在单元分辨率和高分辨率仪器上对总的量化进行敏感LC-MS/MS检测
Jill K Wolken1, Meghan M Peterson1, Wenjing Cao1,2
1University of Wisconsin Hospital and Clinics, Madison, WI 53792, USA.
Journal of clinical medicine
|December 17, 2024
概括
一种新的液体染色学-并联质谱法 (LC-MS/MS) 试验准确地测量了总,提高了临床试验中低度的准确性. 这种方法在多种仪器和样品类型中可靠.
科学领域:
- 临床化学 临床化学
- 分析化学 分析化学
- 质谱测量质量谱测量
背景情况:
- 丸激素是一种重要的雌激素激素,具有广泛的生理作用.
- 现有的免疫测试在低总丸激素度 (<100 ng/dL) 的情况下难以准确,影响女性和儿科的测试.
- 准确测量总丸激素对于各种临床诊断至关重要.
研究的目的:
- 开发和验证一种精确的液体染色学-并联质谱法 (LC-MS/MS) 测定总的方法.
- 为了提高量化低水平的准确性.
- 确保在不同的质谱平台上测试的协调性.
主要方法:
- 血清样本经过稀释和调节.
- 分析物提取使用了支持的液体提取弹.
- 在C18列上进行了染色分离,运行时间为5分钟.
- 根据CLSI指南,对Triple Quad 6500,API 4500和Orbitrap仪器进行了测试验证.
主要成果:
- 实现了0.5 ng/dL的量化极限和2-1200 ng/dL的测量范围.
- 证明了良好的方法验证,当天CV<10%和当天CV<15%.
- 与参考方法相关性很好,在TQ 6500,API 4500和Orbitrap平台上显示一致性.
- 证实了血清分离器和血清激活器管的适用性.
结论:
- 一个强大的和验证的总丸激素LC-MS/MS测定为常规临床使用而建立.
- 该试验提供了准确的量化,特别是在低度下.
- 在三极四极和高分辨率质谱仪之间成功协调,确保了广泛的应用.
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