铁(III)-酞菁配合物的化学发光反应及其在酪氨酸FIA中的应用

T. Ohtomo, Y. Takagai, O. Ohno, S. Igarashi
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引用次数: 0

摘要

研究了金属-酞菁配合物的化学发光特性,建立了l -酪氨酸化学发光检测-流动注射分析(FIA)的分析应用。采用Cu、Fe、Ni、Co、Mg、Pd、Pt和Zn等8种金属-酞菁配合物,研究了铁(III) -酞菁四磺酸(Fe - pts)的CL反应。将Fe-PTS水溶液注入过氧化氢溶液后,立即出现CL信号。此外,还考察了外来物质对Fe-PTS CL系统的影响。铁-酞菁络合物CL强度的降低是由于加入l -酪氨酸等还原剂引起的。利用这种猝灭现象,建立了l -酪氨酸的CL - fia检测方法。在2.5 × 10−7 M ~ 7.5 × 10−6 M的浓度范围内得到校准曲线,采样率为150个样品h−1。在1.0 × 10−6 M条件下,相对标准偏差(RSD)为1.20% (n = 25),检出限(3σ)为8.54 × 10−8 M, EDTA能有效抑制金属离子的干扰。因此,用zn2 +可以抑制l -半胱氨酸的干扰。作为实际样品的应用,测定了补品中的l -酪氨酸。实验值与日本食品研究实验室氨基酸自动分析仪测得的值(1.0 × 10−6 M)基本一致。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Chemiluminescence Reaction of an Iron(III)-Phthalocyanine Complex and Its Application to FIA of L-Tyrosine
Chemiluminescence (CL) of a metal–phthalocyanine complex was studied, and an analytical application of CL detection-flow injection analysis (FIA) of L-tyrosine was developed. The CL reaction of iron (III)–phthalocyanine tetrasulfonic acid (Fe–PTS) was examined using eight metals (Cu, Fe, Ni, Co, Mg, Pd, Pt and Zn)–phthalocyanine complexes. The CL signal immediately appeared, when the Fe-PTS aqueous solution was injected into a hydrogen peroxide solution. Moreover, the influence of foreign substances on the CL system of Fe–PTS was examined. The decrease in the CL intensity of the iron–phthalocyanine complex was caused by adding a reducing agent such as L-tyrosine. The CL detection-FIA of trace amounts of L-tyrosine was then developed using this quenching phenomenon. The calibration curve was obtained in the concentration range 2.5 × 10 −7 M to 7.5 × 10 −6 M, and the sampling rate was 150 samples h −1 . Further, the relative standard deviation (RSD) was 1.20 % (n = 25) for 1.0 × 10 −6 M, and the detection limit (3σ) were 8.54 × 10 −8 M. The interference of metal ions was able to inhibit using EDTA. Therefore, the interference of L-cysteine was able to inhibit using Zn 2+ . As an application to a practical sample, L-tyrosine in a supplement was determined. The experimental value is almost the same as the tabulated one (1.0 × 10 −6 M) measured by amino acid autoanalyzer at the Japan Food Research Laboratories.
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