measure subvolumes of the sep-. arated plasma, and transferthemeasured-subvolumes to respective sample analysis cuvettes where they are reagents and photometrically: analyzed.
BRIEF DEscRIPrIoNoE THE DRAWINGS FIG. 1 is abottom plan view of a rotor'made in accordance withtheinvention. 6 FIG 2 is a' vertical sectional view taken 2--2of FIG. 1. I
' FIGI 3 i'sa top plan view of the rotor of FIG. 1. FIG. 4 is a vertical sectional view taken along line 44 Of FIGQB. i I
w DESCRIPTION OF THE PREFERRED 1 EMBODIMENT Referring now to the drawings, initially to FIGS; 1' and 2, the bottom sideand a first sectional view of a along line 'disk-shap'ed rotor 2 are shown, respectively. In construction, the rotoris' of laminated design with a central, preferably opaque, plastic disk Ssandwichedberic analyzer whichiss'fiitable for use in performing whole blood analyses.
Another more particular object of the invention is to provide an improved rotor for a multistation photometric analyzer suitable for receiving a whole blood sample, centrifuging the whole blood sample to separate its plasma and cellular'co'mponents, measuring discrete plasma subvolumes and transferring the subvolumes to respective sample analysis cuvettes.
Other objects of the invention will be apparent from an examination 'of the following written description of the invention and the appended drawings.
SUMMARY OF THE INVENTION capillary-sized passageway communicating between said static loading chamberand said annulusy'at least one second capillary-sized passageway communicating between said annulus and a centrifugal overflow chamber positioned centripetal to said annulus; third capillary-sized passageways radially folded .to. form'three radially-extending interconnected passageway segments, a firstsegmentextending radially from each cuvette to a point centripetal to said overflow chamber, a second segment extendingfromthe centripetal end of the first segment to a radius about equal to that of the annulus and a third segmentextending from the centrifugal end of the second'segment to a central fluid trans- 'twe'en"top and bottom transpa'rntdisks' 4 and 5. A cirsageways' may' be used in ro tors designed to test. samples", such as sewage effluen'ts; which are not subject to the volumetric restrictions of blood samples. An axially extending loading port ll "provides access to loading ""chamber7 through the-topof the rotor. Also shown in FIG. are second radiallyf'extendingcapillary-sized 7 passageways I-Z cOmmunicating between annulus 9 and and a s'econd-sec tional view of the rotor of FIG. 1 are respective Overflow chambers- 13' designed to limit, the centripetal displacement ofblood within passageways describedin later rference'to- FIGS. 3 and 4.
-'Turning now tO'FIGS. Siaridd whereinthe top side shownja third capillary-sized .pas'sageway14 is radially folded to form three" radially-extending interconnected passageway segmentsfAfirst' segment designated l4'a extends radially from each 'cuvette to a point centripeml to overflow chambers 13'. A second segment designated 14b extends fromthe centripetal end of the first segment to a radius'roughly correspondingto that'of annulus 9. The third segment designated'14c extends from the c'entrifu gal end ofithe second segment to a central fluid transfer cavity in open communication irhce'ntral loading port 11 and the top surface of top 't'raiisparentdisk l,
g v A "and4, annulus 9 communicates with passageways 14 by-means of 'valve contain;- ing connecting passageways 17 extending between the annulus and" the centrifiigal ends of passageway segments 14b and 140. A magnetically opened ball check valve includes a ball traverse chamber 18 of larger diameter than the capillary-sized passageways l4 and 17 to permit ball 19 to close off passage of, liquid between the annulus and passageway 14 during centrifugation, except when an axially located magnet 21 (shown schematically) is brought into position or activated to hold the valve open by drawing ball 19 (of magnetic material) to the centripetal ends of ball traverse chamber OPERATION In operation, a rotor as hereinbefore described is placed in a turntable such as that shown in U.S. Pat. No. 3,798,459 which issued Mar. 19, 1974, in the name of Anderson et al. A gross whole blood sample is loaded, preferably by a hypodermic needle extending through loading port 11 into loading chamber 7 while the rotor is at rest. Suitable reagents are likewise loaded into loading chambers 22 through loading ports 23. Although not shown in FIG. 3, one complete set of loading chamber 22, passageways l4 and 17, etc., is provided for each sample analysis cuvette 6. Only one set of those features is illustrated to simplify the drawing without detracting from a full understanding of the invention.
