| Literature DB >> 33353422 |
Abstract
Burst release of encapsulated drug with release of a significant fraction of payload into release medium within a short period, both in vitro and in vivo, remains a challenge for translation. Such unpredictable and uncontrolled release is often undesirable, especially from the perspective of developing sustained-release formulations. Moreover, a brisk release of the payload upsets optimal release kinetics. This account strives toward understanding burst release noticed in nanocarriers and investigates its causes. Various mathematical models to explain such untimely release were also examined, including their strengths and weaknesses. Finally, the account revisits current techniques of limiting burst release from nanocarriers and prioritizes future directions that harbor potential of fruitful translation by reducing such occurrences.Keywords: Korsmeyer–Peppas model; burst release; controlled release; drug diffusion; drug-delivery system; mathematical modeling; nanocarrier; nanomedicine; pulsatile release system; targeted delivery
Year: 2020 PMID: 33353422 DOI: 10.4155/tde-2020-0099
Source DB: PubMed Journal: Ther Deliv ISSN: 2041-5990