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5-氟尿嘧啶的经颊给药:渗透增强及药代动力学研究

Transbuccal delivery of 5-fluorouracil: permeation enhancement and pharmacokinetic study.

作者信息

Dhiman Munish Kumar, Dhiman Anupama, Sawant Krutika K

机构信息

TIFAC Center of Relevance and Excellence in NDDS, Pharmacy Department, The M.S. University of Baroda, Donor's Plaza, Fatehgunj, Vadodara, Gujarat, India.

出版信息

AAPS PharmSciTech. 2009;10(1):258-65. doi: 10.1208/s12249-009-9203-8. Epub 2009 Mar 12.

Abstract

The purpose of this study was to determine the effect of permeation enhancers on the transbuccal delivery of 5-fluorouracil (FU). The effect of permeation enhancers on in vitro buccal permeability was assessed using sodium deoxycholate (SDC), sodium dodecyl sulphate (SDS), sodium tauroglycocholate (STGC), and oleic acid and their concentrations for absorption enhancement were optimized. STGC appeared to be most effective for enhancing the buccal permeation of FU than the other enhancers. These enhancements by STGC were statistically significant (p < 0.05) compared to control. The order of permeation enhancement was STGC > SDS > SDC > oleic acid. Histological investigations were performed on buccal mucosa and indicated no major morphological changes. The enhancing effect of STGC on the buccal absorption of FU was evaluated from the mucoadhesive gels in rabbits. The absolute bioavailability of FU from mucoadhesive gels containing STGC increased 1.6-fold as compared to the gels containing no permeation enhancer. The mean residence time and mean absorption time considerably increased following administration of gel containing penetration enhancer compared with the gel without penetration enhancer.

摘要

本研究的目的是确定渗透促进剂对5-氟尿嘧啶(FU)经颊给药的影响。使用脱氧胆酸钠(SDC)、十二烷基硫酸钠(SDS)、牛磺胆酸钠(STGC)和油酸评估渗透促进剂对体外颊部渗透性的影响,并优化它们用于增强吸收的浓度。与其他促进剂相比,STGC似乎对增强FU的颊部渗透最有效。与对照组相比,STGC的这些增强作用具有统计学意义(p < 0.05)。渗透增强的顺序为STGC > SDS > SDC > 油酸。对颊黏膜进行了组织学研究,结果表明没有重大的形态学变化。从兔的黏膜黏附凝胶评估了STGC对FU颊部吸收的增强作用。与不含渗透促进剂的凝胶相比,含STGC的黏膜黏附凝胶中FU的绝对生物利用度提高了1.6倍。与不含渗透促进剂的凝胶相比,给予含渗透促进剂的凝胶后,平均驻留时间和平均吸收时间显著增加。

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