WO1997029369A1 - Method and kit for separating plasma from whole blood - Google Patents
Method and kit for separating plasma from whole blood Download PDFInfo
- Publication number
- WO1997029369A1 WO1997029369A1 PCT/NL1997/000046 NL9700046W WO9729369A1 WO 1997029369 A1 WO1997029369 A1 WO 1997029369A1 NL 9700046 W NL9700046 W NL 9700046W WO 9729369 A1 WO9729369 A1 WO 9729369A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- whole blood
- hypodermic syringe
- blood
- diluent
- container
- Prior art date
Links
Classifications
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N33/00—Investigating or analysing materials by specific methods not covered by groups G01N1/00 - G01N31/00
- G01N33/48—Biological material, e.g. blood, urine; Haemocytometers
- G01N33/483—Physical analysis of biological material
- G01N33/487—Physical analysis of biological material of liquid biological material
- G01N33/49—Blood
- G01N33/491—Blood by separating the blood components
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T436/00—Chemistry: analytical and immunological testing
- Y10T436/25—Chemistry: analytical and immunological testing including sample preparation
- Y10T436/25375—Liberation or purification of sample or separation of material from a sample [e.g., filtering, centrifuging, etc.]
Definitions
- the invention relates to a method for separating plasma from whole blood, in which: a) a mixture of whole blood, a blood anticoagulant and a diluent is prepared in a container provided with a sealing cap, and b) the mixture obtained under a) is passed through a filter containing glass fibres.
- Belgian Patent Application 849.898 describes a device for diluting and filtering a sample having a very small volume, such as, for example, a blood sample.
- Said device comprises a container which is made of a flexible plastic material and which contains a liquid diluent for the sample to be treated.
- the container is furthermore provided with a hollow cylindrical neck whose extremity is sealed with a removable stopper, and a cylindrical tube made of a flexible plastic material.
- the internal diameter of the cylindrical tube is essentially equal to the external diameter of the neck.
- the extremity of the cylindrical tube is inserted into a nozzle or fixed on a filter, the nozzle being sealed by a cannula.
- the container may optionally contain a capillary which contains a measured quantity of the sample, for example a blood sample.
- a capillary which contains a measured quantity of the sample
- a blood sample for example, a blood sample.
- the procedure is as follows. First the stopper is removed and the blood sample is transferred to the container either by means of the capillary or directly with the aid of an hypodermic syringe. The cylindrical tube is then mounted on the neck of the container and the device is shaken m such a way that a homogeneous mixture of the blood sample and the diluent is obtained, care being taken to ensure that the filter is not moistened.
- the homogeneous mixture is then filtered by squeezing the container, in which process the homogeneous mixture passes through the filter and a filtrate is obtained which has the desired dilution.
- a disadvantage of said device is that it is unsuitable for separating plasma from quantities of whole blood of, for example, less than 100 ⁇ l because the yield of pure plasma is low when such a small quantity of whole blood is separated.
- a further disadvantage of the device according to Belgian Patent Application 848,898 is that a large dilution has to be used in order to obtain an adequate volume of the homogeneous mixture: the volumetric ratio of the diluent and the blood sample should be between 10:1 and 1000:1. After dilution and filtering, therefore, a very dilute plasma will be obtained, as a result of which only diagnostic tests having a low sensitivity can be carried out .
- Rapid diagnostic means are, for example, substrates which comprise a separating matrix for separating plasma from whole blood and a test reagent.
- substrates which comprise a separating matrix for separating plasma from whole blood and a test reagent.
- a drop of whole blood is applied to the substrate, clear plasma passing through the separating matrix and the blood corpuscles, such as erythrocytes and leucocytes, remaining behind in the matrix.
- the plasma then reacts with the test reagent, in which process a colour change occurs which is then evaluated visually or spectrophotometrically.
- a disadvantage of said rapid diagnostic means is that haemolysis of erythrocytes may occur, in which process haemoglobin is entrained with the plasma and may interfere with the colour reaction.
- a small vacuum tube is a small tube which has a capacity of approximately 7 to 10 ml, which is provided with a stopper made, for example, of rubber and which has to be fitted on an injection needle after the injection needle has been introduced into a vein, for example a vein in the arm (venepuncture) . Because a lower pressure prevails in the small vacuum tube than in the vein, blood will flow out of the vein into the small vacuum tube.
