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用于有效治疗复发性口疮性口炎的盐酸苄达明粘膜粘附口腔膜的设计、开发及体外/离体评价

Design, Development and In vitro/Ex vivo Evaluation of Mucoadhesive Buccal Film of Benzydamine Hydrochloride for the Effective Treatment of Aphthous Stomatitis.

作者信息

Sharma Deepak, Sharma Amit, Garg Rajeev

机构信息

I.K. Gujral Punjab Technical University, Jalandhar, Punjab 144603, India

Department of Pharmaceutics, Rayat Bahra Institute of Pharmacy, Hoshiarpur, Punjab 146104, India

出版信息

Recent Pat Drug Deliv Formul. 2018;12(4):277-294. doi: 10.2174/1872211313666190128151038.

Abstract

BACKGROUND

During the recent two decades, the development of mucoadhesive drug delivery system has been gained tremendous importance to cure many recurrent diseases of the oral cavity. The drug delivery through the buccal route is quite challenging due to limited absorption area, movements of the target region and regular flow of saliva lead to the sub-therapeutic drug level in the buccal region.

OBJECTIVE

The aim is to develop unidirectional release mucoadhesive buccal film for the mucosal delivery of Benzydamine Hydrochloride (WO2016126217Al, EP0812193B1) and evaluate the effects of a different grade of HPMC polymer (US5980942A) with the presumption to prolong the residence time and therapeutic effectiveness at the target site.

METHODS

Mucoadhesive buccal films were prepared by solvent casting evaporation method by employing different grades of HPMC as mucoadhesive and rate controlling polymer. Total twenty-four formulations were developed using ethyl cellulose as a backing layer. The prepared films were subjected to various physicochemical parameters.

RESULTS

The physicochemical parameters were found to be varied according to the type and concentration of polymer used. On the basis of in vitro drug release, desired ex-vivo mucoadhesive time, mucoadhesive force the formulations F4, F9, F14 and F19 were subjected to ex vivo drug permeation study. The F14 film containing 1% w/v of HPMC K50M was considered optimized final formulation due to higher ex vivo drug permeation. Drug-excipient compatibility was confirmed by FTIR and DSC. XRD of final formulation revealed the amorphous nature of drug. SEM indicated the perfect binding between backing and adhesive layer.

CONCLUSION

The developed mucoadhesive buccal film having adequate physicochemical properties was capable to provide prolonged residence time and sustained delivery as compared to existing conventional therapies.

摘要

背景

在最近二十年中,粘膜粘附给药系统的发展对于治疗许多口腔复发性疾病变得极为重要。由于吸收面积有限、靶区域的运动以及唾液的正常流动导致颊部区域药物水平低于治疗剂量,通过颊部途径给药颇具挑战性。

目的

旨在开发用于盐酸苄达明粘膜给药的单向释放粘膜粘附颊膜(WO2016126217Al,EP0812193B1),并评估不同等级的羟丙甲纤维素聚合物(US5980942A)的效果,推测其可延长在靶部位的停留时间和治疗效果。

方法

采用溶剂浇铸蒸发法制备粘膜粘附颊膜,使用不同等级的羟丙甲纤维素作为粘膜粘附和速率控制聚合物。以乙基纤维素作为背衬层,共开发了二十四种制剂。对制备的薄膜进行各种理化参数测定。

结果

发现理化参数根据所用聚合物的类型和浓度而有所不同。基于体外药物释放、所需的体外粘膜粘附时间、粘膜粘附力,对制剂F4、F9、F14和F19进行体外药物渗透研究。含有1% w/v羟丙甲纤维素K50M的F14薄膜由于较高的体外药物渗透率被认为是优化的最终制剂。通过傅里叶变换红外光谱(FTIR)和差示扫描量热法(DSC)确认了药物 - 辅料相容性。最终制剂的X射线衍射(XRD)显示药物为无定形性质。扫描电子显微镜(SEM)表明背衬层和粘附层之间结合良好。

结论

与现有的传统疗法相比,所开发的具有适当理化性质的粘膜粘附颊膜能够提供延长的停留时间和持续释放。

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