己二酸
聚酯纤维
药物输送
甘油
毒品携带者
聚乳酸
材料科学
组合化学
高分子化学
化学
有机化学
纳米技术
聚合物
作者
Sadie M.E. Swainson,Ioanna Danai Styliari,Vincenzo Taresco,Martin C. Garnett
出处
期刊:Polymers
[Multidisciplinary Digital Publishing Institute]
日期:2019-09-25
卷期号:11 (10): 1561-1561
被引量:37
标识
DOI:10.3390/polym11101561
摘要
The enzymatically synthesized poly (glycerol adipate) (PGA) has demonstrated all the desirable key properties required from a performing biomaterial to be considered a versatile "polymeric-tool" in the broad field of drug delivery. The step-growth polymerization pathway catalyzed by lipase generates a highly functionalizable platform while avoiding tedious steps of protection and deprotection. Synthesis requires only minor purification steps and uses cheap and readily available reagents. The final polymeric material is biodegradable, biocompatible and intrinsically amphiphilic, with a good propensity to self-assemble into nanoparticles (NPs). The free hydroxyl group lends itself to a variety of chemical derivatizations via simple reaction pathways which alter its physico-chemical properties with a possibility to generate an endless number of possible active macromolecules. The present work aims to summarize the available literature about PGA synthesis, architecture alterations, chemical modifications and its application in drug and gene delivery as a versatile carrier. Following on from this, the evolution of the concept of enzymatically-degradable PGA-drug conjugation has been explored, reporting recent examples in the literature.
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