特罗洛克
细胞凋亡
活力测定
MTT法
纳米载体
化学
纳米囊
膜联蛋白
脂质过氧化
材料科学
生物物理学
抗氧化剂
生物化学
纳米颗粒
生物
纳米技术
药物输送
有机化学
DPPH
作者
Lu Han,Li-Bo Du,Anil Kumar,Hong-Ying Jia,Xing‐Jie Liang,Qiu Tian,Guangjun Nie,Yang Liu
出处
期刊:Biomaterials
[Elsevier BV]
日期:2012-08-24
卷期号:33 (33): 8517-8528
被引量:50
标识
DOI:10.1016/j.biomaterials.2012.07.034
摘要
A nanocarrier, namely, hydroxylethyl-chitosan nanoparticles was developed in this research for delivering antioxidants with 6-hydroxy-2, 5, 7, 8-tetra-methylchromane-2-carboxylic acid (trolox) as a model antioxidant. The trolox-encapsulated chitosan nanoparticles (trolox-CS NPs) were prepared by modifying chitosan with epoxyethane, which self-assembled into NPs and entrapped trolox, and then characterized by their size, size distribution, morphology and in vitro trolox release profile. Intracellular trafficking of CS NPs was observed. The anti-oxidant effect and potential mechanism of trolox-CS NPs were subsequently investigated in RAW264.7 cells. The effects of trolox-CS NPs on RAW264.7 cells damaged by tert-butylhydroperoxide (t-BHP) were determined by MTT assay for cell viability, MDA assay for membrane lipid peroxidation, JC-1 probe and Annexin V-FITC/PI double staining for mitochondria membrane potential (MMP) and RAW264.7 apoptosis, respectively. The trolox-CS NPs significantly improved cell viability and reduced MDA content compared with those of cells treated with free trolox. The trolox-CS NPs treatment inhibited MMP collapse and RAW264.7 apoptosis more obviously than free trolox. Molecular basis of apoptosis studied by western blotting revealed that trolox-CS NPs may block mitochondria-mediated apoptosis pathway through up-regulation of Bcl-2 and down-regulation of Bax and inhibiting the activation of pro-caspase 3, PARP and Bid.
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