期刊
INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES
卷 126, 期 -, 页码 633-640出版社
ELSEVIER SCIENCE BV
DOI: 10.1016/j.ijbiomac.2018.12.152
关键词
Curdlan; iRGD; siRNA; Receptor-mediated endocytosis; Cancer cells
资金
- National Natural Science Foundation of China [81560568,21875124]
Natural carbohydrate polymer-based nanoparticles have great biocompatibility that is required for the safe delivery of various drugs including nucleic acid therapeutics. Herein, we designed curdlan-based nanoparticles for cancer cell targeted delivery of short interfering RNA (siRNA). iRGD peptide conjugated 6-amino-6-deoxy curdlan specifically delivered siRNA to integrin expressing cancer cells. Incubation of cancer cells with free iRGD peptide competitively blocked cellular uptake of the iRGD functionalized curdlan nanoparticles. Chloroquine but not nystatin inhibited cellular uptake of iRGD functionalized curdlan nanoparticles, indicating that the iRGD peptide conjugated curdlan nanoparticles were internalized through the receptor (clathrin)-mediated endocytosis. Moreover, a disease related gene Plk1 was substantially knocked down by siRNA carried by 6AC-iRGD nanopartides in HepG2 cells. Our data suggested that iRGD functionalized curdlan may provide a biocompatible carrier for siRNA delivery. (C) 2018 Published by Elsevier B.V.
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