Simple and robust differentiation of Ganoderma species by high performance thin-layer chromatography coupled with single quadrupole mass spectrometry QDa.
10.1016/S1875-5364(21)60030-4
- Author:
Shuai YAO
1
;
Jian-Qing ZHANG
1
;
Jin-Jun HOU
1
;
Xiao-Su HU
1
;
Ling WANG
1
;
Juan DA
1
;
Wei RAO
2
;
Dan-Dan WANG
2
;
Yong HUANG
1
;
Wan-Ying WU
3
;
De-An GUO
4
Author Information
1. Shanghai Institute of Materia Medica, Chinese Academy of Sciences, Shanghai 201203, China.
2. Waters Technology (Shanghai) Co., Ltd., Shanghai 201203, China.
3. Shanghai Institute of Materia Medica, Chinese Academy of Sciences, Shanghai 201203, China. Electronic address: wanyingwu@simm.ac.cn.
4. Shanghai Institute of Materia Medica, Chinese Academy of Sciences, Shanghai 201203, China. Electronic address: daguo@simm.ac.cn.
- Publication Type:Journal Article
- Keywords:
Authentication;
Ganoderma;
High performance thin-layer chromatography;
Mass spectrometry QDa
- From:
Chinese Journal of Natural Medicines (English Ed.)
2021;19(4):295-304
- CountryChina
- Language:English
-
Abstract:
In this study, a high performance thin-layer chromatography/single quadrupole mass spectrometry QDa (HPTLC-QDa) method for robust authentication of Ganoderma lucidum, a popular and valuable herbal medicine, has been developed. This method is simple and practical, which allows direct generation of characteristic mass spectra from the HPTLC plates automatically with the application of in situ solvent desorption interface. The HPTLC silica gel plates were developed with toluene-ethyl formate-formic acid (5 : 5 : 0.2, V/V) and all bands were transferred to QDa system directly in situ using 80% methanol with 0.1% formic acid as desorption solvent. The acquired HPTLC-QDa spectra showed that luminous yellow band b3, containing ganoderic acid B/G/H and ganodeneric acid B, the major active components of Ganoderma, could be found only in G. lucidum and G. lucidum (Antler-shaped), but not in G. sinense and G. applanatum. Moreover, bands b13 and b14 with m/z 475/477 and m/z 475/491/495, respectively, could be detected in G. lucidum (Antler-shaped), but not in G. lucidum, thus allowing simple and robust authentication of G. lucidum with confused species. This method is proved to be simple, practical and reproducible, which can be extended to analyze other herbal medicines.
