# US 11,906,433 B2 · System and method for three-dimensional imaging of unstained samples using bright field microscopy

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- Number: US 11,906,433 B2
- Document ID: US11906433B2
- Status: Granted
- Kind: B2
- Application number: 17/550,797
- Filed: 2021-12-14
- Published: 2023-06-15
- Granted: 2024-02-20
- Earliest claimed: 2021-12-14
- Assignees: Instituto Potosino de Investigación Científica y Tecnológica A.C.
- Applicants: Instituto Potosino de Investigación Científica y Tecnológica A.C.
- Inventors: Braulio Gutierrez Medina
- Web page: https://patentgrep.com/patent/US11906433B2

## CPC

- G01N 21/6458: {Fluorescence microscopy (fluorescence microscopes per se G02B21/0076 and G02B21/16)}
- G02B 21/008: {Details of detection or image processing, including general computer control}
- G02B 21/06: Means for illuminating specimens
- G02B 21/16: adapted for ultraviolet illumination {; Fluorescence microscopes (G02B21/0076 takes precedence)}
- G02B 21/244: {using image analysis techniques}
- G02B 21/26: Stages; Adjusting means therefor
- G02B 21/365: {Control or image processing arrangements for digital or video microscopes (G02B21/361, G02B21/362 take precedence)}
- G02B 21/367: {providing an output produced by processing a plurality of individual source images, e.g. image tiling, montage, composite images, depth sectioning, image comparison}
- G01N: INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES (measuring or testing apparatus or processes other than immunoassay, involving enzymes or microorganisms C12M, C12Q)
- G02B: OPTICAL ELEMENTS, SYSTEMS OR APPARATUS

## Abstract

A system and method for optical sectioning in bright field microscopy (OSBM). The system includes a bright field optical microscope having automated change of focus, a substage condenser fitted with an adjustable aperture iris diaphragm, a digital camera that records the microscope image of samples, and one or more digital computers to perform digital image processing. The OSBM method comprises operating the microscope to Kohler illumination, using the iris diaphragm of the condenser to generate contrast in images, acquiring a Z-stack of images of the unstained sample, and applying a sequence of digital image processing filters to the Z-stack, resulting in optical sections from where the final three-dimensional (3D) image of the sample can be reconstructed by computational device. The final 3D images produced by this invention present quality comparable to that of available optical sectioning techniques that require sample labeling, such as light sheet fluorescence microscopy.

## Claims

### Claim 1

A method for three-dimensional imaging using bright field light microscopy, the method comprising the steps of:
a) placing an unstained sample on an optical transparent holder, surrounding the unstained sample in the transparent holder with air or an optically transparent liquid or solid, and then placing the sample in an optical microscope, the optical microscope having automated change of focus, a substage condenser fitted with an adjustable aperture iris diaphragm, a digital camera to record images of said unstained sample created by said microscope, and one or more digital computers to store and process the images of said unstained sample captured by said digital camera;
b) operating said optical microscope in bright field mode;
c) adjusting said optical microscope to Kohler illumination and operating said optical microscope under Kohler illumination;
d) adjusting the aperture of said condenser iris diaphragm of said optical microscope so that contrast is generated in the images of said unstained sample captured by said digital camera of said optical microscope;
e) acquiring a Z-stack of images of said unstained sample;
f) transferring the outputs of said digital camera to said computer or computers;
g) applying to said Z-stack of images a high-pass filter to remove the low spatial frequency components from images;
h) applying a pairwise frame subtraction operation to the resulting image stack of step g);
i) applying a smoothing filter to the resulting image stack of step h);
j) apply a white top hat filter in three dimensions to the resulting image stack of step i); and
k) reporting the result of step (i) in the form of digital image stacks, matrices of numbers, projection images or three-dimensional rendering images.

### Claim 2 (depends on 1)

The method according to claim 1, wherein said unstained sample comprises organic or inorganic material, prokaryotic cells, eukaryotic cells, archaea cells, tissue, polymers, biological polymers, biofilms, transparent materials, or semi-transparent materials.

### Claim 3 (depends on 1)

The method according to claim 1, wherein said unstained sample is free of staining agents and/or free of fluorescent agents.

### Claim 4 (depends on 1)

The method according to claim 1, wherein said unstained sample contains fluorescent agents.

### Claim 5 (depends on 1)

The method according to claim 1, wherein said the transparent holder is a chamber, a microchamber, a cuvette, or a vessel.

### Claim 6 (depends on 1)

The method according to claim 1, wherein said Z-stack of images comprises a collection of images corresponding to different planes of focus within said unstained sample.

### Claim 7 (depends on 1)

The method according to claim 1, wherein said Z-stack of images is acquired by using said automated change of focus to image a set of different planes of focus within said unlabeled sample and using said digital camera to record a bright field image of said sample at each of said different planes of focus.

### Claim 8 (depends on 1)

The method according to claim 1, wherein said high-pass filter, pairwise frame subtraction filter, smoothing filter, and the white top hat filter, are applied to said Z-stack of images by said digital computer or computers.

### Claim 9

An optical sectioning bright field microscopy system comprising:
an optical transparent holder adapted to receive an unstained sample, the optical transparent holder with the unstained sample is surrounded with air or an optically transparent liquid or solid;
an optical microscope, the optical transparent holder with the unstained sample are placed inside the optical microscope, the optical microscope having automated change of focus, a substage condenser fitted with an adjustable aperture iris diaphragm, and a digital camera, said digital camera recording the images of a sample produced by said optical microscope and having an output to provide the information contained in said images of a sample, said optical microscope configured to allow operation in bright field mode and under Kohler illumination, said optical microscope configured to allow adjustment of said iris diaphragm, said optical microscope configured to allow acquisition of Z-stacks of images of said sample by using said automated change of focus of said optical microscope to image a set of different planes of focus within said sample and using said digital camera to record a bright field image representative of each of said different planes of focus;
one or more digital computers configured to receive the output of said digital camera and recognize said output as said Z-stacks of images of said sample, said one or more digital computers configured to apply a high-pass filter, a pairwise frame subtraction filter, a smoothing filter, and a white top hat filter to said Z-stacks of images of said sample resulting in optical section images of the said sample; and
a reporting apparatus in communication with said one or more digital computers, said reporting apparatus configured to provide a report of said optical section images in the form of digital image stacks, matrices of pixel values, projection images or three-dimensional rendered images.

### Claim 10 (depends on 9)

The optical sectioning bright field microscopy system of claim 9, wherein said adjustment of said iris diaphragm allows the generation of contrast in the images of said sample captured by said digital camera of said optical microscope.