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手性荧光衍生化反相高效液相法分离肾上腺素对映体
引用本文:金东日,马奎蓉,张小勇,吴信子,崔胜云,朱玉兰,丰冈利正.手性荧光衍生化反相高效液相法分离肾上腺素对映体[J].色谱,2002,20(4):304-307.
作者姓名:金东日  马奎蓉  张小勇  吴信子  崔胜云  朱玉兰  丰冈利正
作者单位:1. 延边大学理工学院化学系,吉林,延吉,133002
2. 延边大学药学院,吉林,延吉,133002
3. 日本静冈县立大学药学部分析化学系,日本,静冈,422-8526
基金项目:教育部留学回国人员科研启动基金资助项目
摘    要: 以R (- ) /S (+) 4 (N ,N dimethylaminosulfonyl) 7 (3 iso thiocyanatopyrrolidino) 2 ,1,3 benzoxadiazole(DBD PyNCS)为手性荧光衍生化试剂 ,用反相高效液相法 (RP HPLC)对 DL 肾上腺素对映体进行分离。衍生化反应是在含有 7%吡啶的溶剂中 ,6 5℃温度条件下反应 35min ,生成具有荧光特性的肾上腺素非对映体衍生物(λex=4 6 0nm ,λem=5 5 0nm)。生成的非对映体衍生物在流动相为乙腈 水 (体积比为 2 8∶72 ) ,流速为 1 0mL/min时 ,在DiamonsilTMC18柱 (15 0mm× 4 6mmi d ,5 μm)上分离度可达 2 6。

关 键 词:手性荧光衍生化试剂  反相高效液相法  肾上腺素对映体
文章编号:1000-8713(2002)04-0304-04
修稿时间:2002年4月1日

Resolution of the Epinephrine Enantiomers Derivatized with Fluorescent Chiral Reagent by Reversed-Phase High Performance Liquid Chromatography
JIN Dong ri ,MA Kui rong ,ZHANG Xiao yong ,WU Xin zi ,CUI Sheng yun ,ZHU Yu lan ,TOYO'OKA Toshimasa.Resolution of the Epinephrine Enantiomers Derivatized with Fluorescent Chiral Reagent by Reversed-Phase High Performance Liquid Chromatography[J].Chinese Journal of Chromatography,2002,20(4):304-307.
Authors:JIN Dong ri  MA Kui rong  ZHANG Xiao yong  WU Xin zi  CUI Sheng yun  ZHU Yu lan  TOYO'OKA Toshimasa
Institution:Department of Chemistry, Science and Engineering College of Yanbian University, Yanji 133002, China.
Abstract:A new method was developed to separate epinephrine enantiomers derivatized with fluorescent chiral reagent, R-(-)/S-(+)-4-(N, N-dimethylaminosulfonyl)-7-(3-iso-thiocyanatopyrrolidino)-2, 1, 3-benzoxadiazole (DBD-PyNCS), by reversed-phase high performance liquid chromatography, on a Diamonsil C18 column(150 mm x 4.6 mm i.d., 5 microns), with a mobile phase of water-acetonitrile(72:28, volume ratio) and a fluorescent detector at the excitation wavelength of 460 nm and the emission wavelength of 550 nm. The column was eluted at 40 degrees C, with a flow rate of 1 mL/min. At first, let the fluorescent chiral reagent(36 mmol/L, 10 microL) react with epinephrine enantiomers(1 mmol/L, 10 microL), and then 10 microL 20% pyridine acetonitrile solution was added. The resulting mixture was stirred for 1 min and kept at 65 degrees C for 35 min and then a 10 microL aqueous of the diastereomeric derivatives was injected directly into the chromatograph. The diastereomeric compounds were efficiently separated. The Rs value was 2.6 with alpha of 1.07. The k's of L-epinephrine and D-epinephrine were 17.11 and 18.13 respectively. The retention times of L-epinephrine and D-epinephrine were 30.24 min and 31.94 min respectively. The linear range was 0.07 g/L -0.50 g/L (r = 0.9995). The RSD was 4.3%(n = 7). The detection limit was 12 g/L(S/N = 3).
Keywords:fluorescent chiral derivatization reagent  reversed  phase high performance liquid chromatography  epinephrine enantiomer
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