<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Gele T</submitter><funding>Agence Nationale de la Recherche</funding><funding>Agence Nationale de Recherches sur le Sida et les Hépatites Virales</funding><pagination>2282</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9696548</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>14(11)</volume><pubmed_abstract>The development of animal models undergoing long-term antiretroviral treatment (ART) makes it possible to understand a number of immunological, virological, and pharmacological issues, key factors in the management of HIV infection. We aimed to pharmacologically validate a non-human primate (NHP) model treated in the long term with antiretroviral drugs after infection with the pathogenic SIVmac251 strain. A single-dose pharmacokinetic study of tenofovir disoproxil fumarate, emtricitabine, and dolutegravir was first conducted on 13 non-infected macaques to compare three different routes of administration. Then, 12 simian immunodeficiency virus (SIV)-infected (SIV&lt;sup>+&lt;/sup>) macaques were treated with the same regimen for two years. Drug monitoring, virological efficacy, and safety were ev</pubmed_abstract><journal>Pharmaceutics</journal><pubmed_title>Pharmacological Validation of Long-Term Treatment with Antiretroviral Drugs in a Model of SIV-Infected Non-Human Primates.</pubmed_title><pmcid>PMC9696548</pmcid><funding_grant_id>ANR-10-EQPX-02-01</funding_grant_id><funding_grant_id>SIVART ANRS-IDMIT CO1</funding_grant_id><funding_grant_id>ANR-11- INBS-0008</funding_grant_id><pubmed_authors>Desjardins D</pubmed_authors><pubmed_authors>Gele T</pubmed_authors><pubmed_authors>Le Grand R</pubmed_authors><pubmed_authors>Gouget H</pubmed_authors><pubmed_authors>Barrail-Tran A</pubmed_authors><pubmed_authors>Lambotte O</pubmed_authors><pubmed_authors>Dereuddre-Bosquet N</pubmed_authors><pubmed_authors>Furlan V</pubmed_authors></additional><is_claimable>false</is_claimable><name>Pharmacological Validation of Long-Term Treatment with Antiretroviral Drugs in a Model of SIV-Infected Non-Human Primates.</name><description>The development of animal models undergoing long-term antiretroviral treatment (ART) makes it possible to understand a number of immunological, virological, and pharmacological issues, key factors in the management of HIV infection. We aimed to pharmacologically validate a non-human primate (NHP) model treated in the long term with antiretroviral drugs after infection with the pathogenic SIVmac251 strain. A single-dose pharmacokinetic study of tenofovir disoproxil fumarate, emtricitabine, and dolutegravir was first conducted on 13 non-infected macaques to compare three different routes of administration. Then, 12 simian immunodeficiency virus (SIV)-infected (SIV&lt;sup>+&lt;/sup>) macaques were treated with the same regimen for two years. Drug monitoring, virological efficacy, and safety were ev</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Oct</publication><modification>2025-04-04T19:51:56.902Z</modification><creation>2025-04-04T19:51:56.902Z</creation></dates><accession>S-EPMC9696548</accession><cross_references><pubmed>36365101</pubmed><doi>10.3390/pharmaceutics14112282</doi></cross_references></HashMap>