DocumentCode :
1665467
Title :
The research of RGD-conjugated PLA-PLL nanoparticles carriers on targeted delivery to tumor
Author :
Liu, Peifeng ; Qi, Xuelian ; Sun, Ying ; Wang, Hongzhi ; Li, Yaogang ; Duan, Yourong
Author_Institution :
State Key Lab. for Modification of Chem. Fibers & Polymer Mater., Donghua Univ., Shanghai, China
fYear :
2010
Firstpage :
1377
Lastpage :
1378
Abstract :
The development of a more precise targeted delivery system is critical for the advancement of cancer chemotherapy. In this study, we evaluated the effects of RGD-conjugated poly (lactic acid-co-lysine)-(Arginine-Glycine-Aspartic) nanoparticles (PLA -PLL-RGD NPs) on targeted drug delivery for BACP-37 breast cancer. PLA-PLL-RGD NPs were prepared by using the emulsion method. A subsequent MTT assay indicated that the NPs were non-toxic. In vitro, the results of Confocal Laser Scanning Microscopy (CLSM) and Flow cytometry analyses indicated that the PLA-PLL-RGD NPs can bind more significantly to human umbilical vein endothelial cells (HUVECs) compared with PLA-PLL NPs. In vivo, the results of targeted imaging showed that PLA-PLL-RGD can significantly target to BACP-37 breast cancer. These results showed that PLA-PLL-RGD NPs have the potential to be used as targeted delivery carrier.
Keywords :
biochemistry; biological organs; biomedical optical imaging; blood vessels; cancer; cellular biophysics; drugs; emulsions; nanobiotechnology; nanoparticles; optical microscopy; organic compounds; patient treatment; tumours; BACP-37 breast cancer; RGD-conjugated nanoparticles; cancer chemotherapy; confocal laser scanning microscopy; drug delivery; emulsion; flow cytometry; human umbilical vein endothelial cells; poly(lactic acid-co-lysine)-(arginine-glycine-aspartic) nanoparticles; tumor; Breast cancer; Breast neoplasms; Chemical lasers; Humans; In vitro; Microscopy; Nanoparticles; Programmable logic arrays; Targeted drug delivery; Veins;
fLanguage :
English
Publisher :
ieee
Conference_Titel :
Nanoelectronics Conference (INEC), 2010 3rd International
Conference_Location :
Hong Kong
Print_ISBN :
978-1-4244-3543-2
Electronic_ISBN :
978-1-4244-3544-9
Type :
conf
DOI :
10.1109/INEC.2010.5424844
Filename :
5424844
Link To Document :
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