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用于营养补充剂中碱性氨基酸可持续且高速分析的绿色微流控方法

Green Microfluidic Method for Sustainable and High-Speed Analysis of Basic Amino Acids in Nutritional Supplements.

作者信息

Pukleš Iva, Páger Csilla, Sakač Nikola, Šarkanj Bojan, Marković Dean, Sakač Marija Kraševac, Jozanović Marija

机构信息

Department of Chemistry, Josip Juraj Strossmayer University of Osijek, Cara Hadrijana 8, HR-31000 Osijek, Croatia.

Doctoral School of Chemistry, University of Pécs, Ifjúság útja, 7624 Pécs, Hungary.

出版信息

Molecules. 2024 Nov 25;29(23):5554. doi: 10.3390/molecules29235554.

Abstract

Amino acids (AAs) have broad nutritional, therapeutic, and medical significance and thus are one of the most common active ingredients of nutritional supplements. Analytical strategies for determining AAs are high-priced and often limited to methods that require modification of AA polarity or incorporation of an aromatic moiety. The aim of this work was to develop a new method for the determination of L-arginine, L-ornithine, and L-lysine on low-cost microchip electrophoresis instrumentation conjugated with capacitively coupled contactless conductivity detection. A solution consisting of 0.3 M acetic acid and 1 × 10 M iminodiacetic acid has been identified as the optimal background electrolyte, ensuring the shortest possible analysis time. The short migration times of amino acids (t ≤ 64 s) and method simplicity resulted in high analysis throughput with high precision and linearity (R≥ 0.9971). The limit of detection values ranged from 0.15 to 0.19 × 10 M. The accuracy of the proposed method was confirmed by recovery measurements. The results were compared with CE-UV-VIS and HPLC-DAD methods and showed good agreement. This work represents the first successful demonstration of the ME-CD analysis of L-arginine, L-ornithine, and L-lysine in real samples.

摘要

氨基酸具有广泛的营养、治疗和医学意义,因此是营养补充剂中最常见的活性成分之一。测定氨基酸的分析方法价格昂贵,且通常局限于需要改变氨基酸极性或引入芳香基团的方法。本研究的目的是开发一种新方法,用于在与电容耦合非接触式电导检测相结合的低成本微芯片电泳仪器上测定L-精氨酸、L-鸟氨酸和L-赖氨酸。已确定由0.3 M乙酸和1×10 M亚氨基二乙酸组成的溶液为最佳背景电解质,可确保尽可能短的分析时间。氨基酸的迁移时间短(t≤64 s)且方法简单,从而实现了高精度和线性度(R≥0.9971)的高分析通量。检测限范围为0.15至0.19×10 M。通过回收率测量证实了该方法的准确性。将结果与CE-UV-VIS和HPLC-DAD方法进行比较,结果显示出良好的一致性。这项工作首次成功展示了在实际样品中对L-精氨酸、L-鸟氨酸和L-赖氨酸进行微芯片电泳-电导分析。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/43ec/11643986/8f6ca0a04678/molecules-29-05554-g001a.jpg

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