CA2192196C - Modified siphons for improved metering precision - Google Patents

Modified siphons for improved metering precision Download PDF

Info

Publication number
CA2192196C
CA2192196C CA002192196A CA2192196A CA2192196C CA 2192196 C CA2192196 C CA 2192196C CA 002192196 A CA002192196 A CA 002192196A CA 2192196 A CA2192196 A CA 2192196A CA 2192196 C CA2192196 C CA 2192196C
Authority
CA
Canada
Prior art keywords
chamber
siphon
rotor
liquid
inlet
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Lifetime
Application number
CA002192196A
Other languages
French (fr)
Other versions
CA2192196A1 (en
Inventor
Anne R. Kopf-Sill
Carol T. Schembri
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Abaxis Inc
Original Assignee
Abaxis Inc
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Abaxis Inc filed Critical Abaxis Inc
Publication of CA2192196A1 publication Critical patent/CA2192196A1/en
Application granted granted Critical
Publication of CA2192196C publication Critical patent/CA2192196C/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • GPHYSICS
    • G01MEASURING; TESTING
    • G01NINVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N21/00Investigating or analysing materials by the use of optical means, i.e. using sub-millimetre waves, infrared, visible or ultraviolet light
    • G01N21/01Arrangements or apparatus for facilitating the optical investigation
    • G01N21/03Cuvette constructions
    • G01N21/07Centrifugal type cuvettes

Landscapes

  • General Health & Medical Sciences (AREA)
  • Immunology (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Analytical Chemistry (AREA)
  • Biochemistry (AREA)
  • Health & Medical Sciences (AREA)
  • General Physics & Mathematics (AREA)
  • Physics & Mathematics (AREA)
  • Pathology (AREA)
  • Automatic Analysis And Handling Materials Therefor (AREA)
  • Investigating Or Analysing Biological Materials (AREA)
  • Centrifugal Separators (AREA)
  • Optical Measuring Cells (AREA)
  • Sampling And Sample Adjustment (AREA)

Abstract

The present invention provides centrifu-gal force rotors for delivering a premeasured volume of liquid to a chamber in the rotor. In particular the rotors comprise siphons (134) for delivering a premeasured volume of liquid be-tween a first and a second chamber (136) in the rotor. The siphons (134) of the invention are designed such that the inlet (138) of the siphon on the first chamber is radially outward of the siphon outlet (139) on the second cham-ber (136). The first chamber is emptied to a level equivalent to the radial position of the siphon outlet (139).

Description

0 0 o G o BACKGROUND OF TFiE INVENTION
The present invention relates generally to devices and methods for analyzing biological fluids. In particular, it relates to the design and use of improved centrifugal rotors having siphons which allow delivery of a~precise volume of liquid to a chamber in the rotor.
is ~ Biological tests of blood plasma and other biological fluids frequently require that fluids be quickly divided into predetermined volumes for analysis in a variety of optical tests or assays. It is also frequently desirable to separate potentially interfering cellular components of the material from the other fluid grior to testing. Such' measurement and separation steps have previously been typically performed by centrifugation to separate, for instance, blood plasma from the cellular components, followed by manual or automated pipetting of predetermined volumes of the blood plasma into separate test wells. Such procedures are labor intensive and time-consuming. As a result, various automated systems and methods have been proposed for providing multiple aliquots of plasma suitable for testing in a more efficient manner.
A major advance in the analysis of biological fluids has been the use of centrifugal rotors. These rotors are designed to measure volumes of a biological fluid, such as blood, remove cellular components, and mix the fluid with an appropriate diluent for analysis, for example by optical testing. Typically, the rotors provide a plurality of discrete volumes of sample in separate cuvettes in which the sample is optically analyzed.
To ensure accurate and consistent results, such rotors require the delivery of precisely measured volumes of liquid to various chambers in the rotor. This must often be accomplished in circumstances in which the rotor quickly accelerates and decelerates or is otherwise perturbed during operation. This perturbation can often lead to.delivery of inaccurately measured volumes. The present invention addresses these and other needs.
Description of the Background Art U.S. Patent Nos. 4,894,204, and 5,160,?02 disclose siphons for transferring fluids between chambers in a rotor.
U.S. Patent No. 4,244,916 discloses a rotor comprising a plurality of cuvettes positioned radially outward of a central receptacle. Each cuvette is connected to the central receptacle by a duct and comprises a separate air escape orifice. U.S. Patent No. 4,314,968 relates to rotors having cells positioned on the periphery of the rotor. Each cell includes a peripheral orifice for removing fluid introduced into the cell. U.S. Patent No. 4,902,4?9 discloses a multi-cuvette rotor comprising elongated, radially extending cuvettes. Each elongated cuvette comprises a first chamber for receiving a first constituent and a second chamber for receiving a second constituent. A divider structure between the first and second chambers prevents mixing of the constituents before a predetenained time. Mixing occurs as the rotor is spun at a sufficient speed. U.S. Patent No.
4,963,498 discloses devices which rely upon capillaries, chambers, and orifices to pump and mix fluids for optical analysis. U.S. Patent No. 5,0??,013 discloses rotors comprising peripheral cuvettes connected to holding chambers positioned radially inward from the cuvettes.
SUMMARY OF THE INVENTION
The present invention provides centrifugal rotors comprising siphons for delivering a premeasured volume of liquid, typically a biological sample such as plasma, between a first and a second chamber in the rotor.

