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载药核壳结构聚维酮/玉米醇溶蛋白电纺纳米纤维的双相药物释放。

Electrospun drug-loaded core-sheath PVP/zein nanofibers for biphasic drug release.

机构信息

Guangdong Food and Drug Vocational College, Guangzhou 510520, China.

出版信息

Int J Pharm. 2012 Nov 15;438(1-2):232-9. doi: 10.1016/j.ijpharm.2012.08.053. Epub 2012 Sep 5.

Abstract

Core-sheath nanofibers prepared using coaxial electrospinning were investigated for providing biphasic drug release profiles. With ketoprofen (KET) as the model drug, polyvinylpyrrolidone and zein as the sheath polymer and core matrix, respectively, the coaxial process could be carried out smoothly and continuously without any clogging of the spinneret. Scanning electron microscopy and transmission electron microscopy observations demonstrated that the nanofibers were linear with homogeneous structure and had a clear core-sheath structure with an average diameter of 730 ± 190 nm, in which the sheath had a thickness of ca. 90 nm. Differential scanning calorimetric and X-ray diffraction analyses verified that all the components in the core-sheath nanofibers were present in an amorphous state. Attenuated total reflectance Fourier transform infrared spectra demonstrated both the sheath and core matrix had good compatibility with KET owing to hydrogen bonding. In vitro dissolution tests showed that the nanofibers could provide an immediate release of 42.3% of the contained KET, followed by a sustained release over 10h of the remaining drug. The present study exhibited a simple and useful approach to systematically design and fabricate nanostructures using coaxial electrospinning for providing biphasic drug release profiles.

摘要

采用同轴静电纺丝制备的核壳纳米纤维被用于提供双相药物释放曲线。以酮洛芬(KET)为模型药物,聚维酮和玉米醇溶蛋白分别作为鞘聚合物和核基质,同轴过程可以顺利且连续地进行,而不会出现喷丝头堵塞的情况。扫描电子显微镜和透射电子显微镜观察表明,纳米纤维呈线性,具有均匀的结构,具有清晰的核壳结构,平均直径为 730±190nm,其中鞘的厚度约为 90nm。差示扫描量热法和 X 射线衍射分析验证了核壳纳米纤维中的所有成分均处于无定形状态。衰减全反射傅里叶变换红外光谱表明,由于氢键的存在,鞘和核基质都与 KET 具有良好的相容性。体外溶出试验表明,纳米纤维可以立即释放 42.3%的包裹 KET,然后在 10 小时内持续释放剩余的药物。本研究展示了一种简单而有用的方法,通过同轴静电纺丝系统地设计和制造用于提供双相药物释放曲线的纳米结构。

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