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作 者:姚洪菊[1,2] 王绍萍[1] 李德安[1] 付晓艳[1,2]
机构地区:[1]哈尔滨医科大学中国疾病预防控制中心地方病控制中心,哈尔滨150081 [2]卫生部黑龙江省病因流行病学重点实验室
出 处:《公共卫生与预防医学》2014年第6期17-19,共3页Journal of Public Health and Preventive Medicine
基 金:黑龙江省卫生厅科研课题(2009-237);中国疾病预防控制中心地方病控制中心青年启动基金(2013)
摘 要:目的建立高效液相色谱(HPLC)紫外检测器测定T-2毒素的方法,并评价该方法的可操作性,最终推广到下级单位使用。方法采集哈尔滨市市售大米,经过粉碎后,染毒备用。取染毒后大米粉末,加入乙腈水溶液及正己烷萃取,涡旋混合,离心后,移取己烷层氮气吹干,残渣加入甲醇水溶解进样。色谱条件:采用C18常规反相色谱柱(150 mm×4.6 mm,5μm),流动相为甲醇∶水(7∶3),紫外检测波长208 nm,柱温为室温,流速0.5 ml/min。结果 T-2毒素的保留时间为11.6 min;在50~800 ng范围内线性关系良好;样品中T-2毒素的平均回收率为93.00%。结论该方法测定T-2毒素含量,结果准确,可用于粮食中T-2毒素的含量测定。Objective To establish a new HPLC method by UV detection for the assay of T-2 toxin, and evaluate the method of operation, eventually popularize to the subordinate units. Methods Rice on the market of Harbin city was collected, after crushing and exposing to T-2 toxin, rice was extracted by acetonitrile and hexane, then vortexed and centrifuged, the hexane layer was moved and dried by nitrogen evaporation, dissolved by methanol water, finally analyzed by HPLC. T-2 toxin can be separated on the column of C18 ( 150 mm* 4. 6ram, 5 p,m) with the mobile phase methanol-water (7:3 ). UV detection wavelength was 208 nm. The column temperature was at room temperature. The tow rate was 0.Sml/ min. Results This standard curve was linear in the concentration ranged from 50 to 800 ng. The average rate of recovery was 93.00%. Conclusion The retention time of T-2 toxin was 11.6 minutes. This method can determine T-2 toxin content accurately and can be used for the determination of T-2 toxin in grain.
分 类 号:R115[医药卫生—公共卫生与预防医学] R991
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