Accordingly, the present invention provides a centrifugal rotor comprising:
a rotor body comprising a liquid-dispensing chamber, a liquid-receiving chamber, and a siphon;
the siphon being connected to the liquid-dispensing chamber through a siphon inlet and connected to the liquid-receiving chamber through a siphon outlet, the siphon inlet being radially outward of the siphon outlet, said siphon traveling radially inward to a point radially inward of said siphon inlet, and then radially outward to said siphon outlet; the rotor further comprising a cuvette, wherein said cuvette is radially outward of said liquid-dispensing chamber and said liquid-receiving chamber, and;
a distribution ring which permits flow of a liquid to said cuvette from an output siphon connected to the liquid-receiving chamber.
The present invention also provides a centrifugal rotor comprising:
a rotor body comprising a liquid-dispensing chamber, a liquid-receiving chamber, and a siphon;
the siphon being connected to the liquid-dispensing chamber through a siphon inlet and connected to the liguid-receiving chamber through a siphon outlet, the siphon inlet being radially outward of the siphon outlet, said siphon traveling radially inward to a point radially inward of said siphon inlet, and then radially outward to said siphon outlet; the rotor further comprising a distribution ring positioned radially outward of the liquid-receiving chamber; and a delivery channel connecting the distribution ring to the liquid-receiving chamber, said distribution ring being connected to a cuvette through an inlet channel.
The present invention also provides a centrifugal rotor comprising:
a sample chamber containing a liquid;
an unvented receiving chamber positioned radially outward from the sample chamber;
a delivery channel connected to the sample chamber for removing the liquid from the sample chamber under centrifugal force;
a distribution channel directly connected to the delivery channel for removing the liquid from the delivery channel under centrifugal force;
an inlet channel connected to the unvented receiving chamber for receiving the liquid from the sample chamber through the delivery channel and the distribution channel;
wherein, the resistance to flow of the liquid in the delivery channel is greater than the resistance to flow of the liquid in the inlet and distribution channels such that the cross-sectional area of the liquid flowing through the inlet and distribution channels is less than the cross-sectional area of said inlet and distribution channels, whereby spinning the rotor effects the flow of the liquid from the sample chamber through the delivery channel, the distribution channel and the inlet channel to the receiving chamber such that air escapes from the receiving chamber through the inlet channel as the liquid enters the receiving chamber.
In a further aspect, the present invention provides a method of delivering a premeasured volume of liquid from a first chamber to a second chamber in a rotor, the method comprising:
providing a rotor comprising a first chamber with a first volume, a second chamber, and a siphon connected to the first chamber through a siphon inlet and connected to the second chamber through a siphon outlet, the siphon inlet being radially outward of the siphon outlet;
spinning the rotor, thereby introducing an unmeasured volume of liquid into the first chamber;
stopping the rotation of the rotor, thereby priming the siphon connecting the first chamber to the second chamber;
and spinning the rotor, thereby initiating the operation of the siphon and delivering the premeasured volume of the liquid from the first chamber to the second chamber, the premeasured volume being determined by the radial position of the siphon outlet and the first volume of the first chamber.
The siphons of the invention have an elbow that i.s radially inward of the W O 95133986 ' , r '_r ~~rt7S95107145 radially most inward point of the fluid in the first chamber.
As the rotor is spinning the fluid does not flow past the elbow. After the rotor stops, capillary forces "prime" the siphon by pulling fluid just around the elbow. When the rotor ' 5 is restarted, centrifugal force draws the remaining fluid out of the metering chamber into the receiving chamber until the ' level of the fluid in the metering chamber is at the same radial distance as the outlet of the siphon. The siphons of the invention are designed such that the inlet of the siphon on the first chamber is radially outward of the siphon outlet on the second chamber.
The positioning of the inlets and outlets of the siphons of the invention provide a number of advantages. For example, the inlet of the siphon is always positioned radially outward of the final position of the meniscus of the fluid in the first chamber, after fluid has been transferred to the second chamber. Thus, inaccuracy in measurement associated with different shaped menisci in different fluids is minimized since the meniscus is minimized. In addition, one of skill will recognize that all siphons are semi-stable because the train of fluid in a siphon is stable but easily broken if the rotor is perturbed. When the train of fluid is broken, under centrifugal force, the fluid contained in the siphon will flow to the radially most outward point. In prior art siphons this point is the siphon outlet. Thus, the potential exists for the delivery of unmetered volumes of fluid to the receiving chamber. In the siphons of the present invention, the radially most outward point in the siphon is the siphon inlet.
In this design, the problem of delivering unmetered volumes of fluid is avoided because the fluid flows back into the first chamber when the train of fluid is broken.
The chambers connected by the siphons of the invention are used to perform any of a number of functions, such as metering liquids, separating solid components from a sample, mixing diluent with the sample, and the like. In the ' preferred embodiments, the siphons connect a plasma metering chamber to a mixing chamber for mixing the premeasured volume of plasma with diluent.

