کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
1215733 1494076 2014 6 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Simultaneous determination of primary and secondary phenethylamines in biological samples by high-performance liquid chromatographic method with fluorescence detection
ترجمه فارسی عنوان
تعیین همزمان فنیل اتیلامین های اولیه و ثانویه در نمونه های بیولوژیکی با روش کروماتوگرافی مایع با عملکرد بالا با تشخیص فلورسانس
موضوعات مرتبط
مهندسی و علوم پایه شیمی شیمی آنالیزی یا شیمی تجزیه
چکیده انگلیسی


• An HPLC-FD method is reported to determine phenethylamines using TMBB-Su as reagent.
• Both primary and secondary phenethylamines could be analyzed simultaneously.
• Other commonly existing amino acids have no interference with the detection.
• The sensitivity is higher than most of the reports without pretreatment or enrichment.
• BODIPY-based reagent was first applied to analyze compounds in a metabolic pathway.

Phenylalanine is an essential amino acid and its metabolites relate to various physiological and immune functions of living organisms. To monitor the alteration of concentration of primary and secondary phenethylamines including N-methyltyramine, octopamine, tyramine, tyrosine and phenylalanine in the metabolic pathway of phenylalanine, a sensitive and selective reversed-phase high-performance liquid chromatographic method has been developed in this study. The identification and quantification of phenethylamines were performed by fluorescent detection after pre-column derivatization with 1,3,5,7-tetramethyl-8-(N-hydroxysuccinimidyl butyric ester)difluoroboradiaza-s-indacene, an excellent fluorescent probe which could react with both primary and secondary amino groups simultaneously. The derivatization was carried out at 25 °C for 25 min, and the separation was performed on a C18 column within 20 min. The linear ranges were from 2.0 to 100 nM for phenylalanine and tyramine to 5.0 to 250 for tyrosine and octopamine, with the detection limits of 0.1 nM for octopamine, tyramine, tyrosine and phenylalanine and 0.2 nM for N-methyltyramine (signal-to-noise ratio = 3), which allowed for the sure determination of phenethylamines at trace levels in the real samples without complex pretreatment or enrichment during multitudinous samples analysis. The proposed method has been validated by the analysis of the five target compounds in biological samples with spiked recoveries of 96.4–104.4% and the relative standard deviation of 1.0 and 4.4%.

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Journal of Chromatography B - Volume 967, 15 September 2014, Pages 69–74
نویسندگان
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