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首页> 外文期刊>International Journal of Biological Macromolecules: Structure, Function and Interactions >Novel composite blend microbeads of sodium alginate coated with chitosan for controlled release of amoxicillin
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Novel composite blend microbeads of sodium alginate coated with chitosan for controlled release of amoxicillin

机译:海藻酸钠包覆壳聚糖的新型复合掺和微珠可控释阿莫西林

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摘要

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.
机译:海藻酸钠(NaAlg)与羧甲基纤维素钠(NaCMC)含有硅酸镁铝(MAS)颗粒并经壳聚糖包衣的复合掺和微珠已经制备,可在胃环境中实现阿莫西林的控释(CR)。通过X射线衍射(XRD)来研究复合物珠的特征,研究药物的分布,通过DSC来了解热稳定性,并通过傅里叶变换红外(FTIR)光谱来研究化学相互作用以及评估载药制剂的结构。通过扫描电子显微镜(SEM)研究珠的表面形态。通过粒度分析仪研究的载有药物的珠的尺寸分布在745-889μm的范围内。珠粒表现出非常大的封装效率,从52%到92%。珠粒在水中的平衡溶胀以及阿莫西林在pH 1.2介质中的体外释放表明药物释放取决于聚合物共混物的组成,MAS的浓度和肠溶衣的程度。

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