Inverted microscopic imaging system with programmable LED array for multi-contrast label-free imaging

Patent metadata

Field	Value
Publication number	US-12566324-B2
Application number	US-202118026276-A
Country	US
Kind code	B2
Filing date	Aug 18, 2021
Priority date	Sep 24, 2020
Publication date	Mar 3, 2026
Grant date	Mar 3, 2026

Abstract

The invention discloses a miniaturized, low-cost, multi-contrast label-free microscopic imaging system. The imaging system is based on an inverted microscopic structure, a highly integrated optical system is designed by adopting a micro lens having a fixed focal length, and a complex optical system of a traditional microscope system is replaced, such that the whole microscope is highly integrated. The system uses a programmable LED array as an illumination light source; the LED array is controlled by a computer to display different illumination modes, six imaging functions of a bright field, a dark field a rainbow dark field, Rheinberg optical dyeing, differential phase contrast, and quantitative phase imaging are achieved; and diversified unmarked imaging methods are provided for biological applications. The invention provides a matching control system, which can realize system hardware control and algorithm execution and display, comprises functions such as illumination control, camera parameter adjustment quantitative phase reconstruction recovery, two-dimensional/three-dimensional result display, and quantitative profile analysis, and can realize diversified information obtaining and analysis of unmarked samples.

First claim

The invention claimed is:

1 . A miniaturized, low-cost, multi-contrast label-free microscopic imaging system comprising:
an integrated imaging unit comprising an inverted transmission microscopic optical path including a programmable LED array illumination source configured for direct spatial coherence and wavelength modulation, a tube lens, a miniaturized lens, a sample carrier, an area-scan color camera, and a 3D displacement stage, wherein the programmable LED array illumination source, the tube lens, the miniaturized lens, the sample carrier, the area-scan color camera and the 3D displacement stage are arranged in sequence from top to bottom; and a control unit to control an illumination pattern of the programmable LED array illumination source, adjust parameters of the area-scan color camera, control an image acquisition by the area-scan color camera, switch imaging modes, switch a display of 2D/3D imaging results, and perform an analysis of the imaging results.

2 . The miniaturized, low-cost, multi-contrast label-free microscopic imaging system according to claim 1 , wherein the miniaturized lens has a magnification of 6.4×, a numerical aperture (NA) of 0.14, a focal length of 4.25, and a lens aberration of less than 1%.

3 . The miniaturized, low-cost, multi-contrast label-free microscopic imaging system according to claim 2 , wherein the programmable LED array illumination source is configured to produce illumination patterns corresponding to six imaging modes, including: bright-field imaging, dark-field imaging, rainbow dark-field imaging, Rheinberg optical staining imaging, differential phase contrast (DPC) imaging, and quantitative phase imaging (QPI),
wherein the illumination patterns of the six imaging modes match the NA of the miniaturized lens, and assuming the NA of a miniaturized lens of NA obj , the corresponding illumination NA ill for each LED is:

NA
ill

=

sin
[

arctan
⁡
(

R

L
⁢
E
⁢
D

h

)

]

where R LED denotes a distance from each LED to the LED corresponding to a center of the optical axis and h denotes a distance from the programmable LED array illumination source to an upper surface of the sample carrier
wherein the illumination patterns are defined by:
a bright-field illumination pattern comprising a circular illuminated region with an illumination NA less than or equal to the NA of the miniaturized lens;
a dark-field illumination pattern comprising a circular hollow illuminated region with an illumination NA greater than the NA of the miniaturized lens;
a rainbow dark-field illumination pattern comprising the circular hollow illuminated region of the dark-field imaging with rainbow color distribution;
a Rheinberg optical staining illumination pattern comprising a circular illuminated region with LEDs having an illumination NA less than or equal to the NA of the miniaturized lens providing a first color, and LEDs having an illumination NA greater than the NA of the miniaturized lens providing different colors;
a DPC illumination pattern comprising a half-circular illuminated region with an illumination NA less than or equal to the NA of the miniaturized lens; and
a QPI illumination pattern comprising a half-circular illuminated region with an illumination NA less than or equal to the NA of the miniaturized lens.

4 . The miniaturized, low-cost, multi-contrast label-free microscopic imaging system according to claim 3 , wherein the control unit is further configured to perform differential phase contrast (DPC) imaging by applying a differential algorithm to obtain a phase gradient image of the sample in any direction (0˜360°), and
wherein a formula for the differential algorithm is expressed as:

I

l
⁢
r

=

I
l

-

I
r

I
l

+

I
r

where I lr represents a phase gradient of DPC in any axis direction, and I l and I r represent two images acquired with asymmetric illumination in the said axis direction.

5 . The miniaturized, low-cost, multi-contrast label-free microscopic imaging system according to claim 4 , wherein the control unit is further configured to perform quantitative phase imaging (QPI) by a DPC quantitative phase recovery algorithm, comprising the sub-steps of:
acquiring corresponding images from four illumination patterns irradiating a sample along two asymmetric axes; calculating phase gradient images of the sample in the two axes based on the acquired images; calculating a phase transfer function for DPC imaging; solving for a sample phase by deconvoluting a spectrum of the phase gradient images and the phase transfer function using Tikhonov regularization to obtain quantitative phase results of the sample; and repeating the process for QPI.

6 . The miniaturized, low-cost, multi-contrast label-free microscopic imaging system according to claim 5 , wherein the DPC quantitative phase recovery algorithm further comprises, after the sub-step of solving for the sample phase, the sub-step of:
capturing a first, second, third, and fourth image in a cyclic order, wherein each captured image is used to perform the sub-step of calculating the phase transfer function to obtain sample phase gradient image from a current acquisition and a previous acquisition within the cyclic order, thereby achieving quantitative phase imaging output at a highest camera frame rate.

7 . The miniaturized, low-cost, multi-contrast label-free microscopic imaging system according to claim 6 , wherein after the sub-step of repeating, the control unit is further configured to enhance display contrast of the quantitative phase of the sample by at least one of:
histogram filtering, by calculating a histogram of grayscale distribution of pixel values in a reconstructed phase and removing background phase by selecting a range of phase values for display from the histogram; or multi-color pseudo-color display, by selecting a phase color spectrum from a plurality of pseudo-color distributions to display different structural information of the sample.

8 . The miniaturized, low-cost, multi-contrast label-free microscopic imaging system according to claim 5 , the control unit is further configured to generate and store a phase transfer function locally, and to automatically retrieve the stored phase transfer function at system startup.

9 . The miniaturized, low-co

Assignees

• Univ Nanjing Sci & Tech

Inventors

• Chen Qian
• Zuo Chao
• Sun Jiasong
• Feng Shijie
• Zhang Yuzhen
• Gu Guohua

Classifications

• G02B21/008 Primary

  Details of detection or image processing, including general computer control · CPC title

• G02B21/0032

  Optical details of illumination, e.g. light-sources, pinholes, beam splitters, slits, fibers (G02B21/0036 - G02B21/008; means for illumination of specimens in general G02B21/06) · CPC title

• G02B21/0008

  Microscopes having a simple construction, e.g. portable microscopes · CPC title

• G02B21/086

  for transillumination only · CPC title

• G02B21/365

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