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胃部特异性抗幽门螺杆菌疗法:载阿莫西林壳聚糖黏膜黏附微球的制备与评价

Stomach specific anti-helicobacter pylori therapy: preparation and evaluation of amoxicillin-loaded chitosan mucoadhesive microspheres.

作者信息

Patel Jayvadan K, Patel Madhabhai M

机构信息

Shree S. K. Patel College of Pharmaceutical Education and Research, Ganpat University, Kherva-382711, Gujarat, India.

出版信息

Curr Drug Deliv. 2007 Jan;4(1):41-50. doi: 10.2174/156720107779314811.

Abstract

The purpose of this research was to formulate and systematically evaluate in vitro and in vivo performances of mucoadhesive amoxicillin microspheres for the potential use of treating gastric and duodenal ulcers, which were associated with Helicobacter pylori. Amoxicillin mucoadhesive microspheres containing chitosan as mucoadhesive polymer were prepared by simple emulsification phase separation technique using glutaraldehyde as a cross-linking agent. Results of preliminary trials indicate that volume of cross-linking agent, time for cross-linking, polymer-to-drug ratio, and speed of rotation affected characteristics of microspheres. Microspheres were discrete, spherical, free flowing and also showed high percentage drug entrapment efficiency. In vitro mucoadhesive test showed that amoxicillin mucoadhesive microspheres adhered more strongly to gastric mucous layer and could retain in gastrointestinal tract for an extended period of time. A 3(2) full factorial design was employed to study the effect of independent variables, polymer-to-drug ratio (X(1)), and stirring speed (X(2)) on dependent variables i.e. percentage mucoadhesion, t(80), drug entrapment efficiency, particle size and swelling index. The best batch exhibited a high drug entrapment efficiency of 70 % and a swelling index of 1.39; percentage mucoadhesion after 1 h was 79 %. The drug release was also sustained for more than 12 h. The polymer-to-drug ratio had a more significant effect on the dependent variables. The morphological characteristics of the mucoadhesive microspheres were studied using scanning electron microscopy. In vitro release test showed that amoxicillin released slightly faster in pH 1.0 hydrochloric acid than in pH 7.8 phosphate buffer. In vivo H. pylori clearance tests were also carried out by administering amoxicillin mucoadhesive microspheres and powder, to H. pylori infectious Wistar rats under fed conditions at single dose or multiple dose(s) in oral administration. The results showed that amoxicillin mucoadhesive microspheres had a better clearance effect than amoxicillin powder. In conclusion, the prolonged gastrointestinal residence time and enhanced amoxicillin stability resulting from the mucoadhesive microspheres of amoxicillin might make contribution complete eradication of H. pylori.

摘要

本研究的目的是制备并系统评估用于治疗与幽门螺杆菌相关的胃和十二指肠溃疡的黏附性阿莫西林微球的体外和体内性能。以壳聚糖为黏附性聚合物,戊二醛为交联剂,通过简单乳化相分离技术制备了阿莫西林黏附性微球。初步试验结果表明,交联剂体积、交联时间、聚合物与药物比例以及旋转速度会影响微球的特性。微球呈离散状、球形、自由流动,且药物包封率较高。体外黏附试验表明,阿莫西林黏附性微球与胃黏液层的黏附力更强,且能在胃肠道中长时间滞留。采用3(2)全因子设计研究自变量聚合物与药物比例(X(1))和搅拌速度(X(2))对因变量即黏附百分比、t(80)、药物包封率、粒径和溶胀指数的影响。最佳批次的药物包封率高达70%,溶胀指数为1.39;1小时后的黏附百分比为79%。药物释放也持续了12小时以上。聚合物与药物比例对因变量的影响更为显著。采用扫描电子显微镜研究了黏附性微球的形态特征。体外释放试验表明,阿莫西林在pH 1.0盐酸中的释放速度略快于pH 7.8磷酸盐缓冲液。在喂食条件下,对感染幽门螺杆菌的Wistar大鼠单剂量或多剂量口服给予阿莫西林黏附性微球和粉末,进行体内幽门螺杆菌清除试验。结果表明,阿莫西林黏附性微球的清除效果优于阿莫西林粉末。总之,阿莫西林黏附性微球延长的胃肠道停留时间和增强的阿莫西林稳定性可能有助于完全根除幽门螺杆菌。

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