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Preparation of poly(lactic acid)/chitosan nanoparticles for anti-HIV drug delivery applications

机译:聚乳酸/壳聚糖纳米粒的制备及其在抗HIV药物中的应用

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Poly(lactic acid) (PLA)/chitosan (CS) nanoparticles were prepared by emulsion method for anti-HIV drug delivery applications. The prepared PLA/CS nanoparticles were characterized using DLS, SEM, and FTIR. The hydrophilic antiretroviral drug Lamivudine was loaded into PLA/CS nanoparticles. The encapsulation efficiency and in-vitro drug release behaviour of drug loaded PLA/CS nanoparticles were studied using UV spectrophotometer. In addition, the cytotoxicity of the PLA/CS nanoparticles using MTT assay was also studied. The in-vitro drug release studies showed that drug release rate was lower in the acidic pH when compared to alkaline pH. This may due to repulsion between H~+ ions and cationic groups present in the polymeric nanoparticles. Drug release rate was found to be higher in the 6% drug loaded formulation when compared to 3% drug loaded formulation. These results indicated that the PLA/CS nanoparticles are a promising carrier system for controlled delivery of anti-HIV drugs.
机译:通过乳液法制备了聚乳酸(PLA)/壳聚糖(CS)纳米粒子,用于抗HIV药物的递送。使用DLS,SEM和FTIR对制备的PLA / CS纳米颗粒进行表征。将亲水性抗逆转录病毒药物拉米夫定加载到PLA / CS纳米颗粒中。用紫外分光光度计研究了载药PLA / CS纳米粒子的包封率和体外释药性能。另外,还使用MTT分析研究了PLA / CS纳米颗粒的细胞毒性。体外药物释放研究表明,与碱性pH相比,酸性pH的药物释放速率较低。这可能是由于存在于聚合物纳米粒子中的H +离子与阳离子基团之间的排斥。发现载药量为6%的制剂与载药量为3%的制剂相比,药物释放速率更高。这些结果表明,PLA / CS纳米颗粒是用于控制抗HIV药物递送的有前途的载体系统。

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