WO 95/33986 2 ~ 9 219 6. : ~' PC'1'/US95107145 In addition, the rotors of the invention comprise unmodified inlet chanrie~s connecting a distribution ring to cuvettes comprising reagents for optical analysis of a biological sample. The inlet channels are sized such that, as the rotor spins, gas escapes from the cuvette through the inlet channel as the liquid enters the cuvette through the inlet channel. An °'unmodified inlet channel" as used herein refers to a simple inlet channel, typically having a rectangular cross section, which is not modified (e.g., by altering the cross-sectional shape, surface texture, and the like) to provide a pathway for gas to escape from a cuvette that is not otherwise vented.
BRIEF DESCRIPTION OF THE DRAWINGS
Figs. lA-1F are top plan views of a rotor of the invention showing the flow of fluids through the chambers and channels of the rotor as the rotor is spun.
DESCRIPTION OF THE PREFERRED EMBODIMENT
The present invention provides methods and devices for the delivery of liquids to chambers in an analytical rotor. The rotors of the invention comprise siphons which ensure precise delivery of metered volumes of liquid to a desired chamber in the rotor.
The rotors of the invention are suitable for the analysis of any liquid, typically a biological sample such as whole blood or plasma. It is also useful with numerous other biological fluids, such as urine, sputum, semen, saliva, ocular lens fluid, cerebral fluid, spinal fluid, amniotic fluid. Other fluids that can be tested include tissue culture media, food and industrial chemicals, environmental samples and the like.
The rotors typically provide chambers which can separate cellular components from the biological sample (e. g.
whole blood), measure a precise volume of liquid sample (e. g.
plasma), mix the sample with an appropriate diluent and deliver the diluted sample to cuvettes for optical analysis.
The fluid delivered to the cuvettes, undergoes reactions) within the cuvettes, e.g., reaction with a reagent which forms part of an analytical procedure to detect one or more analytas within the fluid. The sample may further be optically analyzed while present in the rotor, either with or without prior reaction.
5 The apparatus of the present invention comprises an analytical rotor having a rotor body which is capable of being mounted on a conventional laboratory centrifuge of the type which is commercially available from suppliers, such a Beckman Instruments, Inc., Spinco Division, Fullerton, California;
Fisher Scientific, Pittsburgh, Pennsylvania; VWR Scientific, San Francisco, California, and the like. Generally, the centrifugal rotor will include a receptacle or other coupling device suitable for mounting on a vertical drive shaft provided by the centrifuge. The particular design of_the receptacle or coupling device will depend on the nature of the centrifuge, and it will be appreciated that the centrifugal rotor of the present invention may be adapted for use with all or most types of centrifuges which are now available or which may become available in the future.
The rotor body comprises a structure which maintains a desired geometric pattern or relationship between a plurality of chambers, interconnecting passages, and vents, as described in more detail below. Various specialized chambers and channels suitable for use in the rotors of the invention 25' aze disclosed in U.S. Patent Nos. 5,061,381; 5,122,284;
5,186,844 and 5,242,606.
Usually, the body will be a substantially solid plate or disk with the chambers and passages formed as spaces - or voids in the otherwise solid matrix. Conveniently, such solid plate structures may be formed by laminating a plurality of separately-formed layers together into a composite structure where the chambers and horizontal passages are generally formed between adjacent layers. The vertical passages may be formed through the layers. The individual layers may be formed by injection molding, machining, or combinations thereof, and will usually be joined together, typically using a suitable adhesive or by ultrasonic welding.
The final enclosed volumes are formed when the layers are brought together.
Of course, the centrifugal rotor could also be formed as a plurality of discrete components, such as tubes, vessels, chambers, etc., arranged in a suitable framework.
Such assemblies of discrete components, however, are generally more difficult to manufacture and are therefore less desirable than those formed within a substantially solid plate.
The rotor body may be formed from a wide variety of to materials and may optionally include two or more materials.
Usually, the materials) will be transparent so that the presence and distribution of the biological fluid, cellular components, and reagents, may be observed within the various internal chambers and passages. Optionally, to the extent analytical chambers, e.g., cuvettes, or other test wells are formed within the rotor, it is desirable to have suitable optical paths formed within the rotor so that the contents of the cuvettes may be observed spectrophotometrically, fluorometrically, or by other optical assessment instruments.
The construction of suitable cuvettes having particular optical paths formed therethrough is disclosed in U.S. Patent No. 5,173,193.
In the preferred embodiment, the rotor is formed with an acrylic resin having suitable optical properties, at least in those areas which define an optical path.
The apparatus and method of the present invention are suitable for performing a wide variety of analytic procedures and assays which are beneficially or necessarily 3o performed on blood plasma and other samples. The analytic procedures may require that the sample be combined with one or more reagents so that some detectable change occurs which may be related to the presence and/or amount of a particular component (analyte) or characteristic of the sample. For instance, the sample may undergo a reaction or other change which results in a change in color, fluorescence, luminescence, or the like, which may be measured by conventional spectrophotometers, fluorometers, light detectors, and the like. In some cases, immunoassays and other specific binding assays may be performed within the cell-free fluid collection chamber or within cuvettes which are connected to the collection chamber. Generally, such assay procedures should be homogeneous and not require a separation step. In other cases, however, it may be possible to accommodate heterogeneous assay systems by providing a means to separate the sample (e.g., blood plasma) from the collection chamber or another test well or cuvette after the immunological reaction step has occurred. One of skill will recognize that the means of analyzing the sample is not an important aspect of the invention. Any of a number of analytical methods can be adapted for use in the rotors of the invention, depending upon the particular sample being analyzed and component being detected.