Once static loading of the whole blood sample and reagents has been completed, the rotor is accelerated to a low speed, typically 300 to 500 rpm, and magnet 21 activated to open the ball check valves by drawing check balls 19 to the centripetal ends of the respective ball traverse chambers 18. Reagents contained in loading chambers 22 pass immediately through passageways 24 to respective sample analysis chambers 6 under the influence of rotation-induced inertial forces. During this initial low speed rotation, the whole blood sample in loading chamber 7 flows outward through passageways 8 into annulus 9 from which it flows radially inwardly into passageways 12, 17 and segments 14b and 140 of passageways 14 to a common radius as determined by radius R where overflow occurs into overflow chambers 13. The gross volume of the statically loaded whole blood sample is selected to cause overflow into chambers 13 without filling those chambers. As indicated above, the common centripetal end of interconnected passageway segments 14a and 14b is centripetal to the radius R defining the overflow level so that no blood spills into the sample analysis cuvettes during this initial low speed centrifugation step.
Following the initial low speed centrifugation step wherein whole blood is caused to rise within passageway segments 14b and 140 to a level corresponding to radius R, magnet 21 is removed or de-energized and rotational speed increased to about 4000 rpm. Ball check 19 moves to the centrifugal end of ball traverse chamber 18 where it blocks passageway 17 as shown in FIG. 4. High speed centrifugation is continued until all red blood cells within passageway segments 14b and 14c sediment into chamber 18 which is sized to hold all the red blood cells in a normal blood sample contained within passageway segments 14b and 140. The plasmared cell interface following sedimentation of the red cells will thus normally be within ball tr'ansfer chamber 18 leaving passageway segments 14b and 14c containing a measured volume of plasma only. The plasma volume is determined by the length and cross section of segments 14b and 14c and the selection of radius R which limits the centripetal level to which the segments are filled.
The volume of clarified plasma contained in passageway segments 14b and 14c is transferred to a respective sample analysis cuvette 6 with the rotor spinning at reduced speed, typically about 1000 rpm, by applying a slight positive air pressure to the central opening in disk 4 to pressurize fluid transfer cavity 15. This slight pressure forces the plasma to flow from passageway segments 14b and through segment 14a and into a sample analysis cuvette where it mixes with reagent previously transferred to the cuvette upon initial rotation. Alternatively, a rinse solution of distilled water could be injected into fluid transfer cavity 15 to displace plasma from passageway segments 14b and 140. Photometric analysis of the cuvette contents is then made while the rotor continues to rotate at about 1000 rpm in accordance with the techniques and principles taught in U.S. Pat. No. 3,555,284 issued Jan. 12, 1971,
in the name of Norman G. Anderson.
The above described preferred embodiment and method of operation are intended to be illustrative only and should not be interpreted in a limiting sense. For example, particulate suspensions other than whole blood could be processed to remove particulates and the clarified supernatant analyzed. It is intended rather, that the invention be limited in scope only by the following claims.
What is claimed is:
1. An improved rotor for a photometric solution analyzer of the rotary cuvette type suitable for use in analyzing whole blood samples comprising a generally disk-shaped member defining:
a. a plurality of sample analysis cuvettes disposed in a circular array for receiving liquid samples and reagents, said disk-shaped member having transparent walls adjacent said sample analysis cuvettes for permitting the passageway of light therethrough;
b. a centrally located static loading chamber having a loading port for receiving gross whole blood samples;
c. a central fluid transfer cavity in open communication with the outside of said disk-shaped member;
(1. a continuous annulus positioned on a radius intermediate said cuvettes and said static loading chamber;
e. at least one first passageway communicating between said annulus and said static loading chamber;
f. at least one overflow chamber positioned intermediate said annulus and said static loading chamber;
g. at least one second passageway communicating between said annulus and said at least one overflow chamber;
h. a plurality of third passageways each of which is radially folded to form three radially extending interconnected passageway segments; a first segment extending radially from a respective sample analysis cuvette to a point centripetal to said overflow chamber, a second segment extending from the centripetal end of said first segment to a radius about equal to that of said annulus, and a third segment extending from the centrifugal end of said second segment to said central fluid transfer cavity; i. a plurality of connecting passageways extending between said annulus and the centrifugal ends of respective second and third segments of said third passageways; j. a magnetically actuated ball trap valve disposed in each of said connecting passageways; and k. means for injecting reagents into said sample analysis cuvettes. 2. The improved rotor of claim 1 wherein said annulus and said first, second, third and connecting passageways are capillary sized.
3. The improved rotor of claim 1 wherein said second and third segments of said third passageways define a preselected sample volume.
4. The improved rotor of claim 1 wherein said magnetically actuated ball trap valve includes a radially oriented ball traverse chamber and a ball of magnetic material disposed within said ball traverse chamber; the centrifugal end of each of said ball traverse chamber being in communication with a respective connecting passageway.
