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载盐酸雷尼替丁的乙基纤维素和聚丙烯酸树脂RS 100漂浮微球:pH调节剂的影响

Ranitidine Hydrochloride-loaded Ethyl Cellulose and Eudragit RS 100 Buoyant Microspheres: Effect of pH Modifiers.

作者信息

Kotagale N R, Parkhe A P, Jumde A B, Khandelwal H M, Umekar M J

机构信息

Smt. Kishoritai Bhoyar College of Pharmacy, Behind Railway Station, New Kamptee, Dist. Nagpur-441 002, India.

出版信息

Indian J Pharm Sci. 2011 Nov;73(6):626-33. doi: 10.4103/0250-474X.100236.

Abstract

A floating type of dosage form of ranitidine hydrochloride in the form of microspheres capable of floating on simulated gastric fluid was prepared by solvent evaporation technique. Microspheres prepared with ethyl cellulose, Eudragit(®) RS100 alone or in combination were evaluated for percent yield, drug entrapment, percent buoyancy and drug release and the results demonstrated satisfactory performance. Microspheres exhibited ranitidine hydrochloride release influenced by changing ranitidine hydrochloride-polymer and ranitidine hydrochloride-polymer-polymer ratio. Incorporation of a pH modifier has been the usual strategy employed to enhance the dissolution rate of weakly basic drug from floating microspheres. Further citric acid, fumaric acid, tartaric acid were employed as pH modifiers. Microspheres prepared with ethyl cellulose, Eudragit(®) RS100 and their combination that showed highest release were utilized to study the effect of pH modifiers on ranitidine hydrochloride release from microspheres which is mainly affected due to modulation of microenvironmental pH. In vitro release of ranitidine hydrochloride from microspheres into simulated gastric fluid at 37° showed no significant burst effect. However the amount of release increased with time and significantly enhanced by pH modifiers. 15% w/w concentration of fumaric acid provide significant drug release from ranitidine hydrochloride microspheres prepared with ranitidine hydrochloride:ethyl cellulose (1:3), ranitidine hydrochloride:Eudragit(®) RS100 (1:2) and ranitidine hydrochloride:ethyl cellulose:Eudragit(®) RS100 (1:2:1) whereas citric acid, tartaric acid showed significant cumulative release at 20% w/w. In all this study suggest that ethyl celluose, Eudragit(®) RS100 alone or in combination with added pH modifiers can be useful in floating microspheres which can be proved beneficial to enhance the bioavailability of ranitidine hydrochloride.

摘要

采用溶剂蒸发技术制备了一种能漂浮在模拟胃液上的盐酸雷尼替丁微球形式的漂浮型剂型。对单独使用乙基纤维素、尤特奇(®)RS100或两者组合制备的微球进行了产率百分比、药物包封率、漂浮百分比和药物释放的评估,结果显示性能良好。微球表现出盐酸雷尼替丁的释放受盐酸雷尼替丁 - 聚合物以及盐酸雷尼替丁 - 聚合物 - 聚合物比例变化的影响。加入pH调节剂一直是提高弱碱性药物从漂浮微球中溶出速率常用的策略。进一步使用柠檬酸、富马酸、酒石酸作为pH调节剂。用乙基纤维素、尤特奇(®)RS100及其组合制备的显示出最高释放率的微球被用于研究pH调节剂对盐酸雷尼替丁从微球中释放的影响,这主要是由于微环境pH的调节所致。在37°下,盐酸雷尼替丁从微球向模拟胃液中的体外释放没有明显的突释效应。然而,释放量随时间增加,并且pH调节剂显著增强了释放量。15% w/w浓度的富马酸能使由盐酸雷尼替丁:乙基纤维素(1:3)、盐酸雷尼替丁:尤特奇(®)RS100(1:2)和盐酸雷尼替丁:乙基纤维素:尤特奇(®)RS100(1:2:1)制备的盐酸雷尼替丁微球有显著的药物释放,而柠檬酸、酒石酸在20% w/w时显示出显著的累积释放。总之,这项研究表明,单独使用乙基纤维素、尤特奇(®)RS100或与添加的pH调节剂组合可用于漂浮微球,这可能有利于提高盐酸雷尼替丁的生物利用度。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c9ac/3480747/eb59b2e8ca38/IJPhS-73-626-g001.jpg

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