Optical bio-discs and fluidic circuits for analysis of cells and methods relating thereto

• US 7,157,049 B2
• Filed: 11/13/2002
• Issued: 01/02/2007
• Est. Priority Date: 11/20/2001
• Status: Expired due to Fees

• Current Assignee: Vindur Technologies, Inc.
• Original Assignee: Nagaoka & Co., Ltd.
• Inventors: Hurt, Susan Newcomb, Selvan, Gowri Pyapali, Chen, YihFar, Urcia, Joseph Roby Iringan, Valencia, Ramoncito Magpantay
• Primary Examiner(s): Le; Long V.
• Assistant Examiner(s): LUM, LEON YUN BON
• Application Number:
  US10/293,214
• Publication Number:
  US 20030219713A1
• Time in Patent Office: 1,511 Days
• Field of Search: 422/50, 422/55, 422 57- 58, 422/64, 422/68.1, 422/82.05, 422/82.09, 422/72, 435 4- 6, 435/7.2, 435/7.24, 435 725- 792, 435/287.1, 435/287.9, 435/288.7, 436/63, 436/164, 436/45, 436/172
• US Class Current: 422/68.1
• CPC Class Codes: B01L 3/5027 by integrated microfluidic structures, i.e. dimensions of channels and chambers are such that surface tension forces are important, e.g. lab-on-a-chip B01L3/5023 takes precedence; micromixers B01F33/30; microreactors for synthesis B01J19/0093; microcapillary devices in general B81B1/00
• CPC Class Codes: G01N 15/1433 using image recognition
• CPC Class Codes: G01N 2015/1486 Counting the particles
• CPC Class Codes: G01N 33/54366 Apparatus specially adapted for solid-phase testing
• CPC Class Codes: G01N 33/80 involving blood groups or blood types or red blood cells white blood cells G01N33/56972
• CPC Class Codes: G01N 35/00069 whereby the sample substrate is of the bio-disk type, i.e. having the format of an optical disk

Abstract

The present invention is directed to optical bio-discs, methods, and optical disc drives for clinical diagnostics. The present invention is further directed to methods for determining the quantity of a specific type of blood cell in a biological sample including on-disc sample preparation and processing, providing a pre-processed sample onto a capture zone, removing portions of the sample that are not bound in the capture zone, and counting bound cells. Also disclosed are fluidic circuits for processing blood samples for use in a cluster designation marker assay in the optical bio-disc.

Claims

1. An optical bio-disc for conducting a cellular assay, said disc comprising:

a rotatable substrate;

a cap portion associated with said substrate; and

a fluidic circuit formed between said substrate and said cap portion, said fluidic circuit comprising;

a mixing chamber, said mixing chamber including an inlet port configured to receive a fluid including RBC'"'"'s;

a RBC capture zone in fluid communication with the mixing chamber so as to receive a fluid therefrom;

a plurality of posts with RBC capture agents coated thereon and located within the RBC capture zone, the posts being configured to capture RBC'"'"'s while allowing passage through said RBC capture zone of non-RBC materials included in the fluid;

a purification chamber in fluid communication with said capture zone, the purification chamber configured to receive mixed fluid communicated from the mixing chamber;

a filter associated with said purification chamber;

an analysis chamber in fluid communication with said purification chamber, said analysis chamber including a capture zone; and

a vent port associated with said analysis chamber.

2. The optical bio-disc according to claim 1 wherein said filter is selected from the group consistingof microspheres and a cellular sieve.

3. The optical bio-disc according to claim 2 wherein said microspheres are coated with a purification agent.

4. The optical bio-disc according to claim 3 wherein said purification agent is selected from the group consisting of monoclonal antibodies, polyclonal antibodies, oligonucleotides, ligands, receptors, and binding agents.

5. The optical bio-disc according to claim 4 wherein said monoclonal antibodies are selected from the group consisting of anti-CD56, anti-CD14, anti-CD19, anti-CD9, anti-CD31, anti-CD41, anti-CD13, and anti-CD43.

6. The optical bio-disc according to claim 1 wherein said capture zone is coated with a capture agent.

7. The optical bio-disc according to claim 6 wherein said capture agent is selected from the group consisting of monoclonal antibodies, polyclonal antibodies, oligonucleotides, ligands, receptors, and binding agents.

8. The optical bio-disc according to claim 7 wherein said monoclonal antibodies are selected from the group consisting of anti-CD4, anti-CD8, and anti-CD2.

9. The optical bio-disc according to claim 1 further comprising a lysis buffer reservoir, a lysis channel connecting said lysis buffer reservoir with said mixing chamber, and a lysis buffer valve located in said lysis channel;

said lysis buffer reservoir being pre-filled with a lysis buffer.

10. The optical bio-disc according to claim 9 further comprising an analysis buffer reservoir, a buffer channel connecting said analysis buffer reservoir with said purification chamber, and an analysis buffer valve located in said buffer channel;

said analysis buffer reservoir being pre-filled with an analysis buffer.

11. The optical bio-disc according to claim 10 further comprising a waste chamber in fluid communication with said analysis chamber and said vent port.

12. The optical bio-disc of claim 11 further comprising a sample mix valve located in the fluidic circuit connecting said mixing chamber and said purification chamber.

13. The optical bio-disc according to claim 1 wherein said posts are distributed throughout said RBC capture zone.

14. The optical bio-disc according to claim 1 wherein said RBC capture agent is lectin.

15. A method of using the optical bio-disc according to claim 1 for a cellular assay, said method of using comprising the steps of:

loading a whole blood sample into said mixing chamber through said inlet port;

loading the bio-disc into an optical reader;

rotating the bio-disc at a sufficient speed and time to move said sample through said RBC capture zone where red blood cells in the sample are captured, through said purification zone where unwanted cells in the sample are captured, and through said analysis chamber where specific cells are captured on the capture zone;

directing an incident beam of electromagnetic radiation to the capture zone;

detecting a beam of electromagnetic radiation formed after the incident beam interacts with the disc at the capture zone;

converting the detected beam into an output signal; and

analyzing the output signal to extract therefrom infonnation relating to the number of cells captured at the capture zone.

20. The optical bio-disc of claim 1, wherein mixing chamber is configured to receive a lysis buffer.

21. The optical bio-disc of claim 20, wherein the bio-disc is configured to transmit the lysis buffer to the mixing chamber after the disc is rotated at a first predetermined speed, and wherein the bio-disc is configured to release the contents of the mixing chamber after the disc is rotated at a second predetermined speed.

16. A method of making an optical bio-disc for use in cellular assays, said method of making comprising the steps of:

forming a rotatable optical disc substrate;

forming a cover disc with similar dimensions to said substrate;

forming a channel layer with cut out portions to form fluidic circuits;

said fluidic circuits including an inlet port, a mixing chamber, a purification chamber, an analysis chamber, a vent port;

a RBC capture zone in fluid communication with the mixing chamber so as to receive a fluid therefrom; and

a plurality of posts with RBC capture agents coated thereon and located within the RBC capture zone;

said posts configured to capture RBC'"'"'s while allowing passage through said RBC capture zone of non-RBC materials; and

said analysis chamber including capture zones;

binding capture probes onto said capture zones;

attaching said channel layer to said substrate;

loading a filter means into said purification chamber;

attaching said cover disc to said channel layer to thereby form the optical bio-disc.

17. The method of claim 16 wherein said attaching steps are achieved by techniques selected from the group comprising adhesives and plastic welding.

18. The method of claim 16 wherein said filter means is selected from the group consisting of microspheres and cellular sieves.

19. The method of claim 18 wherein said filter means is coated with a purification agent.