咖啡酸苯乙酯
分散性
细胞凋亡
槲皮素
细胞毒性
Zeta电位
PLGA公司
粒径
咖啡酸
纳米颗粒
药物输送
化学
材料科学
体外
核化学
生物化学
纳米技术
抗氧化剂
有机化学
物理化学
作者
Reyhan Dilsu Colpan,Ayşegül Demirhan Erdemir
标识
DOI:10.1080/02652048.2021.1948623
摘要
This study aimed to synthesise quercetin- caffeic-acid phenethyl ester (CAPE)-co-loaded poly(lactic-co-glycolic-acid) (PLGA) nanoparticles (QuCaNP) and investigate their anti-cancer activity on human colorectal carcinoma HT-29 cells.QuCaNPs were synthesised using single-emulsion (o/w) solvent evaporation method. Particle size, zeta potential, polydispersity index, in vitro release profile, and surface morphology of QuCaNPs were determined. Cytotoxicity, anti-migration, anti-proliferation and apoptotic activities of QuCaNPs were studied.Mean diameter of QuCaNP was 237.8 ± 9.670 nm, with a polydispersity index (PDI) of 0.340 ± 0.027. Encapsulation efficiency was 74.28% (quercetin) and 65.24% (CAPE). Particle size and drug content of QuCaNP remained stable for 30 days at -20 °C. The half-maximal inhibitory concentration (IC50) values of QuCaNP-treated HT-29 cells were calculated as 11.2 µg/mL (24 h) and 8.2 µg/mL (48 h). QuCaNP treatment increased mRNA levels of caspase-3 (2.38 fold) and caspase-9 (2-fold) and expressions of key proteins in the intrinsic apoptosis pathway in HT-29 cells.Overall, our results demonstrated QuCaNPs exhibits improved anti-cancer activity on HT-29 cells.
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