首页> 外文期刊>Archives of pharmacal research >Determination of plasma dibasic amino acids following trimethylsilyl-trifluoroacyl derivatization using gas chromatography-mass spectrometry.
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Determination of plasma dibasic amino acids following trimethylsilyl-trifluoroacyl derivatization using gas chromatography-mass spectrometry.

机译:用气相色谱 - 质谱法测定三甲基甲硅烷基 - 三氟乙基衍生物后血浆二元氨基酸。

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摘要

A rapid analytical method was developed to quantify dibasic amino acids (ornithine, lysine and arginine) after two-step derivatization procedure with good sensitivity and specificity on human plasma. If early diagnosis has not been made, patients with inborn metabolic disorders such as HHH syndrome, Hyperornithinemia and dibasic aminoaciduria rapidly progress to sudden death, physical defect or mental retardation resulting in storage of the toxic material into the brain. Therefore, it is necessary to develop the analytical method for rapid screening and/or correct confirmation diagnosis. The formation of trimethylsilyl derivative of the carboxylic (COO-) functional group was performed by adding MSTFA. Five μL of methyl orange was added to the residue until the color changed into yellow. Consecutively, the trifluoroacyl derivative of the amino (-NH2) functional group was produced by adding MBTFA. Specific ions was chosen for quantification with following ions; m/z 166 and m/z 212 for ornithine, m/z 180 and m/z 395 for lysine, and m/z 292 and, m/z 519 for arginine. A calibration curve showed a linear relationship for the dibasic amino acids spiked to pooled normal plasma showing R(2) of 0.9955-0.9979 in the range of 0.1-600 ng investigated. The utility of the method for screening and diagnosis was demonstrated by recovery 80-125 % and reproducibility with RSD (9-17 %) at low, medium and high concentration fortified to pooled plasma. Collectively, the present study suggest that this method could be useful for diagnosis, screening, therapeutic monitoring of metabolic disorders on dietary therapy with excellent sensitivity and rapidity.
机译:开发了一种快速分析方法,以在双层衍生化过程中量化二维氨基酸(鸟氨酸,赖氨酸和精氨酸),其血浆具有良好的敏感性和特异性。如果尚未进行早期诊断,患有原始代谢障碍的患者,如HHH综合征,高胆血症和二元氨基遗传症迅速进展到突然死亡,身体缺陷或精神迟缓,导致毒性物质储存到大脑中。因此,有必要开发用于快速筛选和/或正确确认诊断的分析方法。通过添加MSTFA进行羧酸(CoO-)官能团的三甲基甲硅烷基衍生物的形成。将5μl甲基橙加入到残余物中,直至颜色变成黄色。连续地,通过加入MBTFA制备氨基(-NH2)官能团的三氟乙基衍生物。选择特异性离子以用以下离子定量;用于鸟氨酸,M / Z180和M / Z 395的M / Z 166和M / Z 212,用于赖氨酸的M / Z 292和用于精氨酸的M / Z 519。校准曲线显示出掺入的二元氨基酸的线性关系,其掺入汇集的正常血浆,显示0.955-0.9979的R(2),在0.1-600ng的范围内研究。通过恢复筛选和诊断方法的效用,并通过强化池化等离子体的低,中和高浓度的低,中和高浓度的RSD(9-17%)进行效用。本研究表明,该方法可用于诊断,筛选,治疗代谢障碍对膳食疗法的诊断,筛查,治疗监测,具有卓越的敏感性和快速性。

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  • 来源
    《Archives of pharmacal research》 |2013年第3期|共8页
  • 作者

    Hye-Ran Yoon;

  • 作者单位

    Department of Biomedical &

    Pharmaceutical Analyses College of Pharmacy Duksung Women's University;

  • 收录信息
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 药学;
  • 关键词

  • 入库时间 2022-08-20 01:24:16

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