Homocysteine: validation and comparison of two methods using samples from patients with pulmonary hypertension

Detalhes bibliográficos
Autor(a) principal: Barbosa,Tatiana Maria Costa de Campos
Data de Publicação: 2014
Outros Autores: Carvalho,Maria das Graças, Silveira,Josianne Nicácio, Rios,Júnia Garib, Komatsuzaki,Flávia, Godói,Lara Carvalho, Costa,Guilherme Hideki Yoshizane
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Jornal Brasileiro de Patologia e Medicina Laboratorial (Online)
Texto Completo: http://old.scielo.br/scielo.php?script=sci_arttext&pid=S1676-24442014000600402
Resumo: Introduction and objective:The determination of homocysteine plasma levels has been reported as a risk marker of interest in severe diseases involving endothelial injury and associated with the development or progression of atherosclerotic lesions and thrombus formation. The aims of this study were to validate method for quantification of plasma homocysteine by high performance liquid chromatography (HPLC) with fluorimetric detection, and to compare the results obtained from patients with pulmonary hypertension by HPLC with those obtained by spectrophotometric enzymatic cycling (S-Ec) method.Materials and methods:The validation parameters, such as linearity, matrix effect, precision, accuracy, detection and quantitation limits, and robustness of the method were evaluated aiming to demonstrate that it is suitable for the intended use. The data obtained in the quantification of homocysteine using the validated method (HPLC) and the spectrophotometric enzymatic cycling (S-Ec) method, were compared.Results:The method was precise, accurate, and robust; it also had good recovery and showed no matrix effect. The linearity covered a range of 5.0-85.0 µmol/l and the limits of detection and quantification were 1.0 µmol/l and 3.4 µmol/l, respectively. The results obtained for homocysteine determination by HPLC and S-Ec methods were comparable.Conclusion:The validated HPLC method showed good performance for quantification of plasma homocysteine levels, while S-Ec method provided results for homocysteine comparable with those obtained by the validated method; therefore, this methodology is a potential alternative of automated method for clinical laboratories.
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spelling Homocysteine: validation and comparison of two methods using samples from patients with pulmonary hypertensionhomocysteinehigh performance liquid chromatographyspectrophotometric enzymatic cycling methodIntroduction and objective:The determination of homocysteine plasma levels has been reported as a risk marker of interest in severe diseases involving endothelial injury and associated with the development or progression of atherosclerotic lesions and thrombus formation. The aims of this study were to validate method for quantification of plasma homocysteine by high performance liquid chromatography (HPLC) with fluorimetric detection, and to compare the results obtained from patients with pulmonary hypertension by HPLC with those obtained by spectrophotometric enzymatic cycling (S-Ec) method.Materials and methods:The validation parameters, such as linearity, matrix effect, precision, accuracy, detection and quantitation limits, and robustness of the method were evaluated aiming to demonstrate that it is suitable for the intended use. The data obtained in the quantification of homocysteine using the validated method (HPLC) and the spectrophotometric enzymatic cycling (S-Ec) method, were compared.Results:The method was precise, accurate, and robust; it also had good recovery and showed no matrix effect. The linearity covered a range of 5.0-85.0 µmol/l and the limits of detection and quantification were 1.0 µmol/l and 3.4 µmol/l, respectively. The results obtained for homocysteine determination by HPLC and S-Ec methods were comparable.Conclusion:The validated HPLC method showed good performance for quantification of plasma homocysteine levels, while S-Ec method provided results for homocysteine comparable with those obtained by the validated method; therefore, this methodology is a potential alternative of automated method for clinical laboratories.Sociedade Brasileira de Patologia Clínica2014-12-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S1676-24442014000600402Jornal Brasileiro de Patologia e Medicina Laboratorial v.50 n.6 2014reponame:Jornal Brasileiro de Patologia e Medicina Laboratorial (Online)instname:Sociedade Brasileira de Patologia (SBP)instacron:SBP10.5935/1676-2444.20140048info:eu-repo/semantics/openAccessBarbosa,Tatiana Maria Costa de CamposCarvalho,Maria das GraçasSilveira,Josianne NicácioRios,Júnia GaribKomatsuzaki,FláviaGodói,Lara CarvalhoCosta,Guilherme Hideki Yoshizaneeng2015-10-27T00:00:00Zoai:scielo:S1676-24442014000600402Revistahttp://www.scielo.br/jbpmlhttps://old.scielo.br/oai/scielo-oai.php||jbpml@sbpc.org.br1678-47741676-2444opendoar:2015-10-27T00:00Jornal Brasileiro de Patologia e Medicina Laboratorial (Online) - Sociedade Brasileira de Patologia (SBP)false
