Silk fibroin hydrogels and uses thereof
The present specification provides for methods for purifying fibroins, purified fibroins, methods of conjugating biological and synthetic molecules to fibroins, fibroins conjugated to such molecules, methods of making fibroin hydrogels, fibroin hydrogels and fibroin hydrogel formulations useful for a variety of medical uses, including, without limitation uses as bulking agents, tissue space fillers, templates for tissue reconstruction or regeneration, cell culture scaffolds for tissue engineering and for disease models, surface coating to improve medical device function, or drug delivery devices.
1. A method of breast reconstruction or augmentation, the method comprising the steps of
a) implanting a silicone or saline filled breast implant into a site of breast tissue of an individual; and
b) implanting a hydrogel scaffold at the site of implantation, the hydrogel scaffold comprising a substantially sericin-depleted silk fibroin and adipose cells, the hydrogel scaffold formed by:
extracting sericin from a silk fibroin thereby forming the substantially sericin-depleated silk fibroin;
digesting a mixture including the substantially sericin-depleated silk fibroin, thereby forming a digested mixture;
collecting a supernatant of the digested mixture after centrifugation, wherein the supernatant comprises depolymerized silk fibroin;
gelling the supernatant in an ethanol solution comprising ethanol as a gelation enhancer and porogens, thereby forming a silk fibroin hydrogel;
removing the porogens from the silk fibroin hydrogel to form the hydrogel scaffold defined by an array of interconnected pores; and
seeding the hydrogel scaffold with adipose cells,
wherein the adipose cells are autologous with the individual.
2. The method of claim 1 , wherein the hydrogel scaffold is implanted so as to support a lower pole position of the breast implant.
3. The method of claim 1 , wherein the method further comprising the step of at least partially covering the breast implant with the hydrogel scaffold prior to the steps of implanting.
4. . A method of breast reconstruction or augmentation, the method comprising the steps of
(a) implanting a silicone or saline filled breast implant into an individual, and;
(b) implanting a hydrogel scaffold at the site of implantation, the hydrogel scaffold comprising a substantially sericin-depleted silk fibroin and adipose cells autologous to the individual, the hydrogel scaffold formed by:
(i) extracting sericin from a silk fibroin thereby forming the substantially sericin-depleated silk fibroin;
(ii) digesting a mixture including the substantially sericin-depleated silk fibroin, thereby forming a digested mixture, wherein the digested mixture comprises depolymerized silk fibroin;
(iii) gelling the depolymerized silk fibroin in an ethanol solution thereby forming a silk fibroin hydrogel, and;
(iv) seeding the silk fibroin hydrogel with adipose cells autologous to the individual.