Interpenetrating networks of carboxymethyl tamarind gum and chitosan for sustained delivery of aceclofenac

K. Mali, S. Dhawale, R. Dias, V. Havaldar, Pankaj R Kavitake
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引用次数: 17

Abstract

The aim of present investigation was to characterize carboxymethyl tamarind gum (CMTG) based interpenetrating networks (IPNs) of aceclofenac for site specific sustained delivery. The drug loaded IPNs were prepared by using chitosan and CMTG as polymers and gluteraldehyde as crosslinking agent. The IPNs were characterized by Attenuated total reflectance- Fourier transform infrared (ATR-FTIR) spectroscopy, thermal analysis, X-ray powder diffraction and solid state 13C-nuclear magnetic resonance spectroscopy. The prepared IPNs were evaluated for the drug entrapment efficiency and equilibrium swelling. The drug release from IPNs was studied in 0.1NHCl for 2h followed by phosphate buffer pH 6.8 for further 10h and compared with commercial tablet. The results of ATR-FTIR and thermal analysis for blank IPNs indicated intercalation of polymeric chains of crosslinked CMTG and chitosan. The results of solid state characterization revealed that the aceclofenac is compatible with IPNs. Entrapment efficiency of IPNs was found to be increased with increase in crosslinker concentration as well as amount of CMTG. The equilibrium swelling study indicated pH dependent swelling of IPNs. The drug release by IPNs showed sustained release of aceclofenac upto 12h while commercial formulation showed fast release within 8h. From the results, it can be concluded that the IPNs of CMTG and chitosan has potential in development of site specific sustained drug delivery.
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羧甲基罗望子胶和壳聚糖互穿网络对乙酰氯芬酸的持续递送
本研究的目的是表征羧甲基罗米子胶(CMTG)为基础的互穿网络(IPNs)的乙酰氯芬酸位点特异性持续递送。以壳聚糖和CMTG为聚合物,戊二醛为交联剂制备了载药ipn。采用衰减全反射-傅里叶变换红外光谱(ATR-FTIR)、热分析、x射线粉末衍射和固态13c核磁共振光谱对ipn进行了表征。对制备的ipn进行药物包封效率和平衡溶胀评价。研究了IPNs在0.1NHCl中释放2h,然后用pH 6.8的磷酸盐缓冲液再释放10h,并与市售片剂进行了比较。ATR-FTIR和热分析结果表明,空白ipn中插入了交联的CMTG和壳聚糖的聚合物链。固相表征结果表明,乙酰氯芬酸与ipn相容。随着交联剂浓度的增加和CMTG用量的增加,ipn的包封效率提高。平衡溶胀研究表明ipn的溶胀与pH有关。经IPNs释药后,乙酰氯芬酸缓释时间可达12h,而市售制剂释药时间为8h。综上所述,CMTG和壳聚糖的ipn具有开发位点特异性持续给药的潜力。
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