In the case of blood analyses, conventional blood assays are typically preformed. Examples of assays which may be performed include those designed to detect glucose, lactate dehydrogenase, serum glutamic-oxaloacetic transaminase (SGOT), serum glutamic-pyruvic transaminase (SGPT), blood urea nitrogen (HUN), total protein, alkalinity, phosphatase, bilirubin, calcium, chloride, sodium, potassium, magnesium, and the like. This list is not exhaustive and is intended merely as being exemplary of the assays which may be performed using the apparatus and method of the present invention.
Usually, these tests will require that the blood and plasma be combined with one or more reagents which result in an optically detectable, usually photometrically detectable, change in the plasma. The reagents Which are required are well known and amply described in the patent and scientific literature.
The reagents are preferably provided in lyophilized form to increase stability. Ideally, they are provided in the form of lyophilized reagent spheres as described in U.S. Patent No. 5,413,732.
Referring now to Figures lA-F, an analytical rotor comprising the chambers and channels of the present invention can be seen. Figure lA shows the position of a blood sample 102 in the blood application chamber 104 after the sample has been loaded in the rotor body 100. A diluent container in chamber 106 is opened upon mounting of the rotor on the spindle of the centrifuge as described in copending and commonly assigned application, U.S. patent No. 5,275,016.
Fig. 18 shows the position of the diluant 108 and blood sample 102 after the rotor is spun at 4,000 rpm. The blood sample 102 begins to exit the blood application chamber 104 and enters the plasma metering chamber 110. At the same time, diluent 108 empties from the diluent container into the holding chamber 112. The diluent immediately begins to enter the diluent metering chamber 114 through channel 116.
Fig, iC shows the position of the liquids as the rotor 100 continues to spin. Here, the blood sample 102 has emptied the blood application chamber 104 and overflows the plasma metering chamber 110 into the overflow chamber 118 where it flows to the hemoglobin cuvette 120 and the excess blood dump 122. Meanwhile, diluent 108 fills the dilusnt metering chamber 114 and excess flows through channel 124 to diluent-only cuvettes 126 and excess diluent dump 127.
Fig. iD shows the position of the liquids at the conclusion of the first spin. The blood sample 102 has separated into cells 128 and plasma 130. The diluent-only cuvettes 126 are filled and a predetermined amount of diluent remains in the diluent metering chamber 114. The rotor 100 is then stopped and the siphon 132 from the diluent metering chamber 114, as well as the siphon 134 from the plasma metering chamber 110, are allowed to prime, as described above. Siphon 134 is a siphon of the present invention. It is connected to the plasma metering chamber 110 at inlet 138.
The inlet 138 is position radially outward of the siphon outlet 139, through which the siphon 134 empties into the mixing chamber 136.
Fig. lE shows the position of the liquids during the second spin of the rotor. The diluent metering chamber 114 empties into the mixing chamber 136 through siphon 132. A
predetermined amount of plasma 130 is metered into the mixing R'O 95133986 , ~ . ~ PCT/US95107145 chamber 136 and the two fluids are mixed, thereby forming diluted plasma 131. The amount of plasma 130 delivered to the mixing chamber 136 is determined by the position of the outlet 139 on the siphon 134. As can be seen in this figure, the final level of the plasma 133 in the plasma metering chamber 110 is at the same radial position as the outlet 139. Thus, the volume of plasma delievered to the mixing chamber 136 is determined by the volume of the plasma metering chamber 110 between the exit to the overflow chamber 129 and the final level of plasma 133. After the plasma and diluent are mixed in the mixing chamber 136, the rotor is stopped again and the output siphon 140 is primed.
Fig. iF shows the position of the diluted plasma 131 as the rotor is spun during the third spin. This figure illustrates the movement of the diluted plasma 131 through the distribution ring 142 and inlet channels 144 to the cuvettes 146 and excess plasma dump 147. The resistance to flow in the output siphon 140 is selected to be higher than the resistance to flow in the distribution ring 142 and the inlet channels 144 so that air present in the cuvettes 146 can escape as the cuvettes are filled. Specifically, siphon 140 is dimensioned such that the ratio of the cross sectional area of the inlet channels 144 to the cross sectional area of the liquid in them is greater than 2:1, preferably greater than about 4:1. The cross sectional area of the inlet channels 144 is typically the same as or slightly smaller than that of the distribution channel 142 so that gas in the unvented cuvettes escapes through the inlet channels 144 and distribution 142. If the sample is plasma or diluted plasma and the channels are rectangular in cross-section, their dimensions are typically as follows: siphon: 0.150 mm depth, 0.200 mm width;
distribution channel 0.300 mm depth, 0.50omm width; inlet channels: 0.150 depth, 0.500 width.
After the cuvettes have been filled, reagents present in the cuvettes are mixed with the solution and the necessary photometric analyses are made on the sample. Such analyses are carried out as described above according to methods known to those of skill in the art.

