TY - JOUR
T1 - Synthesis, characterization and in vitro cytotoxicity of platinum(II) complexes of selenones [Pt(selenone)2Cl2]
AU - Altoum, Ali Osman S.
AU - Alhoshani, Ali
AU - Alhosaini, Khalid
AU - Altaf, Muhammad
AU - Ahmad, Saeed
AU - Popoola, Saheed A.
AU - Al-Saadi, Abdulaziz A.
AU - Sulaiman, Adam A.
AU - Isab, Anvarhusein A.
N1 - Publisher Copyright:
© 2017 Informa UK Limited, trading as Taylor & Francis Group.
PY - 2017/3/19
Y1 - 2017/3/19
N2 - Platinum(II) complexes with various selenones (L) having the general formula [PtL2Cl2] were prepared and characterized by elemental analysis and, IR and NMR (1H, 13C, and 77Se) spectroscopies. A decrease in the IR frequency of the >C=Se mode and an upfield shift in 13C NMR for the >C=Se resonance of selenones are consistent with their selenium coordination to platinum(II). The NMR data show that the complexes are stable in solution and do not undergo equilibration at 297 K. The geometrical structures of the complexes were predicted theoretically (with DFT method) using Gaussian09 program. DFT calculations predicted that the trans configurations were up to 1.7 kcal/mol more stable than the cis forms in gas phase, while in solution form the cis isomers were predicted to be more stable. The UV–vis spectra of the two complexes, 6 and 7 were also recorded at room temperature for 24 h and it was observed that the complexes were stable and did not undergo decomposition. The in vitro antitumor properties of the complexes as well as of cisplatin were evaluated on two human cancer cell lines, HeLa (cervical cancer cells) and MCF7 (breast cancer cells) using MTT assay. The results indicated that the prepared complexes exerted significant inhibition on the selected cancer cells.
AB - Platinum(II) complexes with various selenones (L) having the general formula [PtL2Cl2] were prepared and characterized by elemental analysis and, IR and NMR (1H, 13C, and 77Se) spectroscopies. A decrease in the IR frequency of the >C=Se mode and an upfield shift in 13C NMR for the >C=Se resonance of selenones are consistent with their selenium coordination to platinum(II). The NMR data show that the complexes are stable in solution and do not undergo equilibration at 297 K. The geometrical structures of the complexes were predicted theoretically (with DFT method) using Gaussian09 program. DFT calculations predicted that the trans configurations were up to 1.7 kcal/mol more stable than the cis forms in gas phase, while in solution form the cis isomers were predicted to be more stable. The UV–vis spectra of the two complexes, 6 and 7 were also recorded at room temperature for 24 h and it was observed that the complexes were stable and did not undergo decomposition. The in vitro antitumor properties of the complexes as well as of cisplatin were evaluated on two human cancer cell lines, HeLa (cervical cancer cells) and MCF7 (breast cancer cells) using MTT assay. The results indicated that the prepared complexes exerted significant inhibition on the selected cancer cells.
KW - anticancer activity
KW - cisplatin
KW - Platinum(II) complexes
KW - selenones
UR - https://www.scopus.com/pages/publications/85012295425
U2 - 10.1080/00958972.2017.1287355
DO - 10.1080/00958972.2017.1287355
M3 - Article
AN - SCOPUS:85012295425
SN - 0095-8972
VL - 70
SP - 1020
EP - 1031
JO - Journal of Coordination Chemistry
JF - Journal of Coordination Chemistry
IS - 6
ER -