5. The improved rotor of claim 1 wherein said means for injecting reagents into said sample analysis cuvettes includes a static reagent loading chamber disposed centripetally to each cuvette, and a radially-extending reagent transfer passageway communicating between the centrifugal end of each reagent loading chamber and a respective cuvette.
|Patente citada||Fecha de presentación||Fecha de publicación||Solicitante||Título|
|US3744974 *||30 Nov 1971||10 Jul 1973||Atomic Energy Commission||Loading disk for photometric analyzer of rotary cuvette type|
|US3744975 *||9 Dic 1971||10 Jul 1973||Atomic Energy Commission||Rotor for multistation photometric analyzer|
|US3795451 *||24 Abr 1973||5 Mar 1974||Atomic Energy Commission||Rotor for fast analyzer of rotary cuvette type|
|Patente citante||Fecha de presentación||Fecha de publicación||Solicitante||Título|
|US4035156 *||21 Ene 1977||12 Jul 1977||The United States Of America As Represented By The United States Energy Research And Development Administration||Filter type rotor for multistation photometer|
|US4148607 *||17 Feb 1976||10 Abr 1979||Hoffmann-La Roche Inc.||Apparatus and analysis for agglutination reaction|
|US4192250 *||1 Dic 1977||11 Mar 1980||Duijn Pieter Van||Valve-centrifuge|
|US4226531 *||29 Ago 1977||7 Oct 1980||Instrumentation Laboratory Inc.||Disposable multi-cuvette rotor|
|US4256696 *||21 Ene 1980||17 Mar 1981||Baxter Travenol Laboratories, Inc.||Cuvette rotor assembly|
|US4284602 *||10 Dic 1979||18 Ago 1981||Immutron, Inc.||Integrated fluid manipulator|
|US4314970 *||27 Ago 1980||9 Feb 1982||Instrumentation Laboratory Inc.||Analysis system|
|US4373812 *||25 Mar 1981||15 Feb 1983||Instrumentation Laboratory Inc.||Cuvette assembly|
|US4431606 *||1 May 1981||14 Feb 1984||Hoffmann-La Roche Inc.||Multicuvette rotor for analyzer|
|US4580896 *||7 Nov 1983||8 Abr 1986||Allied Corporation||Multicuvette centrifugal analyzer rotor with annular recessed optical window channel|
|US4580897 *||31 May 1984||8 Abr 1986||Allied Corporation||Centrifugal analyzer rotors|
|US4580898 *||31 May 1984||8 Abr 1986||Allied Corporation||Analytical system|
|US4663296 *||26 Oct 1983||5 May 1987||Hoffmann-La Roche Inc.||Multicuvette rotor for analyzer|
|US4690899 *||2 Jul 1985||1 Sep 1987||Boehringer Mannheim Gmbh||Process and device for carrying out analytical determinations|
|US4740472 *||5 Ago 1985||26 Abr 1988||The United States Of America As Represented By The United States Department Of Energy||Method and apparatus for automated processing and aliquoting of whole blood samples for analysis in a centrifugal fast analyzer|
|US4756884 *||1 Jul 1986||12 Jul 1988||Biotrack, Inc.||Capillary flow device|
|US4902479 *||7 Nov 1983||20 Feb 1990||Fisher Scientific Company||Centrifugal analyzer rotor|
|US4963498 *||15 Ene 1988||16 Oct 1990||Biotrack||Capillary flow device|
|US4999304 *||28 Dic 1987||12 Mar 1991||Miles Inc.||Dynamic braking centrifuge|
|US5084240 *||13 Jul 1990||28 Ene 1992||Cirrus Diagnostics Inc.||Centrifuge vessel for automated solid-phase immunoassay|
|US5100627 *||30 Nov 1989||31 Mar 1992||The Regents Of The University Of California||Chamber for the optical manipulation of microscopic particles|
|US5160702 *||17 Ene 1989||3 Nov 1992||Molecular Devices Corporation||Analyzer with improved rotor structure|
|US5173193 *||1 Abr 1991||22 Dic 1992||Schembri Carol T||Centrifugal rotor having flow partition|
|US5186844 *||1 Abr 1991||16 Feb 1993||Abaxis, Inc.||Apparatus and method for continuous centrifugal blood cell separation|
|US5242606 *||29 Oct 1991||7 Sep 1993||Abaxis, Incorporated||Sample metering port for analytical rotor having overflow chamber|
|US5300779 *||18 Ago 1992||5 Abr 1994||Biotrack, Inc.||Capillary flow device|
|US5318748 *||8 Abr 1991||7 Jun 1994||Cirrus Diagnostics, Inc.||Centrifuge vessel for automated solid-phase immunoassay having integral coaxial waste chamber|
