Synergistic effects of cisplatin chemotherapy and gold nanorod-mediated hyperthermia on ovarian cancer cells and tumors

被引:1
作者
Mehtala, Jonathan G. [1 ]
Torregrosa-Allen, Sandra [2 ]
Elzey, Bennett D. [3 ]
Jeon, Mansik [4 ]
Kim, Chulhong [4 ]
Wei, Alexander [1 ]
机构
[1] Purdue Univ, Dept Chem, W Lafayette, IN 47907 USA
[2] Mol Discovery & Evaluat Shared Resource, W Lafayette, IN 47907 USA
[3] Dept Comparat Pathobiol, W Lafayette, IN 47907 USA
[4] Pohang Univ Sci & Technol POSTECH, Dept Elect Engn & Creat IT Engn, Pohang 790784, South Korea
关键词
apoptosis; cisplatin; gold nanorods; hyperthermia; ovarian cancer; synergistic effects; CHEMO-PHOTOTHERMAL THERAPY; HOMOLOGOUS RECOMBINATION; CELLULAR UPTAKE; NUCLEAR-MATRIX; DNA-DAMAGE; NANOPARTICLES; TEMPERATURE; TOXICITY; GROWTH; CARCINOMA;
D O I
10.2217/NNM.13.209
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Aim: The synergistic effects of gold nanorod (GNR)-mediated mild hyperthermia (MHT; 42-43 degrees C) and cisplatin (CP) activity was evaluated against chemoresistant SKOV3 cells in vitro and with a tumor xenograft model. Materials & methods: In vitro studies were performed using CP at cytostatic concentrations (5 mu M) and polyethylene glycol-stabilized GNRs, using near-infrared laser excitation for MHT. Results: The amount of polyethylene glycol-GNRs used for environmental MHT was 1 mu g/ml, several times lower than the loadings used in tumor tissue ablation. GNR-mediated MHT increased CP-mediated cytotoxicity by 80%, relative to the projected additive effect, and flow cytometry ana-lysis suggested MHT also enhanced CP-induced apoptosis. In a pilot in vivo study, systemically administered polyethylene glycol-GNRs generated sufficient levels of MHT to enhance CP-induced reductions in tumor volume, despite their heterogeneous distribution in tumor tissue. Conclusion: These studies imply that effective chemotherapies can be developed in combination with low loadings of nanoparticles for localized MHT.
引用
收藏
页码:1939 / 1955
页数:17
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