dc.title.none.fl_str_mv Homocysteine: validation and comparison of two methods using samples from patients with pulmonary hypertension
title Homocysteine: validation and comparison of two methods using samples from patients with pulmonary hypertension
spellingShingle Homocysteine: validation and comparison of two methods using samples from patients with pulmonary hypertension
Barbosa,Tatiana Maria Costa de Campos
homocysteine
high performance liquid chromatography
spectrophotometric enzymatic cycling method
title_short Homocysteine: validation and comparison of two methods using samples from patients with pulmonary hypertension
title_full Homocysteine: validation and comparison of two methods using samples from patients with pulmonary hypertension
title_fullStr Homocysteine: validation and comparison of two methods using samples from patients with pulmonary hypertension
title_full_unstemmed Homocysteine: validation and comparison of two methods using samples from patients with pulmonary hypertension
title_sort Homocysteine: validation and comparison of two methods using samples from patients with pulmonary hypertension
author Barbosa,Tatiana Maria Costa de Campos
author_facet Barbosa,Tatiana Maria Costa de Campos
Carvalho,Maria das Graças
Silveira,Josianne Nicácio
Rios,Júnia Garib
Komatsuzaki,Flávia
Godói,Lara Carvalho
Costa,Guilherme Hideki Yoshizane
author_role author
author2 Carvalho,Maria das Graças
Silveira,Josianne Nicácio
Rios,Júnia Garib
Komatsuzaki,Flávia
Godói,Lara Carvalho
Costa,Guilherme Hideki Yoshizane
author2_role author
author
author
author
author
author
dc.contributor.author.fl_str_mv Barbosa,Tatiana Maria Costa de Campos
Carvalho,Maria das Graças
Silveira,Josianne Nicácio
Rios,Júnia Garib
Komatsuzaki,Flávia
Godói,Lara Carvalho
Costa,Guilherme Hideki Yoshizane
dc.subject.por.fl_str_mv homocysteine
high performance liquid chromatography
spectrophotometric enzymatic cycling method
topic homocysteine
high performance liquid chromatography
spectrophotometric enzymatic cycling method
description Introduction and objective:The determination of homocysteine plasma levels has been reported as a risk marker of interest in severe diseases involving endothelial injury and associated with the development or progression of atherosclerotic lesions and thrombus formation. The aims of this study were to validate method for quantification of plasma homocysteine by high performance liquid chromatography (HPLC) with fluorimetric detection, and to compare the results obtained from patients with pulmonary hypertension by HPLC with those obtained by spectrophotometric enzymatic cycling (S-Ec) method.Materials and methods:The validation parameters, such as linearity, matrix effect, precision, accuracy, detection and quantitation limits, and robustness of the method were evaluated aiming to demonstrate that it is suitable for the intended use. The data obtained in the quantification of homocysteine using the validated method (HPLC) and the spectrophotometric enzymatic cycling (S-Ec) method, were compared.Results:The method was precise, accurate, and robust; it also had good recovery and showed no matrix effect. The linearity covered a range of 5.0-85.0 µmol/l and the limits of detection and quantification were 1.0 µmol/l and 3.4 µmol/l, respectively. The results obtained for homocysteine determination by HPLC and S-Ec methods were comparable.Conclusion:The validated HPLC method showed good performance for quantification of plasma homocysteine levels, while S-Ec method provided results for homocysteine comparable with those obtained by the validated method; therefore, this methodology is a potential alternative of automated method for clinical laboratories.
publishDate 2014
dc.date.none.fl_str_mv 2014-12-01
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
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dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 10.5935/1676-2444.20140048
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dc.publisher.none.fl_str_mv
Sociedade Brasileira de Patologia Clínica
publisher.none.fl_str_mv
Sociedade Brasileira de Patologia Clínica
dc.source.none.fl_str_mv Jornal Brasileiro de Patologia e Medicina Laboratorial v.50 n.6 2014
reponame:Jornal Brasileiro de Patologia e Medicina Laboratorial (Online)
instname:Sociedade Brasileira de Patologia (SBP)
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instname_str Sociedade Brasileira de Patologia (SBP)
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reponame_str Jornal Brasileiro de Patologia e Medicina Laboratorial (Online)
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repository.name.fl_str_mv Jornal Brasileiro de Patologia e Medicina Laboratorial (Online) - Sociedade Brasileira de Patologia (SBP)
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