- Another disadvantage of the method described above is that the separation of the plasma has to be carried out by expert staff or by staff specially trained for the purpose and that special equipment is required. It is therefore not possible to collect whole blood and to separate the plasma therefrom at the same operational site. This is of importance, for example, under circumstances in which urgent help has to be offered and one or more diagnostic tests have to be carried out and special equipment is not available. Thus, for example, a general practitioner or a medical specialist will possibly consider it necessary, when visiting patients at home or in cases where acute help is needed, respectively, to carry out a certain test but will not be in a position to extract the required amount of plasma rapidly and expediently. Another example is the evaluation of new diagnostic blood parameters for which no specific whole blood tests are generally available for a long time.
- US Patent Specification 4,477.575 describes a method for separating plasma from whole blood in which whole blood is applied to a layer of glass fibres.
- a device is also described for separating plasma from whole blood, the device comprising a conical plastic vessel, the top and bottom of the vessel being open. The lowermost part of the vessel is filled with glass fibres.
- the blood is then introduced into the free section of the vessel, after which plasma flows through the layer comprising the glass fibres and can be removed at the bottom with the aid of a capillary.
- US Patent Specification 5.262,067 describes a device for separating plasma from whole blood, in which little haemolysis occurs and in which the device comprises a layer comprising glass fibres coated with polyvinyl alcohol or polyvinyl alcohol/polyvmyl acetate, and a means which causes erythrocytes to aggregate. If an amount of whole blood is applied to the top of the layer, erythrocytes are aggregated and plasma containing little or no haemolysis products passes through the layer.
- This method and device have, however, the disadvantage that they are unsuitable for expediently separating and isolating plasma from small amounts of whole blood so that said plasma can be used for other diagnostic tests.
- the object of the invention is to solve the abovementioned problems and it therefore relates to a method as stated in the preamble, in which a pressure which is lower than the pressure prevailing at ambient temperature prevails in the container.
- the invention also relates to a kit for separating plasma from whole blood.
- the method is particularly suitable for separating plasma from small amounts of whole blood, for example amounts of less than 100 ⁇ l. Such amounts can be collected by means of a heel or finger prick in a particularly patient-friendly manner. In addition, such amounts are in many cases quite sufficient for many diagnostic tests, for example tests for determining the concentration of a metabolite, a hormone or an antibody in blood.
- a capillary which comprises a container provided with, for example, a small elliptical needle having a length of less than 1.5 mm.
- a further advantage of the invention is that plasmas is obtained from the whole blood in a particularly expedient manner and with a very high yield.
- Other advantages of the invention are that no special equipment is necessary, so that the separation of plasma from whole blood can be carried out at the site where the patient is. This last advantage may be of particular importance, for example, for doctors who have to treat patients on the spot and in circumstances already described above.
- a further advantage is that nonspecialists can also separate plasma from whole blood by the method of the invention.
- plasma is obtained which only has to be diluted slightly before it is separated from the whole blood. It has been found that a dilution of 100% is adequate, that is to say that the volumetric ratio of plasma to diluent is no higher than 1:5. preferably no higher than 1:3 and in particular no higher than 1:2. According to the method of the present invention, it is possible to obtain only slightly diluted plasma which is very suitable for carrying out diagnostic tests in which a high sensitivity is desirable.
- the preparation of the mixture of whole blood, the blood anticoagulant and the diluent is carried out in a hypodermic syringe having a volume of, for example, 1 ml.
- the mixture of whole blood and blood anticoagulant is preferably prepared first, after which said mixture s then mixed with the diluent.
- the blood anticoagulant is preferably heparin.
- the diluent may be any buffer solution which is necessary for the desired diagnostic test.
- An example of such a diluent is a phosphate buffer which contains 0.1X by weight of sodium azide and has a pH of approximately 7-2.
- the diluent may also contain one or more standard surface-active agents, preferably non-ionic surface-active agents.
- the diluent may also contain other agents necessary for a particular diagnostic test.
