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:杜雪红[1] 辛晓莹 王计彭 张红医[1] 杨冰 DU Xuehong;XIN Xiaoying;WANG Jipeng;ZHANG Hongyi;YANG Bing(College of Chemistry and Environmental Science,Hebei University,Baoding 071002,China)
机构地区:[1]河北大学化学与环境科学学院,河北保定071002
出 处:《河北大学学报(自然科学版)》2018年第6期596-602,共7页Journal of Hebei University(Natural Science Edition)
基 金:教育部留学回国人员科研启动基金(47批);河北大学校内科研项目(799207022;799207217014);河北大学创新资助项目(hbu2018ss21);河北大学2018年校级大学生创新创业计划项目
摘 要:建立了一种pH依赖型悬浮固化液-液微萃取-HPLC测定尿液中大黄素和大黄酚的方法.该方法选择辛酸钠为萃取剂前体,在加入酸性样品溶液的过程中原位形成萃取剂辛酸.将100μL辛酸钠溶液注入到事先酸化的10mL样品水溶液中,经离心和冰浴后,萃取液固化并浮于溶液上层,取出固化的萃取液并溶解于50μL甲醇供HPLC分析使用.对作为萃取剂的酸种类、辛酸钠体积、离子强度、离心时间等重要因素进行了优化.在最优条件下,大黄素和大黄酚在5~400ng/mL内与峰面积间存在良好的线性关系(R2>0.999),检出限为0.75~0.8ng/mL,相对标准偏差为2.0%~3.2%(n=5).将该方法应用于添加后的尿液样品分析,回收率为82%~110%.该法萃取过程中避免了有机分散溶剂的使用,萃取时间短,操作简单,成本低,绿色环保,非常适于与液相色谱分析联合使用.A method for the determination of anthraquinones in urine was developed by the combination of pH-dependent solidified floating liquid-liquid microextraction with HPLC.Octanoic acid chosen as extraction solvent was dissolved in alkaline solution,and 100μL of it was taken and injected into 10 mL aqueous solution which had been acidified.After centrifugation for 4 min and ice bath for 2 min,the extract was floated on the surface of the aqueous sample.The extract was taken out and dissolved with 50μL methanol for HPLC analysis.The main factors,such as acid type,sodium octanate volume,ion strength and centrifugal time,were systematically investigated.In the optimal conditions,there was a good linear relationship of peak areas for emodin and chrysophanol with their concentrations in the range of 5-400 ng/mL(R 2>0.999),with detection limit 0.75-0.8 ng/mL,and the relative standard deviation 2.0%~3.2%(n=5).The method was applied to the analysis of urine samples,and the recovery after spiking was in the range of 82%and 110%.The extraction process avoids the use of organic dispersive solvents.The advantages of the proposed method are short extraction time,simple operation,low consumption and friendly environment,and very suitable for the combination with liquid chromatography analysis.
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:216.73.216.49