首页> 外文期刊>Journal of chromatography, B. Analytical technologies in the biomedical and life sciences >Determination of midazolam and 1-hydroxymidazolam from plasma by gas chromatography coupled to methane negative chemical ionization mass spectrometry after sublingual administration of midazolam
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Determination of midazolam and 1-hydroxymidazolam from plasma by gas chromatography coupled to methane negative chemical ionization mass spectrometry after sublingual administration of midazolam

机译:咪达唑仑舌下给药后气相色谱-甲烷负化学电离质谱法测定血浆中咪达唑仑和1-羟基咪达唑仑

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摘要

A sensitive and selective gas chromatographic mass spectrometric method for the determination of midazolam and its biologically active metabolite, 1-hydroxymidazolam, in rabbit plasma has been developed and validated. Sample preparation includes mixed-mode solid-phase extraction and derivatization with silylating reagents. Midazolam-d4 was used as an internal standard for the determination of parent drug and its active metabolite. The instrumentation consisted of a capillary column gas chromatography and a single quadrupole mass spectrometer with a negative chemical ionization. The method was found to be valid in terms of selectivity, linearity, precision, accuracy, and recovery over the concentration range of 2-200. ng/ml and 1-100. ng/ml for midazolam and 1-hydroxymidazolam, respectively. For both analytes, the lower limit of quantification was 2. ng/ml. Midazolam was stable in stock solutions stored three months at -20 °C and in human plasma stored for three months at -80 °C. In addition, no degradation of midazolam was found after three freeze-thaw cycles, in short-term stability at room temperature for 24. h, or in post-preparative stability in the autosampler. The validity of the method was further tested by performing a pharmacokinetic study of sublingual administration of midazolam in rabbits. The method will be used in studies related to a formulation development of novel midazolam formulations for use in paediatric anaesthesia.
机译:建立并验证了测定血浆中咪达唑仑及其生物活性代谢物1-羟基咪达唑仑的灵敏且选择性的气相色谱质谱法。样品制备包括混合模式固相萃取和甲硅烷基化试剂衍生化。咪达唑仑-d4用作测定母体药物及其活性代谢物的内标。仪器由毛细管柱气相色谱仪和带有负化学电离的单四极杆质谱仪组成。发现该方法在2-200浓度范围内的选择性,线性,精密度,准确度和回收率方面均有效。 ng / ml和1-100。 ng / ml的咪达唑仑和1-羟基咪达唑仑。对于两种分析物,定量下限均为2 ng / ml。咪达唑仑在-20°C下可存放三个月的原液和在-80°C下可存放三个月的人血浆中稳定。此外,在三个冻融循环后,室温下短期稳定性24小时或自动进样器中的制备后稳定性中,未发现咪达唑仑的降解。通过对咪达唑仑舌下给予家兔进行药代动力学研究,进一步验证了该方法的有效性。该方法将用于与用于儿科麻醉的新型咪达唑仑制剂的制剂开发有关的研究。

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