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Determination of ibuprofen enantiomers in human plasma by HPLC-MS/MS: validation and application in neonates

机译:HPLC-MS / MS法测定人血浆中布洛芬对映体的有效性及在新生儿中的应用

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Aim: An adaptive method to determine ibuprofen enantiomers with limited volume of plasma required is necessary for investigating PK of ibuprofen in neonates. Results: Enantiomer separation was achieved on a Lux cellulose 3 column with mobile phase consisting of methanol water (85: 15, v/v) and formic acid (0.0075%) at isocratic rate of 0.2 ml/min. Calibration curve is linear for each enantiomer at the range of 0.1-60 mu g/ml. Validation was conducted and results met requirements regarding to intra-and inter-run precision, accuracy and recovery. No matrix effect or interference was observed from neonatal plasma or comedications. Only 20 mu l of plasma was requested in this study. Conclusion: This assay was specific and reliable to quantify ibuprofen enantiomers in neonate plasma.
机译:目的:一种确定血浆中布洛芬对映异构体的适应性方法,对于调查新生儿布洛芬的PK是必需的。结果:对映体分离是在Lux纤维素3色谱柱上完成的,流动相由甲醇水(85:15,v / v)和甲酸(0.0075%)组成,等度流速为0.2 ml / min。每个对映体的校准曲线在0.1-60μg / ml范围内呈线性关系。进行了验证,结果符合有关运行内和运行间精度,准确度和回收率的要求。从新生儿血浆或喜剧中未观察到基质效应或干扰。在这项研究中仅要求血浆20微升。结论:该测定方法对定量测定血浆中布洛芬对映体的特异性和可靠性。

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