System and method for calibrating a fluorescence microscope
View Patent ↗A system and method are provided to calibrate fluorescence detection of a fluorescence microscope by using a near-perfectly uniform reflector as a target in combination with temporary removal of the microscope's emission filter. Excitation light is reflected from the near-perfectly uniform reflector back into the microscope's objective optical system and transmitted to a dichroic. A small fraction of the excitation light passes though the dichroic and is measured by a CCD camera or other appropriate measurement device. By measuring the intensity of the residual excitation light at a plurality of points in the field of view, variations in illumination intensity may be determined. Using this, fluorescence detection at different points in the field of view may be readily calibrated.
1. A method for calibrating a fluorescence microscope comprising the steps of:
removing an emission filter from the fluorescence microscope;
placing a reflector as a target of the fluorescence microscope;
measuring excitation light reflected by the reflector; and
adjusting measurements of emission light in response to the measuring of the excitation light.
2. The method of claim 1 further comprising the step of:
placing a neutral density filter in the optical path of the microscope.
3. The method of claim 2 wherein the neutral density filter is placed at the location previously occupied by the emission filter.
4. The method of claim 1 wherein the reflector is a near-perfectly uniform reflector comprising polytetrafluoroethylene.
5. The method of claim 1 wherein the step of measuring further comprises the step of:
creating a map of the intensity of the excitation light reflected from the target, the map depicting the intensity at a number of points in the field of view of the fluorescence microscope.
6. The method of claim 5 wherein each point of the field of view of the fluorescence microscope corresponds to a pixel of a digital image, and the map of the intensity of the excitation light is a digital image.
7. The method of claim 5 wherein the step adjusting measurements of emission light further comprises the steps of:
calculating a map of correction factors from the map of the intensity of the excitation light; and
using the correction factors to adjust measurements of emission light at points in the field of view.
8. The method of claim 1 wherein the fluorescence microscope is an epi-flourescence microscope.
9. The method of claim 1 wherein the fluorescence microscope is a dark-field fluorescence microscope.
10. The method of claim 1 further comprising:
associating the fluorescence microscope with a control calibration chip;
measuring fluorescence emissions of the control calibration chip to create a baseline measurement; and
retaining the baseline measurement and the control calibration chip with the microscope.
11. The method of claim 1 further comprising:
comparing a subsequent measurement of the control calibration chip with the baseline measurement, and adjusting the microscope so the subsequent and the baseline measurements will substantially coincide.
12. A system for calibrating fluorescence detection of a microscope comprising:
a uniform reflector adapted to be used as a target of the microscope;
a neutral density filter adapted to replace an emission filter of the microscope; and
a measurement device for measuring the intensity of excitation light reflected by the uniform reflector, through the neutral density filter, at differing points in a field of view of the microscope, the measurement device further adapted to calculate a correction factor at a plurality of points in the field of view, the correction factor for adjusting measurements of emission light.
13. The system of claim 12 wherein the uniform reflector comprises a material containing polytetrafluoroethylene.
14. The system of claim 12 wherein the microscope is an epi-flourescence microscope.
15. The system of claim 12 wherein the microscope is a dark-field fluorescence microscope.