胶束
体内分布
PEG比率
药物输送
乙二醇
生物利用度
两亲性
药代动力学
药品
毒品携带者
化学
溶解度
血液循环
纳米医学
可生物降解聚合物
共聚物
聚合物
材料科学
药理学
纳米技术
纳米颗粒
有机化学
体外
生物化学
水溶液
医学
经济
传统医学
财务
作者
Yujun Wang,Maling Gou,Changyang Gong,Cheng Wang,Zhiyong Qian,Yunfeng Lin,Feng Luo
标识
DOI:10.2174/138920012800166490
摘要
Micelles assembled from amphiphilic poly(ethylene glycol)/poly(ε -caprolactone) (PEG/PCL) copolymers are promised as safe and effective drug delivery systems. They offer the potential to achieve high solubility of hydrophobic drugs, long blood circulation time and effective delivery to target organs. These advantages contribute to their application as vehicles of a broad variation of therapeutic compounds. In this review, we discussed the safety of the copolymers, release behavior of PEG/PCL micelles in vitro, and pharmacokinetic profiles referring to the optimized fate in vascular system and targeting biodistribution. Keywords: PEG, PCL, micelles, biodegradation, release, long circulation, target
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