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Merck

An intravaginal ring that releases the NNRTI MIV-150 reduces SHIV transmission in macaques.

Science translational medicine (2012-09-08)
Rachel Singer, Paul Mawson, Nina Derby, Aixa Rodriguez, Larisa Kizima, Radhika Menon, Daniel Goldman, Jessica Kenney, Meropi Aravantinou, Samantha Seidor, Agegnehu Gettie, James Blanchard, Michael Piatak, Jeffrey D Lifson, José A Fernández-Romero, Melissa Robbiani, Thomas M Zydowsky
RESUMEN

Microbicides may prevent HIV and sexually transmitted infections (STIs) in women; however, determining the optimal means of delivery of active pharmaceutical ingredients remains a major challenge. We previously demonstrated that a vaginal gel containing the non-nucleoside reverse transcriptase inhibitor MIV-150 partially protected macaques from SHIV-RT (simian/HIV reverse transcriptase) infection, and the addition of zinc acetate rendered the gel significantly protective. We test the activity of MIV-150 without the addition of zinc acetate when delivered from either ethylene vinyl acetate (EVA) or silicone intravaginal rings (IVRs). MIV-150 was successfully delivered, because it was detected in vaginal fluids and tissues by radioimmunoassay in pharmacokinetic studies. Moreover, EVA IVRs significantly protected macaques from SHIV-RT infection. Our results demonstrate that MIV-150-containing IVRs have the potential to prevent HIV infection and highlight the possible use of IVRs for delivering drugs that block HIV and other STIs.

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Sigma-Aldrich
Poly(ethylene-co-vinyl acetate), vinyl acetate 40 wt. %, melt index (41-63 dg/min (190°C/2.16kg)), contains 190-910 ppm inhibitor
Sigma-Aldrich
Poly(ethylene-co-vinyl acetate), vinyl acetate 12 wt. %, melt index 8 g/10 min (190°C/2.16kg)
Sigma-Aldrich
Poly(ethylene-co-vinyl acetate), vinyl acetate 18 wt. %, melt index 8 g/10 min (190°C/2.16kg), contains 200-900 ppm BHT as inhibitor