Trans-palladium complexes with 1-adamantanamine and various halide ions: Synthesis, characterization, DNA and protein binding and in vitro cytotoxicity
The result's identifiers
Result code in IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F60461373%3A22310%2F21%3A43922363" target="_blank" >RIV/60461373:22310/21:43922363 - isvavai.cz</a>
Alternative codes found
RIV/60461373:22330/21:43922363 RIV/60461373:22340/21:43922363
Result on the web
<a href="https://www.sciencedirect.com/science/article/pii/S027753872100440X" target="_blank" >https://www.sciencedirect.com/science/article/pii/S027753872100440X</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.1016/j.poly.2021.115458" target="_blank" >10.1016/j.poly.2021.115458</a>
Alternative languages
Result language
angličtina
Original language name
Trans-palladium complexes with 1-adamantanamine and various halide ions: Synthesis, characterization, DNA and protein binding and in vitro cytotoxicity
Original language description
Research into the antitumor effects of transition metals has been devoted to the decades since the discovery of the cytostatic properties of the platinum complex cisplatin, which despite numerous side effects, is still one of the most prescribed cytostatics. A promising way to develop a new similar complex is to select a suitable ligand. An interesting group of ligands is diamantanoid derivatives, which, due to their high lipophilicity and bulk, show promising pharmacological properties. With this in mind, we have prepared three trans-palladium(II) complexes with bulky 1-adamantanamine and different halide ligands (chlorine, bromine and iodine). The complexes (1-3) were analytically characterized to confirm their structures by FT-IR, 1H and 13C NMR, HR-MS and XRD techniques for the first time. The interaction of DNA with complexes 1-3 was investigated and the affinity to DNA was confirmed by a DNA binding study, gel electrophoresis and electronic circular dichroism. A protein binding study was carried out and a weak interaction with proteins was found. Finally, the anticancer abilities of palladium complexes 1-3, compared to another cytostatic drug oxaliplatin, were tested and confirmed on the cancer cell lines RAW, HeLa, HOC and HL-60, and the healthy cell line MRC-5.
Czech name
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Czech description
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Classification
Type
J<sub>imp</sub> - Article in a specialist periodical, which is included in the Web of Science database
CEP classification
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OECD FORD branch
30502 - Other medical science
Result continuities
Project
<a href="/en/project/GA21-11688S" target="_blank" >GA21-11688S: Core-shell nanoparticles for targeted X-ray-induced photodynamic therapy</a><br>
Continuities
P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)
Others
Publication year
2021
Confidentiality
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Data specific for result type
Name of the periodical
Polyhedron
ISSN
0277-5387
e-ISSN
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Volume of the periodical
209
Issue of the periodical within the volume
November
Country of publishing house
GB - UNITED KINGDOM
Number of pages
9
Pages from-to
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UT code for WoS article
000697059300005
EID of the result in the Scopus database
2-s2.0-85115603345