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首页> 外文期刊>Journal of Applied Polymer Science >Development of sericin/alginate particles by ionic gelation technique for the controlled release of diclofenac sodium
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Development of sericin/alginate particles by ionic gelation technique for the controlled release of diclofenac sodium

机译:不同离子凝胶化技术的硅蛋白/藻酸盐颗粒的研制下双氯芬酸钠控制释放

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摘要

Sericin and alginate particles, prepared by ionic gelation technique, demonstrated to be a promising matrix to controlled release of diclofenac sodium. Ten particle compositions of sericin, alginate, and diclofenac were evaluated. The drug incorporation was confirmed by scanning electron microscopy, Fourier Transform Infrared Spectroscopy, and X-ray diffraction analysis. In vitro dissolution profile was performed to obtain the drug release profile in gastric and enteric medium. The drug release profile indicated that sericin delays the release and alginate contributes to the gastro-resistance of formulations. The blend with composition of 2.5% of sericin, 2.8% of alginate with 2.0% w/v of diclofenac demonstrated to be feasible for drug delivery due the entrapment efficiency of 81.06% and release delay of 360 min, the highest time of all investigated compositions. The mathematical modeling showed that the drug release mechanism is associated to the process of swelling, matrix erosion, and a combination of diffusion and chain relaxation mechanisms. (c) 2017 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2018, 135, 45919.
机译:通过离子凝胶化技术制备的硅粉和海藻酸盐颗粒,证明是对双氯芬酸钠控制释放的有前途的基质。评价了10种颗粒组成的硅蛋白,藻酸盐和双氯芬酸。通过扫描电子显微镜,傅里叶变换红外光谱和X射线衍射分析证实了药物掺入。进行体外溶出曲线以在胃肠和肠溶介质中获得药物释放曲线。药物释放曲线表明,Sericin延迟释放和藻酸盐有助于配方的胃抗性。与组合物的组成的混合物,2.8%的海藻酸盐,含有2.0%w / v的双氯芬酸的含量表明,由于夹带效率为81.06%并释放360分钟,所以所有研究组合物的最高时间可行。数学建模表明,药物释放机制与膨胀,基质腐蚀的过程相关,以及扩散和链松弛机构的组合。 (c)2017 Wiley期刊,Inc.J.Phill。聚合物。 SCI。 2018,135,45919。

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