Identification and quantification of genipin and geniposide from Genipa americana L. by HPLC-DAD using a fused-core column

Detalhes bibliográficos
Autor(a) principal: NÁTHIA-NEVES,Grazielle
Data de Publicação: 2018
Outros Autores: NOGUEIRA,Gislaine Chystina, VARDANEGA,Renata, MEIRELES,Maria Angela de Almeida
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Food Science and Technology (Campinas)
Texto Completo: http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0101-20612018000500116
Resumo: Abstract In this work, it was developed a fast, simple and selective method for quantification of genipin and geniposide from unripe fruits of genipap, which are known as natural colorants, blue and yellow, respectively. The compounds separation was performed in a fused-core C18 column using as mobile phase water (A) and acetonitrile (B) both acidified with 0.1% formic acid, with the following gradient: 0 min, 99% A; 9 min, 75% A; 10 min, 99% A and 13 min, 99% A. The temperature and flow rate that allowed the best chromatographic performance were 35 °C and 1.5 mL/min, respectively, resulting a total run time of 13 min, including column clean-up and re-equilibration. This short analysis time represents an advantage compared to the methods reported in the literature where the running times are 2-5 times greater. The detection wavelength was set at 240 nm. The method validation was performed based on specificity, linearity, detection and quantification limits, precision and accuracy, according to ICH methodology. Finally, the developed method was suitable for monitoring analysis of those compounds content in vegetable samples.
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spelling Identification and quantification of genipin and geniposide from Genipa americana L. by HPLC-DAD using a fused-core columnblue natural colorantmethod validationiridoidsAbstract In this work, it was developed a fast, simple and selective method for quantification of genipin and geniposide from unripe fruits of genipap, which are known as natural colorants, blue and yellow, respectively. The compounds separation was performed in a fused-core C18 column using as mobile phase water (A) and acetonitrile (B) both acidified with 0.1% formic acid, with the following gradient: 0 min, 99% A; 9 min, 75% A; 10 min, 99% A and 13 min, 99% A. The temperature and flow rate that allowed the best chromatographic performance were 35 °C and 1.5 mL/min, respectively, resulting a total run time of 13 min, including column clean-up and re-equilibration. This short analysis time represents an advantage compared to the methods reported in the literature where the running times are 2-5 times greater. The detection wavelength was set at 240 nm. The method validation was performed based on specificity, linearity, detection and quantification limits, precision and accuracy, according to ICH methodology. Finally, the developed method was suitable for monitoring analysis of those compounds content in vegetable samples.Sociedade Brasileira de Ciência e Tecnologia de Alimentos2018-12-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S0101-20612018000500116Food Science and Technology v.38 suppl.1 2018reponame:Food Science and Technology (Campinas)instname:Sociedade Brasileira de Ciência e Tecnologia de Alimentos (SBCTA)instacron:SBCTA10.1590/1678-457x.17317info:eu-repo/semantics/openAccessNÁTHIA-NEVES,GrazielleNOGUEIRA,Gislaine ChystinaVARDANEGA,RenataMEIRELES,Maria Angela de Almeidaeng2019-01-21T00:00:00Zoai:scielo:S0101-20612018000500116Revistahttp://www.scielo.br/ctaONGhttps://old.scielo.br/oai/scielo-oai.php||revista@sbcta.org.br1678-457X0101-2061opendoar:2019-01-21T00:00Food Science and Technology (Campinas) - Sociedade Brasileira de Ciência e Tecnologia de Alimentos (SBCTA)false
dc.title.none.fl_str_mv Identification and quantification of genipin and geniposide from Genipa americana L. by HPLC-DAD using a fused-core column
title Identification and quantification of genipin and geniposide from Genipa americana L. by HPLC-DAD using a fused-core column
spellingShingle Identification and quantification of genipin and geniposide from Genipa americana L. by HPLC-DAD using a fused-core column
NÁTHIA-NEVES,Grazielle
blue natural colorant
method validation
iridoids
title_short Identification and quantification of genipin and geniposide from Genipa americana L. by HPLC-DAD using a fused-core column
title_full Identification and quantification of genipin and geniposide from Genipa americana L. by HPLC-DAD using a fused-core column
title_fullStr Identification and quantification of genipin and geniposide from Genipa americana L. by HPLC-DAD using a fused-core column
title_full_unstemmed Identification and quantification of genipin and geniposide from Genipa americana L. by HPLC-DAD using a fused-core column
title_sort Identification and quantification of genipin and geniposide from Genipa americana L. by HPLC-DAD using a fused-core column
author NÁTHIA-NEVES,Grazielle
author_facet NÁTHIA-NEVES,Grazielle
NOGUEIRA,Gislaine Chystina
VARDANEGA,Renata
MEIRELES,Maria Angela de Almeida
author_role author
author2 NOGUEIRA,Gislaine Chystina
VARDANEGA,Renata
MEIRELES,Maria Angela de Almeida
author2_role author
author
author
dc.contributor.author.fl_str_mv NÁTHIA-NEVES,Grazielle
NOGUEIRA,Gislaine Chystina
VARDANEGA,Renata
MEIRELES,Maria Angela de Almeida
dc.subject.por.fl_str_mv blue natural colorant
method validation
iridoids
topic blue natural colorant
method validation
iridoids
description Abstract In this work, it was developed a fast, simple and selective method for quantification of genipin and geniposide from unripe fruits of genipap, which are known as natural colorants, blue and yellow, respectively. The compounds separation was performed in a fused-core C18 column using as mobile phase water (A) and acetonitrile (B) both acidified with 0.1% formic acid, with the following gradient: 0 min, 99% A; 9 min, 75% A; 10 min, 99% A and 13 min, 99% A. The temperature and flow rate that allowed the best chromatographic performance were 35 °C and 1.5 mL/min, respectively, resulting a total run time of 13 min, including column clean-up and re-equilibration. This short analysis time represents an advantage compared to the methods reported in the literature where the running times are 2-5 times greater. The detection wavelength was set at 240 nm. The method validation was performed based on specificity, linearity, detection and quantification limits, precision and accuracy, according to ICH methodology. Finally, the developed method was suitable for monitoring analysis of those compounds content in vegetable samples.
publishDate 2018
dc.date.none.fl_str_mv 2018-12-01
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
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dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 10.1590/1678-457x.17317
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dc.publisher.none.fl_str_mv Sociedade Brasileira de Ciência e Tecnologia de Alimentos
publisher.none.fl_str_mv Sociedade Brasileira de Ciência e Tecnologia de Alimentos
dc.source.none.fl_str_mv Food Science and Technology v.38 suppl.1 2018
reponame:Food Science and Technology (Campinas)
instname:Sociedade Brasileira de Ciência e Tecnologia de Alimentos (SBCTA)
instacron:SBCTA
instname_str Sociedade Brasileira de Ciência e Tecnologia de Alimentos (SBCTA)
instacron_str SBCTA
institution SBCTA
reponame_str Food Science and Technology (Campinas)
collection Food Science and Technology (Campinas)
repository.name.fl_str_mv Food Science and Technology (Campinas) - Sociedade Brasileira de Ciência e Tecnologia de Alimentos (SBCTA)
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