WO 95133986 ~ ~ ~ ~ PCTIUS95107145 Although the foregoSing invention has been described in detail for purposes of.clarity of understanding, it will be obvious that certain modifications may be practiced within the scope of the appended claims.

Claims (16)

THE EMBODIMENTS OF THE INVENTION IN WHICH AN EXCLUSIVE
PROPERTY OR PRIVILEGE IS CLAIMED ARE DEFINED AS FOLLOWS:
1. A centrifugal rotor comprising:
a rotor body comprising a liquid-dispensing chamber, a liquid-receiving chamber, and a siphon;
the siphon being connected to the liquid-dispensing chamber through a siphon inlet and connected to the liquid-receiving chamber through a siphon outlet, the siphon inlet being radially outward of the siphon outlet, said siphon traveling radially inward to a point radially inward of said siphon inlet, and then radially outward to said siphon outlet; the rotor further comprising a cuvette, wherein said cuvette is radially outward of said liquid-dispensing chamber and said liquid-receiving chamber, and;
a distribution ring which permits flow of a liquid to said cuvette from an output siphon connected to the liquid-receiving chamber.
2. A centrifugal rotor comprising:
a rotor body comprising a liquid-dispensing chamber, a liquid-receiving chamber, and a siphon;
the siphon being connected to the liquid-dispensing chamber through a siphon inlet and connected to the liquid-receiving chamber through a siphon outlet, the siphon inlet being radially outward of the siphon outlet, said siphon traveling radially inward to a point radially inward of said siphon inlet, and then radially outward to said siphon outlet; the rotor further comprising a distribution ring positioned radially outward of the liquid-receiving chamber; and a delivery channel connecting the distribution ring to the liquid-receiving chamber, said distribution ring being connected to a cuvette through an inlet channel.
3. The rotor of claim 2, wherein the inlet channel has a cross sectional area at least about 1.5 times the cross sectional area of the delivery channel.
4. The rotor of claim 3, wherein the cross sectional area of the inlet channel is about 2 times the cross sectional area of the delivery channel.
5. The rotor of claim 3, wherein the cross sectional area of the delivery channel is about 0.03 mm2.
6. The rotor of claim 2, wherein the delivery channel is a siphon.
7. A method of delivering a premeasured volume of liquid from a first chamber to a second chamber in a rotor, the method comprising:
providing a rotor comprising a first chamber with a first volume, a second chamber, and a siphon connected to the first chamber through a siphon inlet and connected to the second chamber through a siphon outlet, the siphon inlet being radially outward of the siphon outlet;
spinning the rotor, thereby introducing an unmeasured volume of liquid into the first chamber;
stopping the rotation of the rotor, thereby priming the siphon connecting the first chamber to the second chamber;
and spinning the rotor, thereby initiating the operation of the siphon and delivering the premeasured volume of the liquid from the first chamber to the second chamber, the premeasured volume being determined by the radial position of the siphon outlet and the first volume of the first chamber.
8. A centrifugal rotor comprising:
a sample chamber containing a liquid;
an unvented receiving chamber positioned radially outward from the sample chamber;
a delivery channel connected to the sample chamber for removing the liquid from the sample chamber under centrifugal force;
a distribution channel directly connected to the delivery channel for removing the liquid from the delivery channel under centrifugal force;
an inlet channel connected to the unvented receiving chamber for receiving the liquid from the sample chamber through the delivery channel and the distribution channel;
wherein, the resistance to flow of the liquid in the delivery channel is greater than the resistance to flow of the liquid in the inlet and distribution channels such that the cross-sectional area of the liquid flowing through the inlet and distribution channels is less than the cross-sectional area of said inlet and distribution channels, whereby spinning the rotor effects the flow of the liquid from the sample chamber through the delivery channel, the distribution channel and the inlet channel to the receiving chamber such that air escapes from the receiving chamber through the inlet channel as the liquid enters the receiving chamber.
9. The rotor of claim 8, wherein the receiving chamber is a cuvette containing reagents necessary for the analysis of a biological sample.
10. The rotor of claim 8, wherein the inlet channel has a cross sectional area at least about 1.5 times the cross sectional area of the delivery channel.
11. The rotor of claim 10, wherein the cross sectional area of the inlet channel is about 2 times the cross sectional area of the delivery channel.
12. The rotor of claim 10, wherein the cross sectional area of the delivery channel is about 0.03 mm2.
13. The rotor of any one of claims 1 to 5, wherein the delivery channel is a siphon.
14. The rotor of any one of claims 1 to 6, wherein the sample chamber is a mixing chamber.
15. The rotor of claim 14, further comprising a diluent splitting chamber positioned radially inward of the mixing chamber and connected to the mixing chamber through a siphon.
16. The rotor of claim 14, further comprising a plasma metering chamber positioned radially inward of the mixing chamber and connected to the mixing chamber through a siphon.
CA002192196A 1994-06-06 1995-06-05 Modified siphons for improved metering precision Expired - Lifetime CA2192196C (en)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US25440694A 1994-06-06 1994-06-06
US08/254,406 1994-06-06
PCT/US1995/007145 WO1995033986A1 (en) 1994-06-06 1995-06-05 Modified siphons for improved metering precision

Publications (2)

Publication Number Publication Date
CA2192196A1 CA2192196A1 (en) 1995-12-14
CA2192196C true CA2192196C (en) 2004-11-23

Family

ID=22964194

Family Applications (1)

Application Number Title Priority Date Filing Date
CA002192196A Expired - Lifetime CA2192196C (en) 1994-06-06 1995-06-05 Modified siphons for improved metering precision

Country Status (4)

Country Link
EP (1) EP0764266A4 (en)
JP (3) JPH10501340A (en)
CA (1) CA2192196C (en)
WO (1) WO1995033986A1 (en)

