Standardization and performance evaluation of manual measurement method for paraoxonase activity

Objectives: We hypothesised that using the traditionallaboratory methods for preparing the kit with chemicalsmay represent sufficient analytic performance with commercialkits, because of the fresh reagents and cost effective.We aimed to apply the paraoxonase (PON1) studyprocedure to the autoanalyser...

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Main Authors: Gökhan Çakırca, Osman Evliyaoğlu, Cemal Polat, Fatma Birgül Işık, Nuriye Mete
Format: Article
Language:English
Published: Dicle University Medical School 2013-01-01
Series:Dicle Medical Journal
Subjects:
Online Access:http://www.diclemedj.org/upload/sayi/27/Dicle%20Med%20J-01603.pdf
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spelling doaj-685cf43f81d14a2badfe1d559b3d61fa2020-11-24T22:29:11ZengDicle University Medical SchoolDicle Medical Journal 1300-29451308-98892013-01-0140221621910.5798/diclemedj.0921.2013.02.0257Standardization and performance evaluation of manual measurement method for paraoxonase activityGökhan ÇakırcaOsman EvliyaoğluCemal PolatFatma Birgül IşıkNuriye MeteObjectives: We hypothesised that using the traditionallaboratory methods for preparing the kit with chemicalsmay represent sufficient analytic performance with commercialkits, because of the fresh reagents and cost effective.We aimed to apply the paraoxonase (PON1) studyprocedure to the autoanalyser and evaluate the analyticperformance of the study.Methods: Thirty five healthy individuals were includedin the study. A total of 100 mL serum pool was createdafter centrifugation of venous blood samples. To assessthe intra-assay variations of PON1 enzyme activities 20samples and for inter-assay variations 30 samples wereprepared from the serum pool and PON1 enzyme activitieswere studied. As well as, 30 samples were studied toevaluate the correlation between the commercial kit andthe manual prepared kit from chemicals.Results: In this study, the mean, standard deviation (SD),percent coefficient of variation (% CV) values of PON1enzyme activities for intra-assay (72.70 U / L, 0.43, 0.59)and inter-assay (74.24 U / L, 3.00, 4.04) were determined.The correlation coefficient between the manual methodand the commercial kit were r = 0.92 and r2 = 0.84.Conclusion: The results of manual kit were showed goodanalytical performance with commercial kit. Therefore,the serum pool which was partially standardized in thisstudy was portionized for using as an internal quality controlserum for future studies in our laboratory. However,the use of standardized control sera, is considered to bemore reliable in routine laboratories.Key words: Paraoxonase, standardization, internal qualitycontrolhttp://www.diclemedj.org/upload/sayi/27/Dicle%20Med%20J-01603.pdfParaoxonasestandardizationinternal quality control
collection DOAJ
language English
format Article
sources DOAJ
author Gökhan Çakırca
Osman Evliyaoğlu
Cemal Polat
Fatma Birgül Işık
Nuriye Mete
spellingShingle Gökhan Çakırca
Osman Evliyaoğlu
Cemal Polat
Fatma Birgül Işık
Nuriye Mete
Standardization and performance evaluation of manual measurement method for paraoxonase activity
Dicle Medical Journal
Paraoxonase
standardization
internal quality control
author_facet Gökhan Çakırca
Osman Evliyaoğlu
Cemal Polat
Fatma Birgül Işık
Nuriye Mete
author_sort Gökhan Çakırca
title Standardization and performance evaluation of manual measurement method for paraoxonase activity
title_short Standardization and performance evaluation of manual measurement method for paraoxonase activity
title_full Standardization and performance evaluation of manual measurement method for paraoxonase activity
title_fullStr Standardization and performance evaluation of manual measurement method for paraoxonase activity
title_full_unstemmed Standardization and performance evaluation of manual measurement method for paraoxonase activity
title_sort standardization and performance evaluation of manual measurement method for paraoxonase activity
publisher Dicle University Medical School
series Dicle Medical Journal
issn 1300-2945
1308-9889
publishDate 2013-01-01
description Objectives: We hypothesised that using the traditionallaboratory methods for preparing the kit with chemicalsmay represent sufficient analytic performance with commercialkits, because of the fresh reagents and cost effective.We aimed to apply the paraoxonase (PON1) studyprocedure to the autoanalyser and evaluate the analyticperformance of the study.Methods: Thirty five healthy individuals were includedin the study. A total of 100 mL serum pool was createdafter centrifugation of venous blood samples. To assessthe intra-assay variations of PON1 enzyme activities 20samples and for inter-assay variations 30 samples wereprepared from the serum pool and PON1 enzyme activitieswere studied. As well as, 30 samples were studied toevaluate the correlation between the commercial kit andthe manual prepared kit from chemicals.Results: In this study, the mean, standard deviation (SD),percent coefficient of variation (% CV) values of PON1enzyme activities for intra-assay (72.70 U / L, 0.43, 0.59)and inter-assay (74.24 U / L, 3.00, 4.04) were determined.The correlation coefficient between the manual methodand the commercial kit were r = 0.92 and r2 = 0.84.Conclusion: The results of manual kit were showed goodanalytical performance with commercial kit. Therefore,the serum pool which was partially standardized in thisstudy was portionized for using as an internal quality controlserum for future studies in our laboratory. However,the use of standardized control sera, is considered to bemore reliable in routine laboratories.Key words: Paraoxonase, standardization, internal qualitycontrol
topic Paraoxonase
standardization
internal quality control
url http://www.diclemedj.org/upload/sayi/27/Dicle%20Med%20J-01603.pdf
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AT cemalpolat standardizationandperformanceevaluationofmanualmeasurementmethodforparaoxonaseactivity
AT fatmabirgulisık standardizationandperformanceevaluationofmanualmeasurementmethodforparaoxonaseactivity
AT nuriyemete standardizationandperformanceevaluationofmanualmeasurementmethodforparaoxonaseactivity
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