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dc.contributor.authorKirtane, Ameya
dc.contributor.authorLanger, Robert S
dc.contributor.authorTraverso, Giovanni
dc.date.accessioned2017-12-01T15:17:04Z
dc.date.available2017-12-01T15:17:04Z
dc.date.issued2016-10
dc.date.submitted2016-09
dc.identifier.issn0022-3549
dc.identifier.issn1520-6017
dc.identifier.urihttp://hdl.handle.net/1721.1/112335
dc.description.abstractThe human immunodeficiency virus has infected millions of people and the epidemic continues to grow rapidly in some parts of the world. Antiretroviral (ARV) therapy has provided improved treatment and prolonged the life expectancy of patients. Moreover, there is growing interest in using ARVs to protect against new infections. Hence, ARVs have emerged as our primary strategy in combating the virus. Unfortunately, several challenges limit the optimal performance of these drugs. First, ARVs often require life-long use and complex dosing regimens. This results in low patient adherence and periods of lapsed treatment manifesting in drug resistance. This has prompted the development of alternate dosage forms such as vaginal rings and long-acting injectables that stand to improve patient adherence. Another problem central to therapeutic failure is the inadequate penetration of drugs into infected tissues. This can lead to incomplete treatment, development of resistance, and viral rebound. Several strategies have been developed to improve drug penetration into these drug-free sanctuaries. These include encapsulation of drugs in nanoparticles, use of pharmacokinetic enhancers, and cell-based drug delivery platforms. In this review, we discuss issues surrounding ARV therapy and their impact on drug efficacy. We also describe various drug delivery–based approaches developed to overcome these issues.en_US
dc.description.sponsorshipBill & Melinda Gates Foundation (Grant OPP1139937)en_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (Grant EB-000244)en_US
dc.language.isoen_US
dc.publisherElsevieren_US
dc.relation.isversionofhttp://dx.doi.org/10.1016/j.xphs.2016.09.015en_US
dc.rightsCreative Commons Attribution-NonCommercial-NoDerivs Licenseen_US
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/en_US
dc.sourceProf. Langer via Erja Kajosaloen_US
dc.titlePast, Present, and Future Drug Delivery Systems for Antiretroviralsen_US
dc.typeArticleen_US
dc.identifier.citationKirtane, Ameya R. et al. “Past, Present, and Future Drug Delivery Systems for Antiretrovirals.” Journal of Pharmaceutical Sciences 105, 12 (December 2016): 3471–3482 © 2016 American Pharmacists Associationen_US
dc.contributor.departmentMassachusetts Institute of Technology. Institute for Medical Engineering & Scienceen_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Chemical Engineeringen_US
dc.contributor.departmentKoch Institute for Integrative Cancer Research at MITen_US
dc.contributor.approverLanger, Robert S.en_US
dc.contributor.mitauthorKirtane, Ameya
dc.contributor.mitauthorLanger, Robert S
dc.contributor.mitauthorTraverso, Giovanni
dc.relation.journalJournal of Pharmaceutical Sciencesen_US
dc.eprint.versionAuthor's final manuscripten_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dspace.orderedauthorsKirtane, Ameya R.; Langer, Robert; Traverso, Giovannien_US
dspace.embargo.termsNen_US
dc.identifier.orcidhttps://orcid.org/0000-0003-4255-0492
mit.licensePUBLISHER_CCen_US
mit.metadata.statusComplete


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