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Adsorption separation of 3b-D-monoglucuronyl-18b-glycyrrhetinic
acid from directional biotransformation products of
glycyrrhizin
Dingqiang Lu1,
2*, Shumin Zhang1, Jun Wang1,
Hui Li1 and Yan Dai1
1College
of Life Science and Pharmaceutical Engineering, Nanjing
University of Technology, Nanjing 210009, P.R. China.
2Jiangsu
Provincial Institute of Materia Medica, Nanjing 210009, P.R.
China.
*Corresponding author. E-mail:
ludingqiang@njut.edu.cn. Tel: 86-25- 8328-5202.
Accepted
22 September, 2008 |
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3β-D-monoglucuronyl-18b-glycyrrhetinic acid (GAMG) can be
obtained on a large scale by directional hydrolysis of
glycyrrhizin (GL) with b-glucuronidases, which has more
physiologically potential application than GL in a wide
range of biological activities. In this study, the
preparative separation of GAMG in hydrolysates of GL by
macroporous resins (NKA-9, D4020, HZ-803, 1300, HP-20 and
X-5) were studied systematically, and the column packed with
selected resin was used to perform dynamic adsorption and
desorption tests to optimize the separation process. The
results shown that NKA-9 resins was the appropriate resin
for the separation of GAMG and GL under pH 5, which
adsorption data fitted to the Freundlich isotherm equation
and pseudo-second-order kinetic model at 25șC. While with
desorption of 70-90% ethanol-water solution, GAMG with the
purity of 85.02% was obtained on a NKA-9 resins packed
column. Comparing with conventional methods, the developed
method can successfully improve product yield and reduce the
consumption of raw materials in the biotransformation
process of GL. The structure identification of each pure
fraction was carried out by 1H and 13C
NMR.
Key words:
3b-D-monoglucuronyl-18b-glycyrrhetinic acid
(GAMG),
glycyrrhizin (GL), adsorption
separation, macroporous resin, directional
bio-transformation.
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