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新型复合混合微球,由海藻酸钠包裹壳聚糖制成,用于阿莫西林的控制释放。

Novel composite blend microbeads of sodium alginate coated with chitosan for controlled release of amoxicillin.

机构信息

Department of Chemistry, Karnatak University, Dharwad, India.

出版信息

Int J Biol Macromol. 2012 Jul-Aug;51(1-2):45-55. doi: 10.1016/j.ijbiomac.2012.04.018. Epub 2012 Apr 24.

Abstract

Composite blend microbeads of sodium alginate (NaAlg) with sodium carboxymethyl cellulose (NaCMC) containing magnesium aluminum silicate (MAS) particles and enteric coated with chitosan have been prepared to achieve controlled release (CR) of amoxicillin in stomach environment. The composite beads have been characterized by X-ray diffraction (XRD) to study drug distribution, DSC for understanding thermal stability and Fourier transform infrared (FTIR) spectroscopy to investigate chemical interactions as well as to assess the structure of the drug-loaded formulations. Surface morphology of the beads was investigated by scanning electron microscopy (SEM). The size distribution of beads loaded with drug as studied by particle size analyzer was in the range of 745-889 μm. The beads exhibited quite widely varying encapsulation efficiencies from 52 to 92%. Equilibrium swelling of the beads measured in water and in vitro release of amoxicillin in pH 1.2 medium suggests that drug release depends on polymer blend composition, concentration of MAS and extent of enteric coating.

摘要

已制备出含有镁铝硅酸盐(MAS)颗粒的海藻酸钠(NaAlg)和羧甲基纤维素钠(NaCMC)的复合混合微球,并对其进行了壳聚糖的肠溶性包衣,以实现阿莫西林在胃部环境中的控制释放(CR)。通过 X 射线衍射(XRD)研究药物分布、差示扫描量热法(DSC)了解热稳定性以及傅里叶变换红外(FTIR)光谱研究化学相互作用和评估载药制剂的结构,对复合微球进行了表征。通过扫描电子显微镜(SEM)研究了微球的表面形态。通过粒度分析仪研究了载药微球的粒径分布范围在 745-889μm 之间。微球的包封效率变化范围较广,为 52%-92%。在水中的平衡溶胀和在 pH1.2 介质中的阿莫西林体外释放表明,药物释放取决于聚合物共混物的组成、MAS 的浓度和肠溶性包衣的程度。

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