食品研究与开发
食品研究與開髮
식품연구여개발
FOOD RESEARCH AND CEVELOPMENT
2014年
24期
112-115
,共4页
黄飞%宁焕焱%奉夏平%胡昆%赵智锋%黄秀丽
黃飛%寧煥焱%奉夏平%鬍昆%趙智鋒%黃秀麗
황비%저환염%봉하평%호곤%조지봉%황수려
高效液相色谱串联质谱%植物源食品%咪唑菌酮%残留量
高效液相色譜串聯質譜%植物源食品%咪唑菌酮%殘留量
고효액상색보천련질보%식물원식품%미서균동%잔류량
HPLC-MS/MS%plant source foods%fenamidone%residue amount
建立采用高效液相色谱串联质谱仪测定植物源食品中咪唑菌酮残留量的分析方法。样品经丙酮提取,固相萃取活性炭柱净化,C18色谱柱分离,以乙腈和5 mmol/L乙酸铵甲醇水(v∶v=40∶60)溶液为流动相进行梯度洗脱,电喷雾正离子(ESI+)模式电离,多反应选择离子监测(MRM)。结果表明:咪唑菌酮在0.05μg/mL~0.8μg/mL范围内呈现良好的线性关系,相关系数(r2)大于0.999。在此范围内加标回收率为80.08%~108.53%,相对标准偏差(RSD)为1.16%~6.03%,检测限为1.0μg/kg。该方法可以满足植物源食品中咪唑菌酮残留量监测的需求。
建立採用高效液相色譜串聯質譜儀測定植物源食品中咪唑菌酮殘留量的分析方法。樣品經丙酮提取,固相萃取活性炭柱淨化,C18色譜柱分離,以乙腈和5 mmol/L乙痠銨甲醇水(v∶v=40∶60)溶液為流動相進行梯度洗脫,電噴霧正離子(ESI+)模式電離,多反應選擇離子鑑測(MRM)。結果錶明:咪唑菌酮在0.05μg/mL~0.8μg/mL範圍內呈現良好的線性關繫,相關繫數(r2)大于0.999。在此範圍內加標迴收率為80.08%~108.53%,相對標準偏差(RSD)為1.16%~6.03%,檢測限為1.0μg/kg。該方法可以滿足植物源食品中咪唑菌酮殘留量鑑測的需求。
건립채용고효액상색보천련질보의측정식물원식품중미서균동잔류량적분석방법。양품경병동제취,고상췌취활성탄주정화,C18색보주분리,이을정화5 mmol/L을산안갑순수(v∶v=40∶60)용액위류동상진행제도세탈,전분무정리자(ESI+)모식전리,다반응선택리자감측(MRM)。결과표명:미서균동재0.05μg/mL~0.8μg/mL범위내정현량호적선성관계,상관계수(r2)대우0.999。재차범위내가표회수솔위80.08%~108.53%,상대표준편차(RSD)위1.16%~6.03%,검측한위1.0μg/kg。해방법가이만족식물원식품중미서균동잔류량감측적수구。
A new method was established to detect the residue amout of fenamidone in plant source foods by high performance liquid chromatography coupled to tandem mass spectrometry (HPLC-MS/MS). The samples were extracted with acetone, then purified by activated carbon column, and detected on C18 column by a gradient elution using acetonitrile (A)-5 mmol/L ammonium acetate methanol aqueous solution (B) as mobile phase. The calibration curve were good linear between the peak areas and concentrations in the range of 0.05 μg/mL-0.8 μg/mL, with correlation coefficients more than 0.999. The average recoveries at this concentration levels ranged from 80.08%to 108.53%, the RSD was in the range of 1.16%to 6.03%. The limits of quantification of fenamidone in plant source foods were below 1.0 μg/kg. It was suitable for the determination of fenamidone residues in plant source foods with high sensitivity and selectivity.