IP Library Granted Patent US 11,029,319
Granted Patent B2
US 11,029,319 · App. 16/157,094 · Granted Jun 8, 2021

Biosensor and application of the same

Inventors: Han-Sheng Chuang (Tainan, TW); Ching-Chuen Chen (New Taipei, TW); Yu-Ting Tseng (Taichung, TW)
Assignee: NATIONAL CHENG KUNG UNIVERSITY
G01N33/6893A61B5/1455A61B5/14507A61B5/6821A61B10/0045G01N21/64G02C7/04G02C11/10A61B2010/0067G01N2333/47G01N2800/164
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Quick Facts
Patent No.
US 11,029,319
App. No.
16/157,094
Granted
Jun 8, 2021
Kind
B2
Abstract

The present invention provides a biosensor and an application of the same. The biosensor includes a substrate, a first polymer layer and a second polymer layer. The first polymer layer includes composite antibodies, each of which includes a first antibody and a labelling molecule. The second polymer layer has an inverse opal photonic crystal structure where gold nanoparticles and second antibodies are distributed. At least one of the composite antibodies, an antigen and at least one of the second antibodies forms a complex in the second polymer layer, and an antigen concentration is obtained by a fluorescence intensity, a degree of red-shift or a change in a visual color of the biosensor.

Claims (15)

1. A biosensor, comprising:

a substrate, wherein the substrate comprises a first region and a second region adjoined to the first region, the second region is located on one side of the first region, a center of the substrate is concentrically surrounded by the first region and the second region in order from outside to inside, a bottom of the first region has a recessed cross section having a first depth, a bottom of the second region has a recessed cross section having an asymmetric U-shape and a second depth, the second depth is greater than the first depth, and a slope of a side wall of the recessed cross section of the second region near the center is greater than a slope of another other side wall of the recessed cross section of the second region near the first region;

a first polymer layer, disposed in the first region, wherein a plurality of composite antibodies are distributed in the first polymer layer, and each of the composite antibodies comprises a labelling molecule and a first antibody connected to the labelling molecule; and

a second polymer layer, disposed in the second region, wherein the second polymer layer has an inverse opal photonic crystal structure, the inverse opal photonic crystal structure comprises a plurality of holes, a plurality of gold nanoparticles and a plurality of second antibodies are disposed on a wall of each of the holes, and the first antibody and the second antibodies recognize the same antigen.

2. The biosensor of claim 1 , wherein the second region is located over the first region.

3. The biosensor of claim 1 , wherein the inverse opal photonic crystal structure is an inverted structure of a face-centered cubic structure of nanobeads, each of the nanobeads has a particle size in a range from 100 nm to 1000 nm, and the gold nanoparticles are distributed on a surface of each of the nanobeads.

4. The biosensor of claim 1 , wherein the labelling molecule comprises a fluorescent molecule, and a particle size of each of the gold nanoparticles is in a range from 5 nm to 80 nm.

5. The biosensor of claim 1 , further comprising a third polymer layer over the first polymer layer.

6. The biosensor of claim 1 , wherein the biosensor is a contact lens, the center of the substrate is an optical zone of the contact lens, the first region and the second region are located in a non-optical zone of the contact lens, at least the second polymer layer is exposed on one surface of the contact lens, and opposes a surface that is in direct contact with an eye.

7. A method of detecting an antigen concentration, comprising:

providing a biosensor described in claim 1 , wherein a substrate of the biosensor comprises a first region and a second region connected to the first region, and the second region is located on one side of the first region;

flowing a biological liquid sample containing an antigen from the second region to the first region of the biosensor, thereby releasing at least one of a plurality of composite antibodies comprising a first antibody and a labelling molecule, and reacting the at least one of the composite antibodies for a period of time with the antigen and at least one of a plurality of second antibodies to form a complex in the second region;

detecting an optical property of the complex in the second region of the biosensor by using a light source having a specific wavelength, wherein the optical property comprises a fluorescence intensity or a visual color; and

obtaining an antigen concentration according to the optical property.

8. The method of claim 7 , wherein the specific wavelength is in a range from 200 nm to 700 nm, and the fluorescence intensity is increased by at least two times based on an inverse opal photonic crystal structure in the second region.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 12, 2018
From: CHUANG, HAN-SHENG; CHEN, CHING-CHUEN; TSENG, YU-TING
To: NATIONAL CHENG KUNG UNIVERSITY
Reel/Frame 047643/0983 →
Continuity (1)
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