期刊
ACTA BIOMATERIALIA
卷 115, 期 -, 页码 383-392出版社
ELSEVIER SCI LTD
DOI: 10.1016/j.actbio.2020.07.045
关键词
Rapamycin; Affinity; Selective PEGylation; Cyclodextrin; Microparticles; Extended drug delivery
资金
- National Institute of Health [R01 GM121477]
Small-molecule drugs are utilized in a wide variety of clinical applications, however, many of these drugs suffer from one or more suboptimal properties that can hinder its delivery or cellular action in vivo, or even shelf an otherwise biologically tolerable drug. While high-throughput screening provides a method to discover drugs with altered chemical properties, directly engineering small-molecule bioconjugates provides an opportunity to specifically modulate drug properties rather than sifting through large drug libraries with seemingly 'random' drug properties. Herein, we propose that selectively tethering a drug molecule to an additional group with favorable properties will improve the drug conjugate's overall properties, such as solubility. Specifically, we outlined the site-specific chemical conjugation of rapamycin (RAP) to an additional high-affinity group to increase the overall affinity the drug has for cyclodextrin-based polymers (pCD). By doing so, we found that RAP's affinity for pCD and RAP's window of delivery from pCD microparticles was tripled without sacrificing RAP's cellular action. This synthesis method was applied to the concept of affinity for pCD, but other prosthetic groups can be used similarly. This study displays potential for increasing drug delivery windows of small-molecule drugs in pCD systems for chronic drug therapies and introduces the idea of altering drug properties to tune polymer-drug interactions. (C) 2020 Acta Materialia Inc. Published by Elsevier Ltd. All rights reserved.
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