用于分析尿液中生长激素释放肽的配位离子喷雾--一项应用研究

Azamat Temerdashev, E. Gashimova, A. Azaryan, Yu-Qi Feng, Sanka N. Atapattu
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引用次数: 0

摘要

本文对离子化技术进行了比较和讨论。使用电喷雾离子源的传统液相色谱法与使用硝酸银作为掺杂剂的配位离子喷雾(CIS-MS)液相色谱法相比,具有更高的稳定性和可重复性。不过,CIS-MS 的灵敏度更高,在非目标应用中可以收集更多数据,这意味着它正在成为一种用于特定应用的仪器。在这项研究中,GHRP-2 和 GHRP-6 的检测限(LOD)被确定为 0.2 纳克/毫升,CIS-MS 的定量下限(LLOQ)为 0.5 纳克/毫升。传统的 ESI-MS 结合弱阳离子交换柱固相萃取,检测限为 1 纳克/毫升,定量下限为 2 纳克/毫升。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Coordination Ion Spray for Analysis of the Growth Hormones Releasing Peptides in Urine—An Application Study
In this article, a comparison of ionization techniques is provided and discussed. Conventional liquid chromatography with an electrospray ionization source shows higher robustness and repeatability in comparison with liquid chromatography coupled with a coordination ion spray (CIS-MS) source using silver nitrate as the dopant. However, the higher sensitivity and possibility to collect more data in untargeted applications mean CIS-MS is emerging as an instrument used in specific applications. During this research, the limit of detection (LOD) for GHRP-2 and GHRP-6 was established at 0.2 ng/mL, and the lower limit of quantification (LLOQ) was 0.5 ng/mL for CIS-MS. For conventional ESI-MS combined with solid-phase extraction on weak cation exchange columns, the limit of detection was found to be 1 ng/mL, and the lower limit of quantification was 2 ng/mL.
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