Compositions comprising low molecular weight silk fibroin fragments and plasticizers

Abstract

Various aspects described herein relate to compositions comprising silk fibroin fragments with particular characteristics and/or properties as well as methods of making and using the same.

What is claimed is: 
     
         1 . A solution for forming a scaffold, the solution comprising silk fibroin fragments and glycerol, the silk fibroin fragments having a weight average molecular weight ranging from about 100 kDa to about 160 kDa, wherein the glycerol and the silk fibroin fragments are present in a weight ratio (glycerol to silk fibroin fragments) of about 1:100 to about 25:100; wherein the solution for forming the scaffold exhibits a glass transition temperature of equal to or less than about −15° C., and wherein the solution for forming the scaffold is sterile; and
 wherein the solution for forming the scaffold, after sublimation, has a relative solubility in a range of about 1% to about 50%. 
 
     
     
         2 . The solution of  claim 1 , wherein the glycerol and the silk fibroin fragments are present in a weight ratio of about 1:100 to about 8:100. 
     
     
         3 . The solution of  claim 1 , wherein the solution further comprises an alcohol and/or a polyol. 
     
     
         4 . A silk fibroin particle comprising silk fibroin fragments and glycerol, wherein the silk fibroin fragments have a weight average molecular weight ranging from about 100 kDa to about 160 kDa, and wherein the silk fibroin particle comprises a porous structure characterized by interconnected pores having an average circle equivalent diameter of about 5 μm to about 60 μm and having an aspect ratio of about 1.0 to about 3.0,
 wherein the silk fibroin particle has an aspect ratio of about 1 to about 3, and 
 wherein the glycerol and the silk fibroin fragments are present in a weight ratio (glycerol to silk fibroin fragments) of 1:100 to about 25:100. 
 
     
     
         5 . The silk fibroin particle of  claim 4 , wherein the silk fibroin particle is formed from a lyophilized scaffold. 
     
     
         6 . The solution of  claim 1 , wherein the solution has been sterilized by vacuum filtration. 
     
     
         7 . The solution of  claim 1 , wherein the silk fibroin fragments have a weight average molecular weight ranging from about 130 kDa to about 160 kDa. 
     
     
         8 . The solution of  claim 1 , wherein no more than about 5% of the total number of the silk fibroin fragments have a molecular weight of about 200 kDa or higher. 
     
     
         9 . The solution of  claim 1 , wherein at least about 60% of the total number of silk fibroin fragments have a molecular weight of about 30 kDa to about 170 kDa. 
     
     
         10 . A silk fibroin scaffold formed from the solution of  claim 1 . 
     
     
         11 . A silk fibroin particle formed from the scaffold of  claim 10 . 
     
     
         12 . The silk fibroin particle of  claim 4 , wherein the silk fibroin particle is formed from a sterile solution. 
     
     
         13 . The silk fibroin particle of  claim 12 , wherein the sterile solution, after sublimation, has a relative solubility in a range of about 1% to about 50%. 
     
     
         14 . The silk fibroin particle of  claim 12 , wherein the sterile solution has a glass transition temperature of equal to or less than about −15° C. 
     
     
         15 . The silk fibroin particle of  claim 4 , wherein the glycerol and the silk fibroin fragments are present in the sterile solution at a weight ratio of 1:100 to about 8:100. 
     
     
         16 . The silk fibroin particle of  claim 12 , wherein the sterile solution has been sterilized by vacuum filtration. 
     
     
         17 . The silk fibroin particle of  claim 4 , wherein the silk fibroin fragments have a weight average molecular weight ranging from about 130 kDa to about 160 kDa. 
     
     
         18 . The silk fibroin particle of  claim 4 , wherein the silk fibroin particle is formed from a sterile solution, wherein the sterile solution, after sublimation, has a relative solubility in a range of about 1% to about 50%, and wherein the sterile solution has a glass transition temperature of equal to or less than about −15° C. 
     
     
         19 . The silk fibroin particle of  claim 18 , wherein the sterile solution has been sterilized by vacuum filtration.