Abstract
Silk is one of the most important materials in the history of medical practice. Owing to its excellent
strength, biocompatibility and degradability, silk from Bombyx mori – which is structured as a
concentric assembly of silk fibroin (SF) coated by a sheath of sericin (SS) – has long been used
for wound treatment. Here, we recapitulate for the first time the topology of native silk fibers using
a radically new materials design-oriented approach to achieve unprecedented porous dermal
patches suitable for controlled drug delivery. The method implies four steps: (1) removing SS; (2)
creating anisotropic macroporosity in SF via ice templating; (3) stabilizing the SF foam with a
methanolic solution of Rifamycin (Rif) antibiotic; and (4) coating Rif-loaded redesigned SF foams
with a SS sheath. The core-shell SS@SF foams exhibit water wicking properties accommodate up
to ~20% lateral deformation. Moreover, monitoring of antibacterial activity against
Staphylococcus aureus revealed that the SS@SF foams’ Rif release extended up to 9 days. We
anticipate that reverse-engineering of silk foams opens exciting new avenues towards the
fabrication of advanced drug eluting silk-based biomaterial platforms with improved performance.
The present approach can be generalizable to re-build multicomponent biological materials with
tunable porosity.
Supplementary materials
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Supporting information preprint
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