Methods and apparatus for scanning small sample volumes

• US 20050264805A1
• Filed: 02/09/2005
• Published: 12/01/2005
• Est. Priority Date: 02/09/2004
• Status: Abandoned Application

• Current Assignee: Blueshift Biotechnologies, Inc. (Danaher Corporation)
• Original Assignee: Blueshift Biotechnologies, Inc. (Danaher Corporation)
• Inventors: Miller, Steven C., Shumate, Christopher B., Comita, Paul B., Cromwell, Evan F.
• Application Number:
  US11/055,244
• Publication Number:
  US 20050264805A1
• Time in Patent Office: Days
• US Class Current: 356/246
• CPC Class Codes: B01L 2300/0806 Standardised forms, e.g. compact disc [CD] format
• CPC Class Codes: B01L 3/5085 for multiple samples, e.g. microtitration plates
• CPC Class Codes: G01N 21/253 for batch operation, i.e. multisample apparatus analytical automats G01N35/00
• CPC Class Codes: G01N 21/6408 with measurement of decay time, time resolved fluorescence
• CPC Class Codes: G01N 21/6445 Measuring fluorescence polarisation
• CPC Class Codes: G01N 21/6452 Individual samples arranged in a regular 2D-array, e.g. multiwell plates
• CPC Class Codes: G01N 35/028 having reaction cells in the form of microtitration plates

Abstract

Methods and apparatus for assaying biological materials employ multi-well substrates as described herein. The substrates include a plurality of wells, typically each of several nanoliters volume or smaller having consistent dimensions and formed in a rigid substrate such as a glass disk. Each well may be provided with a circumferential lip to minimize crosstalk between wells and/or facilitate optical location of the individual wells during interrogation. Samples are provided to the individual wells and assayed by an optical technique employing fluorescence, polarization, reflectance, or the like. A scanning laser system may be employed for this purpose. The substrate may rotate during the scan to allow consistent interrogation of the wells without stopping and starting the rotation. Multiple rotations may also be employed repeatedly interrogate the samples for use in a kinetic study, for example.

Claims

1. An apparatus for collecting optical data pertaining to one or more characteristics of one or more samples, the apparatus comprising:

a light source;

a flat substrate having formed therein a plurality of sample wells, each sample well being configured to hold a sample volume of no more than about 50 nanoliters;

one or more illumination optical elements for directing a light beam from the light source onto the sample wells;

one or more collection optical elements for collecting light originating from within the sample wells and transmitting the collected light to one or more detectors.

2. The apparatus of claim 1, wherein each sample well is configured to hold a sample volume no greater than about 10 nanoliters.

3. The apparatus of claim 1, wherein each sample well is configured to hold a sample volume no greater than about one nanoliter.

4. The apparatus of claim 1, wherein the substrate further includes a substrate cover that seals edges of the individual sample wells.

5. The apparatus of claim 1, wherein the substrate has a substantially circular shape.

6. The apparatus of claim 5, wherein the substrate has a hole in the center of the substrate, allowing the substrate to be placed on a rotating spindle.

7. The apparatus of claim 6, wherein the circular substrate further comprises a reference mark for referencing all sample well locations on the substrate.

8. The apparatus of claim 1, wherein the substrate is a glass substrate.

9. The apparatus of claim 1, wherein a perimeter of a sample well is substantially circular and the diameter of the sample well is significantly larger than a depth of the sample well.

10. The apparatus of claim 9, wherein the diameter of a sample well is in the range of 1-100 micrometers.

11. The apparatus of claim 1, wherein the depth of a sample well is in the range of 10 nanometers to 10 micrometers.

12. The apparatus of claim 1, wherein a perimeter of each sample well is surrounded by a lip for preventing overflow of the sample well and cross talk between the sample wells.

13. The apparatus of claim 12, wherein the lip extends to a height corresponding to about one-tenth to one-third of the depth of the respective sample wells.

14. The apparatus of claim 1, wherein each sample well contains a sample that is unique with respect to the samples in the other sample wells on the substrate.

15. The apparatus of claim 1, wherein the sample contained in a sample well comprises at least one of:

a biological sample and material derived from a biological sample.

16. The apparatus of claim 1, wherein the centers of the sample wells are separated by no more than 100 micrometers.

17. The apparatus of claim 1, wherein the substrate has a surface height variation of not more than about 10 micrometers over a region of the substrate that is readable by the apparatus, and wherein the region that is readable by the apparatus has a roughness of not more than about 10 nanometers.

18. The apparatus of claim 1, wherein the substrate areas between the sample wells are coated with a hydrophobic material and the sample wells are hydrophilic.

19. A method for collecting optical data pertaining to one or more characteristics of one or more samples, comprising:

providing a flat substrate having formed therein a plurality of sample wells, each sample well being configured to hold a sample volume of no more than about 50 nanoliters;

dispensing one or more samples into the plurality of sample wells;

directing a light beam from a light source onto the sample wells;

collecting light originating from within the sample wells and transmitting the collected light to one or more detectors; and

analyzing the signal from the detectors to detect the one or more characteristics of the one or more samples.

20. The method of claim 19, wherein each sample well is configured to hold a sample volume smaller than 10 nanoliters.

21. The method of claim 19, wherein each sample well is configured to hold a sample volume smaller than one nanoliter.

22. The method of claim 19, wherein a perimeter of each sample well is surrounded by a lip for preventing overflow of the sample well and cross talk between the sample wells, and wherein collecting light comprises:

detecting when a focal point of a set of collection optical elements passes across an identifying feature on the substrate; and

collecting light only when a focal point of a set of collection optical elements is located inside the perimeter defined by the lip.

23. The method of claim 22, wherein the identifying feature on the substrate is a lip surrounding a sample well.

24. The method of claim 19, wherein the substrate is substantially circular and wherein collecting light comprises:

rotating the circular substrate past a set of collection optical elements; and

collecting light originating from within the sample well periodically each time the sample well rotates past the collection optical elements.

25. The method of claim 24, wherein the substrate has a hole in the center of the substrate and rotating comprises:

rotating the circular substrate by means of a rotating spindle placed through the hole in the center of the substrate, past a set of collection optical elements.

26. The method of claim 19, wherein the substrate areas between the sample wells are coated with a hydrophobic material and the sample wells are hydrophilic.

27. A substrate for holding one or more biological samples in an apparatus for collecting optical data pertaining to one or more characteristics of the biological samples, the substrate comprising:

a flat transparent glass substrate having formed therein a plurality of sample wells and a set of fiducials against which the location of the sample wells can be determined by the apparatus,

wherein each sample well holds a volume of a biological sample of no more than about 50 nanoliters by one or more of;

gravity, capillary action and surface tension,

wherein each sample well is surrounded by a lip arranged to prevent cross talk between the sample wells,

wherein the substrate areas between the sample wells are coated with a hydrophobic material and the sample wells are hydrophilic; and

a substrate cover that seals edges of the individual sample wells.