Performance of four sources of cholesterol oxidase for serum cholesterol determination by the enzymatic endpoint method

Background: Cholesterol oxidase is used for the determination of serum cholesterol. It can be derived from Streptomyces, Pseudomonas fluorescens, Cellulomonas, and Brevibacterium. This study compared the performance characteristics of four enzymes in the endpoint cholesterol determination. Methods:...

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Main Authors: Porntip H. Lolekha, Pornpen Srisawasdi, Patcharee Jearanaikoon, Nuanchawee Wetprasit, Busarawan Sriwanthana, Martin H. Kroll
Other Authors: Mahidol University
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Published: 2018
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Online Access:https://repository.li.mahidol.ac.th/handle/123456789/21251
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spelling th-mahidol.212512018-07-24T10:56:02Z Performance of four sources of cholesterol oxidase for serum cholesterol determination by the enzymatic endpoint method Porntip H. Lolekha Pornpen Srisawasdi Patcharee Jearanaikoon Nuanchawee Wetprasit Busarawan Sriwanthana Martin H. Kroll Mahidol University Khon Kaen University Ramkhamheng University National Institutes of Health, Bethesda UT Southwestern Medical School Biochemistry, Genetics and Molecular Biology Medicine Background: Cholesterol oxidase is used for the determination of serum cholesterol. It can be derived from Streptomyces, Pseudomonas fluorescens, Cellulomonas, and Brevibacterium. This study compared the performance characteristics of four enzymes in the endpoint cholesterol determination. Methods: Using the Mega analyzer, we studied assay optimization, linearity, precision, recovery, interference, stability, and compared 110 patient samples. Results: The linearity for the four enzymes was up to 13.0 mmol/l at the optimal enzyme activity. The average within-run CVs ranged from 1.6% to 1.9% and between-day ranged from 2.8% to 3.0%, within the NCEP analytical criteria. The analytical recoveries obtained from four reagents (∼ 96.5%) were excellent. The assays using these enzyme sources compared favorably with the commercial method and appeared accurate near the clinical decision cut-points. Hemoglobin concentration at 1.9 g/l interfered with the P. fluorescens cholesterol oxidase. Bilirubin caused a negative interference while lipemia generated a positive interference with all enzyme sources. Reagents were stable up to 6 weeks. Conclusions: Streptomyces, Cellulomonas, and Brevibacterium were essentially analytically equivalent. Streptomyces and Cellulomonas cholesterol oxidase are one-quarter as expensive Brevibacterium. Cellulomonas is a new source of cholesterol oxidase for determining serum cholesterol by the endpoint method. © 2003 Elsevier B.V. All rights reserved. 2018-07-24T03:39:06Z 2018-07-24T03:39:06Z 2004-01-01 Article Clinica Chimica Acta. Vol.339, No.1-2 (2004), 135-145 10.1016/j.cccn.2003.10.005 00098981 2-s2.0-0346995404 https://repository.li.mahidol.ac.th/handle/123456789/21251 Mahidol University SCOPUS https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=0346995404&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
Porntip H. Lolekha
Pornpen Srisawasdi
Patcharee Jearanaikoon
Nuanchawee Wetprasit
Busarawan Sriwanthana
Martin H. Kroll
Performance of four sources of cholesterol oxidase for serum cholesterol determination by the enzymatic endpoint method
description Background: Cholesterol oxidase is used for the determination of serum cholesterol. It can be derived from Streptomyces, Pseudomonas fluorescens, Cellulomonas, and Brevibacterium. This study compared the performance characteristics of four enzymes in the endpoint cholesterol determination. Methods: Using the Mega analyzer, we studied assay optimization, linearity, precision, recovery, interference, stability, and compared 110 patient samples. Results: The linearity for the four enzymes was up to 13.0 mmol/l at the optimal enzyme activity. The average within-run CVs ranged from 1.6% to 1.9% and between-day ranged from 2.8% to 3.0%, within the NCEP analytical criteria. The analytical recoveries obtained from four reagents (∼ 96.5%) were excellent. The assays using these enzyme sources compared favorably with the commercial method and appeared accurate near the clinical decision cut-points. Hemoglobin concentration at 1.9 g/l interfered with the P. fluorescens cholesterol oxidase. Bilirubin caused a negative interference while lipemia generated a positive interference with all enzyme sources. Reagents were stable up to 6 weeks. Conclusions: Streptomyces, Cellulomonas, and Brevibacterium were essentially analytically equivalent. Streptomyces and Cellulomonas cholesterol oxidase are one-quarter as expensive Brevibacterium. Cellulomonas is a new source of cholesterol oxidase for determining serum cholesterol by the endpoint method. © 2003 Elsevier B.V. All rights reserved.
author2 Mahidol University
author_facet Mahidol University
Porntip H. Lolekha
Pornpen Srisawasdi
Patcharee Jearanaikoon
Nuanchawee Wetprasit
Busarawan Sriwanthana
Martin H. Kroll
format Article
author Porntip H. Lolekha
Pornpen Srisawasdi
Patcharee Jearanaikoon
Nuanchawee Wetprasit
Busarawan Sriwanthana
Martin H. Kroll
author_sort Porntip H. Lolekha
title Performance of four sources of cholesterol oxidase for serum cholesterol determination by the enzymatic endpoint method
title_short Performance of four sources of cholesterol oxidase for serum cholesterol determination by the enzymatic endpoint method
title_full Performance of four sources of cholesterol oxidase for serum cholesterol determination by the enzymatic endpoint method
title_fullStr Performance of four sources of cholesterol oxidase for serum cholesterol determination by the enzymatic endpoint method
title_full_unstemmed Performance of four sources of cholesterol oxidase for serum cholesterol determination by the enzymatic endpoint method
title_sort performance of four sources of cholesterol oxidase for serum cholesterol determination by the enzymatic endpoint method
publishDate 2018
url https://repository.li.mahidol.ac.th/handle/123456789/21251
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