DETECTION METHOD AND APPARATUS OF ACTIVATED NEUTROPHILS

• US 20130101996A1
• Filed: 10/17/2012
• Published: 04/25/2013
• Est. Priority Date: 10/25/2011
• Status: Abandoned Application

• Current Assignee: Sysmex Corporation
• Original Assignee: Sysmex Corporation
• Inventors: TAKAGI, Yuri, KONO, Mari
• Application Number:
  US13/654,044
• Publication Number:
  US 20130101996A1
• Time in Patent Office: Days
• US Class Current: 435/6.1
• CPC Class Codes: G01N 15/1468 with spatial resolution of the texture or inner structure of the particle
• CPC Class Codes: G01N 33/5094 for blood cell populations red blood cells G01N33/80

Abstract

To provide a detection method of activated neutrophils enabling the classification of normal leukocytes and the detection of activated neutrophils, a measurement sample in which erythrocytes in a biotic sample are hemolyzed and nucleic acid of leukocytes is stained by a nucleic acid staining fluorochrome is prepared, the sample is irradiated with light, and leukocytes in the biotic sample are classified into at least a cluster containing neutrophils and a cluster containing eosinophils based on scattered light intensity and fluorescence intensity obtained by measuring the scattered light intensity and fluorescence intensity generated from particles in the sample to detect particles present between the cluster containing neutrophils and the cluster containing eosinophils as activated neutrophils.

Claims

1. A detection method of activated neutrophils, comprising:

(a) preparing a measurement sample in which erythrocytes in a biotic sample are hemolyzed and nucleic acid of leukocytes is stained by a nucleic acid staining fluorochrome;

(b) irradiating the prepared measurement sample with light and measuring scattered light intensity and fluorescence intensity generated from particles in the measurement sample;

(c) classifying the leukocytes in the biotic sample into at least a cluster containing neutrophils and a cluster containing eosinophils based on the acquired scattered light intensity and fluorescence intensity; and

(d) detecting particles present between the cluster containing the neutrophils and the cluster containing the eosinophils as activated neutrophils.

2. The method according to claim 1, wherein particles whose fluorescence intensity is equal to that of the cluster containing the neutrophils or less and whose scattered light intensity is between that of the cluster containing the neutrophils and that of the cluster containing the eosinophils in the (d) are detected as the activated neutrophils.

3. The method according to claim 1, wherein the cluster containing the neutrophils further contains basophils.

4. The method according to claim 1, wherein the activated neutrophils have vacuolar degeneration generated in cytoplasm.

5. The method according to claim 1, wherein particles present between the cluster containing the neutrophils and the cluster containing the eosinophils are counted in the (d).

6. The method according to claim 5, wherein if a value counted in the (d) is larger than a predetermined value, the particles are detected as the activated neutrophils.

7. The method according to claim 1, wherein erythrocytes in the measurement sample are hemolyzed by a surfactant.

8. The method according to claim 7, wherein the surfactant is at least one selected from nonionic surfactants and cationic surfactants.

9. The method according to claim 1, wherein the scattered light intensity is side scattered light intensity.

10. A detection apparatus of activated neutrophils, comprising:

a sample preparation unit that prepares a measurement sample by mixing a biotic sample, a fluorochrome to stain nucleic acid, and a hemolyzing agent containing a surfactant that hemolyzes erythrocytes and damages cell membranes of leukocytes to such an extent that the fluorochrome can pass through;

a measuring unit that irradiates the prepared measurement sample with light and measures scattered light intensity and fluorescence intensity generated from particles in the measurement sample; and

a controller configured for performing operations, comprising;

(a) classifying the leukocytes in the biotic sample into at least a cluster containing neutrophils and a cluster containing eosinophils based on the acquired scattered light intensity and fluorescence intensity; and

(b) detecting particles present between the cluster containing the neutrophils and the cluster containing the eosinophils as activated neutrophils.

11. The apparatus according to claim 10, wherein the controller detects particles whose fluorescence intensity is equal to that of the cluster containing the neutrophils or less and whose scattered light intensity is between that of the cluster containing the neutrophils and that of the cluster containing the eosinophils as the activated neutrophils.

12. The apparatus according to claim 10, wherein the controller classifies the leukocytes in the biotic sample into at least the cluster containing the neutrophils and the basophils and the cluster containing the eosinophils based on the acquired scattered light intensity and fluorescence intensity.

13. The apparatus according to claim 10, wherein the controller counts particles present between the cluster containing the neutrophils and the cluster containing the eosinophils.

14. The apparatus according to claim 13, wherein if the counted value is larger than a predetermined value, the controller detects the particles as the activated neutrophils.

15. The apparatus according to claim 10, wherein the scattered light intensity is side scattered light intensity.

16. The apparatus according to claim 10, further comprising:

an output unit that outputs a classification result and a detection result.