Synthesis and Formulation of Powerful ZnO Q-Dots/CNTs@Fe3O4 Nanopackage as a Predominant Anti-HIV-1 Infection

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引用次数: 1

Abstract

Usage of fine and uniform Fe3O4 nanoparticles (NPs) including super-paramagnetic unique properties developed state of the nanobio-formulations in recent years. We have shown a new formulated nanocomposition of super-paramagnetic iron oxide (Fe3O4) NPs (as substrate) with carbon nanotubes (CNTs) (as activator). Besides, ZnO@CNTs was synthesized as a magic assistant/hybrid for ZnO quantum dots nanoparticles (Q-Dots NPs) in this nanopackage. This novel formulated water-based nanofluid product consists of strong stabilizer, suitable dispersant-wetting agent complex and desirable water in oil emulsifier (w/o) package to damage HIV infection (AIDS) type 1. The achieved results demonstrated that smart nanofluid formulation had excellent functions as inhibitor, controller and treatment (Antiretroviral therapy (ART)) for HIV-1 integrase and could act as strong oxidizing agent. The nanofluid product was completely characterized with SEM morphology, TEM images, FTIR spectroscopy, XRD pattern, UV–Vis absorption spectroscopy, EDS and mapping of internal layers for one of the SEM surface morphology. Moreover, HIV-1 replication Assay, RT (reverse transcriptase) Assay, integrase assay, and cytotoxicity tests were performed and compared with Zidovudine (ZDV) and Raltegravir (RAL) as control antiretroviral medications. The specific interaction of this nanopackage with the target RNA and DNA proteins has been very interesting through main redox reactions.
强效ZnO Q-Dots/CNTs@Fe3O4纳米包膜抗hiv -1感染的合成与制备
利用具有超顺磁性的精细均匀的Fe3O4纳米粒子(NPs)是近年来纳米生物制剂的发展方向。我们展示了一种新配方的超顺磁性氧化铁(Fe3O4) NPs(作为底物)和碳纳米管(CNTs)(作为活化剂)的纳米组合物。此外,还合成了ZnO@CNTs作为ZnO量子点纳米粒子(Q-Dots NPs)的神奇助手/杂化物。该新型水基纳米流体产品由强稳定剂、合适的分散剂-润湿剂复合物和油乳化剂(w/o)包装中的理想水组成,可破坏1型HIV感染(AIDS)。研究结果表明,智能纳米流体制剂作为HIV-1整合酶的抑制剂、控制者和治疗(抗逆转录病毒疗法(ART))具有优异的功能,并可作为强氧化剂。利用SEM形貌、TEM图像、FTIR光谱、XRD图谱、UV-Vis吸收光谱、EDS以及其中一种SEM表面形貌的内层图对纳米流体产物进行了全面表征。此外,进行HIV-1复制试验、RT(逆转录酶)试验、整合酶试验和细胞毒性试验,并与齐多夫定(ZDV)和雷替格拉韦(RAL)作为对照抗逆转录病毒药物进行比较。通过主要的氧化还原反应,这种纳米包装与靶RNA和DNA蛋白的特异性相互作用非常有趣。
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