KIZEK, René, Jan VACEK, Libuše TRNKOV, Bořivoj KLEJDUS a Ladislav HAVEL. Využití katalytických reakcí na rtuťových elektrodách pro elektrochemické stanovení metalothioneinu. Chemick Listy. Praha: esk spolenost chemick, 2004, roč. 98, č. 2, s. 166 - 173. ISSN 0009-2770.
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Základní údaje
Originální název Využití katalytických reakcí na rtuťových elektrodách pro elektrochemické stanovení metalothioneinu
Název česky Využití katalytických reakcí na rtuťových elektrodách pro elektrochemické stanovení metalothioneinu
Název anglicky Application of catalytic reactions on a mercury electrode for electrochemical detection of metallothioneins
Autoři KIZEK, René (203 Česká republika), Jan VACEK (203 Česká republika), Libuše TRNKOV (203 Česká republika, garant), Bořivoj KLEJDUS (203 Česká republika) a Ladislav HAVEL (203 Česká republika).
Vydání Chemick Listy, Praha, esk spolenost chemick, 2004, 0009-2770.
Další údaje
Originální jazyk čeština
Typ výsledku Článek v odborném periodiku
Obor 10405 Electrochemistry
Stát vydavatele Česká republika
Utajení není předmětem státního či obchodního tajemství
Impakt faktor Impact factor: 0.348
Kód RIV RIV/00216224:14310/04:00011232
Organizační jednotka Přírodovědecká fakulta
UT WoS 000221682700003
Klíčová slova anglicky metallothionein; electrochemical analysis; catalytic reactions; peak H; Brdicka reaction
Štítky Brdicka reaction, catalytic reactions, electrochemical analysis, metallothionein, Peak H
Změnil Změnila: prof. RNDr. Libuše Trnková, CSc., učo 1027. Změněno: 15. 2. 2005 20:16.
Anotace
Metallothioneins (MTs) belong to a group of oligo- and polypeptides which play an important role in the metabolism of metals in animals, plants and microorganisms. The metabolic function of MTs consists not only in detoxication of an organism but also in the homeostasis of essential metals. This paper reports a novel approach to electroanalysis of MTs. The electrochemical determination of MTs is based on catalytic processes which proceed at very negative potentials on mercury electrodes (from -1.7 V to -1.9 V vs. Ag/AgCl/KCl). These processes accompanied by evolution of hydrogen from supporting electrolyte components, include the Heyrovsky presodium wave and/or Brdicka reaction. It was found that SH groups present in MTs are responsible for catalytic processes. The catalytic signal of a MT at nanomolar concentrations can be detected on mercury electrodes using potentiostatic electrochemical methods. The highest sensitivity in the determination of MTs was observed with a galvanostatic method such as derivative potentiometric stripping analysis (CPSA) which produces the peak H. The coupling of CPSA with the adsorptive transfer stripping technique (AdTS) allows the determination of MTs at a femtomole level in a low amount of sample (5 ěl). Our recent results obtained by AdTS + CPSA show that detection limits for particular MTs can be improved by adding [Co(NH3)6] Cl3 to the sample analyzed. This is probably due to the formation of a complex between [Co(NH3)6] Cl3 and MT. We think that the peak H can be used in physiological studies of metal metabolism.
Anotace anglicky
Metallothioneins (MTs) belong to a group of oligo- and polypeptides which play an important role in the metabolism of metals in animals, plants and microorganisms. The metabolic function of MTs consists not only in detoxication of an organism but also in the homeostasis of essential metals. This paper reports a novel approach to electroanalysis of MTs. The electrochemical determination of MTs is based on catalytic processes which proceed at very negative potentials on mercury electrodes (from -1.7 V to -1.9 V vs. Ag/AgCl/KCl). These processes accompanied by evolution of hydrogen from supporting electrolyte components, include the Heyrovsky presodium wave and/or Brdicka reaction. It was found that SH groups present in MTs are responsible for catalytic processes. The catalytic signal of a MT at nanomolar concentrations can be detected on mercury electrodes using potentiostatic electrochemical methods. The highest sensitivity in the determination of MTs was observed with a galvanostatic method such as derivative potentiometric stripping analysis (CPSA) which produces the peak H. The coupling of CPSA with the adsorptive transfer stripping technique (AdTS) allows the determination of MTs at a femtomole level in a low amount of sample (5 ěl). Our recent results obtained by AdTS + CPSA show that detection limits for particular MTs can be improved by adding [Co(NH3)6] Cl3 to the sample analyzed. This is probably due to the formation of a complex between [Co(NH3)6] Cl3 and MT. We think that the peak H can be used in physiological studies of metal metabolism.
Návaznosti
GA203/02/0422, projekt VaVNázev: Nové směry v elektrochemii nukleových kyselin a jejich aplikace v chemii životního prostředí
Investor: Grantová agentura ČR, Nové směry v elektrochemii nukleových kyselin a jejich aplikace v chemii životního prostředí
IAA1163201, projekt VaVNázev: Využití adsorptivní přenosové a eliminační techniky pro elektrochemickou analýzu oligonukleotidů a nukleových kyselin
Investor: Akademie věd ČR, Využití adsorptivní přenosové a eliminační techniky pro elektrochemickou analýzu oligonukleotidů a nukleových kyselin
VytisknoutZobrazeno: 24. 7. 2024 12:22