황련 추출물의 LC-MS/MS 분석 및 항염증 효과LC-MS/MS analysis and anti-inflammatory effects of crude extract from Coptidis Rhizoma
- Other Titles
- LC-MS/MS analysis and anti-inflammatory effects of crude extract from Coptidis Rhizoma
- Authors
- 김민정; 양예진; 김광연; 김훈환; 손재동; 양주혜; 이동빈; 김우현; 이후장; 박선빈; 박광일
- Issue Date
- Feb-2023
- Publisher
- 대한한의학방제학회
- Keywords
- LC-MS/MS; Anti-inflammatory; Antioxidant; Coptidis Rhizoma.
- Citation
- 대한한의학 방제학회지, v.31, no.1, pp 1 - 10
- Pages
- 10
- Indexed
- KCI
- Journal Title
- 대한한의학 방제학회지
- Volume
- 31
- Number
- 1
- Start Page
- 1
- End Page
- 10
- URI
- https://scholarworks.gnu.ac.kr/handle/sw.gnu/30198
- DOI
- 10.14374/HFS.2023.31.1.1
- ISSN
- 1229-1218
2288-5641
- Abstract
- Objectives : The main aim of this study was to examine the LC-MS/MS used to identify phenolic compounds of CRE(Coptidis Rhizoma 70% EtOH Extract). Also, we investigated antioxidative activities and Anti-inflammatory activities.
Methods : LC-MS/MS Analysis HPLC and LC-MS/MS were performed on a 1260 series HPLC system (Agilent Technologies, Inc., California, USA) and 3200 QTrap tandem mass system (Sciex LLC) operated in positive ion mode (spray voltage set at −4.5 kV). The solvent used was DW and Acetonitrile containing 0.1% formic acid, a gradient system was used at a flow rate of 0.5 mL/min for analysis, and a Prontosil C18 column (length, 250 mm; inner diameter, 4.6 mm; particle size, 5 µm; Phenomenex Co., Ltd., California, USA, Biochoff Chromatography) was used. The solvent conditions used in the mobile phases were 0–10 min at 10–15% B, 10–20 min at 20% B, 20–30 min at 25%, 30–40 min at 40%, 40–50 min at 70%, 50–60 min at 95%, and 60–70 min at 95%. The analysis was performed at a wavelength of 284 nm and a temperature of 35℃. The cell viability was measured using a 3-(4,5-dimethyethiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) assay and 1,1-diphenyl-2-picrylhydrazyl (DPPH) radical scavenging activity. We examined the effects of CRE on the lipopolysaccharide (LPS)-induced production of nitric oxide (NO) in a RAW 264.7 cells Results : The chemical analysis CRE by Liquid chromatography-tandem mass spectrometry (LC-MS/MS) confirmed that Rosmarinic acid, Ferrulic acid, 3-O-feruloylquinic acid, and 5-O-feruloylquinic acid as phenolic components. DPPH radical scavenging activity was the inhibitory activity of CRE showed at 200 μg/mL a statistically significant level. MTT assay demonstrated that the CRE did not have a cytotoxic effect in RAW 264.7 and LPS-induced RAW264.7 cells. Also, CRE reduced NO production in RAW 264.7 cells stimulated with LPS.
Conclusions : Based on these findings, The chemical analysis 4 major components CRE such as Rosmarinic acid, Ferrulic acid, 3-O-feruloylquinic acid, and 5-O-feruloylquinic acid. Moreover, we confirmed that CRE has effects antioxidant and anti-inflammatory. The results demonstrate that CRE can be used as an antioxidant and a powerful chemopreventive ingredient against inflammatory diseases.
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Collections - 수의과대학 > Department of Veterinary Medicine > Journal Articles
- 의학계열 > 수의학과 > Journal Articles

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