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口服多单元和单单元亲水性控释系统的研发与评估

Development and evaluation of oral multiple-unit and single-unit hydrophilic controlled-release systems.

作者信息

Efentakis M, Koutlis A, Vlachou M

机构信息

School of Pharmacy, Department of Pharmaceutical Technology, University of Athens, Panepistimiopolis, Zografou, 157 71 Athens, Greece.

出版信息

AAPS PharmSciTech. 2000 Dec 1;1(4):E34. doi: 10.1208/pt010434.

Abstract

This study compared the release behavior of single-unit (tablets, capsules) and multiple-unit (minitablets in capsules) controlled-release systems of furosemide. The swelling and erosion behaviors of these systems, which contained the swellable hydrophilic polymers sodium alginate (high viscosity) and Carbopol 974P, were compared. Swelling and erosion experiments showed a high degree of swelling and limited erosion for the Carbopol preparations, whereas less swelling but greater erosion was observed for the sodium alginate preparations. The sodium alginate preparations were eroded in 6 hours, while Carbopol preparations exhibited limited erosion within this period of time. These results appear to be attributed to the physicochemical characteristics of the polymers used in this study. Polymer characteristics greatly influenced the release of furosemide (model drug) from the formulations prepared and tested. Sodium alginate had a less pronounced sustained release effect compared with Carbopol (ie, in 8 hours all 3 sodium alginate dosage forms displayed complete release of furosemide, while only 30% of the drug was released from Carbopol dosage forms). Finally, all 3 Carbopol dosage forms (single- and multiple-unit) displayed similar release behavior while sodium alginate dosage forms displayed a different and more distinctive behavior. Minitablets and tablets showed a greater sustained release effect compared with capsules. Evaluation of the release data indicates that the release mechanism for sodium alginate formulations may be attributed to erosion/dissolution, while for Carbopol it may be attributed mainly to polymer relaxation and diffusion of the drug from the polymer surface.

摘要

本研究比较了速尿的单单元(片剂、胶囊)和多单元(胶囊中的微型片)控释系统的释放行为。对这些含有可溶胀亲水性聚合物海藻酸钠(高粘度)和卡波姆974P的系统的溶胀和侵蚀行为进行了比较。溶胀和侵蚀实验表明,卡波姆制剂具有高度的溶胀和有限的侵蚀,而海藻酸钠制剂的溶胀较少但侵蚀较大。海藻酸钠制剂在6小时内被侵蚀,而卡波姆制剂在此时间段内表现出有限的侵蚀。这些结果似乎归因于本研究中使用的聚合物的物理化学特性。聚合物特性极大地影响了速尿(模型药物)从所制备和测试的制剂中的释放。与卡波姆相比,海藻酸钠的缓释作用不太明显(即,在8小时内,所有3种海藻酸钠剂型均显示速尿完全释放,而卡波姆剂型仅释放30%的药物)。最后,所有3种卡波姆剂型(单单元和多单元)表现出相似的释放行为,而海藻酸钠剂型表现出不同且更独特的行为。微型片和片剂与胶囊相比显示出更大的缓释效果。对释放数据的评估表明,海藻酸钠制剂的释放机制可能归因于侵蚀/溶解,而对于卡波姆,其释放机制可能主要归因于聚合物松弛和药物从聚合物表面的扩散。

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