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A HILIC-MS/MS Method for Simultaneous Quantification of the Lysosomal Disease Markers Galactosylsphingosine and Glucosylsphingosine in Mouse Serum

机译:HILIC-MS / MS方法同时定量小鼠血清中的溶酶体疾病标志物半乳糖基鞘氨醇和葡萄糖基鞘氨醇

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摘要

Deficiencies of galactosylceramidase and glucocerebrosidase result in the accumulation of galactosylsphingosine (GalSph) and glucosylsphingosine (GluSph) in Krabbe and Gaucher diseases, respectively. GalSph and GluSph are useful biomarkers for both diagnosis and monitoring of treatment effects. We have developed and validated a sensitive, accurate, high throughput assay for simultaneous determination of the concentration of GalSph and GluSph in mouse serum. GalSph and GluSph and their deuterated internal standards were extracted by protein precipitation in quantitative recoveries, baseline separated by hydrophilic interaction chromatography, and detected by positive-ion electrospray mass spectrometry in multiple reaction monitoring mode. Total run time was 7 minutes. The lower limits of quantification were 0.2 ng/ml for both GalSph and GluSph. Sample stability, assay precision and accuracy, and method robustness were demonstrated. This method has been successfully applied to measurement of these lipid biomarkers in a natural history study in twitcher (Krabbe) mice.
机译:半乳糖基神经酰胺酶和葡萄糖脑苷脂酶的缺乏导致分别在Krabbe和Gaucher病中积累了半乳糖基鞘氨醇(GalSph)和葡萄糖基鞘氨醇(GluSph)。 GalSph和GluSph是用于诊断和监测治疗效果的有用生物标志物。我们已经开发并验证了一种灵敏,准确,高通量的测定方法,可同时测定小鼠血清中GalSph和GluSph的浓度。通过蛋白质沉淀定量回收GalSph和GluSph及其氘代内标,通过亲水相互作用色谱法分离基线,并通过正离子电喷雾质谱法在多反应监测模式下进行检测。总运行时间为7分钟。 GalSph和GluSph的定量下限均为0.2 ng / ml。证明了样品的稳定性,测定的准确性和准确性以及方法的稳健性。在抽搐(Krabbe)小鼠的自然史研究中,该方法已成功应用于这些脂质生物标志物的测量。

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