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 >Simultaneous microdetermination of bosentan, ambrisentan, sildenafil, and tadalafil in plasma using liquid chromatography/tandem mass spectrometry for pediatric patients with pulmonary arterial hypertension
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Simultaneous microdetermination of bosentan, ambrisentan, sildenafil, and tadalafil in plasma using liquid chromatography/tandem mass spectrometry for pediatric patients with pulmonary arterial hypertension

机译:液相色谱/串联质谱法同时测定儿科肺动脉高压患者血浆中的波生坦,安布森坦,西地那非和他达拉非

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摘要

A simultaneous, selective, sensitive, and rapid liquid chromatography/tandem mass spectrometry (LC-MS/MS) method was developed and validated for the quantification of bosentan, ambrisentan, sildenafil, and tadalafil in 50. μL of human blood plasma. Diluted plasma samples were extracted using a solid-phase extraction procedure with 2% formic acid and methanol. The four drugs were separated by high-performance liquid chromatography using a C18 column and an isocratic mobile phase running at a flow rate of 0.2. mL/min for 5. min. The drugs were detected by a tandem mass spectrometer with electrospray ionization using deuterated compounds as internal standards. Calibration curves were generated over the linear concentration range of 2-1000. ng/mL in plasma with a lower limit of quantification of 2. ng/mL for all compounds. Finally, this validated method was applied to a clinical pharmacokinetic study in pediatric patients with pulmonary arterial hypertension (PAH) following the oral administration of PAH drugs. These results indicate that this method is suitable for assessing the risk/benefit of combination therapy in the pediatric population and useful for therapeutic drug monitoring for PAH treatment.
机译:建立了同时,选择性,灵敏和快速的液相色谱/串联质谱(LC-MS / MS)方法,并验证了50.μL人血浆中波生坦,安布森坦,西地那非和他达拉非的定量效果。使用2%甲酸和甲醇,采用固相萃取程序萃取稀释的血浆样品。通过高效液相色谱,使用C18色谱柱和等度流动相,以0.2的流速运行,分离了这四种药物。 mL / min 5分钟。药物是通过串联质谱仪使用氘化化合物作为内标物进行电喷雾电离检测的。在2-1000的线性浓度范围内生成校准曲线。血浆中的ng / mL,所有化合物的定量下限均为2 ng / mL。最后,该经验证的方法被应用于口服PAH药物后患儿肺动脉高压(PAH)的临床药代动力学研究。这些结果表明,该方法适用于评估儿科人群中联合治疗的风险/获益,并可用于监测PAH治疗的治疗药物。

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