首页> 美国卫生研究院文献>International Journal of Molecular Sciences >Emergence of Nanotechnology to Fight HIV Sexual Transmission: The Trip of G2-S16 Polyanionic Carbosilane Dendrimer to Possible Pre-Clinical Trials
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Emergence of Nanotechnology to Fight HIV Sexual Transmission: The Trip of G2-S16 Polyanionic Carbosilane Dendrimer to Possible Pre-Clinical Trials

机译:纳米技术对抗HIV性变速器的出现:G2-S16多阴离子碳硅烷树枝状大分子的临床前试验

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摘要

Development of new, safe, and effective microbicides to prevent human immunodeficiency virus HIV sexual transmission is needed. Unfortunately, most microbicides proved ineffective to prevent the risk of HIV-infection in clinical trials. We are working with G2-S16 polyanionic carbosilane dendrimer (PCD) as a new possible vaginal topical microbicide, based on its short reaction times, wide availability, high reproducibility, and quantitative yields of reaction. G2-S16 PCD exerts anti-HIV activity at an early stage of viral replication, by blocking gp120/CD4/CCR5 interaction, and providing a barrier against infection for long periods of time. G2-S16 PCD was stable at different pH values, as well as in the presence of seminal fluids. It maintained the anti-HIV activity against R5/X4 HIV over time, did not generate any type of drug resistance, and retained the anti-HIV effect when exposed to semen-enhanced viral infection. Importantly, G2-S16 PCD did not modify vaginal microbiota neither in vitro or in vivo. Histopathological examination did not show vaginal irritation, inflammation, lesions, or damage in the vaginal mucosa, after administration of G2-S16 PCD at different concentrations and times in female mice and rabbit animal models. Based on these promising data, G2-S16 PCD could become a good, safe, and readily available candidate to use as a topical vaginal microbicide against HIV.
机译:开发新,安全,有效的杀菌剂,以防止人类免疫缺陷病毒艾滋病病毒性传播。不幸的是,大多数杀菌剂证明是无效的,以防止临床试验中HIV感染的风险。我们正在使用G2-S16多阴离子碳硅烷树突(PCD)作为一种新的可能的阴道外科微生物剂,基于其短反应时间,广泛的可用性,高再重复性和反应的定量产率。 G2-S16 PCD通过阻断GP120 / CD4 / CCR5相互作用,在病毒复制的早期阶段发挥抗HIV活性,并在长时间提供免受感染的屏障。 G2-S16 PCD在不同的pH值下稳定,以及在最精液存在下。它随着时间的推移维持对R5 / X4艾滋病毒的抗HIV活性,未产生任何类型的耐药性,并在暴露于精液增强的病毒感染时保留抗HIV效应。重要的是,G2-S16 PCD既不在体外或体内都没有改变阴道微生物。组织病理学检查未显示阴道粘膜,在母小鼠和兔动物模型中的不同浓度和时间施用G2-S16 PCD后的阴道粘膜。基于这些有前途的数据,G2-S16 PCD可能成为一种良好,安全,易于使用的候选者,以用作针对艾滋病毒的局部阴道微生物剂。

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