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Microwave-Assisted Chitosan-Functionalized Graphene Oxide as Controlled Intracellular Drug Delivery Nanosystem for Synergistic Antitumour Activity.

Authors :
Shu, Mengjun
Gao, Feng
Zeng, Min
Yu, Chulang
Wang, Xue
Huang, Renhua
Yang, Jianhua
Su, Yanjie
Hu, Nantao
Zhou, Zhihua
Liu, Ke
Yang, Zhi
Tan, Hongtao
Xu, Lin
Source :
Nanoscale Research Letters; 4/30/2021, Vol. 16 Issue 1, p1-12, 12p
Publication Year :
2021

Abstract

To achieve better antitumour efficacy, it is urgent to improve anticancer drug delivery efficiency in targeting cancer cells. In this work, chitosan-functionalized graphene oxide (ChrGO) nanosheets were fabricated via microwave-assisted reduction, which were employed to the intracellular delivery nanosystem for anticancer drug agent in breast cancer cells. Drug loading and release research indicated that adriamycin can be efficiently loaded on and released from the ChrGO nanosheets. Less drug release during delivery and better biocompatibility of ChrGO/adriamycin significantly improve its safety and therapeutic efficacy in HER2-overexpressing BT-474 cells. Furthermore, ChrGO/adriamycin in combination with trastuzumab exhibited synergistic antitumour activity in BT-474 cells, which demonstrated superior therapeutic efficacy compared with each drug alone. Cells treated with trastuzumab (5 μg/mL) or equivalent ChrGO/adriamycin (5 μg/mL) each elicited 54.5% and 59.5% cell death, respectively, while the combination treatment with trastuzumab and ChrGO/adriamycin resulted in a dramatic 88.5% cell death. The dual-targeted therapy displayed higher apoptosis, indicating superior therapeutic efficacy due to the presence of different mechanisms of action. The combined treatment of ChrGO/adriamycin and trastuzumab in BT-474 cells induced cell cycle arrest and apoptosis, which ultimately led to the death of augmented cancer cells. This work has provided a facile microwave-assisted fabrication of ChrGO as a controlled and targeted intracellular drug delivery nanosystem, which is expected to be a novel promising therapy for treating HER2-overexpressing breast cancer cells. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
19317573
Volume :
16
Issue :
1
Database :
Complementary Index
Journal :
Nanoscale Research Letters
Publication Type :
Academic Journal
Accession number :
150088265
Full Text :
https://doi.org/10.1186/s11671-021-03525-y