Bicchi C, Cordero C, Rubiolo P, Occelli A
Dipartimento di Scienza e Tecnologia del Farmaco, Via Pietro Giuria 9, I-10125 Torino, Italy.
J Agric Food Chem. 2001 Aug;49(8):3548-52. doi: 10.1021/jf0103673.
This paper reports an HPLC-UV method to determine daminozide residues in apple pulps adopting the recently introduced EU limit of 0.01 mg/kg for baby food preparation (Commission Directive 1999/39/CE). The method is based on alkaline hydrolysis of daminozide to N',N'-dimethylhydrazine (UDMH), which is recovered by distillation and subsequently derivatizated with salicyl aldehyde to salicyl aldehyde-N,N-dimethylhydrazone under strongly basic conditions. The resulting solution was cleaned up with Extrelut 20 NT and dichloromethane as eluent, then analyzed by HPLC with a C18 column and a mobile phase programmed from 50:50 AcCN/H(2)O to 100% AcCN. The salicyl aldehyde-N,N-dimethylhydrazone was selectively detected through two diagnostic UV absorption maxima at 295 and 325 nm, which have strong molar absorbivities. Recoveries of daminozide at 0.01 mg/kg were above 80%. The limits of detection (LODs) of salicyl aldehyde-N,N-dimethylhydrazone expressed as daminozide concentration were 100 pg/microL at 295 nm and 150 pg/microL at 325 nm, and the limits of quantitation (LOQs) of daminozide were 0.0013 mg/kg at 295 nm and 0.0022 mg/kg at 325 nm.
本文报道了一种采用高效液相色谱-紫外检测法(HPLC-UV)测定苹果果肉中氨基三唑残留量的方法,该方法采用了欧盟最近对婴儿食品制剂规定的0.01 mg/kg的限量标准(欧盟委员会指令1999/39/CE)。该方法基于氨基三唑在碱性条件下水解为偏二甲基肼(UDMH),通过蒸馏回收偏二甲基肼,然后在强碱性条件下使其与水杨醛衍生化生成水杨醛-N,N-二甲基腙。所得溶液用Extrelut 20 NT净化,以二氯甲烷为洗脱剂,然后用C18柱进行HPLC分析,流动相由50:50乙腈/水线性梯度变为100%乙腈。通过在295和325 nm处的两个具有强摩尔吸光率的诊断性紫外吸收最大值选择性检测水杨醛-N,N-二甲基腙。0.01 mg/kg的氨基三唑回收率高于80%。以氨基三唑浓度表示的水杨醛-N,N-二甲基腙的检测限(LOD)在295 nm处为100 pg/μL,在325 nm处为150 pg/μL,氨基三唑的定量限(LOQ)在295 nm处为0.0013 mg/kg,在325 nm处为0.0022 mg/kg。