食品研究与开发
食品研究與開髮
식품연구여개발
FOOD RESEARCH AND CEVELOPMENT
2014年
12期
69-72
,共4页
人参蜂王浆口服液%药物残留%HPLC-MS/MS
人參蜂王漿口服液%藥物殘留%HPLC-MS/MS
인삼봉왕장구복액%약물잔류%HPLC-MS/MS
ginseng and royal jelly oral liquid%antibiotics residues%HPLC-MS/MS
建立了同时测定人参蜂王浆口服液中15种抗生素药物(6种喹诺酮类、4种四环素类、3种大环内酯类、2种林可胺类)残留的高效液相色谱-串联质谱(LC-MS/MS)检测方法。该方法采用pH 8.0磷酸盐缓冲液提取样品,提取液经HLB固相萃取柱净化。以甲醇-乙腈-0.1%甲酸作为流动相,C18色谱柱对15种药物进行分离,电喷雾正离子多反应监测模式进行检测。方法检测限为0.02 ng/mL~0.9 ng/mL,线性范围0.08 ng/mL~20 ng/mL,加标回收率为71.8%~87.8%,相对标准偏差为2.2%~7.9%(n=9)。该方法准确、灵敏、简便,适用于人参蜂王浆口服液中四环素等药物残留的测定。
建立瞭同時測定人參蜂王漿口服液中15種抗生素藥物(6種喹諾酮類、4種四環素類、3種大環內酯類、2種林可胺類)殘留的高效液相色譜-串聯質譜(LC-MS/MS)檢測方法。該方法採用pH 8.0燐痠鹽緩遲液提取樣品,提取液經HLB固相萃取柱淨化。以甲醇-乙腈-0.1%甲痠作為流動相,C18色譜柱對15種藥物進行分離,電噴霧正離子多反應鑑測模式進行檢測。方法檢測限為0.02 ng/mL~0.9 ng/mL,線性範圍0.08 ng/mL~20 ng/mL,加標迴收率為71.8%~87.8%,相對標準偏差為2.2%~7.9%(n=9)。該方法準確、靈敏、簡便,適用于人參蜂王漿口服液中四環素等藥物殘留的測定。
건립료동시측정인삼봉왕장구복액중15충항생소약물(6충규낙동류、4충사배소류、3충대배내지류、2충림가알류)잔류적고효액상색보-천련질보(LC-MS/MS)검측방법。해방법채용pH 8.0린산염완충액제취양품,제취액경HLB고상췌취주정화。이갑순-을정-0.1%갑산작위류동상,C18색보주대15충약물진행분리,전분무정리자다반응감측모식진행검측。방법검측한위0.02 ng/mL~0.9 ng/mL,선성범위0.08 ng/mL~20 ng/mL,가표회수솔위71.8%~87.8%,상대표준편차위2.2%~7.9%(n=9)。해방법준학、령민、간편,괄용우인삼봉왕장구복액중사배소등약물잔류적측정。
A HPLC-MS/MS method was established for simultaneous determination of 15 drug residues (6 quinolones,4 tetracyclines,3 macrolides,lincomycin and clindamycin)in Ginseng and Royal Jelly Oral Liquid. Samples were extracted with phosphate buffer solution (pH=8.0)and then purified by Oasis HLB solid phase extraction column. Chromatographic separation was carried out on a C18 column,the mobile phase is methanol-acetonitrile-0.1%formic acid water solution with gradient elution, then detected by MS/MS in the ESI(+)-MRM mode.The limits of detection for the method were 0.02 ng/mL-0.9 ng/mL,The linear plots were obtained between 0.08 ng/mL-20 ng/mL,recoveries ranged from 71.8%-87.8%,and relative standard deviations were in the range of 2.2%-7.9%(n=9).