欢迎登录材料期刊网

材料期刊网

高级检索

建立了被动吸烟儿童尿液中可丁宁的气相色谱-三重四极杆串联质谱( GC-MS / MS)稳定同位素稀释测定方法。尿液经过三氯甲烷提取、净化,采用气相色谱-三重四极杆串联质谱多反应监测( MRM)模式测定,以可丁宁-d3稳定同位素为内标,定量测定和确证被动吸烟儿童尿液中的可丁宁;在0.1~10μg / L 可丁宁质量浓度范围内方法的线性关系良好,相关系数 r﹥0.998;空白尿液中添加可丁宁0.1、1.0和10μg / L,回收率为79.2%~112.8%,相对标准偏差在2.1%~5.8%之间;方法定量限达到0.1μg / L。该方法准确、灵敏、快速,适用于家庭被动吸烟儿童尿液中可丁宁的测定。

An analytical method for the determination of urinary cotinine of children exposed to passive smoking was established based on stable isotope dilution by gas chromatography-triple quadrupole mass spectrometry( GC-MS / MS). The samples were extracted and purified with chloroform. The extracts were determined by GC-MS / MS in multiple reaction monitoring (MRM)mode. The cotinine-d 3 as an isotope internal standard was applied to quantify and con-firm the urinary cotinine of children exposed to passive smoking. The method had a good linear-ity from 0. 1 μg / L to 10 μg / L with the correlation coefficient(r)﹥0. 998. The recoveries of the cotinine in blank urine were from 79. 2% to 112. 8% at spiked levels of 0. 1,1. 0 and 10 μg / L, with relative standard deviations(RSDs)from 2. 1% to 5. 8% . The limit of quantification(LOQ) of the method was 0. 1 μg / L. The developed method is accurate,sensitive,rapid and can be applied to detect urinary cotinine of children exposed to passive smoking at home.

参考文献

[1] Oberg M;Jaakkola M S;Woodward A.[J].LANCET,2011377(9760):139.
[2] Prignot J J.[J].INTERNATIONAL JOURNAL OF ENVIRONMENTAL RESEARCH AND PUBLIC HEALTH,20118:648.
[3] Wu C F;Uang S N;Chiang S Y.[J].Analytical Biochemistry,2012402:2113.
[4] Benowitz N L;Hukkanen J;Jacob P III.[J].Handb Exp Phar-macol,2009192:29.
[5] Knight G J;Wylie P;Holman M S.[J].Clinical Chemistry,198531(01):118.
[6] Park S;Lee D H;Park J G.[J].Clinica Chimica Acta,2010411(17/18):1238.
[7] Wielkoszynski T;Tyrpien K;Szumska M.[J].Journal of Pharmaceutical and Biomedical Analysis,200949(05):1256.
[8] Feyerabend C;Russell M A.[J].Journal of Pharmacy and Pharmacology,199042(06):450.
[9] Church T R;Anderson K E;Le C.[J].BIOMARKERS,201015(04):345.
[10] Matsumoto A;Matsumoto A;Ichiba M.[J].ENVIRONMENTAL HEALTH AND PREVENTIVE MEDICINE,201318(03):244.
[11] Massadeh A M;Gharaibeh A A;Omari K W.[J].Journal of Chromatography Science,200947(02):170.
[12] Mahoney G N;Al Delaimy W.[J].Journal of Chromatography B:Biomedical Sciences and Applications,2001753(02):179.
[13] Gabr R Q;Elsherbiny M E;Somayaji V.[J].Biomedical Chromatography,201125(10):1124.
[14] De Cremer K;Overmeire I V;Van Loco J.[J].Journal of Pharmaceutical and Biomedical Analysis,201376:126.
[15] Xia Y;Xu M;Alexander R R.[J].Journal of Chromatography B,2011879(22):2142.
[16] Hou H;Xiong W;Zhang X.[J].J Anal Methods Chem,20122012:245415.
[17] Marclay F;Saugy M.[J].Journal of Chromatography A,20101217(48):7528.
[18] Da Fonseca B M;Moreno I E D;Magalhaes A R.[J].Journal of Chromatography B,2012889:116.
[19] 徐敦明;陈燕;周爽.[J].色谱,201331(12):1224.
[20] 范忠;刘惠民;谢复炜.[J].烟草科技,2008(09):39.
[21] 周宛虹;王晔;余苓.[J].化学学报,201169(07):803.
上一张 下一张
上一张 下一张
计量
  • 下载量()
  • 访问量()
文章评分
  • 您的评分:
  • 1
    0%
  • 2
    0%
  • 3
    0%
  • 4
    0%
  • 5
    0%