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Herbal Gel Formulation Developed for Anti-Human Immunodeficiency Virus (HIV)-1 Activity Also Inhibits In Vitro HSV-2 Infection

机译:针对抗人类免疫缺陷病毒(HIV)-1活性而开发的草药凝胶制剂也可抑制HSV-2体外感染。

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摘要

Herpes simplex virus-2 (HSV-2) infection is the most common cause of genital ulcers. The impact of ulcers also demonstrates a strong link to the human immunodeficiency virus (HIV) infection. Complications, drug resistance, and side-effects of anti-viral drugs make the treatment of HSV-2 infection challenging. Herbal medicines have shown potential against HSV-2 and HIV infections. In this context, polyherbal gel formulation comprising 50% ethanolic extracts from Acacia catechu, Lagerstroemia speciosa, Terminalia chebula and Phyllanthus emblica has been developed. The gel formulation significantly exhibited virucidal activity against both HIV-1 and HSV-2 infections with IC50, 55.93 ± 5.30 µg/mL and 27.26 ± 4.87 µg/mL, respectively. It also inhibited HSV-2 attachment and penetration to the Vero cells with an IC50 = 46.55 ± 1.25 µg/mL and 54.94 ± 2.52 µg/mL respectively, which were significantly lower than acyclovir. However, acyclovir is more potent in post-infection assay with an IC50 = 0.065 ± 0.01 µg/mL whereas gel formulation showed an IC50 = 469.05 ± 16.65 µg/mL under similar conditions. Gel formulation showed no inhibitory effect on the viability of lactobacilli, human vaginal keratinocyte cells (Vk2/E6E7), and the integrity of the Caco-2 cells monolayer. Gel formulation did not lead to any significant increase in the secretion of pro-inflammatory cytokines and mutagenic index. The proposed gel formulation may be a promising candidate microbicide for the prevention of sexually transmitted HIV-1 and HSV-2.
机译:单纯疱疹病毒2(HSV-2)感染是生殖器溃疡的最常见原因。溃疡的影响还证明与人类免疫缺陷病毒(HIV)感染有很强的联系。抗病毒药物的并发症,耐药性和副作用使HSV-2感染的治疗具有挑战性。草药已显示出抗HSV-2和HIV感染的潜力。在这种情况下,已经开发了包含50%的乙醇提取物的多草药凝胶制剂,所述乙醇提取物来自相思树,紫薇,终端榄仁和余甘子。凝胶制剂对HIV-1和HSV-2感染均具有杀灭病毒活性,IC50分别为55.93±5.30 µg / mL和27.26±4.87 µg / mL。它也抑制HSV-2附着和渗透到Vero细胞,其IC50分别为46.55±1.25 µg / mL和54.94±2.52 µg / mL,显着低于阿昔洛韦。但是,阿昔洛韦在感染后测定中的效价更强,IC50 = 0.065±0.01 µg / mL,而凝胶制剂在相似条件下的IC50 = 469.05±16.65 µg / mL。凝胶制剂对乳杆菌,人阴道角质形成细胞(Vk2 / E6E7)的活力以及Caco-2细胞单层的完整性没有抑制作用。凝胶制剂并未导致促炎细胞因子的分泌和诱变指数的任何显着增加。提出的凝胶制剂可能是用于预防性传播HIV-1和HSV-2的有希望的候选杀微生物剂。

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