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首页> 外文期刊>Talanta: The International Journal of Pure and Applied Analytical Chemistry >Determination of noradrenaline and dopamine in pharmaceutical injection samples by inhibition flow injection electrochemiluminescence of ruthenium complexes
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Determination of noradrenaline and dopamine in pharmaceutical injection samples by inhibition flow injection electrochemiluminescence of ruthenium complexes

机译:阻抑流动注射钌配合物电化学发光法测定药物注射样品中的去甲肾上腺素和多巴胺。

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Two maximal potential-resolved flow injection-electrochemiluminescent (FI-ECL) peaks were observed for Ru(bpy)_3~(2+)/TPrA system at 0.90 and 1.05 V, and for Ru(phen)_3~(2+)/TPrA at 1.01 and 1.25 V (vs. Ag/AgCl) in pH 8.0 phosphate buffer solutions. Sensitive ECL inhibition effects were observed in the presence of noradrenaline and dopamine for both of these systems. Therefore, an FI-ECL inhibition method for determination of noradrenaline and dopamine has been developed. Under optimal conditions, linear responses between logarithm of ECL intensity changes and logarithm of sample concentration were found for noradrenaline in the linear range (LR) of 4 * 10~(-8)-1 * 10~(-5) mol l~(-1) with theoretical detection limit (DL) of 2.5 * 10~(-8) mol l~(-1) for Ru (bpy)_3~(2+)/TPrA system, and in LR of 2 * 10~(-8)-2 * 10~(-5) mol l~(-1) with DL of 7.1 * 10~(-9) mol l~(-1) for Ru(phen)_3~(2+)/TPrA system; and for dopamine in LR of 8 * 10~(-8)-2 * 10~(-5) mol l~(-1) with DL of 5.2 * 10~(-8) mol l~(-1) for Ru(bpy)_3~(2+)/TRrA system, in LR of 4 * 10~(-8)-2 * 10~(-5) mol l~(-1) with DL of 1.5 * 10~(-8) mol l~(-1) for Ru (phen)_3~(2+)/TRrA system. It was applied for determination of commercial pharmaceutical injection samples with satisfied results. The mechanism of the inhibition effects was proposed in the preliminary way.
机译:对于Ru(bpy)_3〜(2 +)/ TPrA系统在0.90和1.05 V以及Ru(phen)_3〜(2 +)/在pH 8.0磷酸盐缓冲溶液中的1.01和1.25 V(vs.Ag/AgCl)下的TPrA。在去甲肾上腺素和多巴胺的存在下,对于这两种系统均观察到了敏感的ECL抑制作用。因此,已经开发了用于测定去甲肾上腺素和多巴胺的FI-ECL抑制方法。在最佳条件下,去甲肾上腺素在4 * 10〜(-8)-1 * 10〜(-5)mol l〜()的线性范围内,ECL强度变化的对数与样品浓度的对数之间存在线性响应。 -1)对Ru(bpy)_3〜(2 +)/ TPrA系统的理论检出限(DL)为2.5 * 10〜(-8)mol l〜(-1),LR为2 * 10〜( -8)-2 * 10〜(-5)mol l〜(-1),对于Ru(phen)_3〜(2 +)/ TPrA的DL为7.1 * 10〜(-9)mol l〜(-1)系统;对于多巴胺,对于Ru的LR为8 * 10〜(-8)-2 * 10〜(-5)mol l〜(-1),而DL为5.2 * 10〜(-8)mol l〜(-1) (bpy)_3〜(2 +)/ TRrA系统,LR为4 * 10〜(-8)-2 * 10〜(-5)mol l〜(-1),DL为1.5 * 10〜(-8对于Ru(phen)_3〜(2 +)/ TRrA系统为mol l〜(-1)。应用于满意的商业药品注射样品的测定。初步提出了抑制作用的机理。

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