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[1]丁婕,何宇敏,王曉萍.血漿中有機(jī)磷液相色譜-質(zhì)譜法測定方法的建立[J].福建醫(yī)藥雜志,2022,44(04):117-120.
 DING Jie,HE Yumin,WANG Xiaoping.Establishment of a liquid chromatography/mass spectrometry method for detecting the plasma concentration of organophosphorus[J].FUJIAN MEDICAL JOURNAL,2022,44(04):117-120.
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血漿中有機(jī)磷液相色譜-質(zhì)譜法測定方法的建立()
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《福建醫(yī)藥雜志》[ISSN:1002-2600/CN:35-1071/R]

卷:
44
期數(shù):
2022年04期
頁碼:
117-120
欄目:
基礎(chǔ)研究
出版日期:
2022-08-15

文章信息/Info

Title:
Establishment of a liquid chromatography/mass spectrometry method for detecting the plasma concentration of organophosphorus
文章編號:
1002-2600(2022)04-0117-04
作者:
丁婕何宇敏王曉萍1
福建醫(yī)科大學(xué)省立臨床醫(yī)學(xué)院 福建省立醫(yī)院急診科 福建省急診醫(yī)學(xué)重點實驗室(福州 350001)
Author(s):
DING Jie HE Yumin WANG Xiaoping
Fujian Provincial Key Laboratory of Emergency Medicine;Department of Emergency Medicine, Fujian Provincial Hospital;Shengli Clinical Medical College of Fujian Medical University, Fuzhou, Fujian 350001, China
關(guān)鍵詞:
液相色譜-質(zhì)譜法有機(jī)磷定量檢測
Keywords:
liquid chromatography/mass spectrometry organophosphorus quantitative detection
分類號:
R.331
文獻(xiàn)標(biāo)志碼:
A
摘要:
目的 建立液相色譜-質(zhì)譜法(liquid chromatography/mass spectrometry,LC/MS)測定血漿中氧化樂果、敵敵畏、克百威、樂果濃度的方法。方法 使用純乙腈沉淀蛋白提取樣品后,利用LC/MS法對提取的樣品進(jìn)行檢測。對建立方法的線性、精密度、加標(biāo)回收率進(jìn)行評價。結(jié)果 氧化樂果在10~200 ng/mL、100~1 000 ng/mL的濃度范圍內(nèi)線性關(guān)系良好,最低定量限為10 ng/mL;敵敵畏、克百威、樂果在50~1 000 ng/mL、1 000~5 000 ng/mL的濃度范圍內(nèi)線性關(guān)系良好,最低定量限均為50 ng/mL;氧化樂果、敵敵畏、克百威、樂果的批內(nèi)精密度均在±10%范圍內(nèi),批間精密度在±15%范圍內(nèi)氧化樂果的回收率在92.89%~98.35%,敵敵畏的回收率為94.36%~98.27%,克百威的回收率為92.74%~97.28%,樂果的回收率為90.36%~96.48%。結(jié)論 建立的LC/MS方法可用于血漿中有機(jī)磷的定性和定量檢測。
Abstract:
Objective To establish a liquid chromatography/mass spectrometry (LC/MS) method for detecting the plasma concentration of organophosphorus.Methods The samples were extracted by acetonitrile,and the extracted samples were detected by LC/MS.The linear of the method, precision and standard recovery rate were evaluated.Results The relationship between the sample concentration and the peak area of mass spectrum response was linear within 10~200 ng/mL,100~1 000 ng/mL in omethoate,and the minimum limit of quantitation was 10 ng/mL;The relationship between the sample concentration and the peak area of mass spectrum response was linear within 50~1 000 ng/mL,1 000~5 000 ng/mL in dichlorvos, carbofuran, dimethoate,and the minimum limit of quantitation was 50 ng/mL.The intraassay precision of omethoate, dichlorvos, carbofuran and dimethoate was within ±10%, and the inter-assay precision was within ±15%.The recovery rate of omethoate, dichlorvos, carbofuran, dimethoate were 92.89%~98.35%, 94.36%~98.27%, 92.74%~97.28%, 90.36%~96.48% respectively. Conclusion The LC/MS method we established can be used for the qualitative and quantitative detection of omethoate, dichlorvos, carbofuran and dimethoate in plasma.

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備注/Memo:
基金項目:福建省自然科學(xué)基金項目(青年創(chuàng)新)(2020J05263)
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更新日期/Last Update: 2022-08-15