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壳聚糖衍生物作为口腔和阴道渗透促进剂的评估。

Assessment of chitosan derivatives as buccal and vaginal penetration enhancers.

作者信息

Sandri Giuseppina, Rossi Silvia, Ferrari Franca, Bonferoni Maria Cristina, Muzzarelli Corrado, Caramella Carla

机构信息

Department of Pharmaceutical Chemistry, University of Pavia, Viale Taramelli 12, 27100, Pavia, Italy.

出版信息

Eur J Pharm Sci. 2004 Feb;21(2-3):351-9. doi: 10.1016/j.ejps.2003.10.028.

Abstract

The aim of the present work was to evaluate the mucoadhesive and penetration enhancement properties via the buccal and vaginal mucosae of four different chitosan derivatives: 5-methyl-pyrrolidinone chitosan (MPC), two low molecular weight chitosans (DC1 and DC2) and a partially reacetylated chitosan (RC). Chitosan HCl was used as a reference. Polymer solutions (4% w/w) were prepared in media simulating the buccal (pH 6.4 buffer or water) and the vaginal (pH 5.0 buffer) environments and subjected to rheological characterization. Acyclovir was added to the polymer solutions at 5% (w/w) concentration. The mucoadhesive properties of the polymer solutions were measured using excised porcine cheek or vaginal mucosa and mucin dispersions to simulate the buccal or vaginal environments, respectively. Drug permeation and penetration tests were carried out using porcine cheek and vaginal mucosae as model membranes. Acyclovir aqueous suspensions prepared in pH 6.4 and 5.0 buffers were used as blanks. Drug release measurements were also carried out in the same conditions employed for the permeation and penetration tests. Methyl-pyrrolidinone chitosan shows the best mucoadhesive and penetration enhancement properties in both buccal and vaginal environments. The capability to enhance the permeation/penetration of acyclovir was decreased by partial depolymerization of chitosan and disappeared after partial reacetylation.

摘要

本研究的目的是评估四种不同壳聚糖衍生物

5-甲基-吡咯烷酮壳聚糖(MPC)、两种低分子量壳聚糖(DC1和DC2)以及一种部分重新乙酰化的壳聚糖(RC),通过颊黏膜和阴道黏膜的黏膜黏附及渗透增强特性。使用盐酸壳聚糖作为对照。在模拟颊部(pH 6.4缓冲液或水)和阴道(pH 5.0缓冲液)环境的介质中制备聚合物溶液(4% w/w),并进行流变学表征。将阿昔洛韦以5%(w/w)的浓度添加到聚合物溶液中。分别使用切除的猪颊黏膜或阴道黏膜以及黏蛋白分散体来模拟颊部或阴道环境,测量聚合物溶液的黏膜黏附特性。以猪颊黏膜和阴道黏膜作为模型膜进行药物渗透和穿透试验。在pH 6.4和5.0缓冲液中制备的阿昔洛韦水悬浮液用作空白对照。在与渗透和穿透试验相同的条件下进行药物释放测量。甲基-吡咯烷酮壳聚糖在颊部和阴道环境中均表现出最佳的黏膜黏附和渗透增强特性。壳聚糖的部分解聚降低了增强阿昔洛韦渗透/穿透的能力,且在部分重新乙酰化后这种能力消失。

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