药物输送
纳米技术
纳米颗粒
前药
药品
脂质体
合理设计
基因传递
材料科学
化学
药理学
生物化学
医学
遗传增强
基因
作者
Jialin Huang,Hong-Zhuan Chen,Xiaoling Gao
标识
DOI:10.1080/1061186x.2017.1419360
摘要
In recent years, lipid-coated calcium-phosphate (LCP) nanoparticle has been developed as a versatile platform for delivery of various therapeutics including gene, protein/peptide, chemotherapeutics and theranostic agents. The high endosomal escape, coupled with the ability to efficiently encapsulate phosphorylated drugs or prodrugs, make LCP become attractive vehicle for drug delivery. Additionally, the principle behind LCP formulation has also allowed rational design of LCP-derived nanoparticles (NPs) with other solid core or lipid membrane to overcome the various drug delivery barriers. Here, we briefly review the history of the development of LCP NPs, highlight the optimisations and modulations in the development process, and summarise the major applications of LCP NPs and LCP-derived NPs in drug delivery.
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