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Virucidal activity of the dendrimer microbicide SPL7013 against HIV-1

journal contribution
posted on 2024-11-01, 17:36 authored by Sushama Telwatte, Katie Moore, Adam Johnson, Tyssen David, Jasminka Sterjovski, Muriel Aldunate, Paul Gorry, Paul RamslandPaul Ramsland, Gareth Lewis, Jeremy Paull, Secondo Sonza, Gilda Tachedjian
Topical microbicides for use by women to prevent the transmission of human immunodeficiency virus (HIV) and other sexually transmitted infections are urgently required. Dendrimers are highly branched nanoparticles being developed as microbicides. SPL7013 is a dendrimer with broad-spectrum activity against HIV type I (HIV-1) and -2 (HIV-2), herpes simplex viruses type-1 (HSV-1) and -2 (HSV-2) and human papillomavirus. SPL7013 [3% (w/w)] has been formulated in a mucoadhesive carbopol gel (VivaGel®) for use as a topical microbicide. Previous studies showed that SPL7013 has similar potency against CXCR4-(X4) and CCR5-using (R5) strains of HIV-1 and that it blocks viral entry. However, the ability of SPL7013 to directly inactivate HIV-1 is unknown. We examined whether SPL7013 demonstrates virucidal activity against X4 (NL4.3, MBC200, CMU02 clade EA and 92UG046 clade D), R5 (Ba-L, NB25 and 92RW016 clade A) and dual-tropic (R5X4; MACS1-spln) HIV-1 using a modified HLA-DR viral capture method and by polyethylene glycol precipitation. Evaluation of virion integrity was determined by ultracentrifugation through a sucrose cushion and detection of viral proteins by Western blot analysis. SPL7013 demonstrated potent virucidal activity against X4 and R5X4 strains, although virucidal activity was less potent for the 92UG046 X4 clade D isolate. Where potent virucidal activity was observed, the 50% virucidal concentrations were similar to the 50% effective concentrations previously reported in drug susceptibility assays, indicating that the main mode of action of SPL7013 is by direct viral inactivation for these strains.

History

Journal

Antiviral Research

Volume

90

Issue

3

Start page

195

End page

199

Total pages

5

Publisher

Elsevier BV

Place published

Netherlands

Language

English

Copyright

© 2011 Elsevier B.V. All rights reserved.

Former Identifier

2006050456

Esploro creation date

2020-06-22

Fedora creation date

2017-06-15

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