- the mixture of whole blood and blood anticoagulant is preferably prepared in a capillary which is suitable for collecting a small amount of blood by means of a heel or finger prick and which contains the blood anticoagulant.
- the mixture of whole blood and blood anticoagulant is then removed with the aid of the hypodermic syringe in which an amount of the diluent has been taken up beforehand.
- it is not preferable according to the invention it will be clear that it is optionally possible to remove the mixture of whole blood and blood anticoagulant first from the capillary using the hypodermic syringe and then to draw up a certain amount of the diluent with the aid of the hypodermic syringe.
- a long and thin hypodermic syringe is used, for example a hypodermic syringe having a length of approximately 7 to approximately 10 cm and a diameter of approximately 3 to approximately 9 mm.
- Suitable hypodermic syringes are, for example, those which have a volume of 3 ml of the type Sherwood Monoject which are provided with a "Luer lock" (reference No. 1100-503497)-
- a hypodermic syringe which has been filled with the diluent and an amount of a gas, a pressure below the ambient pressure, preferably a pressure between 1 and 0.5 bar, prevailing in the hypodermic syringe at ambient temperature, which syringe has been provided with a sealing cap.
- the pressure m the hypodermic syringe at ambient temperature is, in particular, at least 0.5 bar, the hypodermic syringe having a volume of 1 ml and the plunger of the hypodermic syringe being in the fully extended state.
- the sealing cap can be pierced by a capillary and is and remains, even after piercing, essentially impermeable to gases.
- sealing caps are septa and ferrules.
- the sealing caps are preferably made of a material which does not interact with whole blood, the diluent and the gas.
- the sealing caps are preferably made of an inert plastic material or are coated on the inside with an inert plastic material.
- a suitable inert plastic material is, for example, Teflon.
- the hypodermic syringe may be provided with an internal pressure of 0.5 bar by filling it, for example, with a gas having a temperature which is higher than the ambient temperature. After cooling the gas to ambient temperature, a pressure which is lower than the ambient pressure will then be produced in the hypodermic syringe. If the sealing cap is then pricked with the capillary containing the mixture of whole blood and bloo ⁇ anticoagulant, the contents of the capillary will be drawn into the hypodermic syringe.
- hypodermic syringe is filled with a gas which does not interact with the whole blood or a constituent thereof, the blood anticoagulant or the diluent.
- gases are nitrogen, oxygen or air.
- the mixture containing whole blood, the blood anticoagulant and the diluent is introduced into the hypodermic syringe, whose plunger is already in the completely extended state.
- the hypodermic syringe may, if necessary, be rotated horizontally and vertically.
- the hypodermic syringe may also contain media which promote mixing, for example glass beads, so that mixing can be carried out more expediently.
- the sealing cap is removed and the hypodermic syringe is then connected to a container which contains the filter comprising glass fibres.
- the liquid is transferred to the filter by tapping the hypodermic syringe and, after a means of locking the plunger has been broken, preferably by rotating, the contents of the hypodermic syringe are then forced through the filter with the aid of the plunger, a filtrate being obtained in the form of drops which comprises the plasma and contains no haemolysis products.
- drops of plasma are obtained which have a more or less uniform volume. This is achieved by matching the amount and the nature of the surface-active agent used to the properties of the diluent, such as. for example, the pH, the salt concentration and the like.
- kits can be assembled which is suitable for separating a certain amount of plasma which is necessary for the desired diagnostic test.
- the invention therefore also relates to a kit which comprises at least a container which contains an amount of a diluent necessary for a certain diagnostic test, and a filter containing glass fibres, a pressure prevailing in the container which is lower than the pressure prevailing at ambient temperature.
- the kit may also contain a capillary which contains an amount of blood anticoagulant necessary for the blood to be collected.
- the container has a volume which is such that it can contain the amount of whole blood, blood anticoagulant and diluent and, if necessary gas, a pressure of at least 0.5 bar prevailing in the hypodermic syringe at ambient temperature.
- the kit as defined hereinabove to comprise a hypodermic syringe which comprises the container containing diluent or the diluent alone.
- the kit also contains at least one diagnostic test which can be carried out with a small amount of plasma, for example with 40 ⁇ l of plasma.
