TY  - CONF
AU  - Čolović, Mirjana
AU  - Gajski, Goran
AU  - Gerić, M.
AU  - Ma, T.
AU  - Ma, X.
AU  - Kortz, Ulrich
AU  - Krstić, Danijela
PY  - 2021
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/12923
AB  - Polyoxopalladates(II) (POPs) are discrete, anionic palladium(II)- oxo nanoclusters that possess features of both conventional polyoxometalates (POMs) and palladium(II), which were shown to exhibit promising antitumor properties. In this study, in vitro cyto- and genotoxicity evaluation was performed on normal non-target human blood cells using two isostructural POPs with tetravalent metal ions (SnIV, PbIV) encapsulated in the cuboid Pd12-oxo host, Na12[SnO8Pd12(PO4)8]·43H2O (SnPd12) and Na12[PbO8Pd12(PO4)8]·38H2O (PbPd12), with confirmed in vitro antileukemic actions against HL-60 cell line. For this purpose, whole blood samples were exposed to the POPs, at concentrations of ≈ IC50 (24 h) values, resulting in cytotoxicity in HL-60 cells for 24 h at 37 °C. The cytotoxicity studies were performed on human peripheral blood mononuclear cells which were stained with acridine orange and ethidium bromide, and then viewed under a fluorescence microscope. The genotoxicity was tested in whole blood by the alkaline comet assay (microgel electrophoresis). The results of the cytotoxicity evaluation and the comet assay demonstrated that none of the tested POPs, within the investigated concentration range 12.5 – 50 µM, resulted in a statistically significant modulation of blood cell viability as well as DNA damage, expressed as % of tail DNA (relative increase of tail DNA), compared to the untreated controls. Therefore, the promising antileukemic drug candidates, SnPd12 and PbPd12, can be considered as selective and safe from a cytogenotoxicity point of view.
PB  - Belgrade : Society of Physical Chemists of Serbia
C3  - PHYSICAL CHEMISTRY 2021 : 15th international conference on fundamental and applied aspects of physical chemistry : Proceedings
T1  - Cytogenotoxicity assessment of polyoxopalladates(II) as promising antileukemic drug candidates
VL  - 2
SP  - 414
EP  - 417
UR  - https://hdl.handle.net/21.15107/rcub_vinar_12923
ER  - 

@conference{
author = "Čolović, Mirjana and Gajski, Goran and Gerić, M. and Ma, T. and Ma, X. and Kortz, Ulrich and Krstić, Danijela",
year = "2021",
abstract = "Polyoxopalladates(II) (POPs) are discrete, anionic palladium(II)- oxo nanoclusters that possess features of both conventional polyoxometalates (POMs) and palladium(II), which were shown to exhibit promising antitumor properties. In this study, in vitro cyto- and genotoxicity evaluation was performed on normal non-target human blood cells using two isostructural POPs with tetravalent metal ions (SnIV, PbIV) encapsulated in the cuboid Pd12-oxo host, Na12[SnO8Pd12(PO4)8]·43H2O (SnPd12) and Na12[PbO8Pd12(PO4)8]·38H2O (PbPd12), with confirmed in vitro antileukemic actions against HL-60 cell line. For this purpose, whole blood samples were exposed to the POPs, at concentrations of ≈ IC50 (24 h) values, resulting in cytotoxicity in HL-60 cells for 24 h at 37 °C. The cytotoxicity studies were performed on human peripheral blood mononuclear cells which were stained with acridine orange and ethidium bromide, and then viewed under a fluorescence microscope. The genotoxicity was tested in whole blood by the alkaline comet assay (microgel electrophoresis). The results of the cytotoxicity evaluation and the comet assay demonstrated that none of the tested POPs, within the investigated concentration range 12.5 – 50 µM, resulted in a statistically significant modulation of blood cell viability as well as DNA damage, expressed as % of tail DNA (relative increase of tail DNA), compared to the untreated controls. Therefore, the promising antileukemic drug candidates, SnPd12 and PbPd12, can be considered as selective and safe from a cytogenotoxicity point of view.",
publisher = "Belgrade : Society of Physical Chemists of Serbia",
journal = "PHYSICAL CHEMISTRY 2021 : 15th international conference on fundamental and applied aspects of physical chemistry : Proceedings",
title = "Cytogenotoxicity assessment of polyoxopalladates(II) as promising antileukemic drug candidates",
volume = "2",
pages = "414-417",
url = "https://hdl.handle.net/21.15107/rcub_vinar_12923"
}

Čolović, M., Gajski, G., Gerić, M., Ma, T., Ma, X., Kortz, U.,& Krstić, D.. (2021). Cytogenotoxicity assessment of polyoxopalladates(II) as promising antileukemic drug candidates. in PHYSICAL CHEMISTRY 2021 : 15th international conference on fundamental and applied aspects of physical chemistry : Proceedings
Belgrade : Society of Physical Chemists of Serbia., 2, 414-417.
https://hdl.handle.net/21.15107/rcub_vinar_12923

Čolović M, Gajski G, Gerić M, Ma T, Ma X, Kortz U, Krstić D. Cytogenotoxicity assessment of polyoxopalladates(II) as promising antileukemic drug candidates. in PHYSICAL CHEMISTRY 2021 : 15th international conference on fundamental and applied aspects of physical chemistry : Proceedings. 2021;2:414-417.
https://hdl.handle.net/21.15107/rcub_vinar_12923 .

Čolović, Mirjana, Gajski, Goran, Gerić, M., Ma, T., Ma, X., Kortz, Ulrich, Krstić, Danijela, "Cytogenotoxicity assessment of polyoxopalladates(II) as promising antileukemic drug candidates" in PHYSICAL CHEMISTRY 2021 : 15th international conference on fundamental and applied aspects of physical chemistry : Proceedings, 2 (2021):414-417,
https://hdl.handle.net/21.15107/rcub_vinar_12923 .

