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Oxovanadium(IV) complexes of curcumin for cellular imaging and mitochondria targeted photocytotoxicity
被引:56
|作者:
Banik, Bhabatosh
[1
]
Somyajit, Kumar
[2
]
Nagaraju, Ganesh
[2
]
Chakravarty, Akhil R.
[1
]
机构:
[1] Indian Inst Sci, Dept Inorgan & Phys Chem, Bangalore 560012, Karnataka, India
[2] Indian Inst Sci, Dept Biochem, Bangalore 560012, Karnataka, India
关键词:
DNA CLEAVAGE;
ANTICANCER ACTIVITY;
BINDING;
CANCER;
LIGHT;
CYTOTOXICITY;
DEGRADATION;
IRRADIATION;
DELIVERY;
LIGANDS;
D O I:
10.1039/c4dt01487a
中图分类号:
O61 [无机化学];
学科分类号:
070301 ;
081704 ;
摘要:
Oxovanadium(IV) complexes [VO(R-tpy)(cur)](ClO4) (1, 2) of curcumin (Hcur) and terpyridine ligands (R-tpy) where R is phenyl (phtpy in 1) or p-triphenylphosphonium methylphenyl bromide (C6H4CH2PPh3Br) (TPP-phtpy in 2) were prepared and characterized and their DNA photocleavage activity, photocytotoxicity and cellular localization in cancer cells (HeLa and MCF-7) were studied. Acetylacetonate (acac) complexes [VO(R-tpy)(acac)](ClO4) of phtpy (3) and TPP-phtpy (4) were prepared and used as the control species. These complexes showed efficient cleavage of pUC19 DNA in visible light of 454 nm and near-IR light of 705 rim. Complexes 1 and 2 showed significant photocytotoxicity in visible light of 400-700 nm. FACS analysis showed sub-G1/G0 phase cell-cycle arrest in cancer cells when treated with 1 and 2 in visible light in comparison with the dark controls. Fluorescence microscopic studies revealed specific localization of the p-triphenylphosphonium complex 2 in the mitochondria of MCF-7 cancer cells whereas no such specificity was observed for complex 1.
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页码:13358 / 13369
页数:12
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