Families Citing this family (54)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5627041A (en) * 1994-09-02 1997-05-06 Biometric Imaging, Inc. Disposable cartridge for an assay of a biological sample
US6709869B2 (en) 1995-12-18 2004-03-23 Tecan Trading Ag Devices and methods for using centripetal acceleration to drive fluid movement in a microfluidics system
US6143248A (en) * 1996-08-12 2000-11-07 Gamera Bioscience Corp. Capillary microvalve
AU5895898A (en) 1996-12-20 1998-07-17 Gamera Bioscience Corporation An affinity binding-based system for detecting particulates in a fluid
AU7591998A (en) 1997-05-23 1998-12-11 Gamera Bioscience Corporation Devices and methods for using centripetal acceleration to drive fluid movement in a microfluidics system
US6632399B1 (en) 1998-05-22 2003-10-14 Tecan Trading Ag Devices and methods for using centripetal acceleration to drive fluid movement in a microfluidics system for performing biological fluid assays
US6808633B1 (en) 1999-06-23 2004-10-26 Hitachi, Ltd. Centrifugal separator and sample preparation device using the separator
ATE364843T1 (en) 1999-08-11 2007-07-15 Asahi Chemical Ind ANALYSIS CASSETTE AND FLUID FEED CONTROLLER
WO2002043866A2 (en) * 2000-12-01 2002-06-06 Burstein Technologies, Inc. Apparatus and methods for separating components of particulate suspension
WO2002046721A2 (en) 2000-12-08 2002-06-13 Burstein Technologies, Inc. Optical discs for measuring analytes
US7054258B2 (en) 2000-12-08 2006-05-30 Nagaoka & Co., Ltd. Optical disc assemblies for performing assays
US7091034B2 (en) 2000-12-15 2006-08-15 Burstein Technologies, Inc. Detection system for disk-based laboratory and improved optical bio-disc including same
WO2002075312A1 (en) 2001-03-19 2002-09-26 Gyros Ab Characterization of reaction variables
US7429354B2 (en) 2001-03-19 2008-09-30 Gyros Patent Ab Structural units that define fluidic functions
WO2003087827A2 (en) 2001-04-11 2003-10-23 Burstein Technologies, Inc. Multi-parameter assays including analysis discs and methods relating thereto
WO2003018198A1 (en) 2001-08-28 2003-03-06 Gyros Ab Retaining microfluidic microcavity and other microfluidic structures
US6919058B2 (en) 2001-08-28 2005-07-19 Gyros Ab Retaining microfluidic microcavity and other microfluidic structures
US7189368B2 (en) 2001-09-17 2007-03-13 Gyros Patent Ab Functional unit enabling controlled flow in a microfluidic device
JP4301952B2 (en) * 2001-12-14 2009-07-22 アークレイ株式会社 Sample measuring device
EP1459795A4 (en) * 2001-12-28 2011-07-06 Hitachi High Tech Corp Extractor, chemical analyzer, and chemical analyzing method
US7384602B2 (en) 2002-05-08 2008-06-10 Hitachi High-Technologies Corporation Chemical analysis apparatus and genetic diagnostic apparatus
EP1503209A4 (en) * 2002-05-08 2005-07-06 Hitachi High Tech Corp Chemical analyzer and gene diagnosing apparatus
JP4210783B2 (en) 2002-09-26 2009-01-21 アークレイ株式会社 Analysis tool
JP4262466B2 (en) 2002-10-28 2009-05-13 アークレイ株式会社 Analysis tool and analyzer
CN1751239B (en) * 2003-02-19 2010-04-28 独立行政法人科学技术振兴机构 Blood analysis device and blood analysis method
US7390464B2 (en) 2003-06-19 2008-06-24 Burstein Technologies, Inc. Fluidic circuits for sample preparation including bio-discs and methods relating thereto
JP4619224B2 (en) * 2005-07-27 2011-01-26 パナソニック株式会社 Rotational analysis device
