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疏水性和基质厚度对水凝胶-静电纺纤维基质复合材料释放性能的影响。

Effects of hydrophobicity and mat thickness on release from hydrogel-electrospun fiber mat composites.

机构信息

a William G. Lowrie Department of Chemical and Biomolecular Engineering, Department of Biomedical Engineering , The Ohio State University , 125A Koffolt Laboratories, 140 West 19th Ave., Columbus , OH , 43210 , USA .

出版信息

J Biomater Sci Polym Ed. 2013;24(17):2018-30. doi: 10.1080/09205063.2013.822246. Epub 2013 Aug 1.

Abstract

Poly(ethylene glycol) (PEG)-based hydrogel-electrospun fiber mat (EFM) composites are a promising new controlled release system for hydrophilic drugs, providing longer and more linear release characteristics accompanied by a smaller initial burst than traditional hydrogel systems. However, the effect of EFM properties on release characteristics has not yet been examined. Here, we investigated the influence of EFM thickness and hydrophobicity on swelling and release behavior using bovine serum albumin as a model hydrophilic protein. EFMs investigated were comprised of poly(ε-caprolactone) (PCL) at thicknesses of 300, 800, or 1100 μm. Hydrophobicity was adjusted through surface modification: fluorinated PCL, core/shell PCL/PEGPCL, and acrylic acid (AAc)-treated PCL EFMs were examined. EFMs comprised of the external composite surface, forming a sandwich around PEG-poly(lactic acid) (PEGPLA) hydrogels, and significantly restrained hydrogel swelling in the radial direction while increasing swelling in the axial direction. Incorporation of EFMs also reduced initial hydrophilic protein release rates and extended the duration of release. Increased EFM thickness and hydrophobicity were equally correlated with longer and more linear release profiles. Increased thickness most likely increases the diffusional path length, whereas increased hydrophobicity hinders hydrophilic drug diffusion. These composites form a promising new class of tunable release materials having properties superior to those of unmodified hydrogels.

摘要

聚乙二醇(PEG)基水凝胶-电纺纤维垫(EFM)复合材料是一种有前途的新型亲水性药物控释系统,与传统水凝胶系统相比,其具有更长、更线性的释放特性,并伴有较小的初始突释。然而,EFM 性能对释放特性的影响尚未得到检验。在这里,我们研究了 EFM 厚度和疏水性对牛血清白蛋白(BSA)作为模型亲水性蛋白的溶胀和释放行为的影响。所研究的 EFM 由厚度为 300、800 或 1100 μm 的聚己内酯(PCL)组成。通过表面改性调整疏水性:研究了氟化 PCL、PCL/PEGPCL 核壳和丙烯酸(AAc)处理的 PCL EFM。EFM 由外部复合表面组成,在 PEG-聚乳酸(PEGPLA)水凝胶周围形成三明治,显著抑制水凝胶在径向的溶胀,同时增加轴向的溶胀。EFM 的掺入还降低了初始亲水性蛋白的释放速率,并延长了释放时间。EFM 厚度和疏水性的增加与更长、更线性的释放曲线呈正相关。厚度的增加很可能增加了扩散路径长度,而疏水性的增加则阻碍了亲水性药物的扩散。这些复合材料形成了一类有前途的新型可调释材料,其性能优于未改性的水凝胶。

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