- the kit according to the invention may also contain one or more means necessary for carrying out a certain diagnostic test. Examples of such means are test strips for determining the presence of a certain concentration of metabolite, hormone or antibody in the blood and the reagents necessary therefor.
- a preferred embodiment comprises a hypodermic syringe which is provided with a plunger and means or locking the plunger and which optionally contains media which promote mixing, such as glass beads, a nozzle and a sealing cap for sealing the nozzle, a pressure of at least 0.5 bar prevailing in the hypodermic syringe at ambient temperature.
- the hypodermic syringe may be replaced by another suitable container.
- the means of locking the plunger have to be present because, if the said means were not present this underpressure would become lower or even be completely eliminated by moving the plunger.
- the unlocking of the means preferably takes place by means of rotation.
- the nozzle of the hypodermic syringe is preferably provided with a common screw thread, for example a "Luer lock" so that the hypodermic syringe can be connected in a simple manner to the container which contains the filter comprising glass fibres.
- a screw thread another means may also be present for connecting the hypodermic syringe to the holder containing the filter.
- the nozzle is also provided with a sealing cap.
- Said sealing cap may partly or in its entirety be composed of a material which can be pierced by a capillary. The material is also essentially impermeable to gases and also remains impermeable to gases if the material has been pierced several times with a capillary. Examples of such materials are plastic materials, preferably elastic inert plastic materials and, in particular, rubber-like materials. Examples of suitable sealing caps are septa and ferrules.
- An amount of 75 pi of whole blood is collected by a finger prick with the aid of a commercially available capillary containing the standard amount of heparin. This amount of heparin is generally quite sufficient to inhibit the coagulation of the amount of whole blood collected.
- the whole blood has a haematocrit reading of 0.40 and therefore consists of 5 ⁇ l of plasma and 30 ⁇ l of blood cells.
- An amount of 135 ⁇ l of a phosphate buffer having a pH of 7.2 is drawn up with the aid of a hypodermic syringe having a volume of 1 ml.
- the mixture of whole blood and heparin is then removed from the capillary with the aid of the hypodermic syringe and the plunger is pulled out to a volume of 1 ml.
- a filter which comprises glass fibres and has a dead volume of 38 ⁇ l is then mounted on the nozzle of the hypodermic syringe.
- the hypodermic syringe which is now provided with the filter, is rotated several times horizontally and vertically to obtain a good mixing of all the constituents.
- the mixture is transferred to the filter by lightly tapping the hypodermic syringe.
- the plunger is then carefully pressed in, and three completely clear, colourless drops each having a volume of approximately 40 ⁇ l are obtained as filtrate.
- the yield of plasma is therefore 85% .
- Example 1 The test of Example 1 was repeated, with the proviso that a pressure of approximately 0.6 bar prevailed in the hypodermic syringe and, at the same time, the hypodermic syringe was provided with a means for locking the plunger. In this test three completely clear, colourless drops were also obtained which had a total volume of approximately 120 ⁇ l.
