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Removal of Aflatoxin B(1) Using Alfalfa Leaves as an Adsorbent Material: A Comparison between Two In Vitro Experimental Models

An adsorbent material derived from alfalfa leaves was prepared and further characterized, and its efficacy for removing aflatoxin B(1) (AFB(1)) was investigated. Characterization consisted of the use of attenuated total reflectance-Fourier transform infrared spectroscopy (ATR-FTIR), environmental sc...

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Autores principales: Nava-Ramírez, María de Jesús, Vázquez-Durán, Alma, Figueroa-Cárdenas, Juan de Dios, Hernández-Patlán, Daniel, Solís-Cruz, Bruno, Téllez-Isaías, Guillermo, López-Coello, Carlos, Méndez-Albores, Abraham
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10610884/
https://www.ncbi.nlm.nih.gov/pubmed/37888635
http://dx.doi.org/10.3390/toxins15100604
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author Nava-Ramírez, María de Jesús
Vázquez-Durán, Alma
Figueroa-Cárdenas, Juan de Dios
Hernández-Patlán, Daniel
Solís-Cruz, Bruno
Téllez-Isaías, Guillermo
López-Coello, Carlos
Méndez-Albores, Abraham
author_facet Nava-Ramírez, María de Jesús
Vázquez-Durán, Alma
Figueroa-Cárdenas, Juan de Dios
Hernández-Patlán, Daniel
Solís-Cruz, Bruno
Téllez-Isaías, Guillermo
López-Coello, Carlos
Méndez-Albores, Abraham
author_sort Nava-Ramírez, María de Jesús
collection PubMed
description An adsorbent material derived from alfalfa leaves was prepared and further characterized, and its efficacy for removing aflatoxin B(1) (AFB(1)) was investigated. Characterization consisted of the use of attenuated total reflectance-Fourier transform infrared spectroscopy (ATR-FTIR), environmental scanning electron microscopy (ESEM), X-ray fluorescence spectroscopy (XRF), X-ray diffraction (XRD), point of zero charge (pH(pzc)), zeta potential (ζ-potential), UV-Vis diffuse reflectance spectroscopy, and spectral analysis. To determine the adsorption capacity against AFB(1) (250 ng AFB(1)/mL), pH-dependent and avian intestinal in vitro models were used. The adsorbent inclusion percentage was 0.5% (w/w). In general, the pH-dependent model gave adsorption percentages of 98.2%, 99.9%, and 98.2%, evaluated at pH values of 2, 5, and 7, respectively. However, when the avian intestinal model was used, it was observed that the adsorption percentage of AFB(1) significantly decreased (88.8%). Based on the characterization results, it is proposed that electrostatic, non-electrostatic, and the formation of chlorophyll-AFB(1) complexes were the main mechanisms for AFB(1) adsorption. From these results, it can be concluded that the adsorbent derived from alfalfa leaves could be used as an effective material for removing AFB(1) in in vitro digestion models that mimic the physiological reality.
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spelling pubmed-106108842023-10-28 Removal of Aflatoxin B(1) Using Alfalfa Leaves as an Adsorbent Material: A Comparison between Two In Vitro Experimental Models Nava-Ramírez, María de Jesús Vázquez-Durán, Alma Figueroa-Cárdenas, Juan de Dios Hernández-Patlán, Daniel Solís-Cruz, Bruno Téllez-Isaías, Guillermo López-Coello, Carlos Méndez-Albores, Abraham Toxins (Basel) Article An adsorbent material derived from alfalfa leaves was prepared and further characterized, and its efficacy for removing aflatoxin B(1) (AFB(1)) was investigated. Characterization consisted of the use of attenuated total reflectance-Fourier transform infrared spectroscopy (ATR-FTIR), environmental scanning electron microscopy (ESEM), X-ray fluorescence spectroscopy (XRF), X-ray diffraction (XRD), point of zero charge (pH(pzc)), zeta potential (ζ-potential), UV-Vis diffuse reflectance spectroscopy, and spectral analysis. To determine the adsorption capacity against AFB(1) (250 ng AFB(1)/mL), pH-dependent and avian intestinal in vitro models were used. The adsorbent inclusion percentage was 0.5% (w/w). In general, the pH-dependent model gave adsorption percentages of 98.2%, 99.9%, and 98.2%, evaluated at pH values of 2, 5, and 7, respectively. However, when the avian intestinal model was used, it was observed that the adsorption percentage of AFB(1) significantly decreased (88.8%). Based on the characterization results, it is proposed that electrostatic, non-electrostatic, and the formation of chlorophyll-AFB(1) complexes were the main mechanisms for AFB(1) adsorption. From these results, it can be concluded that the adsorbent derived from alfalfa leaves could be used as an effective material for removing AFB(1) in in vitro digestion models that mimic the physiological reality. MDPI 2023-10-08 /pmc/articles/PMC10610884/ /pubmed/37888635 http://dx.doi.org/10.3390/toxins15100604 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Nava-Ramírez, María de Jesús
Vázquez-Durán, Alma
Figueroa-Cárdenas, Juan de Dios
Hernández-Patlán, Daniel
Solís-Cruz, Bruno
Téllez-Isaías, Guillermo
López-Coello, Carlos
Méndez-Albores, Abraham
Removal of Aflatoxin B(1) Using Alfalfa Leaves as an Adsorbent Material: A Comparison between Two In Vitro Experimental Models
title Removal of Aflatoxin B(1) Using Alfalfa Leaves as an Adsorbent Material: A Comparison between Two In Vitro Experimental Models
title_full Removal of Aflatoxin B(1) Using Alfalfa Leaves as an Adsorbent Material: A Comparison between Two In Vitro Experimental Models
title_fullStr Removal of Aflatoxin B(1) Using Alfalfa Leaves as an Adsorbent Material: A Comparison between Two In Vitro Experimental Models
title_full_unstemmed Removal of Aflatoxin B(1) Using Alfalfa Leaves as an Adsorbent Material: A Comparison between Two In Vitro Experimental Models
title_short Removal of Aflatoxin B(1) Using Alfalfa Leaves as an Adsorbent Material: A Comparison between Two In Vitro Experimental Models
title_sort removal of aflatoxin b(1) using alfalfa leaves as an adsorbent material: a comparison between two in vitro experimental models
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10610884/
https://www.ncbi.nlm.nih.gov/pubmed/37888635
http://dx.doi.org/10.3390/toxins15100604
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