首页> 外文期刊>Journal of Pharmaceutical and Biomedical Analysis: An International Journal on All Drug-Related Topics in Pharmaceutical, Biomedical and Clinical Analysis >High-performance liquid chromatography-electrospray ionization mass spectrometry determination of sodium ferulate in human plasma.
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High-performance liquid chromatography-electrospray ionization mass spectrometry determination of sodium ferulate in human plasma.

机译:高效液相色谱-电喷雾电离质谱法测定人血浆中的阿魏酸钠

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摘要

A selective and sensitive high-performance liquid chromatography-electrospray ionization mass spectrometry method has been developed for the determination of sodium ferulate in human plasma. The sample preparation was a liquid-liquid extraction and chromatographic separation was achieved with an Agilent ZORBAX SB-C(18) (3.5 microm, 100 mm x 3.0 mm) column, using a mobile phase of methanol-0.05% acetic acid 40:60 (v/v). Standard curves were linear (r(2)=0.9982) over the concentration range of 0.007-4.63 nM/ml and had acceptable accuracy and precision. The within- and between-batch precisions were within 12% relative standard deviation. The lower limit of quantification (LLOQ) was 0.007 nM/ml. The validated HPLC-ESI-MS method has been used successfully to study sodium ferulate pharmacokinetics, bioavailability and bioequivalence in 20 healthy volunteers.
机译:建立了选择性灵敏的高效液相色谱-电喷雾电离质谱法测定人血浆中的阿魏酸钠。样品制备为液-液萃取,使用Agilent ZORBAX SB-C(18)(3.5 microm,100 mm x 3.0 mm)色谱柱,使用甲醇-0.05%乙酸40:60的流动相进行色谱分离(v / v)。标准曲线在0.007-4.63 nM / ml的浓度范围内是线性的(r(2)= 0.9982),并且具有可接受的准确性和精密度。批内和批间精度在相对标准偏差的12%以内。定量下限(LLOQ)为0.007 nM / ml。经过验证的HPLC-ESI-MS方法已成功用于研究20名健康志愿者中阿魏酸钠的药代动力学,生物利用度和生物等效性。

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