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比索洛尔包衣压片漂浮脉冲释药系统的优化研究

Optimization studies on compression coated floating-pulsatile drug delivery of bisoprolol.

作者信息

Jagdale Swati C, Bari Nilesh A, Kuchekar Bhanudas S, Chabukswar Aniruddha R

机构信息

Department of Pharmaceutics, MAEER's Maharashtra Institute of Pharmacy, MIT Campus, Survey No. 124, Kothrud, Pune, Maharashtra 411 038, India.

出版信息

Biomed Res Int. 2013;2013:801769. doi: 10.1155/2013/801769. Epub 2013 Nov 10.

Abstract

The purpose of the present work was to design and optimize compression coated floating pulsatile drug delivery systems of bisoprolol. Floating pulsatile concept was applied to increase the gastric residence of the dosage form having lag phase followed by a burst release. The prepared system consisted of two parts: a core tablet containing the active ingredient and an erodible outer shell with gas generating agent. The rapid release core tablet (RRCT) was prepared by using superdisintegrants with active ingredient. Press coating of optimized RRCT was done by polymer. A 3² full factorial design was used for optimization. The amount of Polyox WSR205 and Polyox WSR N12K was selected as independent variables. Lag period, drug release, and swelling index were selected as dependent variables. Floating pulsatile release formulation (FPRT) F13 at level 0 (55 mg) for Polyox WSR205 and level +1 (65 mg) for Polyox WSR N12K showed lag time of 4 h with >90% drug release. The data were statistically analyzed using ANOVA, and P < 0.05 was statistically significant. Release kinetics of the optimized formulation best fitted the zero order model. In vivo study confirms burst effect at 4 h in indicating the optimization of the dosage form.

摘要

本研究的目的是设计并优化比索洛尔的包衣漂浮脉冲式药物递送系统。采用漂浮脉冲概念来延长剂型在胃中的滞留时间,使其具有滞后相,随后是突释。所制备的系统由两部分组成:含有活性成分的核心片剂和带有产气剂的可蚀性外壳。通过使用超级崩解剂与活性成分制备速释核心片剂(RRCT)。用聚合物对优化后的RRCT进行压制包衣。采用3²全因子设计进行优化。选择聚氧乙烯WSR205和聚氧乙烯WSR N12K的用量作为自变量。选择滞后时间、药物释放和溶胀指数作为因变量。在聚氧乙烯WSR205水平为0(55毫克)和聚氧乙烯WSR N12K水平为+1(65毫克)时,漂浮脉冲释放制剂(FPRT)F13的滞后时间为4小时,药物释放>90%。使用方差分析对数据进行统计分析,P < 0.05具有统计学显著性。优化制剂的释放动力学最符合零级模型。体内研究证实4小时时有突释效应,表明剂型得到了优化。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2f4d/3842062/fcb13976c425/BMRI2013-801769.001.jpg

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