Quartz crystal microbalance-based biosensor for the detection of α-thalassemia 1 (SEA deletion)

Background: DNA piezoelectric biosensors have become a promising tool in molecular medicine since they do not require any label or staining. Here, a DNA piezoelectric biosensor based on a quartz crystal microbalance (QCM) was created to identify abnormal genes causing α-thalassemia 1 (SEA deletion)....

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Main Authors: Sirinart Chomean, Tiparat Potipitak, Chamras Promptmas, Wanida Ittarat
Other Authors: Mahidol University
Format: Article
Published: 2018
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Online Access:https://repository.li.mahidol.ac.th/handle/123456789/28641
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spelling th-mahidol.286412018-09-24T16:21:31Z Quartz crystal microbalance-based biosensor for the detection of α-thalassemia 1 (SEA deletion) Sirinart Chomean Tiparat Potipitak Chamras Promptmas Wanida Ittarat Mahidol University Biochemistry, Genetics and Molecular Biology Medicine Background: DNA piezoelectric biosensors have become a promising tool in molecular medicine since they do not require any label or staining. Here, a DNA piezoelectric biosensor based on a quartz crystal microbalance (QCM) was created to identify abnormal genes causing α-thalassemia 1 (SEA deletion). Methods: The functionalized gold electrode of the quartz crystal was coated with avidin and the biotinylated DNA probe was attached. The target gene causing α-thalassemia 1 was amplified and hybridized with the immobilized probe. DNA hybridization was indicated by changes in the quartz resonance frequencies. Diagnostic ability of the new α-thalassemia 1 biosensor was validated using both known and unknown blood samples. Specificity was tested using samples of β-thalassemia and α-thalassemia 2. Stability of the sensor was also evaluated. Results: The new biosensor could clearly identify α-thalassemia 1 (SEA deletion), both carrier and disease states, from the normal genotype. Identification accuracy was compatible to the standard gel electrophoresis. It was specific only to α-thalassemia 1 since no cross reaction was found with β-thalassemia and α-thalassemia 2. The sensor could be kept at room temperature up to 6 months with consistent identification accuracy. Conclusions: The label free QCM based biosensor was successfully developed to diagnose an abnormal human globin gene causing α-thalassemia 1 (SEA deletion). Its accuracy, specificity and sensitivity were comparable to the standard method. Its stable diagnostic potency up to 6 months implied its field application in thalassemic control program. © 2010 by Walter de Gruyter Berlin New York. 2018-09-24T08:42:59Z 2018-09-24T08:42:59Z 2010-09-01 Article Clinical Chemistry and Laboratory Medicine. Vol.48, No.9 (2010), 1247-1254 10.1515/CCLM.2010.258 14374331 14346621 2-s2.0-77957292009 https://repository.li.mahidol.ac.th/handle/123456789/28641 Mahidol University SCOPUS https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=77957292009&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
Sirinart Chomean
Tiparat Potipitak
Chamras Promptmas
Wanida Ittarat
Quartz crystal microbalance-based biosensor for the detection of α-thalassemia 1 (SEA deletion)
description Background: DNA piezoelectric biosensors have become a promising tool in molecular medicine since they do not require any label or staining. Here, a DNA piezoelectric biosensor based on a quartz crystal microbalance (QCM) was created to identify abnormal genes causing α-thalassemia 1 (SEA deletion). Methods: The functionalized gold electrode of the quartz crystal was coated with avidin and the biotinylated DNA probe was attached. The target gene causing α-thalassemia 1 was amplified and hybridized with the immobilized probe. DNA hybridization was indicated by changes in the quartz resonance frequencies. Diagnostic ability of the new α-thalassemia 1 biosensor was validated using both known and unknown blood samples. Specificity was tested using samples of β-thalassemia and α-thalassemia 2. Stability of the sensor was also evaluated. Results: The new biosensor could clearly identify α-thalassemia 1 (SEA deletion), both carrier and disease states, from the normal genotype. Identification accuracy was compatible to the standard gel electrophoresis. It was specific only to α-thalassemia 1 since no cross reaction was found with β-thalassemia and α-thalassemia 2. The sensor could be kept at room temperature up to 6 months with consistent identification accuracy. Conclusions: The label free QCM based biosensor was successfully developed to diagnose an abnormal human globin gene causing α-thalassemia 1 (SEA deletion). Its accuracy, specificity and sensitivity were comparable to the standard method. Its stable diagnostic potency up to 6 months implied its field application in thalassemic control program. © 2010 by Walter de Gruyter Berlin New York.
author2 Mahidol University
author_facet Mahidol University
Sirinart Chomean
Tiparat Potipitak
Chamras Promptmas
Wanida Ittarat
format Article
author Sirinart Chomean
Tiparat Potipitak
Chamras Promptmas
Wanida Ittarat
author_sort Sirinart Chomean
title Quartz crystal microbalance-based biosensor for the detection of α-thalassemia 1 (SEA deletion)
title_short Quartz crystal microbalance-based biosensor for the detection of α-thalassemia 1 (SEA deletion)
title_full Quartz crystal microbalance-based biosensor for the detection of α-thalassemia 1 (SEA deletion)
title_fullStr Quartz crystal microbalance-based biosensor for the detection of α-thalassemia 1 (SEA deletion)
title_full_unstemmed Quartz crystal microbalance-based biosensor for the detection of α-thalassemia 1 (SEA deletion)
title_sort quartz crystal microbalance-based biosensor for the detection of α-thalassemia 1 (sea deletion)
publishDate 2018
url https://repository.li.mahidol.ac.th/handle/123456789/28641
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