Development of antipeptide enzyme-linked immunosorbent assay for determination of gelatin in confectionery products

The gelatin sources have become a controversial issue with regard to religious and health concern. Thus,the aims of this study were to develop and evaluate the efficiency of polyclonal antibodies against peptide immunogen of collagen a2 (I) chain for determination of gelatin sources in confectionery...

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Main Authors: Tukiran, Nur Azira, Ismail, Amin, Mustafa, Shuhaimi, Hamid, Muhajir
Format: Article
Language:English
English
English
Published: Wiley-Blackwell 2016
Subjects:
Online Access:http://irep.iium.edu.my/55410/
http://irep.iium.edu.my/55410/
http://irep.iium.edu.my/55410/
http://irep.iium.edu.my/55410/1/Tukiran_et_al-2016-International_Journal_of_Food_Science_%26_Technology.pdf
http://irep.iium.edu.my/55410/7/55410_Development%20of%20antipeptide%20enzyme-linked_WOS.pdf
http://irep.iium.edu.my/55410/8/55410_Development%20of%20antipeptide%20enzyme-linked_SCOPUS.pdf
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spelling iium-554102017-07-18T00:48:57Z http://irep.iium.edu.my/55410/ Development of antipeptide enzyme-linked immunosorbent assay for determination of gelatin in confectionery products Tukiran, Nur Azira Ismail, Amin Mustafa, Shuhaimi Hamid, Muhajir TP Chemical technology The gelatin sources have become a controversial issue with regard to religious and health concern. Thus,the aims of this study were to develop and evaluate the efficiency of polyclonal antibodies against peptide immunogen of collagen a2 (I) chain for determination of gelatin sources in confectionery products by competitive indirect enzyme-linked immunosorbent assay (ELISA). Collagen a2 (I) chain protein showed resistance against heat treatment and detectable in certain commercial products when analysed by sodium dodecyl sulphate–polyacrylamide gel electrophoresis (SDS-PAGE). The established ELISA exhibited low cross-reactivity to fish and chicken gelatin. The IC50 value was 0.39 lg mL �1, and the limit of detection (IC10) was 0.05 lg mL �1. There were no false-positive results from forty-eight commercially processed products. The present method is useful for determination of gelatin in confectionery products. Wiley-Blackwell 2016-01 Article PeerReviewed application/pdf en http://irep.iium.edu.my/55410/1/Tukiran_et_al-2016-International_Journal_of_Food_Science_%26_Technology.pdf application/pdf en http://irep.iium.edu.my/55410/7/55410_Development%20of%20antipeptide%20enzyme-linked_WOS.pdf application/pdf en http://irep.iium.edu.my/55410/8/55410_Development%20of%20antipeptide%20enzyme-linked_SCOPUS.pdf Tukiran, Nur Azira and Ismail, Amin and Mustafa, Shuhaimi and Hamid, Muhajir (2016) Development of antipeptide enzyme-linked immunosorbent assay for determination of gelatin in confectionery products. International Journal of Food Science and Technology, 51 (1). pp. 54-60. ISSN 0950-5423 E-ISSN 1365-2621 http://onlinelibrary.wiley.com/doi/10.1111/ijfs.12971/abstract 10.1111/ijfs.12971
repository_type Digital Repository
institution_category Local University
institution International Islamic University Malaysia
building IIUM Repository
collection Online Access
language English
English
English
topic TP Chemical technology
spellingShingle TP Chemical technology
Tukiran, Nur Azira
Ismail, Amin
Mustafa, Shuhaimi
Hamid, Muhajir
Development of antipeptide enzyme-linked immunosorbent assay for determination of gelatin in confectionery products
description The gelatin sources have become a controversial issue with regard to religious and health concern. Thus,the aims of this study were to develop and evaluate the efficiency of polyclonal antibodies against peptide immunogen of collagen a2 (I) chain for determination of gelatin sources in confectionery products by competitive indirect enzyme-linked immunosorbent assay (ELISA). Collagen a2 (I) chain protein showed resistance against heat treatment and detectable in certain commercial products when analysed by sodium dodecyl sulphate–polyacrylamide gel electrophoresis (SDS-PAGE). The established ELISA exhibited low cross-reactivity to fish and chicken gelatin. The IC50 value was 0.39 lg mL �1, and the limit of detection (IC10) was 0.05 lg mL �1. There were no false-positive results from forty-eight commercially processed products. The present method is useful for determination of gelatin in confectionery products.
format Article
author Tukiran, Nur Azira
Ismail, Amin
Mustafa, Shuhaimi
Hamid, Muhajir
author_facet Tukiran, Nur Azira
Ismail, Amin
Mustafa, Shuhaimi
Hamid, Muhajir
author_sort Tukiran, Nur Azira
title Development of antipeptide enzyme-linked immunosorbent assay for determination of gelatin in confectionery products
title_short Development of antipeptide enzyme-linked immunosorbent assay for determination of gelatin in confectionery products
title_full Development of antipeptide enzyme-linked immunosorbent assay for determination of gelatin in confectionery products
title_fullStr Development of antipeptide enzyme-linked immunosorbent assay for determination of gelatin in confectionery products
title_full_unstemmed Development of antipeptide enzyme-linked immunosorbent assay for determination of gelatin in confectionery products
title_sort development of antipeptide enzyme-linked immunosorbent assay for determination of gelatin in confectionery products
publisher Wiley-Blackwell
publishDate 2016
url http://irep.iium.edu.my/55410/
http://irep.iium.edu.my/55410/
http://irep.iium.edu.my/55410/
http://irep.iium.edu.my/55410/1/Tukiran_et_al-2016-International_Journal_of_Food_Science_%26_Technology.pdf
http://irep.iium.edu.my/55410/7/55410_Development%20of%20antipeptide%20enzyme-linked_WOS.pdf
http://irep.iium.edu.my/55410/8/55410_Development%20of%20antipeptide%20enzyme-linked_SCOPUS.pdf
first_indexed 2023-09-18T21:18:19Z
last_indexed 2023-09-18T21:18:19Z
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