PLGA公司
乙醇酸
纳米颗粒
药物输送
纳米技术
生物相容性材料
可生物降解聚合物
乳酸
药品
聚酯纤维
材料科学
共聚物
化学
聚合物
生物医学工程
有机化学
药理学
医学
生物
细菌
遗传学
作者
Deepti Pandita,Sandeep Kumar,Viney Lather
标识
DOI:10.1016/j.drudis.2014.09.018
摘要
Poly(lactic-co-glycolic acid) (PLGA), a US Food and Drug Administration (FDA)-approved copolymer, has been exploited widely in the design of nanoparticles because it is biodegradable, biocompatible, protects the drug molecules from degradation, and aids in producing sustained and targeted delivery. However, certain constraints associated with PLGA nanoparticles, such as poor drug encapsulation, polymer degradation, and scale-up issues, have led to the development of emerging hybrid PLGA delivery systems. These hybrid nanoparticles are core–shell nanostructures comprising either a PLGA core or a PLGA shell combining multiple functionalities within one system and, thus, exhibiting the complementary characteristics of two different platforms used for the delivery of a wide range of therapeutics and imaging.
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