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使用液相色谱/电喷雾质谱法筛选和定量测定血清中水杨酸、对乙酰氨基酚、茶碱、苯巴比妥、溴戊酰脲、戊巴比妥和异戊巴比妥水平的方法。

Method for screening and quantitative determination of serum levels of salicylic Acid, acetaminophen, theophylline, phenobarbital, bromvalerylurea, pentobarbital, and amobarbital using liquid chromatography/electrospray mass spectrometry.

作者信息

Hori Yasushi, Fujisawa Manami, Shimada Kenji, Hirose Yasuo, Yoshioka Toshiharu

机构信息

Department of Analytical Chemistry, Faculty of Pharmaceutical Sciences, Niigata University of Pharmacy and Applied Life Sciences.

出版信息

Biol Pharm Bull. 2006 Jan;29(1):7-13. doi: 10.1248/bpb.29.7.

Abstract

We investigated a method for the simultaneous screening, identification, and quantitative determination of salicylic acid, acetaminophen, theophylline, barbiturates, and bromvalerylurea, drugs that frequently cause acute poisoning in Japan and therefore require rapid analysis for effective treatment in the clinical setting. The method employs liquid chromatography/electrospray mass spectrometry (LC/MS) of solid-phase extracted serum samples. For LC/MS ionization, the electrospray-ionization method was used, with acetaminophen in the positive-ion mode, and salicylic acid, theophylline, phenobarbital, bromvalerylurea, pentobarbital, amobarbital, and o-acetamidophenol (internal standard) in the negative-ion mode, the base ions were used in each case for quantitative analysis. Quantitation was possible for the following sample concentration ranges: salicylic acid and acetaminophen, 100 to 5 microg/ml; theophylline, 100 to 0.5 microg/ml; and phenobarbital, bromvalerylurea, pentobarbital, and amobarbital, 100 to 1 microg/ml. Using full-scan mass spectrometry, the lower detection limits of 1 microg/ml for salicylic acid and acetaminophen, 0.1 microg/ml for theophylline, and 0.5 microg/ml for phenobarbital, bromvalerylurea, pentobarbital, and amobarbital were adequate for identifying acute poisoning. When each compound was added to serum to a final concentration of 5 microg/ml and solid-phase extraction was performed using Oasis HLB 1-cc (30-mg), the mean recovery rate of each compound was 89.2 to 96.1% (n=5), and the coefficients of variation of the intraday and interday assays were 3.55 to 6.05% (n=5) and 3.68 to 6.38% (n=5), respectively, which are acceptable. When this method of analysis was applied in testing the sera of a female patient who had consumed a large amount of an unknown commercial drug, salicylic acid and bromvalerylurea were identified, and the treatment strategy could be determined in accordance with the serum concentration of those drugs.

摘要

我们研究了一种用于同时筛查、鉴定和定量测定水杨酸、对乙酰氨基酚、茶碱、巴比妥类药物以及溴戊酰脲的方法,这些药物在日本常引发急性中毒,因此在临床环境中需要进行快速分析以实现有效治疗。该方法采用固相萃取血清样本的液相色谱/电喷雾质谱法(LC/MS)。对于LC/MS电离,使用电喷雾电离法,对乙酰氨基酚采用正离子模式,水杨酸、茶碱、苯巴比妥、溴戊酰脲、戊巴比妥、异戊巴比妥和邻乙酰氨基酚(内标)采用负离子模式,每种情况下均使用基峰离子进行定量分析。在以下样本浓度范围内可进行定量:水杨酸和对乙酰氨基酚为100至5微克/毫升;茶碱为100至0.5微克/毫升;苯巴比妥、溴戊酰脲、戊巴比妥和异戊巴比妥为100至1微克/毫升。使用全扫描质谱法,水杨酸和对乙酰氨基酚的最低检测限为1微克/毫升,茶碱为0.1微克/毫升,苯巴比妥、溴戊酰脲、戊巴比妥和异戊巴比妥为0.5微克/毫升,足以鉴定急性中毒情况。当将每种化合物添加到血清中使其终浓度达到5微克/毫升,并使用Oasis HLB 1毫升(30毫克)进行固相萃取时,每种化合物的平均回收率为89.2%至96.1%(n = 5),日内和日间测定的变异系数分别为3.55%至6.05%(n = 5)和3.68%至6.38%(n = 5),这些结果是可接受的。当将这种分析方法应用于检测一名服用了大量未知商业药物的女性患者的血清时,鉴定出了水杨酸和溴戊酰脲,并可根据这些药物的血清浓度确定治疗策略。

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