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首页> 外文期刊>Rapid Communications in Mass Spectrometry: RCM >Identification and quantification of glutathione adducts of clozapine using ultra-high-performance liquid chromatography with orthogonal acceleration time-of-flight mass spectrometry and inductively coupled plasma mass spectrometry
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Identification and quantification of glutathione adducts of clozapine using ultra-high-performance liquid chromatography with orthogonal acceleration time-of-flight mass spectrometry and inductively coupled plasma mass spectrometry

机译:使用正交加速飞行时间质谱和电感耦合等离子体质谱的超高效液相色谱法鉴定和定量氯氮平的谷胱甘肽加合物

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摘要

The application of sulphur-specific detection via ultra-performance liquid chromatography coupled to inductively coupled plasma mass spectrometry (UPLC/ICPMS) to detect and quantify the glutathione (GSH)-adducts produced via the in vitro formation of reactive metabolites is demonstrated. The adducts were formed in human liver microsomes supplemented with unlabelled GSH for clozapine. The calculation of adduct concentration was performed via comparison of the peak areas to calibration curves constructed from omeprazole, a sulphur-containing compound over the range of 0.156 to 15.62 μM of sulphur with a detection limit of 1.02 ng of sulphur on-column. Identification of the adducts was performed using conventional UPLC/time-of-flight (TOF)-MS with the calculation of clozapine intrinsic clearance carried out by high-performance liquid chromatography/tandem mass spectrometry (HPLC/MS/MS). The use of ICPMS in this way appears to offer a novel, rapid and sensitive means of determining the quantity of GSH conjugates with the combined adducts producing 0.9 μM of reactive metabolite out of a total of 3.5 μM of metabolites. The GSH adduct therefore represents 26% of this total produced as a result of the metabolism of drug to reactive species.
机译:通过超高效液相色谱与电感耦合等离子体质谱法(UPLC / ICPMS)结合进行硫特异性检测,以检测和定量通过体外形成反应性代谢产物而产生的谷胱甘肽(GSH)加合物得到了证明。加合物是在补充了氯氮平未标记GSH的人肝微粒体中形成的。加标浓度的计算是通过将峰面积与由奥美拉唑(奥美拉唑)建立的校正曲线进行比较而完成的,该曲线是硫在0.156至15.62μM范围内的含硫化合物,柱上硫的检测限为1.02 ng。使用常规UPLC /飞行时间(TOF)-MS进行加合物的鉴定,并通过高效液相色谱/串联质谱法(HPLC / MS / MS)计算氯氮平的固有清除率。以这种方式使用ICPMS似乎提供了一种新颖,快速和灵敏的方法,可用于确定GSH共轭物的量,以及总3.5μM代谢物中产生0.9μM反应性代谢物的加合物。因此,由于药物代谢成反应性物质,GSH加合物占总产量的26%。

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