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槐豆胶-聚乙烯醇互穿网络用于控制药物释放。

Interpenetrating polymer network of locust bean gum-poly (vinyl alcohol) for controlled release drug delivery.

机构信息

Department of Pharmaceutical Sciences, Birla Institute of Technology, Mesra, Ranchi 835 215, Jharkhand, India.

出版信息

Carbohydr Polym. 2013 Apr 15;94(1):456-67. doi: 10.1016/j.carbpol.2013.01.070. Epub 2013 Jan 30.

Abstract

A novel interpenetrating polymer network (IPN) microspheres of locust bean gum (LBG) and poly (vinyl alcohol) (PVA) was developed for oral controlled release of buflomedil hydrochloride (BH) by emulsion crosslinking method using glutaraldehyde as crosslinker. The effects of gum-polymer ratio, concentration of crosslinker and internal phase viscosity were evaluated thoroughly. Drug entrapment efficiency, particle size distribution, swelling property and in vitro release characteristics with kinetic modelling of microspheres were evaluated. The microspheres were characterised by scanning electron microscopy (SEM), Fourier transform infrared spectroscopy (FT-IR), solid state C(13) NMR, X-ray diffraction study (XRD) and differential scanning colorimetry (DSC). The microspheres showed control release property without showing any incompatibility in IPN device. Hence, IPN microspheres of LBG and PVA can be used as a potential carrier for controlled oral delivery of highly water soluble drugs like BH.

摘要

一种新型的刺梧桐胶(LBG)和聚乙烯醇(PVA)互穿聚合物网络(IPN)微球,通过乳化交联法,以戊二醛为交联剂,制备盐酸丁咯地尔(BH)的口服控释制剂。详细评价了胶-聚合物比、交联剂浓度和内相粘度的影响。评价了微球的药物包封效率、粒径分布、溶胀性能和体外释放特性,并对其进行了动力学建模。通过扫描电子显微镜(SEM)、傅里叶变换红外光谱(FT-IR)、固态 C(13)NMR、X 射线衍射研究(XRD)和差示扫描量热法(DSC)对微球进行了表征。微球表现出控制释放性能,在 IPN 装置中没有表现出任何不相容性。因此,LBG 和 PVA 的 IPN 微球可用作高度水溶性药物如 BH 的口服控释的潜在载体。

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