首页> 外文期刊>Journal of trace elements in medicine and biology: Organ of the Society for Minerals and Trace Elements (GMS) >Chromium determination in osteoblast-like cell culture medium by catalytic cathodic stripping voltammetry with a mercury microelectrode.
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Chromium determination in osteoblast-like cell culture medium by catalytic cathodic stripping voltammetry with a mercury microelectrode.

机译:汞微电极催化阴极溶出伏安法测定成骨样细胞培养基中的铬。

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摘要

A catalytic cathodic stripping voltammetric procedure for the determination of total chromium in osteoblast-like cell culture medium using a mercury film microelectrode (MFM) was optimised. The method is based on the pre-concentration of the Cr(III)-diethylenetriaminepentaacetic acid (DTPA) complex by adsorption at the potential of-1.00 V (vs. Ag/AgC1) in the presence of 10 x 10(-3) mol/L DTPA, 0.70 mol/L sodium nitrate, 0.04 mol/L sodium acetate and 1.0 x 10(-3) mol/L potassium permanganate at pH 5.9-6.0. The limit of detection obtained for a 40 s collection time was 2.80 x 10(-10) mol/L of chromium. The results achieved by stripping voltammetry using the MFM were compared to those obtained by atomic absorption spectrometry (AAS) to ensure the reliability of the electrochemical method. This procedure proved to be an alternative to AAS and valuable in biocompatibility studies performed in vitro using osteoblast-like cells.
机译:优化了使用汞膜微电极(MFM)的催化阴极溶出伏安法测定成骨样细胞培养基中总铬的方法。该方法基于在10 x 10(-3)mol的存在下以-1.00 V(vs. Ag / AgC1)的电位吸附来预浓缩Cr(III)-二亚乙基三胺五乙酸(DTPA)络合物/ L DTPA,0.70 mol / L硝酸钠,0.04 mol / L乙酸钠和1.0 x 10(-3)mol / L高锰酸钾,pH 5.9-6.0。在40 s的收集时间内获得的检出限为2.80 x 10(-10)mol / L铬。将通过使用MFM的溶出伏安法获得的结果与通过原子吸收光谱法(AAS)获得的结果进行比较,以确保电化学方法的可靠性。该方法被证明是AAS的替代方法,并且在体外使用成骨细胞样细胞进行的生物相容性研究中很有价值。

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