Ligand exchange chromatography with chiral mobile phases was established for the separation of theanine enantiomers.The optimum condition was :Polaris C18 column, mobile phase: L-proline: Cu2+=2:1, the concentration of Cu2+ was 0.5βmmol/L, pH6.8, the volume of methanol is 2%, wavelength: 254βnm;flow rate:0.9βml/min, column temperature:30℃. There was a good linearity between peak areas and injection quantities of L-Theanine ranging from 0.09542βμg~4.241βμg and D-Theanine ranging from 0.08486βμg~4.243βμg. The recovery of L-Theanine range from 97.45%~100.4% and D-Theanine range from 97.07%~100.1%.
LI Yin-hua
,
LIU Zhong-hua
,
HUANG Jian-an
. Separation and Quantitation of Theanine Enantiomers on Ligand Exchange Chromatography with Chiral Mobile Phase[J]. Journal of Tea Science, 2006
, 26(4)
: 280
-284
.
DOI: 10.13305/j.cnki.jts.2006.04.009
[1] 肖伟涛, 朱小兰, 陈波, 等. 制备高效液相色谱分离纯化茶氨酸对照品[J]. 中草药, 2004, 35(2): 148~150.
[2] 张莹, 施兆鹏, 施玲.茶氨酸的研究进展[J].天然产物研究与开发, 2003, 15(4): 369~372.
[3] Feibush B, Cohen M J, Karger B L.The role of bonded phase composition on the ligand-exchange chromatography of dansyl-D, L-amino acids[J]. J Chromatogr, 1983, 282(1~2): 3~26.
[4] Davankov V A.Chiral selectors with chelating properties in liquid chromatography:fundamental reflections and selective review of recent developments[J]. J Chromatogr, A, 1994, 666(1~2): 55~76.
[5] Davankov V A, Kurganov A A, Ponomareva T M.Enantioselectivity of complex formation in ligand-exchange chromatographic systems with chiral stationary and/or chiral mobile phases[J]. J Chromatogr, 1988(452): 309~316.