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Authentication of ginkgo biloba herbal products by a novel quantitative real-time PCR approach

dc.contributor.authorGrazina, Liliana
dc.contributor.authorAmaral, Joana S.
dc.contributor.authorCosta, Joana
dc.contributor.authorMafra, Isabel
dc.date.accessioned2018-02-19T10:00:00Z
dc.date.accessioned2021-02-27T16:30:22Z
dc.date.available2018-01-19T10:00:00Z
dc.date.available2021-02-27T16:30:22Z
dc.date.issued2020
dc.description.abstractGinkgo biloba is a widely used medicinal plant. Due to its potential therapeutic effects, it is an ingredient in several herbal products, such as plant infusions and plant food supplements (PFS). Currently, ginkgo is one of the most popular botanicals used in PFS. Due to their popularity and high cost, ginkgo-containing products are prone to be fraudulently substituted by other plant species. Therefore, this work aimed at developing a method for G. biloba detection and quantification. A new internal transcribe spacer (ITS) marker was identified, allowing the development of a ginkgo-specific real-time polymerase chain reaction (PCR) assay targeting the ITS region, with high specificity and sensitivity, down to 0.02 pg of DNA. Additionally, a normalized real-time PCR approach using the delta cycle quantification (ΔCq) method was proposed for the effective quantification of ginkgo in plant mixtures. The method exhibited high performance parameters, namely PCR efficiency, coefficient of correlation and covered dynamic range (50-0.01%), achieving limits of detection and quantification of 0.01% (w/w) of ginkgo in tea plant (Camellia sinensis). The quantitative approach was successfully validated with blind mixtures and further applied to commercial ginkgo-containing herbal infusions. The estimated ginkgo contents of plant mixture samples suggest adulterations due to reduction or almost elimination of ginkgo. In this work, useful and robust tools were proposed to detect/quantify ginkgo in herbal products, which suggests the need for a more effective and stricter control of such products.en_EN
dc.description.sponsorshipThis work was supported by FCT (Fundação para a Ciência e Tecnologia) under the Partnership Agreements UIDB 50006/2020 and UIDB 00690/2020. L. Grazina is grateful to FCT grant (SFRH/BD/132462/2017) financed by POPH-QREN (subsidised by FSE and MCTES).
dc.description.versioninfo:eu-repo/semantics/publishedVersionen_EN
dc.identifier.citationGrazina, Liliana; Amaral, Joana S.; Costa, Joana; Mafra, Isabel (2020) - Authentication of ginkgo biloba herbal products by a novel quantitative real-time PCR approach. Foods. ISSN 2304-8158. 9:9, p. 1-12en_EN
dc.identifier.doi10.3390/foods9091233en_EN
dc.identifier.urihttp://hdl.handle.net/10198/23383
dc.language.isoeng
dc.peerreviewedyesen_EN
dc.relationSafety of Plant Food Supplements: advanced genomic and chemical approaches to assess botanical origin, illegal drugs and contaminants
dc.subjectAdulterationen_EN
dc.subjectAuthenticityen_EN
dc.subjectGinkgo bilobaen_EN
dc.subjectPlant infusionsen_EN
dc.subjectReal-time polymerase chain reactionen_EN
dc.titleAuthentication of ginkgo biloba herbal products by a novel quantitative real-time PCR approachen_EN
dc.typejournal article
dspace.entity.typePublication
oaire.awardTitleSafety of Plant Food Supplements: advanced genomic and chemical approaches to assess botanical origin, illegal drugs and contaminants
oaire.awardURIinfo:eu-repo/grantAgreement/FCT//SFRH%2FBD%2F132462%2F2017/PT
person.familyNameAmaral
person.givenNameJoana S.
person.identifier.ciencia-id5319-7DE8-BEDA
person.identifier.orcid0000-0002-3648-7303
project.funder.identifierhttp://doi.org/10.13039/501100001871
project.funder.nameFundação para a Ciência e a Tecnologia
rcaap.rightsopenAccessen_EN
rcaap.typearticleen_EN
relation.isAuthorOfPublication42be2cf4-adc4-4e7f-ac60-7aab515b38cd
relation.isAuthorOfPublication.latestForDiscovery42be2cf4-adc4-4e7f-ac60-7aab515b38cd
relation.isProjectOfPublication087be544-6360-497c-b38f-7b723cd3a1a2
relation.isProjectOfPublication.latestForDiscovery087be544-6360-497c-b38f-7b723cd3a1a2

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