In Vitro Characterization of a Sustained-Release Formulation for Enfuvirtide
Identifieur interne : 005372 ( Main/Exploration ); précédent : 005371; suivant : 005373In Vitro Characterization of a Sustained-Release Formulation for Enfuvirtide
Auteurs : Sam N. Rothstein [États-Unis] ; Kelly D. Huber [États-Unis] ; Nicolas Sluis-Cremer [États-Unis] ; Steven R. Little [États-Unis]Source :
- Antimicrobial agents and chemotherapy [ 0066-4804 ] ; 2014.
Descripteurs français
- Pascal (Inist)
English descriptors
- KwdEn :
Abstract
Although approved by the U.S. Food and Drug Administration, enfuvirtide is rarely used in combination antiretroviral therapies (cART) to treat HIV-1 infection, primarily because of its intense dosing schedule that requires twice-daily subcutaneous injection. Here, we describe the development of enfuvirtide-loaded, degradable poly(lactic-co-glycolic) acid microparticles that provide linear in vitro release of the drug over an 18-day period. This sustained-release formulation could make enfuvirtide more attractive for use in cART.
Affiliations:
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Le document en format XML
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<front><div type="abstract" xml:lang="en">Although approved by the U.S. Food and Drug Administration, enfuvirtide is rarely used in combination antiretroviral therapies (cART) to treat HIV-1 infection, primarily because of its intense dosing schedule that requires twice-daily subcutaneous injection. Here, we describe the development of enfuvirtide-loaded, degradable poly(lactic-co-glycolic) acid microparticles that provide linear in vitro release of the drug over an 18-day period. This sustained-release formulation could make enfuvirtide more attractive for use in cART.</div>
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