色谱
色譜
색보
CHINESE JOURNAL OF CHROMATOGRAPHY
2014年
10期
1104-1110
,共7页
许森%李秀琴%罗锡明%张庆合
許森%李秀琴%囉錫明%張慶閤
허삼%리수금%라석명%장경합
同位素稀释质谱法%克伦特罗%猪肉%国际比对
同位素稀釋質譜法%剋倫特囉%豬肉%國際比對
동위소희석질보법%극륜특라%저육%국제비대
isotopic dilution mass spectrometry( IDMS)%clenbuterol%porcine meat%interna-tional comparison
建立了同位素稀释质谱法( IDMS)测定猪肉中克伦特罗含量的高准确度方法,并应用于亚太计量规划组织(Asia Pacific Metrology Programme,APMP)开展的国际比对“猪肉中克伦特罗含量测定”(APMP. QM-S6)。本研究考察了影响测定结果的喷雾电压值、流动相、色谱柱、提取条件、净化条件等主要因素并进行了优化,并对测定结果的不确定度进行了评定。结果表明:流动相组成以及 pH 值会影响克伦特罗的质谱响应以及最优的电喷雾电压值;样品溶剂会影响克伦特罗的色谱保留,甲醇溶剂会引起严重的溶剂效应,甚至导致峰分裂;克伦特罗易在固相萃取柱及亲水性滤膜上吸附,且吸附材料和滤膜上吸附的杂质有可能被洗脱,引起基质效应,干扰测定。提取效率最高的方法是采用0.1%( v/v)甲酸乙腈溶液为提取溶剂,通过匀浆进行提取。方法检出限(以信噪比大于3计)为0.2μg/kg。比对样品中克伦特罗的含量为5.18μg/kg±0.50μg/kg(k=2),比对结果与参考值等效一致,取得国际互认。该方法准确可靠,可为猪肉中克伦特罗的日常检测提供参考。
建立瞭同位素稀釋質譜法( IDMS)測定豬肉中剋倫特囉含量的高準確度方法,併應用于亞太計量規劃組織(Asia Pacific Metrology Programme,APMP)開展的國際比對“豬肉中剋倫特囉含量測定”(APMP. QM-S6)。本研究攷察瞭影響測定結果的噴霧電壓值、流動相、色譜柱、提取條件、淨化條件等主要因素併進行瞭優化,併對測定結果的不確定度進行瞭評定。結果錶明:流動相組成以及 pH 值會影響剋倫特囉的質譜響應以及最優的電噴霧電壓值;樣品溶劑會影響剋倫特囉的色譜保留,甲醇溶劑會引起嚴重的溶劑效應,甚至導緻峰分裂;剋倫特囉易在固相萃取柱及親水性濾膜上吸附,且吸附材料和濾膜上吸附的雜質有可能被洗脫,引起基質效應,榦擾測定。提取效率最高的方法是採用0.1%( v/v)甲痠乙腈溶液為提取溶劑,通過勻漿進行提取。方法檢齣限(以信譟比大于3計)為0.2μg/kg。比對樣品中剋倫特囉的含量為5.18μg/kg±0.50μg/kg(k=2),比對結果與參攷值等效一緻,取得國際互認。該方法準確可靠,可為豬肉中剋倫特囉的日常檢測提供參攷。
건립료동위소희석질보법( IDMS)측정저육중극륜특라함량적고준학도방법,병응용우아태계량규화조직(Asia Pacific Metrology Programme,APMP)개전적국제비대“저육중극륜특라함량측정”(APMP. QM-S6)。본연구고찰료영향측정결과적분무전압치、류동상、색보주、제취조건、정화조건등주요인소병진행료우화,병대측정결과적불학정도진행료평정。결과표명:류동상조성이급 pH 치회영향극륜특라적질보향응이급최우적전분무전압치;양품용제회영향극륜특라적색보보류,갑순용제회인기엄중적용제효응,심지도치봉분렬;극륜특라역재고상췌취주급친수성려막상흡부,차흡부재료화려막상흡부적잡질유가능피세탈,인기기질효응,간우측정。제취효솔최고적방법시채용0.1%( v/v)갑산을정용액위제취용제,통과균장진행제취。방법검출한(이신조비대우3계)위0.2μg/kg。비대양품중극륜특라적함량위5.18μg/kg±0.50μg/kg(k=2),비대결과여삼고치등효일치,취득국제호인。해방법준학가고,가위저육중극륜특라적일상검측제공삼고。
A method was developed for the determination of clenbuterol in porcine meat by iso-topic dilution mass spectrometry( IDMS). National Institute of Metrology of China( NIM)par-ticipated in the international comparison activity organized by Asia Pacific Metrology( APMP) and got an international mutual recognition result using this method. The important factors of the method,such as the spray voltage,mobile phase,chromatographic column,extraction, purification and filtration conditions were investigated to acquire optimum conditions. The opti-mization results showed that the composition and pH value of the mobile phase had effects on the response of the mass spectrum of clenbuterol and the optimal value of the spray voltage. The solvent of sample had influences on the chromatographic retention behavior of clenbuterol. It was found that methanol caused a serious solvent effect,even made chromatographic peak split. Since clenbuterol was easily adsorbed on hydrophilic filter membranes and solid phase extraction columns,there were interference suppressions for the quantification of clenbuterol because of the eluate of the solid phase extraction columns. The homogenate method with extraction solvent of 0. 1% ( v/v ) formic acid in acetonitrile had the highest extraction efficiency. The limit of the detection(LOD,S/N﹥3)of the method was 0.2 μg/kg. The determination results of clenbuterol in the porcine meat by this method were 5. 18 μg/kg±0. 50μg/kg( k=2). This method is accurate,reliable,reproducible,and suitable for the determina-tion of clenbuterol with trace quantity in porcine meat.