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. 2017 Apr 7;39(5):1233–1241. doi: 10.3892/ijmm.2017.2945

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Copyright: © Son et al.

This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made.

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HPLC analysis of Ac and aqueous fraction produced by solid fermentation of Ganoderma lucidum on Artemisia capillaris (afAc/Gl). Sample extract (10 µg/ml) was used for treatment as described in the Materials and methods. Caffeic acid and chlorogenic acid were used as standard materials for HPLC. (A) Measurement of caffeic acid and other compounds in Ac or afAc/Gl extract. No peak was observed on the designated retension time period in afAc/Gl extract. (B) Detection of chlorogenic acid on Ac or afAc/Gl extract. Lane a, Gl; lane b, Ac; lane c, afAc/Gl; lane d, standard (caffeic acid or chlorogenic acid).

HPLC analysis of Ac and aqueous fraction produced by solid fermentation of Ganoderma lucidum on Artemisia capillaris (afAc/Gl). Sample extract (10 µg/ml) was used for treatment as described in the Materials and methods. Caffeic acid and chlorogenic acid were used as standard materials for HPLC. (A) Measurement of caffeic acid and other compounds in Ac or afAc/Gl extract. No peak was observed on the designated retension time period in afAc/Gl extract. (B) Detection of chlorogenic acid on Ac or afAc/Gl extract. Lane a, Gl; lane b, Ac; lane c, afAc/Gl; lane d, standard (caffeic acid or chlorogenic acid).