前药
共聚物
顺铂
己内酯
可生物降解聚合物
药品
聚合物
药物输送
材料科学
两亲性
动态光散射
纳米颗粒
化学
纳米技术
有机化学
药理学
生物化学
外科
化疗
医学
作者
Bapurao Surnar,Pramod P. Subash,M. Jayakannan
标识
DOI:10.1002/zaac.201400030
摘要
Abstract A carboxylic acid substituted amphiphilic diblock copolymer scaffold with a hydrophilic PEG‐chain and hydrophobic biodegradable poly(caprolactone) (PCL), which forms a cisplatin anticancer drug is reported herein. Cisplatin [ cis ‐dichloro‐diammine platinum(II), CDDP] was anchored on the polymer backbone through Pt–OOC–PCL chemical linkage that enabled self‐assembly of the prodrug to produce 110 ± 10 nm nanoparticles in water. These drug loaded nanoparticles were characterized by dynamic light scattering, electron microscopy, and X‐ray diffraction. The polymer‐drug conjugate burst instantaneously in saline and PBS to release 35 % of the cisplatin drug for immediate administration. The remaining drug that retained in the polymer scaffold underwent slow and controlled release to deliver the drug over a period of 6–7 d. In the presence of esterase enzyme; the biodegradable PCL aliphatic ester backbone broke completely to release 100 % loaded drugs within a few hours. This biodegradable diblock copolymer design strategy opens up new platform for cisplatin‐polymer drug delivery approach.
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