Next generation 3D-printed intravaginal ring for prevention of HIV and unintended pregnancy

Globally, there are 20 million adolescent girls and young women living with HIV who have limited access to long-acting, effective, women-controlled preventative methods. Additionally, although there are many contraceptive methods available, globally, half of all pregnancies remain unintended. Here w...

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Veröffentlicht in:Biomaterials 2023-10, Vol.301, p.122260-122260, Article 122260
Hauptverfasser: Young, Isabella C., Srinivasan, Priya, Shrivastava, Roopali, Janusziewicz, Rima, Thorson, Allison, Cottrell, Mackenzie L., Sellers, Rani S., Sykes, Craig, Schauer, Amanda, Little, Dawn, Kelley, Kristen, Kashuba, Angela D.M., Katz, David, Pyles, Richard B., García-Lerma, J. Gerardo, Vincent, Kathleen L., Smith, James, Benhabbour, S. Rahima
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Sprache:eng
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Zusammenfassung:Globally, there are 20 million adolescent girls and young women living with HIV who have limited access to long-acting, effective, women-controlled preventative methods. Additionally, although there are many contraceptive methods available, globally, half of all pregnancies remain unintended. Here we report the first 3D-printed multipurpose prevention technology (MPT) intravaginal ring (IVR) for HIV prevention and contraception. We utilized continuous liquid interface production (CLIP™) to fabricate MPT IVRs in a biocompatible silicone-based resin. Etonogestrel (ENG), ethinyl estradiol (EE), and islatravir (ISL) were loaded into the silicone poly(urethane) IVR in a controlled single step drug loading process driven by absorption. ENG/EE/ISL IVR promoted sustained release of drugs for 150 days in vitro and 14 days in sheep. There were no adverse MPT IVR-related findings of cervicovaginal toxicity or changes in vaginal biopsies or microbiome community profiles evaluated in sheep. Furthermore, ISL IVR in macaques promoted sustained release for 28 days with ISL-triphosphate levels above the established pharmacokinetic benchmark of 50–100 fmol/106 PBMCs. The ISL IVR was found to be safe and well tolerated in the macaques with no observed mucosal cytokine changes or alterations in peripheral CD4 T-cell populations. Collectively, the proposed MPT IVR has potential to expand preventative choices for young women and girls. [Display omitted] •ENG/EE/ISL were loaded into the IVR in a single step using a controlled solvent-mediated loading process.•ENG/EE/ISL IVRs exhibited sustained release for 150 days in vitro and 14 days in sheep.•ISL IVRs exhibited sustained release in macaques for 28 days above the PK benchmark.•IVRs showed no signs of toxicity in sheep, modeled human vaginal mucosa, and macaques.
ISSN:0142-9612
1878-5905
1878-5905
DOI:10.1016/j.biomaterials.2023.122260