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采用高效液相色谱-串联质谱法(HPLC-MS/MS)测定碘海醇清除率。

Determination of iohexol clearance by high-performance liquid chromatography-tandem mass spectrometry (HPLC-MS/MS).

作者信息

Lee Soo-Youn, Chun Mi-Ryung, Kim Dae-Joong, Kim Jong Won

机构信息

Department of Laboratory Medicine, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, South Korea.

出版信息

J Chromatogr B Analyt Technol Biomed Life Sci. 2006 Jul 24;839(1-2):124-9. doi: 10.1016/j.jchromb.2006.03.057. Epub 2006 May 3.

Abstract

We have developed a simple, rapid, and accurate HPLC-MS/MS method for the determination of iohexol in serum. The column used was a Zorbax Eclipse XDB-C8 (100 mm x 2.1 mm i.d., 3.5 microm). Mobile phases consisted of water containing 2mM ammonium acetate and 0.1% formic acid (A) and methanol containing 2 mM ammonium acetate and 0.1% formic acid (B). After simple protein precipitation with ZnSO4, serum samples were mixed with I.S. (bromperidol) and centrifuged for 3 min. The obtained extraction recovery at three levels was 94.6-107.4%. Quantitative analysis was performed in the multiple reaction-monitoring mode (m/z 822.0-->804.0 for iohexol, 420.1-->122.7 for I.S.) with the total running time of 3 min for each sample. The assay was linear between 0.5 and 1500 microg/mL (r2 > 0.997). The intra- and inter-assay coefficient of variations were 2.4-6.2% and 5.5-6.5%, respectively. Our method provided sufficient analytical range and specificity for the 210 clinical samples analyzed.

摘要

我们开发了一种简单、快速且准确的HPLC-MS/MS方法来测定血清中的碘海醇。所用色谱柱为Zorbax Eclipse XDB-C8(100 mm×2.1 mm内径,3.5微米)。流动相由含2 mM醋酸铵和0.1%甲酸的水(A)以及含2 mM醋酸铵和0.1%甲酸的甲醇(B)组成。用硫酸锌进行简单的蛋白沉淀后,将血清样品与内标(溴哌利多)混合并离心3分钟。三个浓度水平下获得的提取回收率为94.6 - 107.4%。在多反应监测模式下进行定量分析(碘海醇的m/z为822.0→804.0,内标的m/z为420.1→122.7),每个样品的总运行时间为3分钟。该测定在0.5至1500微克/毫升之间呈线性(r2>0.997)。批内和批间变异系数分别为2.4 - 6.2%和5.5 - 6.5%。我们的方法为所分析的210份临床样品提供了足够的分析范围和特异性。

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