Malik Nadia Shamshad, Ahmad Mahmood, Minhas Muhamad Usman, Tulain Ruqia, Barkat Kashif, Khalid Ikrima, Khalid Qandeel
Department of Pharmacy, Capital University of Science & Technology, Islamabad, Pakistan.
Faculty of Pharmacy, University of Central Punjab, Lahore, Pakistan.
Front Chem. 2020 Feb 4;8:50. doi: 10.3389/fchem.2020.00050. eCollection 2020.
This study investigated the use of pure polymer chitosan (CS), xanthan gum (XG), monomer 2-acrylamido-2-methylpropane sulfonic acid (AMPS) and initiator potassium persulfate (KPS) as drug carrier system crosslinked through N' N'-methylene bis-acrylamide (MBA) for controlled drug delivery of acyclovir (ACV). ACV is highly effective and selective antiviral drugs used for prophylaxis and treatment against herpes simplex viruses (HSV) infections. Present oral marketed formulations are associated with number of side effects and shortcomings which hampered its clinical effectiveness. Hydrogels (FCX1-FCX9) composed of CS, XG, AMPS, MBA, and KPS were prepared by free radical polymerization technique and characterized through FTIR, PXRD, thermal analysis and SEM. Swelling dynamics and drug release behavior was also investigated. FTIR studies confirmed that ACV was successfully encapsulated into hydrogel polymeric network. SEM revealed porous structure whereas thermal analysis showed enhanced thermal stability of polymeric network. PXRD indicated amorphous dispersion of ACV during preparation process. Swelling dynamics and ACV release behavior from developed hydrogels was dependent on pH of the medium and concentration of pure reactants used. Korsmeyer-Peppas model was best fit to regression coefficient. The present work demonstrated a potential for developing a pH sensitive hydrogel for an antiviral drug ACV by using pure polymers CS, XG, and monomer AMPS.
本研究考察了使用纯聚合物壳聚糖(CS)、黄原胶(XG)、单体2-丙烯酰胺基-2-甲基丙烷磺酸(AMPS)和引发剂过硫酸钾(KPS)作为药物载体系统,通过N,N'-亚甲基双丙烯酰胺(MBA)交联用于阿昔洛韦(ACV)的控释给药。ACV是用于预防和治疗单纯疱疹病毒(HSV)感染的高效且选择性抗病毒药物。目前市售的口服制剂存在多种副作用和缺点,这限制了其临床疗效。通过自由基聚合技术制备了由CS、XG、AMPS、MBA和KPS组成的水凝胶(FCX1-FCX9),并通过傅里叶变换红外光谱(FTIR)、粉末X射线衍射(PXRD)、热分析和扫描电子显微镜(SEM)对其进行了表征。还研究了水凝胶的溶胀动力学和药物释放行为。FTIR研究证实ACV成功包封在水凝胶聚合物网络中。SEM显示出多孔结构,而热分析表明聚合物网络的热稳定性增强。PXRD表明在制备过程中ACV为无定形分散状态。所制备水凝胶的溶胀动力学和ACV释放行为取决于介质的pH值和所用纯反应物的浓度。Korsmeyer-Peppas模型与回归系数拟合最佳。本研究表明,通过使用纯聚合物CS、XG和单体AMPS开发用于抗病毒药物ACV的pH敏感水凝胶具有潜力。