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变性乳清蛋白粉作为一种新型基质辅料:用于药物缓释应用的黏附片的设计与评价

Denatured Whey Protein Powder as a New Matrix Excipient: Design and Evaluation of Mucoadhesive Tablets for Sustained Drug Release Applications.

作者信息

Hsein Hassana, Garrait Ghislain, Tamani Fahima, Beyssac Eric, Hoffart Valérie

机构信息

Univ Clermont 1, UFR Pharmacie, EA4678, Laboratoire de Biopharmacie, Clermont-Ferrand, F-63001, France.

出版信息

Pharm Res. 2017 Feb;34(2):365-377. doi: 10.1007/s11095-016-2067-1. Epub 2016 Dec 21.

Abstract

PURPOSE

In earlier study, we proposed denatured whey protein (DWP) powder obtained by atomization as a new excipient to promote oral drug delivery. In this work, we evaluate the possibility to formulate tablets based on DWP powders and to characterize their role as a matrix mucoadhesive excipient.

METHODS

Tablets containing increased amount of DWP (10 to 30%) were produced by direct compression after mixing with theophylline, microcrystalline cellulose, Aerosil® and magnesium stearate. Dissolution behaviors of obtained tablets were evaluated in different USP buffers (pH 1.2, 4.5 and 6.8) and in simulated gastric and intestinal fluids and mechanisms analyzed by multiple mathematical models. Swelling, erosion and mucoadhesion were also evaluated. Finally, release and absorption were studied in the artificial digestive system (TIM 1).

RESULTS

Tablets based on DWP and containing 300 mg of theophylline were obtained by direct compression. These tablets exhibited controlled release driven by diffusion starting from 15% DWP content whatever the pH studied. They also showed a great extent of swelling and water uptake while matrix weight loss was limited. Addition of enzymes accelerated drug release which became governed by erosion according to Peppas model.

CONCLUSIONS

The present study shows that DWP powders can be successfully used as a pharmaceutical excipient, and in particular as a matrix mucoadhesive controlled release tablets.

摘要

目的

在早期研究中,我们提出将通过雾化获得的变性乳清蛋白(DWP)粉末作为一种新型辅料来促进口服药物递送。在本研究中,我们评估了基于DWP粉末制备片剂的可能性,并表征其作为基质粘膜粘附性辅料的作用。

方法

将DWP(10%至30%)含量增加的片剂与茶碱、微晶纤维素、Aerosil®和硬脂酸镁混合后直接压片制备。在不同的USP缓冲液(pH 1.2、4.5和6.8)以及模拟胃液和肠液中评估所得片剂的溶出行为,并通过多种数学模型分析其机制。还评估了片剂的膨胀、侵蚀和粘膜粘附性。最后,在人工消化系统(TIM 1)中研究药物的释放和吸收情况。

结果

通过直接压片获得了基于DWP且含有300 mg茶碱的片剂。无论研究的pH值如何,从DWP含量为15%开始,这些片剂均表现出由扩散驱动的控释特性。它们还表现出很大程度的膨胀和吸水性,而基质重量损失有限。添加酶会加速药物释放,根据Peppas模型,此时药物释放由侵蚀作用主导。

结论

本研究表明,DWP粉末可成功用作药物辅料,尤其是作为基质粘膜粘附性控释片剂的辅料。

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