Department of Biomedical Information Sciences, Graduate School of Information Sciences, Hiroshima City University, 3-4-1 Ozuka-higashi, Asaminami-ku, Hiroshima, 731-3194, Japan.
Sci Rep. 2022 Mar 2;12(1):3427. doi: 10.1038/s41598-022-07408-9.
A one-step analysis method was developed for four types of amino acids using a microfluidic paper-based analytical device fabricated from chromatography filtration paper and laminate films. Aminoacyl-tRNA synthetase was used to detect each amino acid. The obtained laminated paper-based analytical device (LPAD) contained four enzymatic reaction areas. Colorimetric detection was performed based on the molybdenum blue reaction. A model method for the simple, easy, and simultaneous detection of several amino acid concentrations was suggested, in contrast to the conventional methods such as HPLC or LC-MS. The method provided a selective quantification at the ranges of 3.6-100 μM for tryptophan, 10.1-100 μM for glycine, 5.9-100 μM for histidine and 5.6-100 μM for lysine with a detection limit of 1.1 μM, 3.3 μM, 1.9 μM and 1.8 μM, respectively. LPAD fabrication was considerably simple, and the subsequent detection process was easy and required a short period of time (within 15 min).
开发了一种使用由色谱过滤纸和层压膜制成的微流控纸基分析器件对四种类型的氨基酸进行一步分析的方法。使用氨酰-tRNA 合成酶检测每种氨基酸。所获得的层压纸基分析器件 (LPAD) 包含四个酶反应区域。基于钼蓝反应进行比色检测。与 HPLC 或 LC-MS 等传统方法相比,提出了一种简单、易用且可同时检测几种氨基酸浓度的模型方法。该方法在色氨酸的 3.6-100 μM、甘氨酸的 10.1-100 μM、组氨酸的 5.9-100 μM 和赖氨酸的 5.6-100 μM 范围内提供了选择性定量,检测限分别为 1.1 μM、3.3 μM、1.9 μM 和 1.8 μM。LPAD 的制造相当简单,随后的检测过程简单,所需时间短(<15 分钟)。