PLGA公司
阿霉素
化学
药物输送
体内
细胞毒性
生物物理学
癌细胞
壳聚糖
纳米医学
药品
两亲性
药理学
体外
纳米颗粒
生物化学
癌症
纳米技术
材料科学
化疗
有机化学
生物
生物技术
聚合物
遗传学
共聚物
作者
Sheng-Jyun Huang,Tzu-Hao Wang,Ya-Hsuan Chou,Huimin Wang,Tsai‐Ching Hsu,Jia-Le Yow,Bor‐Show Tzang,Wen‐Hsuan Chiang
标识
DOI:10.1016/j.ijbiomac.2022.04.209
摘要
To achieve effective intracellular anticancer drug release for boosted antitumor efficacy, the acidity-responsive nanovehicles for doxorubicin (DOX) delivery were fabricated by tailor-made co-assembly of amphiphilic PEGylated chitosan20k and hydrophobic poly(lactic-co-glycolic acid) (PLGA) segments at pH 8.5. The attained DOX-loaded PEGylated chitosan20k/PLGA nanoparticles (DOX-PC20kPNs) were characterized to have a spherical shape composed of drug-encapsulated chitosan20k/PLGA-constituted solid core surrounded by hydrophilic PEG shells. Compared to non-pH-sensitive DOX-loaded PLGA nanoparticles (DOX-PNs), the DOX-PC20kPNs displayed outstanding colloidal stability under serum-containing condition and tended to swell in weak acidic milieu upon increased protonation of chitosan20k within hybrid cores, thus accelerating drug release. The in vitro cellular uptake and cytotoxicity studies revealed that the DOX-PC20kPNs after being endocytosed by prostate TRAMP-C1 cancer cells rapidly liberated drug, thus promoting drug accumulation in nuclei to enhance anticancer potency. Moreover, the hydrated PEG shells of DOX-PC20kPNs remarkably reduced their uptake by macrophage-like RAW264.7 cells. Importantly, in vivo animal findings showed that the DOX-PC20kPNs exhibited the capability of inhibiting TRAMP-C1 tumor growth superior to free hydrophobic DOX molecules and DOX-PNs, demonstrating the great potential in cancer chemotherapy.
科研通智能强力驱动
Strongly Powered by AbleSci AI