分析化学
分析化學
분석화학
CHINESE JOURNAL OF ANALYTICAL CHEMISTRY
2015年
2期
282-287
,共6页
麦沛明%余胜兵%吴西梅%苏广宁%钟秀华%朱炳辉
麥沛明%餘勝兵%吳西梅%囌廣寧%鐘秀華%硃炳輝
맥패명%여성병%오서매%소엄저%종수화%주병휘
分散液-液微萃取%生物碱%鼠药%气相色谱-质谱%同时测定
分散液-液微萃取%生物堿%鼠藥%氣相色譜-質譜%同時測定
분산액-액미췌취%생물감%서약%기상색보-질보%동시측정
Dispersive liquid-liquid micro-extraction%Alkaloids%Rat poison%Gas chromatography-mass spectrometry%Simultaneous determination
建立了分散液-液微萃取( Dispersive liquid-liquid micro-extraction, DLLME)与气相色谱-质谱( GC-MS)联用同时测定中毒样品中3种鼠药(毒鼠强、溴鼠灵、溴敌隆)和5种有毒生物碱(莨菪碱、东莨菪碱碱、钩吻碱、士的宁、马钱子碱)的方法。100μL萃取剂氯仿与600μL分散剂甲醇混合后,迅速注入样品,萃取过程在乳化体系中完成;以8000 r/min离心5 min,使两相分层,取下层有机相进行GC-MS分析。考察了萃取剂、分散剂的种类和体积、萃取时间、pH值及盐浓度对萃取效率的影响。在优化条件下,各目标物在水样、尿样、黄酒样的检出限为0.003~1.0μg/L,在米饭样品检出限为0.002~0.2μg/kg;各目标物低、中、高加标回收率为81.0%~110%,精密度均小于7%。本方法灵敏度高,快捷高效,适用于中毒样品中有毒生物碱和鼠药的同时测定。
建立瞭分散液-液微萃取( Dispersive liquid-liquid micro-extraction, DLLME)與氣相色譜-質譜( GC-MS)聯用同時測定中毒樣品中3種鼠藥(毒鼠彊、溴鼠靈、溴敵隆)和5種有毒生物堿(莨菪堿、東莨菪堿堿、鉤吻堿、士的寧、馬錢子堿)的方法。100μL萃取劑氯倣與600μL分散劑甲醇混閤後,迅速註入樣品,萃取過程在乳化體繫中完成;以8000 r/min離心5 min,使兩相分層,取下層有機相進行GC-MS分析。攷察瞭萃取劑、分散劑的種類和體積、萃取時間、pH值及鹽濃度對萃取效率的影響。在優化條件下,各目標物在水樣、尿樣、黃酒樣的檢齣限為0.003~1.0μg/L,在米飯樣品檢齣限為0.002~0.2μg/kg;各目標物低、中、高加標迴收率為81.0%~110%,精密度均小于7%。本方法靈敏度高,快捷高效,適用于中毒樣品中有毒生物堿和鼠藥的同時測定。
건립료분산액-액미췌취( Dispersive liquid-liquid micro-extraction, DLLME)여기상색보-질보( GC-MS)련용동시측정중독양품중3충서약(독서강、추서령、추활륭)화5충유독생물감(랑탕감、동랑탕감감、구문감、사적저、마전자감)적방법。100μL췌취제록방여600μL분산제갑순혼합후,신속주입양품,췌취과정재유화체계중완성;이8000 r/min리심5 min,사량상분층,취하층유궤상진행GC-MS분석。고찰료췌취제、분산제적충류화체적、췌취시간、pH치급염농도대췌취효솔적영향。재우화조건하,각목표물재수양、뇨양、황주양적검출한위0.003~1.0μg/L,재미반양품검출한위0.002~0.2μg/kg;각목표물저、중、고가표회수솔위81.0%~110%,정밀도균소우7%。본방법령민도고,쾌첩고효,괄용우중독양품중유독생물감화서약적동시측정。
A novel method for simultaneous determination of 3 rat poisons ( tetramine, bromadiolone, brodifacoum) and 5 toxic alkaloids ( hyoscyamine, scopolamine, gelsemine, strychnine, brucine ) in toxic samples by dispersive liquid-liquid micro-extraction ( DLLME ) coupled with gas chromatography-mass spectrometry was established. A mixture extractant containing 100 μL trichloromethane and 600 μL methanol was injected into the prepared sample to form an emulsion and the extraction process was accomplished. After centrifuged at 8000 r/min for 5 min, the settled drop of trichloromethane solvent was transferred to a conical insert within a GC autosampler vessel, and analyzed by GC-MS. Factors affecting extraction efficiency such as the type and volume of extractant, dispersive agent, extraction time, pH value and salt concentration of extraction system were studied. The limits of detection(LODs) were from 0. 003 to 1 μg/L in water sample, urine sample and rice wine sample. LODs were from 0. 002 to 0. 2 μg/kg in rice sample. The recoveries of toxic samples were in the range of 81. 0%-110%. The relative standard deviations( RSDs) were lower than 7%. The proposed method was sensitive, effective, and suitable for the simultaneous determination of toxic alkaloids and rat poisons in food poisoning sample.