Optical interrogation system and method for increasing a read-out speed of a spectrometer

• US 7,705,336 B2
• Filed: 08/07/2006
• Issued: 04/27/2010
• Est. Priority Date: 08/08/2005
• Status: Expired due to Fees

• Current Assignee: Corning Incorporated
• Original Assignee: Corning Incorporated
• Inventors: Piech, Garrett A., Webb, Michael B.
• Primary Examiner(s): Epps; Georgia Y
• Assistant Examiner(s): Ko; Tony
• Application Number:
  US11/500,048
• Publication Number:
  US 20070031291A1
• Time in Patent Office: 1,359 Days
• Field of Search: 250/208.1, 25055901-55943, 250/226
• US Class Current: 250/559.05
• CPC Class Codes: G01J 3/2803 using photoelectric array detector
• CPC Class Codes: G01N 21/7743 the reagent-coated grating coupling light in or out of the waveguide

Abstract

A typical use of linear or two dimensional spectrometers is to expose the detector area, and then shift the photo-electric charges out of the device in a serial fashion. If the illuminating signal is spatially narrow relative to the size of the array, this will drive down the percent of the detector that is utilized, as only a relatively small number of pixels are used to detect the beam. The present invention proposes a method which capitalizes on this spatial under-utilization, and alters the clocking scheme to maximize the read-out speed of the pixels containing signal information. This type of clocking scheme raises the optical power saturation level of the spectrometer. Such an improvement in optical power handling is beneficial for spectrometer based detection of resonant waveguide grating biochemical binding, since in such systems the performance is frequently limited by spectrometer saturation.

Claims

1. A method for increasing a read-out speed of a 1-D detector within an optical interrogation system, the optical interrogation system includes a launch system and a receive system, wherein said launch system directs a light beam towards a biosensor, and wherein said receive system includes a 1-D detector which receives a light beam out-coupled from said biosensor, the method comprising the steps of:

blocking a plurality of pixels located within said 1-D detector such that only a subset of pixels receive the light beam out-coupled from said biosensor;

transferring a set of charges/voltages associated with the received light beam from the subset of pixels located within said 1-D detector before outputting from said 1-D detector a signal representative of a previously transferred set of charges/voltages associated with a previously received light beam; and

processing the signal in a first-in and first-out sequence to determine an optical response corresponding to the previously transferred set of charges/voltages, wherein said optical response indicates whether or not there was a biological substance/bio-chemical interaction on top of said biosensor.

2. An optical interrogation system, comprising:

a launch system including;

a light source that directs a light beam towards a biosensor; and

a receive system including;

an optical shutter

a detector comprising;

a subset of pixels that receives an out-coupled light beam from said biosensor, wherein the optical shutter blocks a plurality of pixels located within said detector such that only the subset of pixels receive the light beam out-coupled from said biosensor;

a controller that causes a set of charges/voltages associated with the received light beam to be transferred out from said subset of pixels before a voltage signal representative of a previously transferred set of charges/voltages associated with a previously received light beam is outputted from said detector; and

an analog/digital converter that converts the voltage signal into a digital signal representative of the previously transferred set of charges/voltages; and

a processor that processes the digital signal in a first-in and first-out sequence to determine an optical response corresponding to the previously transferred set of charges/voltages, wherein said optical response indicates whether or not there was a biological substance/bio-chemical interaction on top of said biosensor.

3. The optical interrogation system of claim 2, wherein said 1-D detector is:

a 1-D spectrometer;

a 1-D CCD detector;

or

a 1-D CMOS detector.

4. The optical interrogation system of claim 2, wherein said receive system further includes a reference detector that receives a portion of the light beam directed towards the biosensor.

5. The optical interrogation system of claim 2, wherein said biosensor is a resonant waveguide grating biosensor.

6. The optical interrogation system of claim 2, wherein said biosensor is incorporated within a well of a microplate.

7. A method for increasing a read-out speed of a 1-D detector within an optical interrogation system, the optical interrogation system includes a launch system and a receive system, wherein said launch system directs a light beam towards a biosensor, and wherein said receive system includes a 1-D detector which receives a light beam out-coupled from said biosensor, the method comprising the steps of:

blocking a plurality of pixels located within said 1-D detector such that only a subset of pixels receive the light beam out-coupled from said biosensor;

transferring a set of charges/voltages associated with the received light beam from the subset of pixels located within said 1-D detector before outputting from said 1-D detector a signal representative of a previously transferred set of charges/voltages associated with a previously received light beam;

processing the signal in a first-in and first-out sequence to determine an optical response corresponding to the previously transferred set of charges/voltages, wherein said optical response indicates whether or not there was a biological substance/bio-chemical interaction on top of said biosensor;

wherein the combination of the blocking and transferring steps improve the processing step by;

extending an optical power saturation limit of the 1-D detector by transferring more charges out per unit time than is possible without the blocking and transferring steps, where the extended optical power saturation limit results in higher signal-to-noise ratio, SNR, measurements which makes it easier to detect a change in a position of the optical response of the biosensor.

8. A method for increasing a read-out speed of a 1-D detector within an optical interrogation system, the optical interrogation system includes a launch system and a receive system, wherein said launch system directs a light beam towards a biosensor, and wherein said receive system includes a 1-D detector which receives a light beam out-coupled from said biosensor, the method comprising the steps of:

blocking a plurality of pixels located within said 1-D detector such that only a subset of pixels receive the light beam out-coupled from said biosensor;

transferring a set of charges/voltages associated with the received light beam from the subset of pixels located within said 1-D detector before outputting from said 1-D detector a signal representative of a previously transferred set of charges/voltages associated with a previously received light beam;

processing the signal in a first-in and first-out sequence to determine an optical response corresponding to the previously transferred set of charges/voltages, wherein said optical response indicates whether or not there was a biological substance/bio-chemical interaction on top of said biosensor;

wherein the combination of the blocking and transferring steps improve the processing step by;

extending an optical power saturation limit of the 1-D detector by transferring more charges out per unit time than is possible without the blocking and transferring steps, where the extended optical power saturation limit results in higher signal-to-noise ratio, SNR, measurements which makes it easier to detect a change in a position of the optical response of the biosensor; and

reducing an overall pixel clock rate in the 1-D detector more than is possible without the blocking and transferring steps, where the reduced pixel clock rate averages down electrical noise from the 1-D detector; and

limiting the extending step and the reducing step based on a specific application to trade-off benefits of extending the optical power saturation limit of the 1-D detector and reducing the overall pixel clock rate in the 1-D detector.

9. The method of claim 8, wherein said processing step further includes cropping the signal into individual signals and using a peak finding algorithm to process each individual signal to locate the optical response.

10. The method of claim 8, wherein said processing step further includes accumulating multiple signals associated with previously transferred sets of charges/voltages and using a peak finding algorithm on the accumulated signals to monitor a movement of the optical response over time which indicates when the biological substance/bio-chemical interaction occurred on the top of said biosensor.