检索规则说明:AND代表“并且”;OR代表“或者”;NOT代表“不包含”;(注意必须大写,运算符两边需空一格)
检 索 范 例 :范例一: (K=图书馆学 OR K=情报学) AND A=范并思 范例二:J=计算机应用与软件 AND (U=C++ OR U=Basic) NOT M=Visual
作 者:董爱军[1] 杨鑫[1] 张英春[1] 张华[1] 井晶[1]
机构地区:[1]哈尔滨工业大学食品科学与工程学院,黑龙江哈尔滨150090
出 处:《食品工业科技》2013年第24期64-66,69,共4页Science and Technology of Food Industry
摘 要:建立了测定秋葵干蔬中β-胡萝卜紊的高效液相色谱法。样品皂化后,采用反相高效液相色谱-紫外可见检测器进行测定,外标法定量。色谱柱为C18柱(250mm×4.6mm,i.d.5μm),流动相为乙腈-甲醇-乙酸乙酯(88:10:2),流速1mL/min,检测波长453nm。结果表明,β-胡萝卜素在0.1-10.0mg/L浓度范围内呈现良好的线性关系,相关系数为0.996;β-胡萝卜素的回收率为82.4%~94.0%,相对标准偏差(RSD)为2.28%-5.43%;秋葵干蔬中β-胡萝卜素的检出限(LOD)为0.08mg/kg,定量下限(LOQ)为0.26mg/kg。本方法的准确度和精密度都很高,能够满足实际测定需要。Okra was a popular health food in the world,and it could be used for many purposes,such as a vegetable,soup ingredient and fat substitute in chocolate. In this paper,a method was developed for the determination of β-carotene in dried okra by reverse phase high performance liquid chromatography(RP- HPLC). After the sample was extracted with ethanol,the mixture was saponified at room temperature overnight, and then the saponification liquid was extracted with n-hexane. The extract was separated on a C18 column (250mm×4.6mm,5μm) at 30℃,which was eluted with acetonitrile-methyl alcohol-ethyl acetate(88:10:2,v:v:v) at a rate of lmL/min,and the signal was detected at 453nm. The results showed that:β-carotene was linear over the concentration range of 0.1-10.0mg/L with a correlation coefficient of 0.996 ;the recovery of β-carotene in dried okra was 82.4%-94.0%,the relative standard deviations(RSD) was 2.28%-5.43%,the limit of detection (LOD) of β-carotene in dried okra was 0.08mg/kg,the limit of quantification(LOQ) was 0.26mg/kg. This method was reliable and accurate,and it could meet the demands of actual measurement.
分 类 号:TS207.3[轻工技术与工程—食品科学]
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在链接到云南高校图书馆文献保障联盟下载...
云南高校图书馆联盟文献共享服务平台 版权所有©
您的IP:216.73.216.214