US2014039159A1PendingUtilityA1

Electroactive biopolymer optical and electro-optical devices and method of manufacturing the same

Assignee: UNIV TUFTSPriority: Nov 3, 2006Filed: Jul 11, 2013Published: Feb 6, 2014
Est. expiryNov 3, 2026(~0.3 yrs left)· nominal 20-yr term from priority
G02B 2006/1213G02B 1/041B29D 11/0074G02B 1/045G02B 1/046B29D 11/00663G02B 1/005C07K 14/43586G02B 2006/12104D10B 2401/20G02B 2006/12107G01N 2333/43578B82Y 20/00G02B 2006/12171G02B 2006/12102D01F 4/02G01N 33/544B29C 39/02G02B 5/18G02B 1/06G01N 33/5436G02B 6/138G02B 1/04D10B 2211/04G01N 33/54373G01N 33/54386
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Claims

Abstract

A method of manufacturing a biopolymer optical device includes providing a polymer, providing a substrate, casting the polymer on the substrate, and enzymatically polymerizing an organic compound to generate a conducting polymer between the provided polymer and the substrate. The polymer may be a biopolymer such as silk and may be modified using organic compounds such as tyrosines to provide a molecular-level interface between the provided bulk biopolymer of the biopolymer optical device and a substrate or other conducting layer via a tyrosine-enzyme polymerization. The enzymatically polymerizing may include catalyzing the organic compound with peroxidase enzyme reactions. The result is a carbon-carbon conjugated backbone that provides polymeric “wires” for use in polymer and biopolymer optical devices. An all organic biopolymer electroactive material is thereby provided that provides optical functions and features.

Claims

exact text as granted — not AI-modified
1 - 26 . (canceled) 
     
     
         27 . A device comprising a biopolymer,
 wherein the biopolymer is modified to have an additional function,   wherein the additional function is a cell binding domain, a redox trigger, a phosphorylation trigger, or a combination thereof; and,   wherein the device is an optical or electro-optical device.   
     
     
         28 . The device of  claim 27 , wherein the cell binding domain is an RGD domain. 
     
     
         29 . The device of  claim 27 , wherein the redox trigger is a methionine. 
     
     
         30 . The device of  claim 27 , wherein the optical or electro-optical device is selected from the group consisting of:
 diffraction gratings, photonic crystals, optofluidic devices, waveguides, lenses, microlens arrays, pattern generators, beam reshapers, electro-optical collectors, solar collectors, and mechanical actuators with optical readout.   
     
     
         31 . The device of any one of  claims 27 - 30 , wherein the biopolymer is selected from the group consisting of:
 silk fibroin, chitosan, collagen, gelatin, agarose, chitin, polyhydroxyalkanoates, pullan, starch, cellulose, hyaluronic acid, polydimethylsiloxane (PDMS), and combinations thereof.   
     
     
         32 . A method of manufacturing a device comprising a modified biopolymer, the method comprising steps of:
 providing a substrate;   providing a biopolymer solution;   casting the biopolymer solution on the substrate;   catalyzing a reaction to alter the biopolymer to provide a modified biopolymer having an additional functional feature,   wherein the additional functional feature is a conducting wire, a cell binding domain, a redox trigger, a phosphorylation trigger, or a combination thereof.   
     
     
         33 . The method of  claim 32 , wherein the step of catalyzing comprises chemical coupling, enzymatic reaction, or combination thereof. 
     
     
         34 . The method of  claim 32 , wherein the step of catalyzing comprises polymerization. 
     
     
         35 . The method of  claim 32 , wherein the step of catalyzing comprises addition of an organic compound. 
     
     
         36 . The method of  claim 35 , wherein the organic compound is an aromatic moiety, tyrosine, methionine, or combination thereof. 
     
     
         37 . The method of  claim 32 , wherein the step of catalyzing comprises a peroxidase, a lipase, an amylose, an organophosphate dehydrogenase, a restriction endonuclease, s ribonuclease, a DNA polymerases, a glucose oxidase, a laccase, or a combination thereof. 
     
     
         38 . The method of any one of  claims 32 - 37 , wherein the biopolymer is selected from the group consisting of:
 silk fibroin, chitosan, collagen, gelatin, agarose, chitin, polyhydroxyalkanoates, pullan, starch, cellulose, hyaluronic acid, polydimethylsiloxane (PDMS), and combinations thereof.   
     
     
         39 . The method of  claim 32 , wherein the substrate is a template for at least one of an electro-optical collector, a solar collector, a mechanical actuator with optical readout, a lens, a microlens array, an optical grating, a pattern generator, and a beam reshaper.

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