J 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.