Abstract
Description
Claims
Priority Applications (7)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
AU16752/97A AU1675297A (en) | 1996-02-09 | 1997-02-10 | Method and kit for separating plasma from whole blood |
DK97902735T DK1021715T3 (en) | 1996-02-09 | 1997-02-10 | Method and kit for separating whole blood plasma |
US09/117,790 US6245244B1 (en) | 1996-02-09 | 1997-02-10 | Method and kit for separating plasma from whole blood |
AT97902735T ATE224541T1 (en) | 1996-02-09 | 1997-02-10 | METHOD AND KIT FOR SEPARATING PLASMA FROM WHOLE BLOOD |
DE69715687T DE69715687T2 (en) | 1996-02-09 | 1997-02-10 | METHOD AND KIT FOR DEPOSITING PLASMA FROM WHOLE BLOOD |
EP97902735A EP1021715B1 (en) | 1996-02-09 | 1997-02-10 | Method and kit for separating plasma from whole blood |
HK01100600A HK1032107A1 (en) | 1996-02-09 | 2001-01-27 | Method and kit for separating plasma from whole blood |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
NL1002296 | 1996-02-09 | ||
NL1002296 | 1996-02-09 |
Publications (1)
Publication Number | Publication Date |
---|---|
WO1997029369A1 true WO1997029369A1 (en) | 1997-08-14 |
Family
ID=19762278
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/NL1997/000046 WO1997029369A1 (en) | 1996-02-09 | 1997-02-10 | Method and kit for separating plasma from whole blood |
Country Status (10)
Country | Link |
---|---|
US (1) | US6245244B1 (en) |
EP (1) | EP1021715B1 (en) |
AT (1) | ATE224541T1 (en) |
AU (1) | AU1675297A (en) |
DE (1) | DE69715687T2 (en) |
DK (1) | DK1021715T3 (en) |
ES (1) | ES2182022T3 (en) |
HK (1) | HK1032107A1 (en) |
PT (1) | PT1021715E (en) |
WO (1) | WO1997029369A1 (en) |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0937981A2 (en) * | 1998-02-19 | 1999-08-25 | Fuji Photo Film Co., Ltd. | Method of separating serum from whole blood |
WO2002040993A1 (en) | 2000-11-17 | 2002-05-23 | Best Quality B.V. | Device for treating a fluid-like sample, such as a whole blood, with treatment fluid, use of such a device and kit containing such a device |
EP1221614A2 (en) * | 2001-01-05 | 2002-07-10 | Leisure, Inc. | Instrument and method for blood separation, and preparing method, quantifying method and preserving container for biological sample |
US6936473B2 (en) | 2000-01-05 | 2005-08-30 | Leisure, Inc. | Method of preparing a biological sample for quantification |
Families Citing this family (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6695803B1 (en) | 1998-10-16 | 2004-02-24 | Mission Medical, Inc. | Blood processing system |
EP3645998B1 (en) | 2017-06-26 | 2023-11-15 | Mendoza, Estevan | Sample filtration device and method |
USD920534S1 (en) | 2018-12-21 | 2021-05-25 | CanaryQ, Inc. | Blood sample filtration device |
Citations (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
BE849898A (en) * | 1976-12-28 | 1977-06-28 | DILUTION AND FILTRATION DEVICE | |
FR2335267A1 (en) * | 1975-12-19 | 1977-07-15 | Sherwood Medical Ind Inc | FLUID COLLECTOR DEVICE |
US4263922A (en) * | 1979-08-31 | 1981-04-28 | American Hospital Supply Corporation | Method and device for collecting, transporting, and delivering micro samples of blood |
GB2232599A (en) * | 1989-06-08 | 1990-12-19 | Summers Dr Julie Andrea | One-step blood to plasma device |
EP0439917A1 (en) * | 1989-12-01 | 1991-08-07 | Sangstat Medical Corporation | Apparatus for detection and semi-quantitative measurement of analytes |
EP0550950A2 (en) * | 1992-01-10 | 1993-07-14 | Sanwa Kagaku Kenkyusho Co., Ltd. | Process and device for separating blood serum and plasma |
Family Cites Families (8)
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US4632901A (en) * | 1984-05-11 | 1986-12-30 | Hybritech Incorporated | Method and apparatus for immunoassays |
US5362654A (en) * | 1984-07-20 | 1994-11-08 | Sangstat Medical Corporation | Self-contained quantitative assay |
US5135719A (en) * | 1986-10-29 | 1992-08-04 | Biotrack, Inc. | Blood separation device comprising a filter and a capillary flow pathway exiting the filter |
US4874691A (en) * | 1987-10-16 | 1989-10-17 | Quadra Logic Technologies Inc. | Membrane-supported immunoassays |
