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Cited 6 time in webofscience Cited 5 time in scopus
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Mass spectrometry-based ginsenoside profiling: Recent applications, limitations, and perspectivesopen access

Authors
Kim, Hyun WooKim, Dae HyunRyu, ByeolChung, You JinLee, KyunghaKim, Young ChangLee, Jung WooKim, Dong HwiJang, WoojongCho, WoohyeonShim, HyeonahSung, Sang HyunYang, Tae-JinKang, Kyo Bin
Issue Date
Mar-2024
Publisher
고려인삼학회
Keywords
Chemical profiling; Genetic variation; Ginseng; Ginsenoside; Mass spectrometry
Citation
Journal of Ginseng Research, v.48, no.2, pp 149 - 162
Pages
14
Indexed
SCIE
SCOPUS
KCI
Journal Title
Journal of Ginseng Research
Volume
48
Number
2
Start Page
149
End Page
162
URI
https://scholarworks.dongguk.edu/handle/sw.dongguk/22710
DOI
10.1016/j.jgr.2024.01.004
ISSN
1226-8453
2093-4947
Abstract
Ginseng, the roots of Panax species, is an important medicinal herb used as a tonic. As ginsenosides are key bioactive components of ginseng, holistic chemical profiling of them has provided many insights into understanding ginseng. Mass spectrometry has been a major methodology for profiling, which has been applied to realize numerous goals in ginseng research, such as the discrimination of different species, geographical origins, and ages, and the monitoring of processing and biotransformation. This review summarizes the various applications of ginsenoside profiling in ginseng research over the last three decades that have contributed to expanding our understanding of ginseng. However, we also note that most of the studies overlooked a crucial factor that influences the levels of ginsenosides: genetic variation. To highlight the effects of genetic variation on the chemical contents, we present our results of untargeted and targeted ginsenoside profiling of different genotypes cultivated under identical conditions, in addition to data regarding genome-level genetic diversity. Additionally, we analyze the other limitations of previous studies, such as imperfect variable control, deficient metadata, and lack of additional effort to validate causation. We conclude that the values of ginsenoside profiling studies can be enhanced by overcoming such limitations, as well as by integrating with other -omics techniques. © 2024
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