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用于口腔给药的壳聚糖/乙基纤维素粘膜粘附双层制剂的设计与评价

Design and evaluation of chitosan/ethylcellulose mucoadhesive bilayered devices for buccal drug delivery.

作者信息

Remuñán-López C, Portero A, Vila-Jato J L, Alonso M J

机构信息

Department of Pharmacy and Pharmaceutical Technology, Faculty of Pharmacy, The University of Santiago de Compostela, Campus Sur, 15706-Santiago de Compostela, Spain.

出版信息

J Control Release. 1998 Nov 13;55(2-3):143-52. doi: 10.1016/s0168-3659(98)00044-3.

Abstract

This paper describes the preparation of new buccal bilayered devices comprising a drug-containing mucoadhesive layer and a drug-free backing layer, by two different methods. Bilaminated films were produced by a casting/solvent evaporation technique and bilayered tablets were obtained by direct compression. The mucoadhesive layer was composed of a mixture of drug and chitosan, with or without an anionic crosslinking polymer (polycarbophil, sodium alginate, gellan gum), and the backing layer was made of ethylcellulose. The double-layered structure design was expected to provide drug delivery in a unidirectional fashion to the mucosa and avoid loss of drug due to wash-out with saliva. Using nifedipine and propranolol hydrochloride as slightly and highly water-soluble model drugs, respectively, it was demonstrated that these new devices show promising potential for use in controlled delivery of drugs to the oral cavity. The uncrosslinked chitosan-containing devices absorbed a large quantity of water, gelled and then eroded, allowing drug release. The bilaminated films showed a sustained drug release in a phosphate buffer (pH 6.4). Furthermore, tablets that displayed controlled swelling and drug release and adequate adhesivity were produced by in situ crosslinking the chitosan with polycarbophil.

摘要

本文描述了通过两种不同方法制备新型口腔双层装置的过程,该装置由含药粘膜粘附层和无药背衬层组成。通过流延/溶剂蒸发技术制备了双层膜,并通过直接压片获得了双层片剂。粘膜粘附层由药物与壳聚糖的混合物组成,含有或不含有阴离子交联聚合物(聚卡波非、海藻酸钠、结冷胶),背衬层由乙基纤维素制成。双层结构设计预期能以单向方式向粘膜递送药物,并避免因唾液冲刷而导致药物流失。分别使用硝苯地平和盐酸普萘洛尔作为低水溶性和高水溶性模型药物,结果表明这些新型装置在药物向口腔的控释应用中显示出有前景的潜力。未交联的含壳聚糖装置吸收大量水分,形成凝胶然后侵蚀,从而实现药物释放。双层膜在磷酸盐缓冲液(pH 6.4)中显示出药物的持续释放。此外,通过壳聚糖与聚卡波非原位交联制备出具有可控溶胀和药物释放以及足够粘附性的片剂。

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