Herbal Gel Formulation Developed for Anti-Human Immunodeficiency Virus (HIV)-1 Activity Also Inhibits In Vitro HSV-2 Infection
Autor: | Reshmi Nair, Ajay Kesharwani, Aakanksha Agarwal, Satish K. Gupta, Suja Kizhiyedath Polachira, Nripendra N. Mishra |
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Jazyk: | angličtina |
Rok vydání: | 2018 |
Předmět: |
0301 basic medicine
Keratinocytes Drug Compounding Herpesvirus 2 Human viruses lcsh:QR1-502 Drug resistance Pharmacology Virus Replication pro-inflammatory cytokines Antiviral Agents viability of lactobacilli Article lcsh:Microbiology Proinflammatory cytokine 03 medical and health sciences Mice Virology Microbicide Chlorocebus aethiops Medicine Animals Humans anti-HIV-1 activity IC50 Vero Cells Chromatography High Pressure Liquid Mucous Membrane business.industry Plant Extracts anti-HSV-2 activity In vitro Terminalia chebula 030104 developmental biology Infectious Diseases Phyllanthus emblica Vagina herbal gel formulation Vero cell HIV-1 Cytokines Female Inflammation Mediators business Gels |
Zdroj: | Viruses, Vol 10, Iss 11, p 580 (2018) Viruses Volume 10 Issue 11 |
ISSN: | 1999-4915 |
Popis: | 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 µ g/mL and 27.26 ± 4.87 µ g/mL, respectively. It also inhibited HSV-2 attachment and penetration to the Vero cells with an IC50 = 46.55 ± 1.25 µ g/mL and 54.94 ± 2.52 µ g/mL respectively, which were significantly lower than acyclovir. However, acyclovir is more potent in post-infection assay with an IC50 = 0.065 ± 0.01 µ g/mL whereas gel formulation showed an IC50 = 469.05 ± 16.65 µ g/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. |
Databáze: | OpenAIRE |
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