Antioxidant Profiling of Ginger via Reaction Flow Chromatography

Author:

Zhou Xian1ORCID,Power Declan12,Jones Andrew3,Acquaviva Agustín4,Dennis Gary R.3,Shalliker R. Andrew34,Li Chunguang1,Soliven Arianne13

Affiliation:

1. NICM Health Research Institute, Western Sydney University, Penrith, Australia

2. School of Medicine, Western Sydney University, Campbelltown, Australia

3. Australian Centre for Research on Separation Science (ACROSS), School of Science and Health, Western Sydney University, Parramatta, Australia

4. Laboratorio de Investigación y Desarrollo de Métodos Analíticos (LIDMA), Facultad de Ciencias Exactas, Universidad Nacional de La Plata, La Plata, Argentina

Abstract

Reaction flow (RF) chromatography is a powerful and efficient approach that utilizes conventional high-performance liquid chromatography (HPLC)–ultraviolet (UV)–visible detection. This technique exploits a novel column end-fitting and an extra HPLC pump that delivers a reagent specific for selective detection, in particular the antioxidant profiling of natural products. This study employed RF for the first time to identify antioxidants in a commercial ginger sample. This demonstrated the previously validated assay's ease and power to extract information about the natural product's antioxidant properties. Due to the simplicity involved with data analysis and peak matching process, the following information was revealed between the chemical and antioxidant profiles: three of the strongest antioxidant activity peaks in the ginger sample (593 nm) did not correlate with the three most abundant chemical profile peaks (UV absorbance at 254 and 280 nm); the ratio of seven antioxidant peaks may be potentially used for food authenticity purposes, and future research should target these peaks for the early discovery of novel antioxidants sourced in ginger. Utilization of this previously validated assay provided the resolution of numerous peaks in the ginger extract and information associated with their antioxidant attributes and chemical abundance. This approach is more informative than total antioxidant assays that lack compound specificity information. Furthermore, it is superior to mass spectrometric (MS) assays that cannot evaluate each compound's antioxidant strength, and does not involve the expense involved in the acquisition and maintenance of the MS detection hardware, and does not require the high level of expertise needed to conduct the MS data analysis.

Funder

Australian Research Council

Publisher

SAGE Publications

Subject

Complementary and alternative medicine,Plant Science,Drug Discovery,Pharmacology,General Medicine

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