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Crystallinity modulated silk fibroin electrospun nanofibers based floating scaffold as a candidate for controlled release of felodipine

丝素 静电纺丝 材料科学 控制释放 纳米纤维 药物输送 肿胀 的 结晶度 溶解试验 化学工程 溶解 丝绸 复合材料 纳米技术 聚合物 乙基纤维素 工程类
作者
Shailesh Dugam,Sopan Nangare,Anil H. Gore,Sarika Wairkar,P.S. Patil,Latika Choudary,Namdeo Jadhav
出处
期刊:International Journal of Polymeric Materials [Taylor & Francis]
卷期号:71 (18): 1393-1406 被引量:7
标识
DOI:10.1080/00914037.2021.1981318
摘要

Floating gastro-retentive delivery approach provides a significant pathway for controlled release of drug with increase gastric residence. In this study, we report crystallinity modulated electrospun silk fibroin nanofibers (SF-NFs) floating scaffolds for the controlled release of felodipine (FD). The alteration in the crystallinity behavior due to changes in the structural conformation of SF helps to customize the release kinetics of FD-loaded SF-NFs scaffolds. Additionally, FD-loaded SF scaffolds system having a density less than the acidic gastric fluid explore as a new tactic for floating drug delivery system. The prepared FD-loaded SF nanofibers (FD-loaded SF-NFs) were characterized by spectral, thermal, and diffractometric techniques, scanning electron microscopy, floating profile, in-vitro degradation, mucoadhesion, and in-vitro dissolution studies, etc. The optimized batch had the least porosity and swelling, was annealed with ethanol and water for crystallinity modulation of SF-NFs to get controlled release of FD. Spectral, thermal, and diffractometric analyses could unveil the molecular dispersion of FD, coupled with amorphous form stabilization in NF. Excellent floating profile and satisfactory mucoadhesion of FD-SF-NFs also endorsed the formation of a novel floating drug delivery system. Temporal control over FD release was elucidated by in-vitro dissolution, demonstrating controlled release due to crystallinity modulation of SF-NFs. In conclusion, crystallinity-modulated electrospun NFs fabricated from SF waste could be used as a customizable carrier for drug delivery to the gastric region.
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