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采用模型可溶性和不溶性药物经口腔黏膜给药的新型制剂。

Novel films for drug delivery via the buccal mucosa using model soluble and insoluble drugs.

机构信息

Department of Pharmaceutical, Chemical and Environmental Sciences, School of Science, University of Greenwich, Chatham Maritime, Kent, UK.

出版信息

Drug Dev Ind Pharm. 2012 Oct;38(10):1207-20. doi: 10.3109/03639045.2011.644294. Epub 2011 Dec 29.

Abstract

Bioadhesive buccal films are innovative dosage forms with the ability to adhere to the mucosal surface and subsequently hydrate to release and deliver drugs across the buccal membrane. This study aims to formulate and characterize stable carrageenan (CAR) based buccal films with desirable drug loading capacity. The films were prepared using CAR, poloxamer (POL) 407, various grades of PEG (plasticizer) and loaded with paracetamol (PM) and indomethacin (IND) as model soluble and insoluble drugs, respectively. The films were characterized by texture analysis, thermogravimetric analysis (TGA), DSC, scanning electron microscopy, X-ray powder diffraction (XRPD), and in vitro drug release studies. Optimized films were obtained from aqueous gels comprising 2.5% w/w κ-CAR 911, 4% w/w POL 407 and 6% w/w (PM) and 6.5% w/w (IND) of PEG 600 with maximum drug loading of 1.6% w/w and 0.8 % w/w for PM and IND, respectively. TGA showed residual water content of approximately 5% of films dry weight. DSC revealed a T(g) at 22.25 and 30.77°C for PM and IND, respectively, implying the presence of amorphous forms of both drugs which was confirmed by XRPD. Drug dissolution profiles in simulated saliva showed cumulative percent release of up to 45 and 57% of PM and IND, respectively, within 40 min of contact with dissolution medium simulating saliva.

摘要

生物黏附颊膜是一种创新的剂型,能够黏附在黏膜表面,随后水合释放并通过颊膜输送药物。本研究旨在制备并表征具有理想载药能力的卡拉胶(CAR)基颊膜。使用 CAR、泊洛沙姆(POL)407、不同等级的 PEG(增塑剂)制备薄膜,并分别将对乙酰氨基酚(PM)和吲哚美辛(IND)作为模型可溶性和不溶性药物载入其中。通过质构分析、热重分析(TGA)、差示扫描量热法(DSC)、扫描电子显微镜、X 射线粉末衍射(XRPD)和体外药物释放研究对薄膜进行了表征。从包含 2.5%w/w κ-CAR 911、4%w/w POL 407 和 6%w/w(PM)和 6.5%w/w(IND)PEG 600 的水性凝胶中获得了优化的薄膜,其最大载药量分别为 1.6%w/w 和 0.8%w/w PM 和 IND。TGA 显示薄膜干重约 5%的残余含水量。DSC 分别显示 PM 和 IND 的 T(g)在 22.25 和 30.77°C,表明两种药物均存在无定形形式,XRPD 也证实了这一点。在模拟唾液的溶解介质中接触 40 分钟后,药物溶解曲线显示 PM 和 IND 的累积释放率分别高达 45%和 57%。

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