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Determination of Total Chromium in Biological Samples by Automated Reagent Injection Chemiluminescence Analysis

机译:试剂自动进样化学发光分析法测定生物样品中总铬

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摘要

A sensitive method for the determination of total chromium in real samples by flow injection-chemiluminescence (FI-CL) analysis was proposed. It was found that the CL intensity from luminol-lysozyme reaction could be markedly quenched, and the decrease of CL intensity was linear with the logarithm of Cr(III) concentrations over the range of 5.0 to 4000 pg mL~(-1) with a detection limit of 2.0 pg mL~(-1) (3σ) and relative standard deviations (RSDs) of 3.0, 2.6, and 2.0% for 10, 100, and 1000 pg mL~(-1) Cr(III) (n = 7), respectively. At a flow rate of 2.0 mL min-1, the whole process including sampling and washing could be accomplished within 36 s. The proposed CL method was successfully applied to the determination of total chromium in pharmaceutical capsules, a dietary supplement, and spiked human serum samples, with recoveries from 92.2 to 108.4% and RSDs of less than 4.0%. Using the homemade FI-CL model, the binding constant (K = 4.38 × 106 L mol-1) and the binding sites (n ≈ 1) of Cr(III) to lysozyme were given.
机译:提出了一种通过流动注射化学发光(FI-CL)分析法测定实际样品中总铬的灵敏方法。结果表明,鲁米诺-溶菌酶反应产生的CL强度可以被明显淬灭,并且CL强度的下降与Cr(III)浓度在5.0至4000 pg mL〜(-1)范围内的对数呈线性关系。 10、100和1000 pg mL〜(-1)Cr(III)的检出限为2.0 pg mL〜(-1)(3σ),相对标准偏差(RSD)为3.0、2.6和2.0%(n = 7)。以2.0 mL min-1的流速,整个过程(包括采样和清洗)可在36 s内完成。所提出的CL方法已成功地用于测定药物胶囊,膳食补充剂和加标的人血清样品中的总铬,回收率从92.2%至108.4%,RSD小于4.0%。使用自制的FI-CL模型,给出了Cr(III)与溶菌酶的结合常数(K = 4.38×106 L mol-1)和结合位点(n≈1)。

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