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一种采用同位素稀释气相色谱/质谱联用选择离子监测法测定血清和尿液中尼古丁的固相萃取方法。

A solid phase extraction method for determination of nicotine in serum and urine by isotope dilution gas chromatography/mass spectrometry with selected ion monitoring.

作者信息

Baskin L B, Anderson R W, Charlson J R, Hurt R D, Lawson G M

机构信息

Department of Pathology, University of Texas Southwestern Medical Center, Dallas 75235-9073, USA.

出版信息

Ann Clin Biochem. 1998 Jul;35 ( Pt 4):522-7. doi: 10.1177/000456329803500406.

Abstract

A rapid method for measuring nicotine concentration in serum and urine is described. Deuterated nicotine is used as an internal standard. Nicotine and deuterated nicotine are extracted using a copolymeric-bonded phase silica column. The extract is analysed by gas chromatography coupled with mass spectrometry (GC/MS) operating in selected ion monitoring mode. The method has a lower limit of detection of approximately 2 micrograms/L and is linear to at least 2000 micrograms/L. Within-run percentage coefficients of variation (% CV) are < 4 in both assays over a nicotine concentration range of 10-2000 micrograms/L. Between-run % CV in the serum assay are 5.4, 5.2, 4.8 and 5.9, respectively, at nicotine concentrations of 10, 15, 25, and 50 micrograms/L. Between-run % CV in the urine assay are 5.9, 4.5, 2.7 and 5.2, respectively, at nicotine concentrations of 100, 250, 500, and 2000 micrograms/L. The absolute recovery of nicotine is 61 +/- 6% (mean +/- SD) over the range of 10-250 micrograms/L. The assay has been used to measure serum nicotine concentrations and 24-h urinary excretion of nicotine to monitor the extent of replacement in subjects receiving transdermal nicotine therapy for smoking cessation.

摘要

本文描述了一种快速测定血清和尿液中尼古丁浓度的方法。氘代尼古丁用作内标。尼古丁和氘代尼古丁采用共聚键合相硅胶柱进行萃取。萃取物通过气相色谱 - 质谱联用仪(GC/MS)在选择离子监测模式下进行分析。该方法的检测下限约为2微克/升,线性范围至少为2000微克/升。在10 - 2000微克/升的尼古丁浓度范围内,两种分析方法的批内变异系数(% CV)均<4。在血清分析中,尼古丁浓度为10、15、25和50微克/升时,批间% CV分别为5.4、5.2、4.8和5.9。在尿液分析中,尼古丁浓度为100、250、500和2000微克/升时,批间% CV分别为5.9、4.5、2.7和5.2。在10 - 250微克/升范围内,尼古丁的绝对回收率为61±6%(平均值±标准差)。该检测方法已用于测量血清尼古丁浓度和24小时尿尼古丁排泄量,以监测接受经皮尼古丁治疗戒烟的受试者的替代程度。

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