TY - JOUR
T1 - Nanolayer biomaterial coatings of silk fibroin for controlled release
AU - Wang, Xianyan
AU - Hu, Xiao
AU - Daley, Andrea
AU - Rabotyagova, Olena
AU - Cebe, Peggy
AU - Kaplan, David L.
N1 - Funding Information:
This work was supported by NIH (EB002520 and EB003210) and the NSF (DMR). We thank Anthony B. Barry, Wyeth BioPharma, for his critical assessment of this work. We also thank Ms. Yenhsi Lin, surface engineering and molecular assembly laboratory, Iowa State University, for assistance with the coating thickness measurements.
PY - 2007/8/28
Y1 - 2007/8/28
N2 - An all-aqueous, stepwise deposition process with silk fibroin protein for the assembly of nanoscale layered controlled release coatings was exploited. Model compounds, Rhodamine B, Even Blue and Azoalbumin, representing small molecule drugs and therapeutically relevant proteins were incorporated in the nanocoating process and their loading and release behavior was quantified. In addition, the structure and morphology of the coatings were characterized. Release studies in vitro showed that control of β-sheet crystal content and the multilayer structure of the silk coatings correlated with the release properties of the incorporated compounds. In particular, higher crystallinity and a thicker silk capping layer suppressed the initial burst of release and prolonged the duration of release. These novel coatings and deposition approach provide a unique option to regulate structure and morphology, and thus release kinetics. The results also suggest these systems as a promising framework for surface engineering of biomaterials and medical devices to regulate the release of drugs, when considered with the all-aqueous process involved, the conformal nature of the coatings, the robust material properties of silk fibroin, and the degradability and biocompatibility of this family of protein.
AB - An all-aqueous, stepwise deposition process with silk fibroin protein for the assembly of nanoscale layered controlled release coatings was exploited. Model compounds, Rhodamine B, Even Blue and Azoalbumin, representing small molecule drugs and therapeutically relevant proteins were incorporated in the nanocoating process and their loading and release behavior was quantified. In addition, the structure and morphology of the coatings were characterized. Release studies in vitro showed that control of β-sheet crystal content and the multilayer structure of the silk coatings correlated with the release properties of the incorporated compounds. In particular, higher crystallinity and a thicker silk capping layer suppressed the initial burst of release and prolonged the duration of release. These novel coatings and deposition approach provide a unique option to regulate structure and morphology, and thus release kinetics. The results also suggest these systems as a promising framework for surface engineering of biomaterials and medical devices to regulate the release of drugs, when considered with the all-aqueous process involved, the conformal nature of the coatings, the robust material properties of silk fibroin, and the degradability and biocompatibility of this family of protein.
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U2 - 10.1016/j.jconrel.2007.06.006
DO - 10.1016/j.jconrel.2007.06.006
M3 - Article
C2 - 17628161
AN - SCOPUS:34547699279
SN - 0168-3659
VL - 121
SP - 190
EP - 199
JO - Journal of Controlled Release
JF - Journal of Controlled Release
IS - 3
ER -