US5064541A (en) * | 1989-04-07 | 1991-11-12 | Abbott Laboratories | Devices and methods for the collection of a predetermined volume of plasma or serum |
US5147780A (en) * | 1989-12-01 | 1992-09-15 | Sangstat Medical Corporation | Multiwell stat test |
US5589399A (en) * | 1994-10-21 | 1996-12-31 | First Medical, Inc. | System and method for plasma separation and measurement |
US5725774A (en) * | 1995-04-07 | 1998-03-10 | Lxn Corp. | Whole blood separation method and devices using the same |
-
1997
- 1997-02-10 ES ES97902735T patent/ES2182022T3/en not_active Expired - Lifetime
- 1997-02-10 DE DE69715687T patent/DE69715687T2/en not_active Expired - Lifetime
- 1997-02-10 US US09/117,790 patent/US6245244B1/en not_active Expired - Fee Related
- 1997-02-10 AT AT97902735T patent/ATE224541T1/en not_active IP Right Cessation
- 1997-02-10 AU AU16752/97A patent/AU1675297A/en not_active Abandoned
- 1997-02-10 WO PCT/NL1997/000046 patent/WO1997029369A1/en active IP Right Grant
- 1997-02-10 DK DK97902735T patent/DK1021715T3/en active
- 1997-02-10 EP EP97902735A patent/EP1021715B1/en not_active Expired - Lifetime
- 1997-02-10 PT PT97902735T patent/PT1021715E/en unknown
-
2001
- 2001-01-27 HK HK01100600A patent/HK1032107A1/en not_active IP Right Cessation
Patent Citations (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2335267A1 (en) * | 1975-12-19 | 1977-07-15 | Sherwood Medical Ind Inc | FLUID COLLECTOR DEVICE |
BE849898A (en) * | 1976-12-28 | 1977-06-28 | DILUTION AND FILTRATION DEVICE | |
US4263922A (en) * | 1979-08-31 | 1981-04-28 | American Hospital Supply Corporation | Method and device for collecting, transporting, and delivering micro samples of blood |
GB2232599A (en) * | 1989-06-08 | 1990-12-19 | Summers Dr Julie Andrea | One-step blood to plasma device |
EP0439917A1 (en) * | 1989-12-01 | 1991-08-07 | Sangstat Medical Corporation | Apparatus for detection and semi-quantitative measurement of analytes |
EP0550950A2 (en) * | 1992-01-10 | 1993-07-14 | Sanwa Kagaku Kenkyusho Co., Ltd. | Process and device for separating blood serum and plasma |
Cited By (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0937981A2 (en) * | 1998-02-19 | 1999-08-25 | Fuji Photo Film Co., Ltd. | Method of separating serum from whole blood |
EP0937981A3 (en) * | 1998-02-19 | 2001-02-14 | Fuji Photo Film Co., Ltd. | Method of separating serum from whole blood |
US6225130B1 (en) | 1998-02-19 | 2001-05-01 | Fuji Photo Film Co., Ltd. | Method of separating serum from whole blood |
US6936473B2 (en) | 2000-01-05 | 2005-08-30 | Leisure, Inc. | Method of preparing a biological sample for quantification |
WO2002040993A1 (en) | 2000-11-17 | 2002-05-23 | Best Quality B.V. | Device for treating a fluid-like sample, such as a whole blood, with treatment fluid, use of such a device and kit containing such a device |
NL1016646C2 (en) * | 2000-11-17 | 2002-05-29 | Best Quality B V | Device for treating a fluid-like sample, such as whole blood, with treatment fluid, use of such a device, and kit comprising such a device. |
US7144382B2 (en) | 2000-11-17 | 2006-12-05 | Best Quality B.V. | Device for treating a fluid-like sample such as a whole blood, with treatment fluid, use of such a device and kit containing such a device |
EP1221614A2 (en) * | 2001-01-05 | 2002-07-10 | Leisure, Inc. | Instrument and method for blood separation, and preparing method, quantifying method and preserving container for biological sample |
EP1221614A3 (en) * | 2001-01-05 | 2003-11-05 | Leisure, Inc. | Instrument and method for blood separation, and preparing method, quantifying method and preserving container for biological sample |
Also Published As
Publication number | Publication date |
---|---|
ES2182022T3 (en) | 2003-03-01 |
EP1021715B1 (en) | 2002-09-18 |
DE69715687D1 (en) | 2002-10-24 |
PT1021715E (en) | 2003-03-31 |
US6245244B1 (en) | 2001-06-12 |
DE69715687T2 (en) | 2003-01-30 |
ATE224541T1 (en) | 2002-10-15 |
DK1021715T3 (en) | 2002-10-21 |
HK1032107A1 (en) | 2001-07-06 |
EP1021715A1 (en) | 2000-07-26 |
AU1675297A (en) | 1997-08-28 |
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