Identification and quantification of genipin and geniposide from Genipa americana L. by HPLC-DAD using a fused-core column
Autor(a) principal: | |
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Data de Publicação: | 2018 |
Outros Autores: | , , |
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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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 |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0101-20612018000500116 |
url |
http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0101-20612018000500116 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
10.1590/1678-457x.17317 |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
text/html |
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) |
repository.mail.fl_str_mv |
||revista@sbcta.org.br |
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1752126322957615104 |