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作 者:王英[1,2] 王永生[2] 曹晓娟 邓雪飞 王湘屏 段荣
机构地区:[1]湖南省衡阳市中心血站,湖南衡阳421001 [2]南华大学公共卫生学院,湖南衡阳421001
出 处:《中国卫生检验杂志》2009年第3期565-566,573,共3页Chinese Journal of Health Laboratory Technology
基 金:湖南省自然科学基金课题(03JJY3030);湖南省卫生厅科研基金课题(B2003-077)
摘 要:目的:建立了一种同时检测尿中α-萘酚、β-萘酚和1-羟基芘(1-OHP)的反相高效液相色谱的方法。方法:采用Diamonsil^TMC18(5μm,150×4.6 nm)色谱柱,以V(甲醇):V(乙酸铵缓冲液)=70:30为流动相,在波长280 nm处检测,流速为0.7 ml/min。结果:当α-萘酚、β-萘酚和1-羟基芘的质量浓度分别为0.3600~18.72 mg/L,0.3600~18.72 mg/L,0.2700~11.88 mg/L时,峰高和质量浓度呈很好的线性关系,相对标准差分别为0.9%、2.2%、3.2%(n=5),平均回收率分别为100.3%、103.1%、99.4%。结论:方法准确快速,可用于人尿中α-萘酚、β-萘酚和1-羟基芘的同时测定。Objective:To develop a reversed-phase high performance liquid chromatography method for assaying 1-naphthol,2-naphthol and 1-hydroxypyrene(1-OHP).Methods:1-naphthol,2-naphthol and 1-OHP were separated on Diamonsil^TMC18(5 μm,150×4.6 nm)and detected at 280 nm by using methanol-ammonium acetate buffer solution(70:30,v:v) as mobile phase when the column temperature was 35.0℃ and the flow rate was 0.7 ml/min.Results:The calibration curves of а-naphthol,β-naphthol and 1-OHP showed good linearities in the ranges of 0.3600~18.72 mg/L,0.3600~18.72 mg/L,0.2700~11.88 mg/L,respectively.The relative standard deviations(RSD) were 0.9%,2.2%,3.2%(n=5)and the average recoveries were 100.3%,103.1%,99.4% respectively.Conclusion:The method is accurate and suitable for the identification and quantification of these compositions in urine.
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