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作 者:付朝晖[1] 黄雪祥[1] 肖宏瑞[1] 黄金祥[1]
机构地区:[1]中国疾病控制中心职业卫生与中毒控制所,北京100050
出 处:《卫生研究》2005年第2期255-256,共2页Journal of Hygiene Research
基 金:科技部"十五"科技攻关项目 (No .2 0 0 1BA70 4B0 6)
摘 要:为给临床上治疗有机磷中毒提供参考依据 ,建立了高效液相色谱法测定大鼠血浆中氯解磷定含量的方法。本方法固定相采用BECKMANC18色谱柱 (ODSdp5u 4 . 6mm× 2. 5cm) ,流动相为乙腈 :(0 . 0 2mol LNaH2 PO4 ,加入 0 .2 %的 1 辛烷基磺酸钠 ,磷酸调节pH至 3 0 ) (体积比 7. 5∶92 .5 ) ,996PDA检测器 ,检测波长为 2 96nm或 2 5 4nm ,保留时间定性 ,峰面积定量。氯解磷定测定的线性范围 1 .0~ 5 0 μg ml,检测限为 0 . 5 μg ml(S N =2 ) ,该方法测得的氯解磷定的回收率为 76 %~ 84 % ,批内 ,批间测定RSD1. 35 % ,2 . 73%Objective\ To provide a reference for clinically curi ng organophosphrous compounds Poisoning. A high performance liquid chromatograph y method has been developed f or determination of pralidoxime chloride in rat plasma. BECKMAN ODS C 18 co lumn, Waters Model 510 HPLC pump and 996 photodiode Detector were used. The mobi le phase consisted of 7.5% acetonitrite and 92.5% (20nmol/L NaH 2PO 4, 0.2% C 8H 17SO 3 Na, pH3.0, adjusted by H 3PO 4 Solution) the flow rate wa s 1.0mol/min. detection wavelength was set at 296. The samples were pretreated with acetonitrite. The results show a good liner correlation between pralidoxime chloride concentration(from 1.0~5.0μg/ml) and absorption intensity. The det ection limit is 0.5μg/ml with signal to noise ratio of 2. The intra-assay and inter-assay coefficients of variation were 1.35% and 2.73%. The recoveries f or plasma were in ranges of 76%~84%.
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