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依托度酸温敏型直肠给药系统的体外和体内特性。

In vitro and in vivo characteristics of a thermogelling rectal delivery system of etodolac.

机构信息

Department of Pharmaceutics, College of Pharmacy, King Saud University, 11495 Riyadh, Saudi Arabia.

出版信息

AAPS PharmSciTech. 2009;10(3):724-31. doi: 10.1208/s12249-009-9261-y. Epub 2009 May 29.

Abstract

Rectal etodolac-Poloxamer gel systems composed of Poloxamer and bioadhesive polymers were developed and evaluated. Hydroxypropylmethyl cellulose, poly)vinyl) pyrrolidone, methyl cellulose, hydroxyethylcellulose, and carbopol were examined as mucoadhesive polymers. The characteristics of the rectal gels differed according to the properties of mucoadhesive polymers. The physicochemical properties such as gelation temperature, gel strength, and bioadhesive force of various formulations were investigated. The analysis of release mechanism showed that the release of etodolac was proportional to the square root of time, indicating that etodolac might be released from the suppositories by Fickian diffusion. The anti-inflammatory effect of etodolac-Poloxamer gel system was also studied in rats. Moreover, liquid suppository of etodolac did not cause any morphological damage to the rectal tissues. These results suggested that in situ gelling liquid suppository with etodolac and mucoadhesive polymer was a physically safe, convenient, and effective rectal dosage form for etodolac.

摘要

开发并评价了由泊洛沙姆和生物黏附聚合物组成的直肠依托度酸-泊洛沙姆凝胶系统。考察了羟丙甲纤维素、聚维酮、甲基纤维素、羟乙基纤维素和卡波姆作为黏膜黏附聚合物的性能。直肠凝胶的特性因黏膜黏附聚合物的性质而异。考察了各种制剂的物理化学性质,如胶凝温度、凝胶强度和生物黏附力。释放机制的分析表明,依托度酸的释放与时间的平方根成正比,表明依托度酸可能通过菲克扩散从栓剂中释放。还在大鼠中研究了依托度酸-泊洛沙姆凝胶系统的抗炎作用。此外,依托度酸的液体栓剂不会对直肠组织造成任何形态损伤。这些结果表明,含有依托度酸和黏膜黏附聚合物的原位凝胶化液体栓剂是一种物理安全、方便且有效的依托度酸直肠给药剂型。

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