Low cost biosensor-based molecular differential diagnosis of α-thalassemia (Southeast Asia deletion)

Background: Thalassemias are genetic hematologic diseases which the homozygous form of α-thalassemia can cause either death in utero or shortly after birth. It is necessary to accurately identify high-risk heterozygous couples. We developed a quartz crystal microbalance (QCM) to identify the abnorma...

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Main Authors: Nantawan Wangmaung, Chamras Promptmas, Sirinart Chomean, Chularat Sanchomphu, Wanida Ittarat
Other Authors: Mahidol University
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Published: 2018
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Online Access:https://repository.li.mahidol.ac.th/handle/123456789/31298
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spelling th-mahidol.312982018-10-19T12:23:05Z Low cost biosensor-based molecular differential diagnosis of α-thalassemia (Southeast Asia deletion) Nantawan Wangmaung Chamras Promptmas Sirinart Chomean Chularat Sanchomphu Wanida Ittarat Mahidol University Biochemistry, Genetics and Molecular Biology Medicine Background: Thalassemias are genetic hematologic diseases which the homozygous form of α-thalassemia can cause either death in utero or shortly after birth. It is necessary to accurately identify high-risk heterozygous couples. We developed a quartz crystal microbalance (QCM) to identify the abnormal gene causing the commonly found α-thalassemia1, [Southeast Asia (SEA) deletion]. This work is an improved method of our previous study by reducing both production cost and analysis time. Methods: A silver electrode on the QCM surface was immobilized with a biotinylated probe. The α-globin gene fragment was amplified and hybridized with the probe. Hybridization was indicated by changes of quartz oscillation. Each drying step was improved by using an air pump for 30min instead of the overnight air dry. The diagnostic potency of the silver QCM was evaluated using 70 suspected samples with microcytic hypochromic erythrocytes. Results: The silver QCM could clearly identify samples with abnormal α-globin genes, either homozygous or heterozygous, from normal samples. Thirteen out of 70 blood samples were identified as carrier of α-thalassemia1 (SEA deletion). Results were consistent with the standard agarose gel electrophoresis. Using silver instead of gold QCM could reduce the production expense 10-fold. An air pump drying the QCM surface could reduce the analysis time from 3 days to 4 h. Conclusions: The silver thalassemic QCM was specific, sensitive, rapid, cheap and field applicable. It could be used as a one-step definite diagnosis of α-thalassemia1 (SEA deletion) with no need for the preliminary screening test. 2018-10-19T04:39:03Z 2018-10-19T04:39:03Z 2013-06-01 Article Clinical Chemistry and Laboratory Medicine. Vol.51, No.6 (2013), 1199-1205 10.1515/cclm-2012-0732 14374331 14346621 2-s2.0-84882302030 https://repository.li.mahidol.ac.th/handle/123456789/31298 Mahidol University SCOPUS https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84882302030&origin=inward
institution Mahidol University
building Mahidol University Library
continent Asia
country Thailand
Thailand
content_provider Mahidol University Library
collection Mahidol University Institutional Repository
topic Biochemistry, Genetics and Molecular Biology
Medicine
spellingShingle Biochemistry, Genetics and Molecular Biology
Medicine
Nantawan Wangmaung
Chamras Promptmas
Sirinart Chomean
Chularat Sanchomphu
Wanida Ittarat
Low cost biosensor-based molecular differential diagnosis of α-thalassemia (Southeast Asia deletion)
description Background: Thalassemias are genetic hematologic diseases which the homozygous form of α-thalassemia can cause either death in utero or shortly after birth. It is necessary to accurately identify high-risk heterozygous couples. We developed a quartz crystal microbalance (QCM) to identify the abnormal gene causing the commonly found α-thalassemia1, [Southeast Asia (SEA) deletion]. This work is an improved method of our previous study by reducing both production cost and analysis time. Methods: A silver electrode on the QCM surface was immobilized with a biotinylated probe. The α-globin gene fragment was amplified and hybridized with the probe. Hybridization was indicated by changes of quartz oscillation. Each drying step was improved by using an air pump for 30min instead of the overnight air dry. The diagnostic potency of the silver QCM was evaluated using 70 suspected samples with microcytic hypochromic erythrocytes. Results: The silver QCM could clearly identify samples with abnormal α-globin genes, either homozygous or heterozygous, from normal samples. Thirteen out of 70 blood samples were identified as carrier of α-thalassemia1 (SEA deletion). Results were consistent with the standard agarose gel electrophoresis. Using silver instead of gold QCM could reduce the production expense 10-fold. An air pump drying the QCM surface could reduce the analysis time from 3 days to 4 h. Conclusions: The silver thalassemic QCM was specific, sensitive, rapid, cheap and field applicable. It could be used as a one-step definite diagnosis of α-thalassemia1 (SEA deletion) with no need for the preliminary screening test.
author2 Mahidol University
author_facet Mahidol University
Nantawan Wangmaung
Chamras Promptmas
Sirinart Chomean
Chularat Sanchomphu
Wanida Ittarat
format Article
author Nantawan Wangmaung
Chamras Promptmas
Sirinart Chomean
Chularat Sanchomphu
Wanida Ittarat
author_sort Nantawan Wangmaung
title Low cost biosensor-based molecular differential diagnosis of α-thalassemia (Southeast Asia deletion)
title_short Low cost biosensor-based molecular differential diagnosis of α-thalassemia (Southeast Asia deletion)
title_full Low cost biosensor-based molecular differential diagnosis of α-thalassemia (Southeast Asia deletion)
title_fullStr Low cost biosensor-based molecular differential diagnosis of α-thalassemia (Southeast Asia deletion)
title_full_unstemmed Low cost biosensor-based molecular differential diagnosis of α-thalassemia (Southeast Asia deletion)
title_sort low cost biosensor-based molecular differential diagnosis of α-thalassemia (southeast asia deletion)
publishDate 2018
url https://repository.li.mahidol.ac.th/handle/123456789/31298
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