基于壳聚糖的新型纳米抗病毒药物

Julio C. Garay-Jimenez
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摘要

摘要:本文研究了14种低聚壳聚糖类似物的合成及其对人类免疫缺陷病毒(HIV)、呼吸道合胞病毒(RSV)和柯萨奇病毒的抗病毒潜力筛选。利用核磁共振(NMR)和红外光谱(FTIR)技术对合成的低聚壳聚糖类似物进行了表征。采用HIV-1 p24抗原捕获法进行HIV-1 p24酶联免疫吸附测定,以估计病毒的感染性损失。结果表明,与低聚壳聚糖UN102类似物相比,硫酸化低聚壳聚糖缺乏抗病毒活性。其余的UN102类似物包括n -硫醇(UN105)、n -戊二酰(UN106)、n -叠氮(UN111)、n -邻苯二酰(UN114)和n -柠檬酸类似物(UN117),均表现出抗病毒活性。UN102还能降低RSV引起的病毒感染。此外,还发现UN102与引起自身免疫性心肌炎的柯萨奇病毒结合。研究结果对开发新型抗病毒药物具有重要意义。
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A New Range of Chitosan Based Nano-antiviral Agents
ABSTRACT The current study involves the synthesis of fourteen analogs of oligochitosan and their screening for antiviral potential against human immunodeficiency virus (HIV), respiratory syncytial virus (RSV) and Coxsackie virus. The synthesized oligochitosan analogs were characterized by nuclear magnetic resonance (NMR) and FTIR techniques. HIV-1 p24 ELISA was performed using HIV-1 p24 antigen capture assay in order to estimate the viral infectivity loss. It was observed that sulfated oligochitosan was devoid of antiviral activity as compared to oligochitosan UN102 analog. The rest of UN102 analogs which include N-thiol (UN105), N-glutaryl (UN106), N-Azido (UN111) and N-phthaloyl (UN114) and N-citric analog (UN117) exhibited antiviral activity against HIV. The UN102 also decreased viral infection caused by RSV. In addition, UN102 was found to bind Coxsackie virus, which causes autoimmune myocarditis. The findings were of great interest to proceed for the development of novel antiviral agents.
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