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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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 |
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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) |
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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. |
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Mahidol University |
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Mahidol University Nantawan Wangmaung Chamras Promptmas Sirinart Chomean Chularat Sanchomphu Wanida Ittarat |
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Article |
author |
Nantawan Wangmaung Chamras Promptmas Sirinart Chomean Chularat Sanchomphu Wanida Ittarat |
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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) |
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2018 |
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https://repository.li.mahidol.ac.th/handle/123456789/31298 |
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1763498184353513472 |