Volume 20, Issue 12 pp. 1573-1578
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Tetra-substituted Amino Aluminum Phthalocyanine as a New Red-region Fluorescent Substrate for Horseradish Peroxidase Based Enzyme-linked Immunosorbent Assay

Huang-Haoa Yang

Huang-Haoa Yang

Key Laboratory of Analytical Science of Ministry of Education, Department of Chemistry, Xiamen University, Xiamen, Fujian 361005, China

Department of Material Science, Xiamen University, Xiamen, Fujian 361005, China

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Dong-Hui Li

Dong-Hui Li

Cancer Research Center, Xiamen University, Xiamen, Fujian 361005, China

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Xiao-Lan Chen

Xiao-Lan Chen

Key Laboratory of Analytical Science of Ministry of Education, Department of Chemistry, Xiamen University, Xiamen, Fujian 361005, China

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Hui-Ying Qu

Hui-Ying Qu

Key Laboratory of Analytical Science of Ministry of Education, Department of Chemistry, Xiamen University, Xiamen, Fujian 361005, China

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Ma-Tai Ding

Ma-Tai Ding

Department of Material Science, Xiamen University, Xiamen, Fujian 361005, China

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Jin-Gou Xu

Jin-Gou Xu

Key Laboratory of Analytical Science of Ministry of Education, Department of Chemistry, Xiamen University, Xiamen, Fujian 361005, China

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First published: 26 August 2010
Citations: 2

Abstract

The use of tetra-substituted ammo aluminum phthalocyanine (TAAIPc) as a new red-region fluorescent substrate for horseradish peroxidase (HRP)-based enzyme-linked immunosorbent assay was investigated. TAAIPc displayed an excitation maximum at 610 nm and emission maximum at 678 nm in a strong acidic medium. In the presence of HRP, trace amounts of H2O2 could rapidly and significantly react with TAAIPc, thus quenching the fluorescence of TAAIPc. The Michaelis-Menten parameters Km and Vmax were measured to be 2.82 × 10−6 mol/L−1 and 6.0 × 10−9 mol·L−1, respectively. In this paper, TAAIPc was used in an HRP-based enzyme-linked immunosorbent assay (ELISA) of α-fetoprotein (AFP) in human serum with satisfactory results. AFP could be determined in the concentration range of 0.5–200 ng/mL with a detection limit of 0.2 ng/mL, which was close to that of radioimmunoassay. The advantage of proposed method was strongly minimizing the interference resulting from background fluorescence or scattering light and had a high analytical sensitivity.

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