首页|液液萃取—高效液相色谱串联质谱法测定血清中可替宁及3-羟基可替宁含量

液液萃取—高效液相色谱串联质谱法测定血清中可替宁及3-羟基可替宁含量

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目的 建立全自动固体介质液液萃取—高效液相色谱串联质谱法(HPLC-MS/MS)同时测定血清中可替宁及 3-羟基可替宁含量的检测方法.方法 采用液液萃取进行前处理,样品中加入 50 μL氢氧化钾溶液,50 μL同位素内标溶液,混匀加入到固体介质液液萃取 96 孔板中,先后加入 2 次 750 μL萃取溶剂(5%异丙醇二氯甲烷混合液)后,收集萃取液,氮气吹干,100 μL纯水复溶后上机测定.以 HSS T3 液相色谱柱(2.1 mm×100 mm,1.8 μm)、0.05%氨水溶液和乙腈为流动相进行梯度洗脱分离目标物.采用正离子电喷雾模式电离,多反应离子监测方式(MRM)检测,保留时间和离子对定性,内标法定量.结果 2 种目标物在 0.1~50、5~300 μg/L范围内线性关系好,相关系数(r)均优于 0.999 0;可替宁与 3-羟基可替宁方法检出限分别为 0.016 与 0.023 μg/L;2 种化合物在添加水平为 2.0、15.0、40.0 μg/L 时,平均回收率为 86.4%~117.2%,相对标准偏差(RSD)为 2.03%~8.03%.结论 该方法样品前处理有机试剂消耗少,可实现自动化操作,准确性、精密度及灵敏度均较好,适用于吸烟及非吸烟人群血清中可替宁及 3-羟基可替宁含量的检测.
Determination of cotinine and 3-hydroxycotinine in serum using liquid-liquid extraction-high performance liquid chromatography-tandem mass spectrometry
Objective To establish a method for the simultaneous determination of the contents of cotinine and 3-hydroxycotinine in serum using automatic liquid-liquid extraction-high performance liquid chromatography-tandem mass spectrometry(HPLC-MS/MS)in a solid medium.Methods The sample was pretreated with liquid-liquid extraction by adding 50 μL of potassium hydroxide solution and 50 μL of isotope internal standard.The solution was mixed well and added into a 96-well plate used for liquid-liquid extraction in a solid medium.After 750 μL of extraction solvent(5%isopropanol dichloromethane mixture)was added twice at an interval of time,the extraction solution was collected and blow-dried with nitrogen gas.The sample was reconstituted with 100 μL of pure water and then loaded onto the machine for determination.The compounds of interest were separated on an HSS T3 liquid-phase column(2.1 mm×100 mm,1.8 μm),with 0.05%ammonia solution and acetonitrile used as a mobile phase for gradient elution separation.The sample underwent positive electrospray ionization and multiple reaction monitoring.The retention time and ion pairs were measured using quali-tative method,and quantitative measurements were performed using the internal standard method.Results The two compounds of in-terest had a good linear relationship within the ranges of 0.1-50 and 5-300 μg/L,with a correlation coefficient(r)of greater than 0.999 0.The limits of detection of cotinine and 3-hydroxycotinine were 0.016 and 0.023 μg/L,respectively.The average recoveries of the two compounds were between 86.4%and 117.2%,with relative standard deviations falling between 2.03%and 8.03%,when the spiking levels were 2.0,15.0,and 40.0 μg/L.Conclusion The pretreatment of samples using this method consumes less organic reagents,most steps can be automated,and it is accurate,precise,and sensitive,making it suitable for the determination of the con-tent of cotinine and 3-hydroxycotinine in the serum of smokers and non-smokers.

high performance liquid chromatography-tandem mass spectrometryserumcotinine3-hydroxycotinine

张志荣、张来颖、李韵冰、刘裕婷、王玉江、陈曦

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北京市丰台区疾病预防控制中心,北京 100071

中国疾病预防控制中心环境与健康相关产品安全所

高效液相色谱—串联质谱 血清 可替宁 3-羟基可替宁

2024

环境卫生学杂志
中国疾病预防控制中心

环境卫生学杂志

CSTPCD
影响因子:0.735
ISSN:2095-1906
年,卷(期):2024.14(2)
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