Giakisikli Georgia, Ayala Quezada Alejandro, Tanaka Junpei, Anthemidis Aristidis N, Murakami Hiroya, Teshima Norio, Sakai Tadao
Anal Sci. 2015;31(5):383-9. doi: 10.2116/analsci.31.383.
A fully automated sequential injection column preconcentration method for the on-line determination of trace vanadium, cadmium and lead in urine samples was successfully developed, utilizing electrothermal atomic absorption spectrometry (ETAAS). Polyamino-polycarboxylic acid chelating resin (Nobias chelate PA-1) packed into a handmade minicolumn was used as a sorbent material. Effective on-line retention of chelate complexes of analytes was achieved at pH 6.0, while the highest elution effectiveness was observed with 1.0 mol L(-1) HNO3 in the reverse phase. Several analytical parameters, like the sample acidity, concentration and volume of the eluent as well as the loading/elution flow rates, have been studied, regarding the efficiency of the method, providing appropriate conditions for the analysis of real samples. For a 4.5 mL sample volume, the sampling frequency was 27 h(-1). The detection limits were found to be 3.0, 0.06 and 2.0 ng L(-1) for V(V), Cd(II) and Pb(II), respectively, with the relative standard deviations ranging between 1.9 - 3.7%. The accuracy of the proposed method was evaluated by analyzing a certified reference material (Seronorm(TM) trace elements urine) and spiked urine samples.
利用电热原子吸收光谱法(ETAAS)成功开发了一种全自动顺序注射柱预富集方法,用于在线测定尿液样本中的痕量钒、镉和铅。将填充到自制微型柱中的聚氨基多羧酸螯合树脂(Nobias螯合PA-1)用作吸附材料。在pH 6.0时实现了分析物螯合物的有效在线保留,而在反相中用1.0 mol L(-1) HNO3观察到最高的洗脱效率。关于该方法的效率,研究了几个分析参数,如样品酸度、洗脱液浓度和体积以及进样/洗脱流速,为实际样品分析提供了合适的条件。对于4.5 mL的样品体积,进样频率为27 h(-1)。发现V(V)、Cd(II)和Pb(II)的检测限分别为3.0 ng L(-1)、0.06 ng L(-1)和2.0 ng L(-1),相对标准偏差在1.9% - 3.7%之间。通过分析有证标准物质(Seronorm(TM)微量元素尿液)和加标尿液样本评估了该方法的准确性。