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用于测定人血清或血浆中抗精神病药物顺式(Z)-氟哌噻吨的灵敏气-液色谱法。

Sensitive gas-liquid chromatographic method for the assay of the neuroleptic drug cis(Z)-flupentixol in human serum or plasma.

作者信息

Ulrich S

机构信息

Institute of Clinical Pharmacology, University Hospital Magdeburg, Germany.

出版信息

J Chromatogr B Biomed Appl. 1995 Jun 9;668(1):31-40. doi: 10.1016/0378-4347(95)00057-p.

Abstract

A gas-liquid chromatographic (GLC) assay suitable for the analysis of the cis(Z)-stereoisomer of the antipsychotic drug flupentixol in human serum or plasma was developed. The minimal quantifiable concentration was 0.5 ng/ml and the day-to-day coefficient of variation was 11.2% at 1 ng/ml and 8.7% at 10 ng/ml. Following addition of perphenazine as the internal standard (I.S.) and aqueous NaOH, samples (2 ml) are extracted with n-hexane-isoamyl alcohol (98.5:1.5, v/v) (solvent), back-extracted to 0.1 M HCl and after one washing-step and addition of aqueous NaOH again extracted into 100 microliters solvent. After evaporation to dryness, the extract is reconstituted in 20 microliters solvent and evaporated to approximative 10 microliters. A 4-microliter aliquot is injected cool on-column onto the GLC system. A gas chromatograph HP 5890 with on-column injection port, nitrogen-phosphorus detector (NPD), a HP-1 25 m x 0.32 mm I.D., 0.52 micron capillary and hydrogen (3 ml/min, automated pressure control) as the carrier gas was applied. The negative influence of light on the assay was measured and discussed. The suitability of this method for clinical pharmacokinetic studies and therapeutic drug monitoring (TDM) was determined by the analysis of serum samples of 12 schizophrenic patients.

摘要

开发了一种适用于分析人血清或血浆中抗精神病药物氟哌噻吨顺式(Z)-立体异构体的气-液色谱(GLC)测定法。最低可定量浓度为0.5 ng/ml,日间变异系数在1 ng/ml时为11.2%,在10 ng/ml时为8.7%。加入奋乃静作为内标(I.S.)和氢氧化钠水溶液后,取2 ml样品用正己烷-异戊醇(98.5:1.5,v/v)(溶剂)萃取,反萃取至0.1 M盐酸中,经过一步洗涤并再次加入氢氧化钠水溶液后,再萃取至100微升溶剂中。蒸发至干后,提取物用20微升溶剂复溶并蒸发至约10微升。取4微升等分试样冷进样到GLC系统中。使用配有柱上进样口、氮磷检测器(NPD)、HP-1 25 m×0.32 mm内径、0.52微米毛细管以及氢气(3 ml/min,自动压力控制)作为载气的HP 5890气相色谱仪。测定并讨论了光照对该测定法的负面影响。通过分析12例精神分裂症患者的血清样本,确定了该方法用于临床药代动力学研究和治疗药物监测(TDM)的适用性。

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