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Herbal Gel Formulation Developed for Anti-Human Immunodeficiency Virus (HIV)-1 Activity Also Inhibits In Vitro HSV-2 Infection.
Mishra, Nripendra Nath; Kesharwani, Ajay; Agarwal, Aakanksha; Polachira, Suja Kizhiyedath; Nair, Reshmi; Gupta, Satish Kumar.
Afiliación
  • Mishra NN; Reproductive Cell Biology Laboratory, National Institute of Immunology, Aruna Asaf Ali Marg, New Delhi 110 067, India. nripbiochem@gmail.com.
  • Kesharwani A; Reproductive Cell Biology Laboratory, National Institute of Immunology, Aruna Asaf Ali Marg, New Delhi 110 067, India. biotechajay@gmail.com.
  • Agarwal A; Reproductive Cell Biology Laboratory, National Institute of Immunology, Aruna Asaf Ali Marg, New Delhi 110 067, India. agarwalaksh24@gmail.com.
  • Polachira SK; Corporate R & D Centre, HLL Lifecare Limited, Akkulum, Thiruvananthapuram, Kerala 695 017, India. sujakp@lifecarehll.com.
  • Nair R; Corporate R & D Centre, HLL Lifecare Limited, Akkulum, Thiruvananthapuram, Kerala 695 017, India. reshmiraj2004@gmail.com.
  • Gupta SK; Reproductive Cell Biology Laboratory, National Institute of Immunology, Aruna Asaf Ali Marg, New Delhi 110 067, India. skgupta@nii.ac.in.
Viruses ; 10(11)2018 10 24.
Article en En | MEDLINE | ID: mdl-30352961
ABSTRACT
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.
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Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Antivirales / Extractos Vegetales / VIH-1 / Herpesvirus Humano 2 / Geles Límite: Animals / Female / Humans Idioma: En Revista: Viruses Año: 2018 Tipo del documento: Article País de afiliación: India

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Antivirales / Extractos Vegetales / VIH-1 / Herpesvirus Humano 2 / Geles Límite: Animals / Female / Humans Idioma: En Revista: Viruses Año: 2018 Tipo del documento: Article País de afiliación: India