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作 者:王穗萍[1] 夏延斌[1] 彭进[2] 郑瑶瑶[1] 熊科[1] 杨峰[1] 陆微微[1]
机构地区:[1]湖南农业大学食品科技学院,长沙410000 [2]常德市疾病预防控制中心,常德415000
出 处:《分析试验室》2007年第12期39-43,共5页Chinese Journal of Analysis Laboratory
基 金:农业部948专项经费(2003T18)项目资助
摘 要:建立了高效液相色谱法测定高油脂辣椒制品中3种主要辣味成分的方法。样品以70%乙醇提取,采用反相高效液相色谱分离,紫外检测器;根据色谱峰的保留时间定性,以外标峰面积法定量辣椒素(C)、二氢辣椒素(DC)、去甲二氢辣椒素(NDC),结果以斯氏指数(SHU)计。NDC的色谱行为与C极其类似,NDC可采用C的标准曲线定量。采用色谱柱,ZORBAX SB-C18;流动相,V(甲醇)∶V(水)=70∶30;UV检测波长,230 nm;辣椒素和二氢辣椒素RSD分别为1%,1.5%(n=5);回收率分别为97.5%、94.5%。辣椒素和二氢辣椒素在0.001-0.1 mg/mL范围内线性良好;LOD 0.1 mg/L,LOQ 0.5 mg/L。供试品溶液稳定,12 h内测定RSD为1%。方法满足辣味水平评价要求。A method was developed for the determination of capsaicinoids in highly oil-containing pepper products by high performance liquid chromatography; so that the pungency level can be measured accurately. The sample was extracted with 70% ethanol. The analysis was performed on a C18 column (250 × 4.6 mm i.d. 5 tan) with 70:30 MeOH-water as the mobile phase at a flow rote of 0.8 mL/min and detected at 230 nm. The column temperature was 30℃. The injection volume was 20 μ/L. The determination of capsaicin (C), dihydrocapsaicin (DC) and nordihydro- capsaicin (NDC) were processed by peak area and external standard method. The three compounds demonstrated good linear relationship (r 〉 0.999) in the range of 0.001 -0.1 mg/mL. Due to the similar chromatographic behavior, NDC can use the standard curve of C. The LOD was 0.1 mg/L. The LOQ was 0.5 mg/L. The precisions of C and DC were good with the RSDs of 1% and 1.5 % respectively ( n = 5). The recoveries for C and DC are 97.5 % and 94.5 % respectively.
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