TY  - CONF
AU  - Čolović, Mirjana B.
AU  - Bondžić, Aleksandra M.
AU  - Kortz, Ulrich
AU  - Vasić, Vesna M.
AU  - Krstić, Danijela Z.
PY  - 2016
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/9208
AB  - The in  vitroinfluence  of  five  polyoxotungstates  containing  various  central atoms    on    acetylcholinesterase    (AChE)    activity    was    investigated. K6[PV3W9O40] × 3H2O, K6H2[TiW11CoO40] × 13H2O, (NH4)14[NaP5W30O110]    ×    31H2O,    K7[SiV3W9O40]    ×    10H2O,    and K7[Ti2PW10O40]   induced   the   enzyme   inhibition   in   a   concentration-dependent  manner.  Inhibitory  power  of  the  investigated  compounds  was evaluated  using  IC50values.  K7[SiV3W9O40]  ×  10H2O  affected  AChE activity with lowest potency (IC50 = 4.80 × 10-4mol/L). K6H2[TiW11CoO40] ×  13H2O  and  K7[Ti2PW10O40]  exhibited  high  affinity  toward  the  enzyme, inducing half-maximuminhibition at micromolar concentrations (1.14 × 10-6and 1.04 × 10-6mol/L, respectively), while the same effect was achieved in the  presence  of  about  fifty  times  higher  concentration  of  K6[PV3W9O40]  × 3H2O.  Finally,  (NH4)14[NaP5W30O110]  ×  31H2O  was  foundas  the  most potent   inhibitor   of   AChE   activity   (IC50 = 6.36   ×   10-7mol/L),   and consequently the most promising candidate for the treatment of neurological diseases associated with acetylcholine leakage.
PB  - Belgrade : Society of Physical Chemists of Serbia
C3  - PHYSICAL CHEMISTRY 2016 : 13th international conference on fundamental and applied aspects of physical chemistry : Proceedings
T1  - Modulation of acetylcholinesterase activity induced by polyoxotungstates
VL  - 1
SP  - 451
EP  - 454
UR  - https://hdl.handle.net/21.15107/rcub_vinar_9208
ER  - 

@conference{
author = "Čolović, Mirjana B. and Bondžić, Aleksandra M. and Kortz, Ulrich and Vasić, Vesna M. and Krstić, Danijela Z.",
year = "2016",
abstract = "The in  vitroinfluence  of  five  polyoxotungstates  containing  various  central atoms    on    acetylcholinesterase    (AChE)    activity    was    investigated. K6[PV3W9O40] × 3H2O, K6H2[TiW11CoO40] × 13H2O, (NH4)14[NaP5W30O110]    ×    31H2O,    K7[SiV3W9O40]    ×    10H2O,    and K7[Ti2PW10O40]   induced   the   enzyme   inhibition   in   a   concentration-dependent  manner.  Inhibitory  power  of  the  investigated  compounds  was evaluated  using  IC50values.  K7[SiV3W9O40]  ×  10H2O  affected  AChE activity with lowest potency (IC50 = 4.80 × 10-4mol/L). K6H2[TiW11CoO40] ×  13H2O  and  K7[Ti2PW10O40]  exhibited  high  affinity  toward  the  enzyme, inducing half-maximuminhibition at micromolar concentrations (1.14 × 10-6and 1.04 × 10-6mol/L, respectively), while the same effect was achieved in the  presence  of  about  fifty  times  higher  concentration  of  K6[PV3W9O40]  × 3H2O.  Finally,  (NH4)14[NaP5W30O110]  ×  31H2O  was  foundas  the  most potent   inhibitor   of   AChE   activity   (IC50 = 6.36   ×   10-7mol/L),   and consequently the most promising candidate for the treatment of neurological diseases associated with acetylcholine leakage.",
publisher = "Belgrade : Society of Physical Chemists of Serbia",
journal = "PHYSICAL CHEMISTRY 2016 : 13th international conference on fundamental and applied aspects of physical chemistry : Proceedings",
title = "Modulation of acetylcholinesterase activity induced by polyoxotungstates",
volume = "1",
pages = "451-454",
url = "https://hdl.handle.net/21.15107/rcub_vinar_9208"
}

Čolović, M. B., Bondžić, A. M., Kortz, U., Vasić, V. M.,& Krstić, D. Z.. (2016). Modulation of acetylcholinesterase activity induced by polyoxotungstates. in PHYSICAL CHEMISTRY 2016 : 13th international conference on fundamental and applied aspects of physical chemistry : Proceedings
Belgrade : Society of Physical Chemists of Serbia., 1, 451-454.
https://hdl.handle.net/21.15107/rcub_vinar_9208

Čolović MB, Bondžić AM, Kortz U, Vasić VM, Krstić DZ. Modulation of acetylcholinesterase activity induced by polyoxotungstates. in PHYSICAL CHEMISTRY 2016 : 13th international conference on fundamental and applied aspects of physical chemistry : Proceedings. 2016;1:451-454.
https://hdl.handle.net/21.15107/rcub_vinar_9208 .

Čolović, Mirjana B., Bondžić, Aleksandra M., Kortz, Ulrich, Vasić, Vesna M., Krstić, Danijela Z., "Modulation of acetylcholinesterase activity induced by polyoxotungstates" in PHYSICAL CHEMISTRY 2016 : 13th international conference on fundamental and applied aspects of physical chemistry : Proceedings, 1 (2016):451-454,
https://hdl.handle.net/21.15107/rcub_vinar_9208 .