Light microscope and method for determining a wavelength-dependent refractive index of a sample medium

Patent metadata

Field	Value
Publication number	US-10684221-B2
Application number	US-201615769286-A
Country	US
Kind code	B2
Filing date	Oct 11, 2016
Priority date	Nov 9, 2015
Publication date	Jun 16, 2020
Grant date	Jun 16, 2020

Abstract

With the method of the invention a wavelength-dependent refractive index of a specimen medium, which is examined with a light microscope, is determined. With the light microscope, a specimen measurement at the specimen medium which has an unknown refractive index is performed, wherein illumination light is radiated to the specimen medium and detection light coming from the specimen medium is measured. With the specimen measurement, a specimen measurement focus position of the illumination and/or detection light is measured. Using a mathematical model, in which a focus position of illumination and/or detection light is defined in dependence of a refractive index of a medium, the refractive index of the specimen medium is derived from the specimen measurement focus position. Furthermore, a light microscope for carrying out the method is described.

First claim

The invention claimed is:

1. A method for determining a wavelength-dependent refractive index of a specimen medium which is examined with a light microscope, the method comprising:
performing with the light microscope a specimen measurement of the specimen medium which has an unknown refractive index, wherein illumination light is radiated to the specimen medium and detection light coming from the specimen medium is measured;
measuring a specimen measurement focus position of the illumination or detection light in the specimen medium by means of the specimen measurement;
using a mathematical model, in which a focus position of illumination or detection light in the specimen medium is defined in dependence of a refractive index of a medium, for deriving the refractive index of the specimen medium from the specimen measurement focus position in the specimen medium.

2. The method as defined in claim 1 ,
characterized in that the mathematical model is formed by an equation in which a focus position depends linearly from a refractive index plus a constant (Offset).

3. The method as defined in claim 1 ,
further comprising performing at least one calibration measurement with the light microscope for determining at least one parameter of the mathematical model, wherein in the calibration measurement:
a medium with known refractive index is illuminated with illumination light,
detection light coming from the medium with known refractive index is measured for obtaining at least one microscope image, and
a calibration measurement focus position of the illumination or detection light is determined from the at least one microscope image, and

calculating at least one parameter of the mathematical model based on the known refractive index and the determined calibration measurement focus position.

4. The method as defined in claim 3 ,
wherein an illumination beam path of the illumination light is transverse to a detection beam path of the detection light,
the illumination light is focusedly radiated into the medium with known refractive index or the specimen medium,
determining during the calibration measurement the location in the at least one microscope image at which location the illumination light has a minimal cross-section, and using that location as calibration measurement focus position, or recording during the specimen measurement at least one specimen image and determining in that image at which location the illumination light has a minimal cross-section, and using this location as specimen measurement focus position.

5. The method as defined in claim 4 ,
further comprising
performing at least two calibration measurements which differ from each other at least in the emission of the illumination light such that:
for one of the calibration measurements, the calibration measurement focus position of the illumination light is in travel direction in front of an image field center, and
for another of the calibration measurements, the calibration measurement focus position of the illumination light is in travel direction behind the image field center.

6. The method as defined in claim 1 ,
further comprising performing at least two calibration measurements,
wherein the calibration measurements differ from each other in one or more of the following ways:
using different media with a respectively known refractive index;
using different specimen vessels with geometries that differ from each other in known ways;
using different microscope settings which influence the calibration measurement focus position.

7. The method as defined in claim 6 ,
wherein the different microscope settings which are used for the at least two calibration measurements differ in one or more of the following ways:
the microscope settings differ in the wavelength of the respectively emitted illumination light;
the microscope settings differ in the wavelength of the recorded detection light;
the microscope settings differ in a numerical aperture with which the illumination light is radiated into the medium;
the microscope settings differ in an illumination direction in which the illumination light is radiated into the medium;
the microscope settings differ in a zoom setting of detection optics and thus in an image field size.

8. The method as defined in claim 1 ,
further comprising recording several microscope images in each calibration measurement, wherein for the several microscope images, detection optics of the light microscope image different height planes,
determining the microscope image of maximal sharpness out of the microscope images,
using the height plane that corresponds to the microscope image of maximal sharpness as calibration measurement focus position.

9. The method as defined in claim 1 ,
further comprising recording in the specimen measurement several specimen images for which detection optics of the light microscope image different height planes,
determining the specimen image of maximal sharpness out of the specimen images,
using the height plane that corresponds to the microscope image of maximal sharpness as specimen measurement focus position.

10. The method as defined in claim 1 ,
further comprising at least one of:
radiating the illumination light as structured illumination light into the medium with known refractive index during the at least one calibration measurement, or
radiating the illumination light as structured illumination light into the specimen medium during the specimen measurement,
wherein an illumination beam path is transverse to a detection beam path and a cross-section of the structured illumination light varies in the travel direction of the structured illumination light.

11. The method as defined in claim 1 ,
further comprising
outputting the determined refractive index of the specimen medium or outputting a certain instruction to a user or to a control and evaluation unit for automatic or non-automatic adjustment of a microscope setting, in dependence of the determined refractive index of the specimen medium.

12. A light microscope comprising
an illumination light source for emitting illumination light in direction of a specimen medium to be examined,
a detection objective and a camera device for measuring detection light coming from the specimen medium, and
an illumination objective configured to produce a focus of the illumination light within the specimen medium, wherein the illumination objective and the detection objective are formed by different objectives or one and the same objective,
wherein the light microscope comprises a control and evaluation unit in which a mathematical model is included in which a focus position of illumination or detection light in the specimen medium is expressed in dependence of a refractive index of the specimen medium, and
the control and evaluation unit is configured to determine the focus position of illumination or detection light in the specimen medium and to determine the refractive index of the specimen medium from the focus position of illumination or detection light in the specimen medium, with the help of the mathematical model.

13. The light microscope as defined in claim 12 ,
wherein the control and evaluation unit is furthermore configured to:
perform a specimen measurement at a specimen medium with unknown refractive index,
determine by means of the specimen measurement a specimen measurement focus position of the illumination or detection light,
use the determined specimen measurement focus position as focus position to be input for determining the refractive index of the specimen medium.

14. A method for

Assignees

• Zeiss Carl Microscopy Gmbh

Inventors

• Bergter Annette
• Lippert Helmut

Classifications

• G02B21/367

  providing an output produced by processing a plurality of individual source images, e.g. image tiling, montage, composite images, depth sectioning, image comparison · CPC title

• G02B21/0076

  arrangements using fluorescence or luminescence · CPC title

• G02B21/365

  Control or image processing arrangements for digital or video microscopes (G02B21/361, G02B21/362 take precedence) · CPC title

• G01N21/274

  Calibration, base line adjustment, drift correction · CPC title

• G01N21/4133 Primary

  Refractometers, e.g. differential · CPC title