DE102005048260A1 (en) * 2005-10-07 2007-04-12 Albert-Ludwigs-Universität Freiburg A method and apparatus for handling a liquid sample using rotation with a time-varying rotary vector
DE102005048233A1 (en) * 2005-10-07 2007-04-12 Albert-Ludwigs-Universität Freiburg Apparatus and method for handling a liquid sample using a siphon structure
JP4531677B2 (en) * 2005-10-24 2010-08-25 パナソニック株式会社 Assay method, sensor device for implementing the same, and measuring device for sensor device
JPWO2007116909A1 (en) * 2006-04-04 2009-08-20 パナソニック株式会社 Sample solution analysis panel
EP2126119A4 (en) * 2007-03-02 2014-07-16 Corbett Res Pty Ltd Apparatus and method for nucleic acid amplification
KR100858091B1 (en) 2007-04-24 2008-09-10 삼성전자주식회사 Centrifugal force-based microfluidic device having sample distribution structure and microfluidic system including the microfluidic device
EP2072131B1 (en) 2007-12-13 2015-04-22 Roche Diagnostics GmbH Microfluid element for mixing a fluid into a reagent
WO2009111461A2 (en) * 2008-03-04 2009-09-11 University Of Utah Research Foundation Microfluidic flow cell
CN101981455B (en) 2008-07-17 2013-07-03 松下电器产业株式会社 Analyzing device, and analyzing method using the analyzing device
KR101099495B1 (en) * 2008-10-14 2011-12-28 삼성전자주식회사 Centrifugal force-based microfluidic device, method of manufacturing the same and sample analysis method using the same
GB2464721C (en) 2008-10-23 2013-08-14 Biosurfit Sa Jet deflection device
GB2466644B (en) * 2008-12-30 2011-05-11 Biosurfit Sa Liquid handling
JP5174723B2 (en) 2009-03-12 2013-04-03 パナソニック株式会社 Analytical device
GB2476474B (en) 2009-12-22 2012-03-28 Biosurfit Sa Surface plasmon resonance detection system
GB2479139A (en) 2010-03-29 2011-10-05 Biosurfit Sa A liquid distribution and metering device
EP2486978A1 (en) 2010-10-28 2012-08-15 Roche Diagnostics GmbH Microfluid test carrier for separating a fluid volume in partial volumes
EP2455162A1 (en) 2010-10-29 2012-05-23 Roche Diagnostics GmbH Microfluidic element for analysing a fluid sample
BR112013022889B8 (en) * 2011-03-08 2022-12-20 Univ Laval CENTRIPETAL FLUIDIC DEVICE FOR TESTING COMPONENTS OF A BIOLOGICAL MATERIAL IN A FLUID, TEST APPARATUS AND TESTING METHOD USING SUCH CENTRIPETAL FLUIDIC DEVICE
ES2755078T3 (en) 2011-05-18 2020-04-21 Diasorin S P A Systems and methods for volumetric measurement in a sample processing device
ES2870874T3 (en) 2011-05-18 2021-10-27 Diasorin S P A Systems and methods for detecting the presence of a selected volume of material in a sample processing device
WO2012158988A1 (en) 2011-05-18 2012-11-22 3M Innovative Properties Company Systems and methods for valving on a sample processing device
WO2013083822A1 (en) 2011-12-08 2013-06-13 Biosurfit S.A. Sequential aliqoting and determination of an indicator of sedimentation rate
US9145579B2 (en) 2012-07-24 2015-09-29 Panasonic Healthcare Co., Ltd. Analyzing device
CA3026548C (en) 2013-04-15 2022-01-04 Becton, Dickinson And Company Medical device for collection of a biological sample
USD799715S1 (en) 2015-10-23 2017-10-10 Gene POC, Inc. Fluidic centripetal device
EP3474993A4 (en) * 2016-06-27 2019-12-18 Abaxis, Inc. Devices with modified conduits
US20200238279A1 (en) * 2017-03-08 2020-07-30 Northwestern University Devices, systems, and methods for specimen preparation and analysis using capillary and centrifugal forces

