Isolation and high-performance liquid chromatography analysis of chettaphanin I in extracts from Cladogynos orientalis roots

Importance of the work: Cladogynos orientalis Zipp. ex Span. is a Thai traditional plant that has been used for antiflatulence and anti-stomach pain effects.Objectives: To isolate and quantitative analysis of chettaphanin I in C. orientalis root extracts and fractions. Materials & Methods: Chett...

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Bibliographic Details
Main Author: Kongkiatpaiboon S.
Other Authors: Mahidol University
Format: Article
Published: 2023
Subjects:
Online Access:https://repository.li.mahidol.ac.th/handle/123456789/83385
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Institution: Mahidol University
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Summary:Importance of the work: Cladogynos orientalis Zipp. ex Span. is a Thai traditional plant that has been used for antiflatulence and anti-stomach pain effects.Objectives: To isolate and quantitative analysis of chettaphanin I in C. orientalis root extracts and fractions. Materials & Methods: Chettaphanin I was isolated from the root extract of C. orientalis using chromatographic techniques and structurally identified using spectroscopic and spectrometric techniques. A high-performance liquid chromatography (HPLC) method was developed and validated for the quantitative analysis of chettaphanin I in the root extracts and fractions from this plant. Results: It was found that the root ethanol extract contained a higher amount of chettaphanin I than the root decoction extract (2.97 ± 0.14% weight per weight (w/w) and 1.82 ± 0.12% w/w, respectively, in the dried extract). Using a solvent-solvent extraction process from the root decoction extract, the obtained aqueous fraction contained a significant amount of chettaphanin I (6.19 ± 0.36% w/w of dried extract) while the dichoromethane fraction contained a very low amount. Main finding: Chettaphanin I was a compound mainly found in the roots of C. orientalis which could be used as a marker for the quality control of raw materials and root extracts of this plant. HPLC method was developed and validated for quantitative analysis of chettaphanin I.