The patent badge is an abbreviated version of the USPTO patent document. The patent badge does contain a link to the full patent document.

The patent badge is an abbreviated version of the USPTO patent document. The patent badge covers the following: Patent number, Date patent was issued, Date patent was filed, Title of the patent, Applicant, Inventor, Assignee, Attorney firm, Primary examiner, Assistant examiner, CPCs, and Abstract. The patent badge does contain a link to the full patent document (in Adobe Acrobat format, aka pdf). To download or print any patent click here.

Date of Patent:
Feb. 23, 2021

Filed:

Oct. 30, 2018
Applicant:

The Chinese University of Hong Kong, Hong Kong, CN;

Inventors:

Li Zhang, Hong Kong, CN;

Yabin Zhang, Hong Kong, CN;

Lidong Yang, Hong Kong, CN;

Kai Fung Chan, Hong Kong, CN;

Lin Zhang, Hong Kong, CN;

Ka Kei William Wu, Hong Kong, CN;

Assignee:
Attorney:
Primary Examiner:
Int. Cl.
CPC ...
C12Q 1/04 (2006.01); G01N 1/10 (2006.01); A61B 5/145 (2006.01); C12Q 1/24 (2006.01); C12M 1/26 (2006.01); A61B 34/30 (2016.01);
U.S. Cl.
CPC ...
C12Q 1/04 (2013.01); A61B 5/14503 (2013.01); C12M 1/268 (2013.01); C12Q 1/24 (2013.01); G01N 1/10 (2013.01); A61B 34/30 (2016.02);
Abstract

Disclosed are materials, devices, methods and systems for the detection of target molecules in test samples using microrobots. The target molecules may be bacterial toxins. The microrobots may include biohybrid materials such as porous spore core, a middle layer coated on the spore core for the actuation and steering in a fluid and further conjugation with a functional probe, and a sensing probe anchored onto middle layer for attaching to the targeted molecules in a fluid to respond to fluorescent tracking. A system for detecting bacterial toxin, is disclosed and comprises an intelligent motion control system based on automated fluorescent recognition and detection methods, which can propel and guide the microrobots to realize the automated motion in a pre-designed path and perform the real-time monitoring when integrating with an inverted fluorescent microscope or a fluorescent emission multi-reader.


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