Silicon Oxycarbide Porous Particles and Film Coating as Strategies for Tenofovir Controlled Release in Vaginal Tablets for HIV Prevention.
Araceli Martín-IllanaRaul Cazorla-LunaFernando Notario-PerezRoberto Ruiz-CaroJuan RubioAitana TamayoMaría Dolores VeigaPublished in: Pharmaceutics (2022)
Sustained release of antiretroviral drugs is currently the most encouraging strategy for the prevention of the sexual transmission of HIV. Vaginal tablets based on hydrophilic gelling polymers are an interesting dosage form for this purpose, since they can be developed to modify the release of the drug depending on the tablet swelling. Tenofovir is a drug with proven activity in the prevention of HIV-1 infection, and it is possible to have it loaded in the surface of γ-aminopropyl trimethoxy silane-functionalized oxycarbide particles. These particles can be incorporated into the tablets, thus providing a sustained release of the drug. Moreover, the presence of the particles modifies the microstructure of the gel formed, as observed in scanning electron microscopy and Hg porosimetry studies, resulting into a gel with a narrow pore size distribution between 10 and 100 µm. This implies a lower volume of fluid incorporated into the gel during swelling studies, and therefore improved mucoadhesion times in ex vivo test. The coating of the formulations with Eudragit ® RS modifies the swelling behavior of the tablets, which not only is decreased in magnitude but also extended in time, and as consequence the drug release is also prolonged for up to 7 days.
Keyphrases
- antiretroviral therapy
- electron microscopy
- hiv infected
- drug release
- hiv positive
- human immunodeficiency virus
- hiv aids
- drug delivery
- hiv infected patients
- wound healing
- hyaluronic acid
- drug induced
- hepatitis c virus
- adverse drug
- case control
- mental health
- high resolution
- hiv testing
- multiple sclerosis
- men who have sex with men
- cancer therapy
- electronic health record
- room temperature
- ionic liquid
- molecularly imprinted