2017
Platinum nanoparticles induce damage to DNA and inhibit DNA replication
NEJDL, Lukas, Jiri KUDR, Amitava MOULICK, Dagmar HEGEROVA, Branislav RUTTKAY-NEDECKY et. al.Základní údaje
Originální název
Platinum nanoparticles induce damage to DNA and inhibit DNA replication
Autoři
NEJDL, Lukas (203 Česká republika), Jiri KUDR (203 Česká republika), Amitava MOULICK (203 Česká republika), Dagmar HEGEROVA (203 Česká republika), Branislav RUTTKAY-NEDECKY (203 Česká republika), Jaromír GUMULEC (203 Česká republika, garant, domácí), Kristyna CIHALOVA (203 Česká republika), Kristyna SMERKOVA (203 Česká republika), Simona DOSTALOVA (203 Česká republika), Sona KRIZKOVA (203 Česká republika), Marie NOVOTNA (203 Česká republika), Pavel KOPEL (203 Česká republika) a Vojtech ADAM (203 Česká republika)
Vydání
Plos one, San Francisco, Public Library of Science, 2017, 1932-6203
Další údaje
Jazyk
angličtina
Typ výsledku
Článek v odborném periodiku
Obor
30105 Physiology
Stát vydavatele
Spojené státy
Utajení
není předmětem státního či obchodního tajemství
Impakt faktor
Impact factor: 2.766
Kód RIV
RIV/00216224:14110/17:00100237
Organizační jednotka
Lékařská fakulta
UT WoS
000405649600050
Klíčová slova anglicky
Platinum nanoparticles; DNA
Štítky
Příznaky
Mezinárodní význam, Recenzováno
Změněno: 8. 3. 2018 12:37, Soňa Böhmová
Anotace
V originále
Sparsely tested group of platinum nanoparticles (PtNPs) may have a comparable effect as complex platinum compounds. The aim of this study was to observe the effect of PtNPs in in vitro amplification of DNA fragment of phage., on the bacterial cultures (Staphylococcus aureus), human foreskin fibroblasts and erythrocytes. In vitro synthesized PtNPs were characterized by dynamic light scattering (PtNPs size range 4.8-11.7 nm), zeta potential measurements (-15 mV at pH 7.4), X-ray fluorescence, UV/vis spectrophotometry and atomic absorption spectrometry. The PtNPs inhibited the DNA replication and affected the secondary structure of DNA at higher concentrations, which was confirmed by polymerase chain reaction, DNA sequencing and DNA denaturation experiments. Further, cisplatin (CisPt), as traditional chemotherapy agent, was used in all parallel experiments. Moreover, the encapsulation of PtNPs in liposomes (LipoPtNPs) caused an approximately 2.4x higher of DNA damage in comparison with CisPt, LipoCisPt and PtNPs. The encapsulation of PtNPs in liposomes also increased their antibacterial, cytostatic and cytotoxic effect, which was determined by the method of growth curves on S. aureus and HFF cells. In addition, both the bare and encapsulated PtNPs caused lower oxidative stress (determined by GSH/GSSG ratio) in the human erythrocytes compared to the bare and encapsulated CisPt. CisPt was used in all parallel experiments as traditional chemotherapy agent.