Antioxidant activity of the melanoidin fractions formed from D-Glucose and D-Fructose with L-Asparagine in the Maillard reaction

Melanoidins formed at the last stage of the Maillard reaction have been shown to possess certain functional properties, such as antioxidant activity. In order to gain more insight into these functional properties, soluble model systems melanoidins from L - Asparagine with D - glucose or D - fructose...

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Main Authors: A.P Echavarría, J. Pagán, A. Ibarz
Format: Article
Language:English
Published: Universidad Nacional de Trujillo 2013-01-01
Series:Scientia Agropecuaria
Online Access:http://www.redalyc.org/articulo.oa?id=357633710005
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spelling doaj-48c619cf028c4d328c9434fe731262c72020-11-24T21:58:33ZengUniversidad Nacional de TrujilloScientia Agropecuaria2077-99172306-67412013-01-01414554Antioxidant activity of the melanoidin fractions formed from D-Glucose and D-Fructose with L-Asparagine in the Maillard reactionA.P EchavarríaJ. PagánA. IbarzMelanoidins formed at the last stage of the Maillard reaction have been shown to possess certain functional properties, such as antioxidant activity. In order to gain more insight into these functional properties, soluble model systems melanoidins from L - Asparagine with D - glucose or D - fructose fractionating by ultrafiltration were analyzed. The fractionating/concentration sequence of the melanoidin fraction (1 - 300 kDa) enabled five fractions to be produced. Additionally, the absorption of melanoidins was measured at different wavelengths (280, 325, 405) and browning at 420 nm. The fractionati on effect of melanoidin systems on the color intensity, UV - absorbance scan wavelengths (nm), CIE, L*, a*, b* parameters and antioxidant activity were measured. For this purpose, antioxidant activity was evaluated through the free radical scavenging activit y, including 1,1 - diphenyl - 2 - picryl - hydrazil (DPPH) and 2,20 - azinobis (3 - ethylbenothiazoline - 6 - sulfonic acid), diammonium salt (ABTS). The results showed that the absorption of the melanoidins formed from Glucose/L - Asn was higher than for those derived from Fructose/L - Asn. On the other hand, their antioxidant power was lower than that for melanoidins formed from Fructose/L - Asn systems.http://www.redalyc.org/articulo.oa?id=357633710005
collection DOAJ
language English
format Article
sources DOAJ
author A.P Echavarría
J. Pagán
A. Ibarz
spellingShingle A.P Echavarría
J. Pagán
A. Ibarz
Antioxidant activity of the melanoidin fractions formed from D-Glucose and D-Fructose with L-Asparagine in the Maillard reaction
Scientia Agropecuaria
author_facet A.P Echavarría
J. Pagán
A. Ibarz
author_sort A.P Echavarría
title Antioxidant activity of the melanoidin fractions formed from D-Glucose and D-Fructose with L-Asparagine in the Maillard reaction
title_short Antioxidant activity of the melanoidin fractions formed from D-Glucose and D-Fructose with L-Asparagine in the Maillard reaction
title_full Antioxidant activity of the melanoidin fractions formed from D-Glucose and D-Fructose with L-Asparagine in the Maillard reaction
title_fullStr Antioxidant activity of the melanoidin fractions formed from D-Glucose and D-Fructose with L-Asparagine in the Maillard reaction
title_full_unstemmed Antioxidant activity of the melanoidin fractions formed from D-Glucose and D-Fructose with L-Asparagine in the Maillard reaction
title_sort antioxidant activity of the melanoidin fractions formed from d-glucose and d-fructose with l-asparagine in the maillard reaction
publisher Universidad Nacional de Trujillo
series Scientia Agropecuaria
issn 2077-9917
2306-6741
publishDate 2013-01-01
description Melanoidins formed at the last stage of the Maillard reaction have been shown to possess certain functional properties, such as antioxidant activity. In order to gain more insight into these functional properties, soluble model systems melanoidins from L - Asparagine with D - glucose or D - fructose fractionating by ultrafiltration were analyzed. The fractionating/concentration sequence of the melanoidin fraction (1 - 300 kDa) enabled five fractions to be produced. Additionally, the absorption of melanoidins was measured at different wavelengths (280, 325, 405) and browning at 420 nm. The fractionati on effect of melanoidin systems on the color intensity, UV - absorbance scan wavelengths (nm), CIE, L*, a*, b* parameters and antioxidant activity were measured. For this purpose, antioxidant activity was evaluated through the free radical scavenging activit y, including 1,1 - diphenyl - 2 - picryl - hydrazil (DPPH) and 2,20 - azinobis (3 - ethylbenothiazoline - 6 - sulfonic acid), diammonium salt (ABTS). The results showed that the absorption of the melanoidins formed from Glucose/L - Asn was higher than for those derived from Fructose/L - Asn. On the other hand, their antioxidant power was lower than that for melanoidins formed from Fructose/L - Asn systems.
url http://www.redalyc.org/articulo.oa?id=357633710005
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AT jpagan antioxidantactivityofthemelanoidinfractionsformedfromdglucoseanddfructosewithlasparagineinthemaillardreaction
AT aibarz antioxidantactivityofthemelanoidinfractionsformedfromdglucoseanddfructosewithlasparagineinthemaillardreaction
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