dc.creatorZhou, Xian
dc.creatorPower, Declan
dc.creatorJones, Andrew
dc.creatorAcquaviva, Agustín
dc.creatorDennis, Gary R.
dc.creatorShalliker, R. Andrew
dc.creatorLi, Chunguang
dc.creatorSoliven, Arianne
dc.date.accessioned2022-06-15T18:56:15Z
dc.date.accessioned2022-10-15T11:54:28Z
dc.date.available2022-06-15T18:56:15Z
dc.date.available2022-10-15T11:54:28Z
dc.date.created2022-06-15T18:56:15Z
dc.date.issued2021-07
dc.identifierZhou, Xian; Power, Declan; Jones, Andrew; Acquaviva, Agustín; Dennis, Gary R.; et al.; Antioxidant profiling of ginger via reaction flow chromatography; Natural Products; Natural Product Communications; 16; 9; 7-2021; 1-6
dc.identifier1934-578X
dc.identifierhttp://hdl.handle.net/11336/159862
dc.identifierCONICET Digital
dc.identifierCONICET
dc.identifier.urihttps://repositorioslatinoamericanos.uchile.cl/handle/2250/4383154
dc.description.abstractReaction 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.
dc.languageeng
dc.publisherNatural Products
dc.relationinfo:eu-repo/semantics/altIdentifier/doi/http://dx.doi.org/10.1177/1934578X211035286
dc.relationinfo:eu-repo/semantics/altIdentifier/url/https://journals.sagepub.com/doi/10.1177/1934578X211035286
dc.rightshttps://creativecommons.org/licenses/by-nc/2.5/ar/
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectANTIOXIDANT
dc.subjectFERRIC REDUCING ANTIOXIDANT POWER ASSAY
dc.subjectGINGER
dc.subjectPOST COLUMN DERIVATIZATION
dc.subjectREACTION FLOW CHROMATOGRAPHY
dc.subjectSELECTIVE DETECTION
dc.titleAntioxidant profiling of ginger via reaction flow chromatography
dc.typeinfo:eu-repo/semantics/article
dc.typeinfo:ar-repo/semantics/artículo
dc.typeinfo:eu-repo/semantics/publishedVersion


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