Preparation of an Immunoaffinity Column with Amino-Silica Gel Microparticles and Its Application in Sample Cleanup for Aflatoxin Detection in Agri-Products

This study established an immunoaffinity column for selective extraction of aflatoxins in agri-products. Specifically, the immunoaffinity column was developed by covalently coupling monoclonal antibody 1C11 against aflatoxins to amino-silica gel microparticles and then packing these into a cartridge...

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Main Authors: Xiaofeng Hu, Wen Zhang, Qi Zhang, Fei Ma, Peiwu Li, Ran Chen
Format: Article
Language:English
Published: MDPI AG 2013-02-01
Series:Molecules
Subjects:
Online Access:http://www.mdpi.com/1420-3049/18/2/2222
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spelling doaj-ea22de2c7a3c4740b3e866138e146d622020-11-25T01:46:24ZengMDPI AGMolecules1420-30492013-02-011822222223510.3390/molecules18022222Preparation of an Immunoaffinity Column with Amino-Silica Gel Microparticles and Its Application in Sample Cleanup for Aflatoxin Detection in Agri-ProductsXiaofeng HuWen ZhangQi ZhangFei MaPeiwu LiRan ChenThis study established an immunoaffinity column for selective extraction of aflatoxins in agri-products. Specifically, the immunoaffinity column was developed by covalently coupling monoclonal antibody 1C11 against aflatoxins to amino-silica gel microparticles and then packing these into a cartridge. The extraction conditions were thoroughly optimized in terms of loading, washing and eluting solutions. Under the optimal conditions, the immunoaffinity column had a capacity of 200 ng of aflatoxins. The detection limits (S/N = 3) for aflatoxin G1, B1, G2 and B2 were 0.03, 0.07, 0.05 and 0.09 μg·kg−1, and the corresponding quantification limits (S/N = 10) were 0.10, 0.25, 0.18 and 0.30 μg·kg−1, respectively. The recoveries of aflatoxins in samples were 90.1%–104.4% and RSDs were <4.4%. The developed method was further applied to the determination of aflatoxins in peanut, vegetable oil and tea samples, and the results indicated that peanut (26.9%), vegetable oils (28.0%) and tea (5.3%) samples were contaminated with aflatoxins, with levels ranging from 0.49 to 20.79 μg·kg−1.http://www.mdpi.com/1420-3049/18/2/2222aflatoxinsimmunoaffinity columnamino-silica gelmicroparticle conjugateagri-productsHPLC
collection DOAJ
language English
format Article
sources DOAJ
author Xiaofeng Hu
Wen Zhang
Qi Zhang
Fei Ma
Peiwu Li
Ran Chen
spellingShingle Xiaofeng Hu
Wen Zhang
Qi Zhang
Fei Ma
Peiwu Li
Ran Chen
Preparation of an Immunoaffinity Column with Amino-Silica Gel Microparticles and Its Application in Sample Cleanup for Aflatoxin Detection in Agri-Products
Molecules
aflatoxins
immunoaffinity column
amino-silica gel
microparticle conjugate
agri-products
HPLC
author_facet Xiaofeng Hu
Wen Zhang
Qi Zhang
Fei Ma
Peiwu Li
Ran Chen
author_sort Xiaofeng Hu
title Preparation of an Immunoaffinity Column with Amino-Silica Gel Microparticles and Its Application in Sample Cleanup for Aflatoxin Detection in Agri-Products
title_short Preparation of an Immunoaffinity Column with Amino-Silica Gel Microparticles and Its Application in Sample Cleanup for Aflatoxin Detection in Agri-Products
title_full Preparation of an Immunoaffinity Column with Amino-Silica Gel Microparticles and Its Application in Sample Cleanup for Aflatoxin Detection in Agri-Products
title_fullStr Preparation of an Immunoaffinity Column with Amino-Silica Gel Microparticles and Its Application in Sample Cleanup for Aflatoxin Detection in Agri-Products
title_full_unstemmed Preparation of an Immunoaffinity Column with Amino-Silica Gel Microparticles and Its Application in Sample Cleanup for Aflatoxin Detection in Agri-Products
title_sort preparation of an immunoaffinity column with amino-silica gel microparticles and its application in sample cleanup for aflatoxin detection in agri-products
publisher MDPI AG
series Molecules
issn 1420-3049
publishDate 2013-02-01
description This study established an immunoaffinity column for selective extraction of aflatoxins in agri-products. Specifically, the immunoaffinity column was developed by covalently coupling monoclonal antibody 1C11 against aflatoxins to amino-silica gel microparticles and then packing these into a cartridge. The extraction conditions were thoroughly optimized in terms of loading, washing and eluting solutions. Under the optimal conditions, the immunoaffinity column had a capacity of 200 ng of aflatoxins. The detection limits (S/N = 3) for aflatoxin G1, B1, G2 and B2 were 0.03, 0.07, 0.05 and 0.09 μg·kg−1, and the corresponding quantification limits (S/N = 10) were 0.10, 0.25, 0.18 and 0.30 μg·kg−1, respectively. The recoveries of aflatoxins in samples were 90.1%–104.4% and RSDs were <4.4%. The developed method was further applied to the determination of aflatoxins in peanut, vegetable oil and tea samples, and the results indicated that peanut (26.9%), vegetable oils (28.0%) and tea (5.3%) samples were contaminated with aflatoxins, with levels ranging from 0.49 to 20.79 μg·kg−1.
topic aflatoxins
immunoaffinity column
amino-silica gel
microparticle conjugate
agri-products
HPLC
url http://www.mdpi.com/1420-3049/18/2/2222
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