|US5650334 *||31 Ago 1995||22 Jul 1997||First Medical, Inc.||Fluorescent labelling compositions and methods for their use|
|US5693233 *||4 Dic 1995||2 Dic 1997||Abaxis||Methods of transporting fluids within an analytical rotor|
|US5919711 *||7 Ago 1997||6 Jul 1999||Careside, Inc.||Analytical cartridge|
|US6162400 *||12 Ago 1998||19 Dic 2000||Agilent Technologies, Inc.||Apparatus for controlling reactions|
|US6299839||31 Ago 1995||9 Oct 2001||First Medical, Inc.||System and methods for performing rotor assays|
|US6395553 *||23 Oct 2000||28 May 2002||Agilent Technologies, Inc.||Method for controlling reactions|
|US7247486 *||14 May 2002||24 Jul 2007||Agilent Technologies, Inc.||Method and apparatus for controlling reactions|
|US7635585 *||31 May 2002||22 Dic 2009||Jae Chern Yoo||Micro valve apparatus using micro bead and method for controlling the same|
|US7897398 *||25 Jul 2008||1 Mar 2011||Panasonic Corporation||Centrifugal analysis device with improved mixing and method using the device|
|US7935522 *||4 Abr 2006||3 May 2011||Gyros Patent Ab||Microfabricated apparatus for cell based assays|
|US8241891||9 Nov 2009||14 Ago 2012||Samsung Electronics Co., Ltd.||Micro valve apparatus using micro bead and method for controlling the same|
|US8343428 *||24 Oct 2008||1 Ene 2013||Rohm Co., Ltd.||Microchip and method of using the same|
|US8367424 *||14 Oct 2008||5 Feb 2013||Rohm Co., Ltd.||Microchip and method of using the same|
|US20020132355 *||14 May 2002||19 Sep 2002||Schembri Carol T.||Method and apparatus for controlling reactions|
|US20040155213 *||31 May 2002||12 Ago 2004||Yoo Jae Chern||Micro valve apparatus using micro bead and method for controlling the same|
|US20060194273 *||4 Abr 2006||31 Ago 2006||Gyros Patent Ab||Microfabricated apparatus for cell based assays|
|US20070134799 *||31 Ene 2007||14 Jun 2007||Schembri Carol T||Method and apparatus for controlling reactions|
|US20090098658 *||14 Oct 2008||16 Abr 2009||Rohm Co., Ltd.||Microchip and Method of Using the Same|
|US20090111675 *||24 Oct 2008||30 Abr 2009||Rohm Co., Ltd.||Microchip and Method of Using the Same|
|US20100055771 *||9 Nov 2009||4 Mar 2010||Jae Chern Yoo||Micro valve apparatus using micro bead and method for controlling the same|
|US20130115148 *||9 May 2013||Rohm Co., Ltd.||Microchip and Method of Using the Same|
|EP0039825A1 *||29 Abr 1981||18 Nov 1981||F. HOFFMANN-LA ROCHE & CO. Aktiengesellschaft||Cuvette rotor for analyzer and method of operation of said cuvette rotor|
|EP0062907A1 *||8 Abr 1982||20 Oct 1982||Jean Guigan||Method and apparatus for delivering a predetermined amount of sample liquid to a cell|
|EP0167171A2 *||5 Jul 1985||8 Ene 1986||Boehringer Mannheim Gmbh||Method and device for performing analytical determinations|
|EP0167175A2 *||5 Jul 1985||8 Ene 1986||Boehringer Mannheim Gmbh||Device for washing a substance present in a field with a washing liquid in several washing steps and for transporting the washing fluid, emerging from said field, after the last washing step to a cuvette|
|EP0532591A1 *||31 May 1991||24 Mar 1993||Abaxis, Inc.||Analytical rotors and methods for analysis of biological fluids|
|EP0631125A1 *||9 May 1990||28 Dic 1994||Lockheed Martin Energy Systems, Inc.||Rotor and method for automatically processing liquids for laboratory and bioanalysis purposes|
|WO1990015321A2 *||9 May 1990||13 Dic 1990||Martin Marietta Energy Systems||Rotor and method for automatically processing liquids for laboratory and bioanalysis purposes|
|WO1999008095A1 *||28 Jul 1998||18 Feb 1999||Careside Inc||Analytical cartridge|
|WO1999058956A1 *||25 Mar 1999||18 Nov 1999||Careside Inc||Electrochemical analytical cartridge|
|Clasificación de EE.UU.||422/50, 356/39, 494/10, 422/72, 494/17|
|Clasificación internacional||G01N21/03, G01N21/07|