Determination of tetracaine hydrochloride by fluorescence quenching method with some aromatic amino acids as probes.

J Fluoresc

Education Ministry Key Laboratory on Luminescence and Real-Time Analysis, School of Chemistry and Chemical Engineering, Southwest University, Chongqing, 400715, People's Republic of China.

Published: January 2012

AI Article Synopsis

  • A new method using fluorescence quenching has been developed to measure the concentration of tetracaine hydrochloride (TA·HCl) using aromatic amino acids as probes.
  • In an acidic medium (pH 6.3), amino acids like tryptophan, tyrosine, and phenylalanine interact with TA·HCl, resulting in reduced fluorescence due to various molecular interactions.
  • The method demonstrates linear relationships between fluorescence intensity and TA·HCl concentration with detection limits of around 0.37 to 0.41 μg/mL, indicating good selectivity and effective detection arising from static quenching processes.

Article Abstract

A novel fluorescence quenching method for the determination of tetracaine hydrochloride (TA·HCl) concentration with some aromatic amino acids as fluorescence probe has been developed. In pH 6.3 acidic medium, tryptophane (Trp), tyrosine (Tyr) or phenylalanine (Phe) can react with tetracaine hydrochloride to form an ion-association complex by electrostatic attraction, aromatic stacking interaction and Van der Waals' force, which lead to fluorescence quenching of above amino acids. The maximum fluorescence excitation and emission wavelengths of them are located at 278, 274, 258 nm and 354, 306, 285 nm, respectively. The relative fluorescence intensity (F (0)/F) is proportional to the TA·HCl concentration in certain range. The linear ranges and detection limits are 1.2-5.0 μg/mL and 0.37 μg/mL for Tyr-TA·HCl system, 1.3-6.0 μg/mL and 0.38 μg/mL for Trp-TA·HCl system, and 1.4-6.0 μg/mL and 0.41 μg/mL for Phe-TA·HCl system. The optimum reaction conditions, influencing factors and the effect of coexisting substances are investigated. And the results show the method has a good selectivity. Judging from the effect of temperature, the Stern-Volmer plots and fluorescence lifetime determination, the quenching of fluorescence of amino acids by TA·HCl is a static quenching process.

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Source
http://dx.doi.org/10.1007/s10895-011-0938-8DOI Listing

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