多西紫杉醇
肺癌
癌症研究
细胞毒性
耐受性
医学
整合素
肿瘤科
材料科学
药理学
化疗
内科学
化学
不利影响
体外
生物化学
受体
作者
Yan Zou,Yinping Sun,Beibei Guo,Yaohua Wei,Yifeng Xia,Zhenyuan Huangfu,Fenghua Meng,Jan C. M. van Hest,Jiandong Yuan,Zhiyuan Zhong
标识
DOI:10.1021/acsami.0c01069.s001
摘要
Docetaxel
(DTX) widely used for treating nonsmall cell lung cancer
(NSCLC) patients is associated with dose-limiting side effects, especially
neurotoxicity and myelosuppression. Here, we have developed cyclic
cNGQGEQc peptide-directed polymersomal docetaxel (cNGQ-PS-DTX) as
a targeted and multifunctional formulation for NSCLC. cNGQ-PS-DTX
carrying 8.1 wt % DTX had a size of 93 nm, neutral surface charge,
high stability, and glutathione-triggered DTX release behavior. Cytotoxicity
studies demonstrated a clearly better antitumor activity of cNGQ-PS-DTX
in α3β1 integrin overexpressing
A549 human lung cancer cells than free DTX and nontargeted PS-DTX.
cNGQ-PS-DTX showed a remarkably high tolerability (over 8 times better
than free DTX) and slow elimination in mice. Importantly, cNGQ-PS-DTX
exhibited greatly improved tumor accumulation and higher suppression
of subcutaneous and orthotopic A549 xenografts as compared to PS-DTX
and free DTX controls. α3β1 integrin-targeting
polymersomal docetaxel emerges as an advanced nanotherapeutic for
NSCLC treatment.
科研通智能强力驱动
Strongly Powered by AbleSci AI