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

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...

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Main Authors: Tatiana Maria Costa de Campos Barbosa, Maria das Graças Carvalho, Josianne Nicácio Silveira, Júnia Garib Rios, Flávia Komatsuzaki, Lara Carvalho Godói, Guilherme Hideki Yoshizane Costa
Format: Article
Language:English
Published: Sociedade Brasileira de Patologia Clínica 2014-12-01
Series:Jornal Brasileiro de Patologia e Medicina Laboratorial
Subjects:
Online Access:http://www.scielo.br/scielo.php?script=sci_arttext&pid=S1676-24442014000600402&lng=en&tlng=en
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spelling doaj-8484b54001d045368625b9f187ac43562020-11-24T22:40:42ZengSociedade Brasileira de Patologia ClínicaJornal Brasileiro de Patologia e Medicina Laboratorial1678-47742014-12-0150640240910.5935/1676-2444.20140048S1676-24442014000600402Homocysteine: validation and comparison of two methods using samples from patients with pulmonary hypertensionTatiana Maria Costa de Campos BarbosaMaria das Graças CarvalhoJosianne Nicácio SilveiraJúnia Garib RiosFlávia KomatsuzakiLara Carvalho GodóiGuilherme Hideki Yoshizane CostaIntroduction 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.http://www.scielo.br/scielo.php?script=sci_arttext&pid=S1676-24442014000600402&lng=en&tlng=enhomocisteínacromatografia líquida de alta eficiênciametodologia espectrofotométrica enzimática cíclica
collection DOAJ
language English
format Article
sources DOAJ
author Tatiana Maria Costa de Campos Barbosa
Maria das Graças Carvalho
Josianne Nicácio Silveira
Júnia Garib Rios
Flávia Komatsuzaki
Lara Carvalho Godói
Guilherme Hideki Yoshizane Costa
spellingShingle Tatiana Maria Costa de Campos Barbosa
Maria das Graças Carvalho
Josianne Nicácio Silveira
Júnia Garib Rios
Flávia Komatsuzaki
Lara Carvalho Godói
Guilherme Hideki Yoshizane Costa
Homocysteine: validation and comparison of two methods using samples from patients with pulmonary hypertension
Jornal Brasileiro de Patologia e Medicina Laboratorial
homocisteína
cromatografia líquida de alta eficiência
metodologia espectrofotométrica enzimática cíclica
author_facet Tatiana Maria Costa de Campos Barbosa
Maria das Graças Carvalho
Josianne Nicácio Silveira
Júnia Garib Rios
Flávia Komatsuzaki
Lara Carvalho Godói
Guilherme Hideki Yoshizane Costa
author_sort Tatiana Maria Costa de Campos Barbosa
title Homocysteine: validation and comparison of two methods using samples from patients with pulmonary hypertension
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
publisher Sociedade Brasileira de Patologia Clínica
series Jornal Brasileiro de Patologia e Medicina Laboratorial
issn 1678-4774
publishDate 2014-12-01
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.
topic homocisteína
cromatografia líquida de alta eficiência
metodologia espectrofotométrica enzimática cíclica
url http://www.scielo.br/scielo.php?script=sci_arttext&pid=S1676-24442014000600402&lng=en&tlng=en
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