Show simple item record

dc.creatorPantelić, Nebojša Đ.
dc.creatorZmejkovski, Bojana
dc.creatorKolundžija, Branka
dc.creatorCrnogorac, Marija Đorđić
dc.creatorVujić, Jelena M.
dc.creatorDojčinović, Biljana
dc.creatorTrifunović, Srećko R.
dc.creatorStanojković, Tatjana
dc.creatorSabo, Tibor
dc.creatorKaluđerović, Goran N.
dc.date.accessioned2019-06-03T08:10:12Z
dc.date.available2019-04-04
dc.date.issued2017
dc.identifier.issn0162-0134
dc.identifier.urihttp://cer.ihtm.bg.ac.rs/handle/123456789/2931
dc.description.abstractFour novel gold(III) complexes of general formulae [AuCl2{(S,S)-R(2)eddl}]PF6 (R(2)eddl = O,O'-dialkyl-(S,S)-ethylenediamine-N,N'-di-2-(4-methyl)pentanoate, R= n-Pr, n-Bu, n-Pe, i-Bu; 1-4, respectively), were synthesized and characterized by elemental analysis, UV/Vis, IR, and NMR spectroscopy, as well as high resolution mass spectrometry. Density functional theory calculations pointed out that (R,R)-N,N'-configuration diastereoisomers were energetically the most favorable. Duo to high cytotoxic activity complex 3 was chosen for stability study in DMSO, no decomposition occurs within 24 h, and for the reaction with ascorbic acid in which was reduced immediately. Additionally, 3 interacts with bovine serum albumin (BSA) as proven by UV/Vis spectroscopy. In vitro antitumor activity was determined against human cervix adenocarcinoma (HeLa), human myelogenous leukemia (K562), and human melanoma (Fem-x) cancer cell lines, as well as against non-cancerous human embryonic lung fibroblast cells MRC-5. The highest activity was observed against K562 cells (IC50: 5.04-6.51 mu M). Selectivity indices showed that these complexes are less toxic than cisplatin. 3 had a similar viability kinetics on HeLa cells as cisplatin. Drug accumulation studies in HeLa cells showed that the total gold uptake increased much faster than that of cisplatin pointing out that 3 more efficiently enters the cells than cisplatin. Furthermore, morphological and cell cycle analysis reveal that gold(III) complexes induced apoptosis in time- and dose-dependent manner.
dc.publisherElsevier Science Inc, New York
dc.relationinfo:eu-repo/grantAgreement/MESTD/Basic Research (BR or ON)/172035/RS//
dc.relationinfo:eu-repo/grantAgreement/MESTD/Basic Research (BR or ON)/172016/RS//
dc.relationinfo:eu-repo/grantAgreement/MESTD/Basic Research (BR or ON)/175011/RS//
dc.rightsembargoedAccess
dc.sourceJournal of Inorganic Biochemistry
dc.subjectApoptosis
dc.subjectBiological reactivity
dc.subjectGold(III) complexes
dc.subjectMetal uptake
dc.subjectR 2 edda-type ligands
dc.titleIn vitro antitumor activity, metal uptake and reactivity with ascorbic acid and BSA of some gold(III) complexes with N,N′-ethylenediamine bidentate ester ligands
dc.typearticle
dc.rights.licenseBY-NC-ND
dcterms.abstractЗмејковски, Бојана Б.; Колунджија, Бранка; Дојчиновић, Биљана; Пантелић, Небојша Ђ.; Црногорац, Марија Ђорђић; Вујић, Јелена М.; Трифуновић, Срећко Р.; Станојковић, Татјана; Сабо, Тибор; Калуђеровић, Горан Н.;
dc.citation.volume172
dc.citation.spage55
dc.citation.epage66
dc.citation.rankM22
dc.description.otherThis is the peer-reviewed version of the following article: Pantelić, N.; Zmejkovski, B. B.; Kolundžija, B.; Crnogorac, M. Đ.; Vujić, J. M.; Dojčinović, B.; Trifunović, S. R.; Stanojković, T. P.; Sabo, T. J.; Kaluđerović, G. N. In Vitro Antitumor Activity, Metal Uptake and Reactivity with Ascorbic Acid and BSA of Some Gold(III) Complexes with N,N′-Ethylenediamine Bidentate Ester Ligands. Journal of Inorganic Biochemistry 2017, 172, 55–66. [https://doi.org/10.1016/j.jinorgbio.2017.04.001]
dc.description.other[http://cer.ihtm.bg.ac.rs/handle/123456789/2248]
dc.identifier.pmid28433833
dc.identifier.doi10.1016/j.jinorgbio.2017.04.001
dc.identifier.fulltexthttp://cer.ihtm.bg.ac.rs/bitstream/id/7133/acc_jib_2017.pdf
dc.identifier.scopus2-s2.0-85017584556
dc.identifier.wos000404000300007
dc.type.versionacceptedVersion


Files in this item

Thumbnail

This item appears in the following Collection(s)

Show simple item record