Comparison of Metabolomics Approaches for Evaluating the Variability of Complex Botanical Preparations: Green Tea (Camellia Sinensis) As a Case Study
Overview
Authors
Affiliations
A challenge that must be addressed when conducting studies with complex natural products is how to evaluate their complexity and variability. Traditional methods of quantifying a single or a small range of metabolites may not capture the full chemical complexity of multiple samples. Different metabolomics approaches were evaluated to discern how they facilitated comparison of the chemical composition of commercial green tea [Camellia sinensis (L.) Kuntze] products, with the goal of capturing the variability of commercially used products and selecting representative products for in vitro or clinical evaluation. Three metabolomic-related methods-untargeted ultraperformance liquid chromatography-mass spectrometry (UPLC-MS), targeted UPLC-MS, and untargeted, quantitative HNMR-were employed to characterize 34 commercially available green tea samples. Of these methods, untargeted UPLC-MS was most effective at discriminating between green tea, green tea supplement, and non-green-tea products. A method using reproduced correlation coefficients calculated from principal component analysis models was developed to quantitatively compare differences among samples. The obtained results demonstrated the utility of metabolomics employing UPLC-MS data for evaluating similarities and differences between complex botanical products.
A new database to guide reference material selection for dietary supplement and nutrition science.
Kuszak A, Hosbas Coskun S, Wise S Anal Bioanal Chem. 2025; .
PMID: 39812795 DOI: 10.1007/s00216-024-05664-4.
Mechanisms of intestinal pharmacokinetic natural product-drug interactions.
Oyanna V, Clarke J Drug Metab Rev. 2024; 56(3):285-301.
PMID: 39078118 PMC: 11606768. DOI: 10.1080/03602532.2024.2386597.
Green Tea Catechins Decrease Solubility of Raloxifene In Vitro and Its Systemic Exposure in Mice.
Oyanna V, Bechtold B, Lynch K, Ridge Call M, Graf T, Oberlies N Pharm Res. 2024; 41(3):557-566.
PMID: 38302834 PMC: 10939713. DOI: 10.1007/s11095-024-03662-w.
Clarke J, Judson S, Tian D, Kirby T, Tanna R, Matula-Pentek A Clin Transl Sci. 2023; 16(10):1779-1790.
PMID: 37639334 PMC: 10582660. DOI: 10.1111/cts.13578.
Oh J, Muthu M, Pushparaj S, Gopal J Molecules. 2023; 28(5).
PMID: 36903395 PMC: 10004647. DOI: 10.3390/molecules28052151.