IP Library Granted Patent US 9,599,891
Granted Patent B2
US 9,599,891 · App. 12/741,066 · Granted Mar 21, 2017

Fabrication of silk fibroin photonic structures by nanocontact imprinting

Inventors: David L. Kaplan (Concord, MA); Fiorenzo G. Omenetto (Lexington, MA); Luca Dal Negro (Cambridge, MA)
Assignees: TRUSTEES OF TUFTS COLLEGE; TRUSTEES OF BOSTON UNIVERSITY
G03F7/0002B29D11/00B29D11/00346B82Y10/00B82Y20/00B82Y40/00C07K14/435G02B6/1225
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Quick Facts
Patent No.
US 9,599,891
App. No.
12/741,066
Granted
Mar 21, 2017
Kind
B2
Abstract

A method of manufacturing a nanopatterned biophotonic structure includes forming a customized nanopattern mask on a substrate using E-beam lithography, providing a biopolymer matrix solution, depositing the biopolymer matrix solution on the substrate, and drying the biopolymer matrix solution to form a solidified biopolymer film. A surface of the film is formed with the nanopattern mask, or a nanopattern is machined directly on a surface of the film using E-beam lithograpy such that the biopolymer film exhibits a spectral signature corresponding to the E-beam lithograpy nanopattern. The resulting bio-compatible nanopatterned biophotonic structures may be made from silk, may be biodegradable, and may be bio-sensing devices. The biophotonic structures may employ nanopatterned masks based on non-periodic photonic lattices, and the biophotonic structures may be designed with specific spectral signatures for use in probing biological substances, including displaying optical activity in the form of opalescence.

Claims (31)

1. A method of manufacturing a biophotonic nano-material, the method comprising steps of:

providing a substrate having a lithographically nanopatterned structure on a surface thereof;

providing an aqueous silk-fibroin solution;

depositing the solution on the lithographically nanopatterned surface of the substrate;

drying the solution to form a solidified silk-fibroin film haying a surface in contact with the nanopatterned surface of the substrate, which film is characterized by beta-sheet secondary structure and by a nanopatterned imprint in the contacted surface of the film transferred from the nanopatterned surface of the substrate; and

mechanically removing the film from the substrate,

wherein the film is characterized in that when it is exposed to photonic radiation it exhibits it spectral response corresponding to the lithographically nanopatterned imprint, and

wherein the biophotonic nano-material is characterized such that when a biological material selected from the group consisting of red blood cells, horseradish peroxidase, a nucleic acid, cells, an antibody, enzymes, peroxidase, lipase, amylose, organophosphate dehydrogenase, ligases, restriction endonuclease, ribonucleases, DNA polymerases, glucose oxidase, laccase, viruses, proteins, peptides, amino acids, DNA, RNA, RNAi, nucleotides, bacteriorhodopsin, and protorhodopsin is embedded in the film or coated on its surface, one or both of its structure and its biological activity is not materially degraded, reduced, and/or inhibited.

2. The method of claim 1 , wherein prior to the step of providing the substrate, the method comprises:

spin-coating a resist on the surface of the substrate;

e-beam writing the nanopattern on the resist;

developing the resist to selectively remove areas of it;

evaporating a metal layer onto the surface of the substrate; and

removing the resist to expose a metal island array, thereby forming the nanopatterned structure on the surface of the substrate.

3. The method of claim 1 , wherein the biophotonic nano-material is biocompatible.

4. The method of claim 1 , wherein the biophotonic nano-material is biodegradable.

5. The method of claim 1 , wherein the nanopatterned structure comprises an array of at least one of holes and pits.

6. The method of claim 5 , wherein the holes are spaced apart from 50 nm to 500 nm, inclusive.

7. The method of claim 5 , when the nanopatterned structure comprises holes, the holes are spaced apart from 50 nm to 500 nm, inclusive.

8. The method of claim 1 , wherein the nanopatterned structure is based on non-periodic photonic lattices.

9. The method of claim 1 , wherein the spectral response exhibited is the form of an opalescent response.

10. The method of claim 1 , wherein the step of providing an aqueous silk-fibroin solution comprises providing a solution in which is present at approximately 1 wt % to 30 wt % inclusive.

11. The method of claim 1 , wherein the nanopatterned structure is a template for an optical device.

12. The method of claim 11 , wherein the optical device is at least one of a lens, a microlens array, an optical grating, a pattern generator, and a beam reshaper.

13. The method of claim 11 , wherein the optical device is an arrangement of geometrical features.

14. The method of claim 11 , wherein the arrangement of geometrical features is holes and/or pits.

15. The method of claim 1 , wherein the nanopatterned structure is a template for a biosensing device.

16. The method of claim 1 , wherein the nanopatterned structure comprises 100 nm diameter Cr nanoparticles on a Si substrate.

17. The method of claim 16 , wherein the Cr nanoparticles are spaced from 20 nm to 250 nm, inclusive.

18. The method of claim 1 , further comprising a step of coating the biophotonic nano-material with one or more components selected from the group consisting of: red blood cells, horseradish peroxidase, a nucleic acid, cells, an antibody, enzymes, peroxidase, lipase, amylose, organophosphate dehydrogenase, ligases, restriction endonucleases, ribonucleases, DNA polymerases, glucose oxidase, laccase, viruses, proteins, peptides, amino acids, DNA, RNA, RNAi, nucleotides, bacteriorhodopsin, and protorhodopsin.

19. The method of claim 1 , the step of providing the aqueous silk-fibroin solution, comprises adding to the aqueous silk-fibroin solution one or more components selected from the group consisting of: red blood cells, horseradish peroxidase, a nucleic acid, cells, an antibody, enzymes, peroxidase, lipase, amylose, organophosphate dehydrogenase, ligases, restriction endonucleases, ribonucleases, DNA polymerases, glucose oxidase, laccase, viruses, proteins, peptides, amino acids, DNA, RNA, RNAi, nucleotides, bacteriorhodopsin, and protorhodopsin and thereby embedding the biophotonic nano-material.

Assignments (3)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 3, 2017
From: KAPLAN, DAVID L.; OMENETTO, FIORENZO G.
To: TRUSTEES OF TUFTS COLLEGE
Reel/Frame 041170/0559 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 3, 2017
From: DAL NEGRO, LUCA
To: TRUSTEES OF BOSTON UNIVERSITY
Reel/Frame 041170/0708 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 16, 2011
From: OMENETTO, FIORENZO
To: TUFTS UNIVERSITY/TRUSTEES OF TUFTS COLLEGE
Reel/Frame 026757/0659 →
Continuity (2)
Provisional Application 60985310 · Nov 5, 2007
Related Publication 20120121820A1 · May 17, 2012