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Abstract
Most pharmaceuticals are given using short-acting formulations that require frequent administration, which can negatively affect patient compliance and increase failure risks associated with inconsistent use. By contrast, long-acting release formulations can achieve sustained release of drugs for weeks, months or years. In this Review, we discuss long-acting drug delivery formulations that release drugs for at least 1 month and that have received approval from the US Food and Drug Administration (FDA), with an emphasis on materials used in their formulation. We highlight different slow-release mechanisms, including dissolution-based, biodegradation-based (preformed and in situ-formed), non-degradable implantable and hydrogel-based formulations, and investigate the clinical applications of long-acting drug delivery formulations, including long-acting contraceptives, extended sex hormone suppression, opioid and alcohol addiction treatments and localized drug delivery to the eye. Finally, we summarize release mechanisms, delivery duration, pharmaceutical forms, administration routes, indications, manufacturers and inactive ingredients of 63 FDA-approved long-acting drug products. We conclude by looking at the future challenges and opportunities for long-acting drug delivery formulations.
Long-acting drug delivery formulations enable sustained and prolonged drug release at the site of action or for systemic delivery, overcoming the need for frequent and repeated drug administration. This Review discusses US Food and Drug Administration (FDA)-approved long-acting drug delivery formulations, highlighting different slow-release mechanisms and delivery platforms, and the materials used to achieve them.
Details
; Tang, Jie 2 ; Lee, Dennis 3
; Tice, Thomas R 4
; Schwendeman, Steven P 5 ; Prausnitz, Mark R 6
1 Georgia Institute of Technology, School of Chemical and Biomolecular Engineering, Atlanta, USA (GRID:grid.213917.f) (ISNI:0000 0001 2097 4943); Wuhan University, School of Pharmaceutical Sciences, Wuhan, China (GRID:grid.49470.3e) (ISNI:0000 0001 2331 6153)
2 University of Michigan, Department of Pharmaceutical Sciences, Ann Arbor, USA (GRID:grid.214458.e) (ISNI:0000000086837370); Biointerfaces Institute, University of Michigan, Ann Arbor, USA (GRID:grid.214458.e) (ISNI:0000000086837370)
3 Bill and Melinda Gates Foundation, Seattle, USA (GRID:grid.418309.7) (ISNI:0000 0000 8990 8592)
4 Evonik Corporation, Birmingham, USA (GRID:grid.418309.7)
5 University of Michigan, Department of Pharmaceutical Sciences, Ann Arbor, USA (GRID:grid.214458.e) (ISNI:0000000086837370)
6 Georgia Institute of Technology, School of Chemical and Biomolecular Engineering, Atlanta, USA (GRID:grid.213917.f) (ISNI:0000 0001 2097 4943)




