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Cellular uptake mechanism and intracellular fate of hydrophobically modified pullulan nanoparticles
Jiang, Liqin ; Li, Xuemin ; Liu, Lingrong ; Zhang, Qiqing ; Zhang QQ(张其清)
刊名http://dx.doi.org/10.2147/IJN.S44342
2013
关键词ASSEMBLED HYDROGEL NANOPARTICLE ARTIFICIAL MOLECULAR CHAPERONE CHOLESTEROL-BEARING PULLULAN DRUG-DELIVERY SYSTEMS CHITOSAN NANOPARTICLES CONTROLLED ASSOCIATION ACETATE NANOPARTICLES CANCER-TREATMENT POLYSACCHARIDE PROTEIN
英文摘要Ministry of Education of The People's Republic of China [20101106110042]; The cellular uptake mechanism and intracellular fate of self-assembled nanoparticles (NPs) of cholesterol-modified pullulan (CHSP) by human hepatocellular carcinoma (HepG2) cells were investigated. Covalent conjugation with fluorescein isothiocyanate (FITC) yielded stably labeled CHSP (FITC-CHSP), which was successfully formulated into NPs (mean particle size 63.0 +/- 1.9 nm) by dialysis. A cytotoxicity assay clearly indicated that the CHSP NPs did not show significant toxicity in HepG2 cells. The effects of NP concentration, incubation time, and temperature on the cellular uptake of the NPs were systematically evaluated by fluorometry, and the results suggested that cellular uptake of the NPs was concentration-, time-, and temperature-dependent. In vitro experiments with endocytic inhibitors revealed that clathrin-mediated endocytosis and macropinocytosis were involved in the internalization of CHSP NPs. The intracellular trafficking study demonstrated that CHSP NPs were entrapped in the lysosomes at 1 hour after incubation; colocalization of NPs with either the Golgi apparatus or the endoplasmic reticula was not observed during the entire course of the study. These results suggested that the CHSP NPs may serve as a versatile carrier for intracellular delivery of therapeutic agents.
语种英语
出版者DOVE MEDICAL PRESS LTD
内容类型期刊论文
源URL[http://dspace.xmu.edu.cn/handle/2288/93444]  
专题医学院-已发表论文
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GB/T 7714
Jiang, Liqin,Li, Xuemin,Liu, Lingrong,et al. Cellular uptake mechanism and intracellular fate of hydrophobically modified pullulan nanoparticles[J]. http://dx.doi.org/10.2147/IJN.S44342,2013.
APA Jiang, Liqin,Li, Xuemin,Liu, Lingrong,Zhang, Qiqing,&张其清.(2013).Cellular uptake mechanism and intracellular fate of hydrophobically modified pullulan nanoparticles.http://dx.doi.org/10.2147/IJN.S44342.
MLA Jiang, Liqin,et al."Cellular uptake mechanism and intracellular fate of hydrophobically modified pullulan nanoparticles".http://dx.doi.org/10.2147/IJN.S44342 (2013).
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