2012
DOI: 10.1007/s10800-012-0404-6
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Chromium–protein complexation studies by adsorptive cathodic stripping voltammetry and MALDI-TOF–MS

Abstract: A methodology using stripping voltammetry has been elaborated to enable sensitive and reliable protein-chromium complexation measurements. Disturbing effects caused by adsorption of proteins on the mercury electrode were addressed. At low concentrations of proteins (\60-85 nM), chromium-protein complexation measurements were possible. Chromium(VI) complexation was quantitatively determined using differently sized, charged, and structured proteins: serum albumin (human and bovine), lysozyme, and mucin. Generate… Show more

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Cited by 12 publications
(18 citation statements)
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“…Previously, a lower chromium complexation capacity was observed for LSZ compared with BSA at a given molar concentration [68]. However, at a given mass concentration, LSZ revealed a higher complexation capacity to chromium compared with BSA [68]. In this study, a mass concentration of 2.2 g/L LSZ induced no significant enhancement of released metals compared with PBS for 316L (Fig.…”
Section: Resultssupporting
confidence: 41%
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“…Previously, a lower chromium complexation capacity was observed for LSZ compared with BSA at a given molar concentration [68]. However, at a given mass concentration, LSZ revealed a higher complexation capacity to chromium compared with BSA [68]. In this study, a mass concentration of 2.2 g/L LSZ induced no significant enhancement of released metals compared with PBS for 316L (Fig.…”
Section: Resultssupporting
confidence: 41%
“…4. Previously, a lower chromium complexation capacity was observed for LSZ compared with BSA at a given molar concentration [68]. However, at a given mass concentration, LSZ revealed a higher complexation capacity to chromium compared with BSA [68].…”
Section: Resultsmentioning
confidence: 96%
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“…The determination limit of the diluted samples in this study was 0.4 µg L −1 Cr(VI). Analytical details are given elsewhere . The exposure conditions (phosphate buffer, pH 7.4, closed vessels with relatively low amounts of dissolved oxygen) are optimal to avoid any transformation of Cr(III) to Cr(VI) and vice versa .…”
Section: Methodsmentioning
confidence: 99%
“…A Metrohm 797 VA Computrace instrument with a hanging mercury drop working electrode, a Ag/AgCl (saturated KCl) reference electrode, and a platinum auxiliary electrode were used for measurement of samples (2 mL) in the supporting electrolyte (2.5 mL: 0.2 M sodium acetate, 0.05 M diethylenetriaminepentaacetate (DTPA), 2.5 M sodium nitrate) diluted by ultrapure water (8 mL, 18.2 MXcm) to 10.5 mL solution and adjusted to a pH of 6.2 ± 0.1 with 30% ultrapure NaOH. The detailed procedure is described in (Hedberg et al, 2012a).…”
Section: Chromium Speciationmentioning
confidence: 99%