Method for controlling or regulating a microscope illumination

Patent metadata

Field	Value
Publication number	US-11774739-B2
Application number	US-201716463017-A
Country	US
Kind code	B2
Filing date	Nov 22, 2017
Priority date	Nov 22, 2016
Publication date	Oct 3, 2023
Grant date	Oct 3, 2023

Abstract

A method for regulating a light source of a microscope that illuminates an object, said method including specifying an intended value of an energy parameter of illumination radiation on the object; producing illumination radiation; providing an objective for focusing illumination radiation onto the object; ascertaining a transmission property of the objective for the illumination radiation; output coupling a component of the illumination radiation upstream of the objective as measurement radiation and measuring an actual value of the energy parameter of the measurement radiation; providing a relationship between energy parameters of the measurement radiation and energy parameters of the illumination radiation on the object, and setting the light source in such a way that the actual value of the energy parameter measured for the measurement radiation corresponds to the intended value of the energy parameter according to the relationship.

First claim

The invention claimed is:

1. A method for controlling or regulating a light source of a microscope for illuminating an object with illumination radiation, comprising the following steps:
defining a setpoint value of an energy parameter of the illumination radiation on the object, wherein the setpoint value indicates with what intensity or power the object is intended to be illuminated;
generating the illumination radiation by means of the light source;
providing an objective for focusing the illumination radiation onto the object;
coupling out a proportion of the illumination radiation upstream of the objective as measurement radiation and measuring an actual value of the energy parameter of the measurement radiation;
ascertaining a transmission property of the objective for the illumination radiation by at least one of measuring the transmission property of the objective, reading the transmission property from a database for the objective and reading the transmission property from memory associated with the objective;
providing a relationship between energy parameter of the measurement radiation and energy parameter of the illumination radiation on the object, wherein the relationship is dependent on the magnitude of the proportion and the transmission property of the objective; and
setting the light source in such a way that the actual value of the energy parameter measured for the measurement radiation corresponds, within a tolerance range, to the setpoint value of the energy parameter of the illumination radiation on the object in accordance with the relationship; and
wherein the microscope is configured to perform reflected light microscopy and further comprising performing the reflected light microscopy.

2. The method as claimed in claim 1 , characterized in that ascertaining the transmission property and/or measuring the actual value are/is carried out in a wavelength-dependent manner and/or the relationship is wavelength-dependent.

3. The method as claimed in claim 1 , characterized in that for taking account of the transmission property of the objective for the relationship, the type of the light source and/or an excitation filter, which filters the illumination radiation, are/is ascertained.

4. The method as claimed in claim 3 , characterized in that the actual value of the energy parameter of the measurement radiation is measured in a predefined partial wavelength range of the illumination radiation, wherein an instantaneous value of the energy parameter on the object in the entire wavelength range is deduced from this indication taking account of the type of the light source and/or the excitation filter.

5. The method as claimed claim 1 , characterized in that transmission properties of optical elements arranged between the objective and the output coupling location and/or transmission properties of an immersion medium present between the object and the objective are furthermore ascertained and taken into account for the relationship.

6. The method as claimed in claim 1 , characterized in that the measurement radiation is guided through a monitoring stop, wherein an opening of the monitoring stop is set in such a way that it corresponds to an effective aperture of the objective.

7. The method as claimed in claim 1 , characterized in that the actual value of the energy parameter of the measurement radiation is monitored continuously and the light source is regulated.

8. The method as claimed in claim 1 , characterized in that an area of a spot of the measurement radiation is determined and the relationship is corrected with regard to an effective aperture of the objective ( 14 ) and/or the area.

9. The method as claimed in claim 1 , characterized in that an electronic image of the object is generated, wherein an exposure time is synchronized with an exposure time of the process of measuring the actual value.

10. The method as claimed in claim 1 , characterized in that a shutter is provided between the objective and a beam splitter device that couples out the measurement radiation, and the shutter is opened if the actual value corresponds to the setpoint value within the tolerance range.

11. The method as claimed in claim 1 , characterized in that a temporal profile of the setpoint value and/or of the actual value of a value derived therefrom is stored.

Assignees

• Zeiss Carl Microscopy Gmbh

Inventors

• Gögler Michael
• Ohrt Thomas

Classifications

• G02B21/06 Primary

  Means for illuminating specimens · CPC title

• G02B21/0096

  with photometer devices (photometers per se G01J) · CPC title

• G02B21/16

  adapted for ultraviolet illumination {; Fluorescence microscopes (G02B21/0076 takes precedence)} · CPC title

• G02B21/365

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