Alginate-polyvinyl alcohol based interpenetrating polymer network for prolonged drug therapy, Optimization and in-vitro characterization

被引:108
作者
Anwar, Hina [1 ]
Ahmad, Mahmood [1 ]
Minhas, Muhammad Usman [1 ]
Rehmani, Sahrish [1 ]
机构
[1] Islamia Univ Bahawalpur, Fac Pharm & Alternat Med, Khawaja Fareed Campus,Railway Rd, Bahawalpur 63100, Punjab, Pakistan
关键词
Sodium alginate; Interpenetrating polymer network; Swelling index; Prolonged drug delivery; Release kinetics; RESPONSE-SURFACE METHODOLOGY; CONTROLLED-RELEASE; SODIUM ALGINATE; SULFONIC-ACID) HYDROGELS; ORAL DELIVERY; ACID; HYDROCHLORIDE; CARRAGEENAN; DESIGN; SYSTEM;
D O I
10.1016/j.carbpol.2017.02.080
中图分类号
O69 [应用化学];
学科分类号
070301 [无机化学];
摘要
A new natural and synthetic polymeric blend to form interpenetrating polymer network (IPN) hydrogels was synthesized utilizing sodium alginate and PVA as polymers by free radical polymerization employing 2-Acylamido-2-methylpropane-sulfonic acid as monomer (AMPS) and tramadol HCl as model drug through 32 level full factorial design to evaluate the impact of selected independent factors i.e. polymer (sodium alginate) and monomer (AMPS) contents on swelling index at 18th hour, percent drug release at 18th hour, time required for 80% drug release and drug entrapment efficiency as dependent variables. FTIR, SEM, sol-gel analysis, equilibrium swelling studies and in-vitro release kinetics were performed for in-vitro characterization of formulated IPN hydrogels. In-vitro studies carried out at pH 1.2 and pH 7.4 revealed pH independent swelling and drug release from polymeric IPN, providing controlled drug release for an extended period of time with improved entrapment efficiency, thereby concluding that this polymeric blend may be a promising system for the prolonged drug delivery. (C) 2017 Elsevier Ltd. All rights reserved.
引用
收藏
页码:183 / 194
页数:12
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