Method for performing automated hematology and cytometry analysis

• US 5,631,165 A
• Filed: 06/07/1995
• Issued: 05/20/1997
• Est. Priority Date: 08/01/1994
• Status: Expired due to Term

• Current Assignee: Abbott Laboratories Incorporated
• Original Assignee: Abbott Laboratories Incorporated
• Inventors: Stuart, John P., Lobban, Peter E., Chupp, Vernon L., Larue, Roderick W., Kim, Young R.
• Primary Examiner(s): Le, Long V.
• Application Number:
  US08/488,532
• Time in Patent Office: 713 Days
• Field of Search: 436/8, 436/10, 436/17, 436/18, 436/522, 436/579, 436/523, 436/805, 436/43, 436/49, 436/63, 436/54, 436/164, 436/165, 436/172, 436/174, 436/175, 436/179, 436/180, 422/68.1, 422/73, 422/63, 422/65, 422/67, 422/82.01-82.09, 435/808, 435/809, 435/767, 435/973, 435/724, 356/39, 356/73, 356/335, 356/336, 364/413.07, 364/413.08
• US Class Current: 436/43
• CPC Class Codes: B01F 25/3132 by using two or more injector devices
• CPC Class Codes: B01F 25/31324 arranged concentrically
• CPC Class Codes: G01N 1/14 Suction devices, e.g. pumps; Ejector devices
• CPC Class Codes: G01N 15/14 Optical investigation techniques, e.g. flow cytometry
• CPC Class Codes: G01N 15/1404 Handling flow, e.g. hydrodynamic focusing
• CPC Class Codes: G01N 2015/014 Reticulocytes
• CPC Class Codes: G01N 2015/018 Platelets
• CPC Class Codes: G01N 2015/1413 Hydrodynamic focussing
• CPC Class Codes: G01N 2035/00356 Holding samples at elevated temperature (incubation)
• CPC Class Codes: G01N 2035/00524 Mixing by agitating sample carrier
• CPC Class Codes: G01N 2035/1032 Dilution or aliquotting
• CPC Class Codes: G01N 35/0092 Scheduling
• CPC Class Codes: G01N 35/10 Devices for transferring samples or any liquids to, in, or from, the analysis apparatus, e.g. suction devices, injection devices G01N35/0099 takes precedence
• CPC Class Codes: G01N 35/1004 Cleaning sample transfer devices
• CPC Class Codes: G01N 35/109 with two horizontal degrees of freedom
• CPC Class Codes: Y10S 436/805 Optical property
• CPC Class Codes: Y10T 436/11 Automated chemical analysis
• CPC Class Codes: Y10T 436/119163 with aspirator of claimed structure
• CPC Class Codes: Y10T 436/25 including sample preparation
• CPC Class Codes: Y10T 436/25125 Digestion or removing interfering materials
• CPC Class Codes: Y10T 436/2575 : Volumetric liquid transfer

Abstract

A device for analyzing a whole blood sample is provided. The device comprises a conventional hematology analyzer integrated with a fluorescence cytometry analyzer. A controller is provided for controlling the analyzers, obtaining and utilizing data from both and reporting a quantitative result. Methods are also provided for analyzing a whole blood sample. One such method comprises the steps of performing on a single instrument an analysis of impedance associated with the blood sample, an analysis of light scatter associated with the blood sample, and an analysis of fluorescence associated with the blood sample. Data is collected and utilized. A result is reported.

Claims

1. An automated method for distinguishing and differentiating cells in a whole blood sample with an automated instrument system capable of performing both hematology and fluorescent cytometry analysis to which the whole blood sample is provided, the automated method comprising the steps of:

(a) selecting a series of one or more tests to be performed on the whole blood sample, and correlating the tests to be performed to the sample;

(b) aspirating a volume of the whole blood sample;

(c) dispensing an aliquot of the whole blood sample into at least three sample receiving vessels;

(d) diluting one or more first aliquots of the whole blood sample with a diluent reagent in at least one of the at least three sample receiving vessels, thereby producing a diluted sample;

(e) lysing at least one second aliquot of the whole blood sample with a lysing reagent in at least one of the at least three sample receiving vessels, thereby producing a lysed sample;

(f) transporting at least one aliquot of the diluted sample through a first flow transducer of the automated instrument system;

(g) detecting and counting red blood cells in the at least one aliquot of diluted sample with the first flow transducer;

(h) transporting at least one aliquot of the lysed sample through a second flow transducer;

(i) detecting multi-angle light scatter from the aliquot of lysed sample and counting and differentiating white blood cells or cell surface antigens in the aliquot of lysed sample with the second flow transducer;

(j) detecting multi-angle light scatter and fluorescence from the lysed sample or the diluted sample and counting and differentiating nucleated red blood cells or reticulocytes and cell surface antigens in the lysed sample or the diluted sample with the second flow transducer;

(k) storing data for the tests performed on the whole blood sample; and

(l) reporting results of each test performed on the whole blood sample,

wherein the automated instrument system automatedly performs method steps (a) through (l) without physically separating cells from the whole blood sample or an aliquot thereof and results of the hematology analysis are utilized in at least reporting of results of the fluorescent cytometry analysis.

2. The method of claim 1 further comprising the steps of:

(m) combining a third aliquot of the whole blood sample with fluorescent-labelled monoclonal antibodies for a sufficient time to allow the fluorescent-labelled monoclonal antibodies to become attached to a cell surface antigen on the cells in the third aliquot of the whole blood sample, thereby producing a labelled sample in at least one of the at least three sample receiving vessels;

(n) lysing the labelled sample with a lysing reagent without thereafter separating unlysed cells in the third aliquot, thereby producing a lysed and labelled sample in the at least one of the at least three sample receiving vessels;

(o) transporting the lysed and labelled sample through the second flow transducer; and

(p) detecting multi-angle light scatter and fluorescence and counting and differentiating sub populations of lymphocytes in the lysed and labelled sample.

3. The method of claim 2 further comprising the steps of:

(q) staining an aliquot of the diluted sample thereby producing a stained aliquot of whole blood sample;

(r) transporting the stained aliquot through the second flow transducer, wherein reticulocytes in the stained aliquot are counted and differentiated.

4. The method of claim 1 wherein the first flow transducer comprises an impedance flow cell.

5. The method of claim 4 wherein data detected by the impedance flow cell is utilized to produce a quantitative red blood cell result.

6. The method of claim 1 wherein an aliquot of the diluted sample is transported by the automated instrument system through the second flow transducer and multi-angle light scatter is detected to count and to differentiate platelets in the aliquot of diluted sample.

7. The method of claim 1 wherein the nucleated red blood cells and the white blood cells are counted and differentiated from the lysed sample.

8. The automated method of claim 1 wherein a reported quantitative white blood cell result is obtained from the multi-angle light scatter and fluorescent detected data.

9. The automated method of claim 8 wherein the white blood cell result comprises a five-part differential.

10. The automated method of claim 9 wherein the five-part differential further comprises a percentage of nucleated red blood cells.