Suppr超能文献

卡马西平单向释放口腔贴片的制剂及其透过猪口腔黏膜的渗透研究。

Formulation of unidirectional release buccal patches of carbamazepine and study of permeation through porcine buccal mucosa.

作者信息

Govindasamy Parthasarathy, Kesavan Bhaskar Reddy, Narasimha Jayaveera Korlakunta

机构信息

R.R College of Pharmacy, Chikkabanavara, Bangalore-560 090, India.

出版信息

Asian Pac J Trop Biomed. 2013 Dec;3(12):995-1002. doi: 10.1016/S2221-1691(13)60192-6.

Abstract

OBJECTIVE

To achieve transbuccal release of carbamazepine by loading in unidirectional release mucoadhesive buccal patches.

METHODS

Buccal patches of carbamazepine with unidirectional drug release were prepared using hydroxypropyl methyl cellulose, polyvinyl alcohol, polyvinyl pyrrolidone and ethyl cellulose by solvent casting method. Water impermeable backing layer (Pidilite® Biaxially-oriented polypropylene film) of patches provided unidirectional drug release. They were evaluated for thickness, mass uniformity, surface pH and folding endurance. Six formulations FA2, FA8, FA10, FB1, FB14 and FB16 (folding endurance above 250) were evaluated further for swelling studies, ex vivo mucoadhesive strength, ex vivo mucoadhesion time, In vitro drug release, ex vivo permeation, accelerated stability studies and FTIR and XRD spectral studies.

RESULTS

The ex vivo mucoadhesion time of patches ranged between 109 min (FA10) to 126 min (FB14). The ex vivo mucoadhesive force was in the range of 0.278 to 0.479 kg/m/s. The In vitro drug release studies revealed that formulation FA8 released 84% and FB16 released 99.01% of drug in 140 min.

CONCLUSIONS

The prepared unidirectional buccal patches of carbamazepine provided a maximum drug release within specified mucoadhesion period and it indicates a potential alternative drug delivery system for systemic delivery of carbamazepine.

摘要

目的

通过将卡马西平载入单向释放的黏膜黏附性口腔贴片来实现其经颊释放。

方法

采用溶剂浇铸法,使用羟丙基甲基纤维素、聚乙烯醇、聚乙烯吡咯烷酮和乙基纤维素制备具有单向药物释放功能的卡马西平口腔贴片。贴片的不透水背衬层(Pidilite® 双向拉伸聚丙烯薄膜)实现药物单向释放。对其厚度、质量均匀性、表面pH值和耐折性进行评估。进一步对六种配方FA2、FA8、FA10、FB1、FB14和FB16(耐折性超过250)进行溶胀研究、体外黏膜黏附强度、体外黏膜黏附时间、体外药物释放、体外渗透、加速稳定性研究以及傅里叶变换红外光谱(FTIR)和X射线衍射(XRD)光谱研究。

结果

贴片的体外黏膜黏附时间在109分钟(FA10)至126分钟(FB14)之间。体外黏膜黏附力在0.278至0.479千克/米/秒范围内。体外药物释放研究表明,配方FA8在140分钟内释放了84%的药物,FB16释放了99.01%的药物。

结论

所制备的卡马西平单向口腔贴片在规定的黏膜黏附期内实现了最大药物释放,表明其是卡马西平全身给药的一种潜在替代给药系统。

相似文献

本文引用的文献

8
Effect of freezing and type of mucosa on ex vivo drug permeability parameters.冷冻和解冻对药物体外渗透参数的影响。
AAPS PharmSciTech. 2011 Jun;12(2):587-92. doi: 10.1208/s12249-011-9621-2. Epub 2011 May 4.

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验