Family Cites Families (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2572533B1 (en) * 1984-10-26 1986-12-26 Guigan Jean METHOD FOR CARRYING OUT THE MEDICAL ANALYSIS OF A LIQUID SAMPLE USING AT LEAST ONE LIQUID REAGENT AND DEVICE FOR CARRYING OUT THE METHOD
FR2575293B1 (en) * 1984-12-21 1987-03-20 Inovelf Sa DYNAMIC PIPETTING ROTOR FOR CENTRIFUGAL ANALYSIS DEVICE
FR2579756B1 (en) * 1985-03-26 1987-05-07 Guigan Jean METHOD FOR PERFORMING BIOLOGICAL ANALYSIS USING IMMUNOLOGICAL REACTIONS AND DEVICE FOR CARRYING OUT SAID METHOD
US4999304A (en) * 1987-12-28 1991-03-12 Miles Inc. Dynamic braking centrifuge
US5160702A (en) * 1989-01-17 1992-11-03 Molecular Devices Corporation Analyzer with improved rotor structure
US5256376A (en) * 1991-09-12 1993-10-26 Medical Laboratory Automation, Inc. Agglutination detection apparatus
US5304348A (en) * 1992-02-11 1994-04-19 Abaxis, Inc. Reagent container for analytical rotor
WO1993019827A1 (en) * 1992-04-02 1993-10-14 Abaxis, Inc. Analytical rotor with dye mixing chamber
US5591643A (en) 1993-09-01 1997-01-07 Abaxis, Inc. Simplified inlet channels

Also Published As

Publication number Publication date
EP0764266A1 (en) 1997-03-26
EP0764266A4 (en) 1998-08-05
WO1995033986A1 (en) 1995-12-14
JP2008157960A (en) 2008-07-10
JP4178169B2 (en) 2008-11-12
CA2192196A1 (en) 1995-12-14
JPH10501340A (en) 1998-02-03
JP2006317467A (en) 2006-11-24

Similar Documents

Publication Publication Date Title
CA2192196C (en) Modified siphons for improved metering precision
US6235531B1 (en) Modified siphons for improved metering precision
US5591643A (en) Simplified inlet channels
US5518930A (en) Simultaneous cuvette filling with means to isolate cuvettes
US5173193A (en) Centrifugal rotor having flow partition
CA2129967C (en) Reagent container for analytical rotor
US5472603A (en) Analytical rotor with dye mixing chamber
US5122284A (en) Apparatus and method for optically analyzing biological fluids
US5186844A (en) Apparatus and method for continuous centrifugal blood cell separation
JP4707035B2 (en) Mixing in microfluidic devices
CA2082827C (en) Analytical rotors and methods for analysis of biological fluids
JP3256542B2 (en) Sample metering port of analysis rotor
JP2007502979A5 (en)
CA2346975C (en) Analytical rotors and methods for analysis of biological fluids

Legal Events

Date Code Title Description
EEER Examination request
MKEX Expiry

Effective date: 20150605