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首页> 外文期刊>Journal of chromatography, B. Analytical technologies in the biomedical and life sciences >Determination of tobramycin in serum using liquid chromatography-tandem mass spectrometry and comparison with a fluorescence polarisation assay
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Determination of tobramycin in serum using liquid chromatography-tandem mass spectrometry and comparison with a fluorescence polarisation assay

机译:液相色谱-串联质谱法测定血清中的妥布霉素并与荧光偏振法比较

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摘要

We have developed a tandem mass spectrometry (LC-MS-MS) method for measuring tobramycin concentrations in serum samples and have compared it with a fluorescence polarisation immunoassay. After protein precipitation with acetonitrile supernatant was injected into the LC-MS-MS system. A C_(18) cartridge (4 * 2 mm) was eluted with a step gradient of 20-100% methanol containing HFBA. The retention times were, tobramycin 1.05 min and sisomycin 1.05 min. The MRM transitions were: m/z 467.8 > 163 (tobramycin) and m/z 447.8 > 160 (sisomycin). The limit of quantification was 0.15 mg/l and the assay was linear up to 50 mg/l. Assay precision was <6% within and between batch.
机译:我们已经开发了一种串联质谱(LC-MS-MS)方法来测量血清样品中妥布霉素的浓度,并将其与荧光偏振免疫分析法进行了比较。用乙腈沉淀蛋白质后,将上清液注入LC-MS-MS系统。用含HFBA的20-100%甲醇的逐步梯度洗脱C_(18)色谱柱(4 * 2 mm)。保留时间为妥布霉素1.05分钟和西霉素1.05分钟。 MRM转换为:m / z 467.8> 163(妥布霉素)和m / z 447.8> 160(西霉素)。定量限为0.15 mg / l,测定线性至50 mg / l。批内和批间的测定精度<6%。

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