The development and validation of an analytical method for doxycycline quantification in human plasma - doi:10.5020/18061230.2007.p193

Detalhes bibliográficos
Autor(a) principal: Aguiar, Geysa
Data de Publicação: 2012
Outros Autores: Kano, Eunice Kazue, Rolim, Clarice Madalena Bueno, Serra, Cristina Helena dos Reis, Ferraz, Humberto Gomes, Porta, Valentina
Tipo de documento: Artigo
Idioma: por
Título da fonte: Revista Brasileira em Promoção da Saúde
Texto Completo: https://ojs.unifor.br/RBPS/article/view/1025
Resumo: The aim of this study was to develop and validate a simple, quick and sensitive assay for determination of doxycycline concentration in human plasma by High Performance Liquid Chromatography (HPLC). Doxycycline and Oxytetracycline (internal standard) were extracted from 0,5 mL human plasma into ethyl acetate. The HPLC system was operated isocratically at controlled temperature (30°C) with reversed phase Phenomenex Luna C8 column (150 mm x 4.6mm i.d.; 4 ?m particle size) and using a mobile phase consisting in water: acetonitrile: tetrahydrofuran (80:15:5 v/v/v) adjusted to pH 2.5, at a flow rate of 1.0 mL/min. Detection was achieved with a UV detector at 357 nm. Method validation investigated parameters such as the sensitivity, linearity (r2= 0.9946), precision, accuracy, recovery and stability. The limit of quantification was 0,25 ?g/mL. Under the assay conditions, doxycycline and oxytetracycline had retention times of 7,5 and 2,4 minutes, respectively. No interferences with endogenous compounds or with anticoagulant were observed. The mean recovery of doxycycline was 84.57%, and 80.73% for the intern standard at working concentration (20?g/mL). The method showed to be precise and accurate both for analyses held in a same day (intra-day) as in different days (inter-days). A good stability of doxycycline and oxytetracycline was observed during extraction and analysis, when stored over a fourmonth period at -20°C, on the auto sample during 24 hours and to 3 freeze-thaw cycles. The present method is suitable for sensitive, precise and accurate determination of doxycycline concentrations in human plasma, within the limits established for this type of analyses
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spelling The development and validation of an analytical method for doxycycline quantification in human plasma - doi:10.5020/18061230.2007.p193Desenvolvimento e validação de método analítico para quantificação de doxiciclina em plasma humano - doi:10.5020/18061230.2007.p193DoxiciclinaCromatografia LíquidaPlasmaEstudos de Validação.The aim of this study was to develop and validate a simple, quick and sensitive assay for determination of doxycycline concentration in human plasma by High Performance Liquid Chromatography (HPLC). Doxycycline and Oxytetracycline (internal standard) were extracted from 0,5 mL human plasma into ethyl acetate. The HPLC system was operated isocratically at controlled temperature (30°C) with reversed phase Phenomenex Luna C8 column (150 mm x 4.6mm i.d.; 4 ?m particle size) and using a mobile phase consisting in water: acetonitrile: tetrahydrofuran (80:15:5 v/v/v) adjusted to pH 2.5, at a flow rate of 1.0 mL/min. Detection was achieved with a UV detector at 357 nm. Method validation investigated parameters such as the sensitivity, linearity (r2= 0.9946), precision, accuracy, recovery and stability. The limit of quantification was 0,25 ?g/mL. Under the assay conditions, doxycycline and oxytetracycline had retention times of 7,5 and 2,4 minutes, respectively. No interferences with endogenous compounds or with anticoagulant were observed. The mean recovery of doxycycline was 84.57%, and 80.73% for the intern standard at working concentration (20?g/mL). The method showed to be precise and accurate both for analyses held in a same day (intra-day) as in different days (inter-days). A good stability of doxycycline and oxytetracycline was observed during extraction and analysis, when stored over a fourmonth period at -20°C, on the auto sample during 24 hours and to 3 freeze-thaw cycles. The present method is suitable for sensitive, precise and accurate determination of doxycycline concentrations in human plasma, within the limits established for this type of analysesO objetivo deste estudo foi desenvolver e validar método simples, rápido e sensível para determinação de doxiciclina em plasma humano por cromatografia líquida de alta eficiência (CLAE). A doxiciclina e oxitetraciclina (padrão interno), foram extraídas de 0,5 mL de plasma com acetato de etila. Utilizaram-se o sistema de CLAE com bomba isocrática, com temperatura controlada (30°C) e coluna cromatográfica Phenomenex® Luna C8 (15,0 cm x 4,6 mm; partícula 4 ?m). A fase móvel, constituída por mistura de água, acetonitrila e tetrahidrofurano (80:15:5 v/v/v), teve pH ajustado para 2,5 sendo bombeada para o sistema cromatográfico em fluxo de 1,0 mL/min. Utilizou-se detector ultravioleta com comprimento de onda de 357 nm. Investigaram-se os seguintes parâmetros de validação: especificidade, linearidade (r2 = 0,9946), precisão, exatidão, recuperação e estabilidade. O limite de quantificação encontrado foi de 0,25?g/mL. Nas condições do ensaio, doxiciclina e oxitretaciclina apresentaram tempo de retenção de 7,5 e 2,4 minutos, respectivamente. Não foram observadas interferências com compostos endógenos ou com anticoagulante. Obtevese recuperação média para doxiciclina de 84,57% e de 80,73% para o padrão interno na concentração de 20 ?g/mL. O método mostrou-se preciso e exato tanto em análises realizadas no mesmo dia (intra-dia) quanto em dias diferentes (inter-dias). As amostras mantiveramse estáveis no tempo e condições de análise, por pelo menos 120 dias, à temperatura de -20°C, durante a injeção no cromatógrafo (24 horas) e quando analisadas após três ciclos de congelamento e descongelamento. O método desenvolvido demonstrou-se adequado à quantificação de doxiciclina em amostras de plasma humano, apresentando sensibilidade, precisão e exatidão dentro dos limites estabelecidos para análises deste tipoUniversidade de Fortaleza2012-01-04info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionapplication/pdfhttps://ojs.unifor.br/RBPS/article/view/102510.5020/1025Brazilian Journal in Health Promotion; Vol. 20 No. 3 (2007); 193-198Revista Brasileña en Promoción de la Salud; Vol. 20 Núm. 3 (2007); 193-198Revista Brasileira em Promoção da Saúde; v. 20 n. 3 (2007); 193-1981806-1230reponame:Revista Brasileira em Promoção da Saúdeinstname:Universidade de Fortaleza (Unifor)instacron:UFORporhttps://ojs.unifor.br/RBPS/article/view/1025/2185Aguiar, GeysaKano, Eunice KazueRolim, Clarice Madalena BuenoSerra, Cristina Helena dos ReisFerraz, Humberto GomesPorta, Valentinainfo:eu-repo/semantics/openAccess2012-01-10T12:18:48Zoai:ojs.ojs.unifor.br:article/1025Revistahttps://periodicos.unifor.br/RBPS/oai1806-12301806-1222opendoar:2012-01-10T12:18:48Revista Brasileira em Promoção da Saúde - Universidade de Fortaleza (Unifor)false
dc.title.none.fl_str_mv The development and validation of an analytical method for doxycycline quantification in human plasma - doi:10.5020/18061230.2007.p193
Desenvolvimento e validação de método analítico para quantificação de doxiciclina em plasma humano - doi:10.5020/18061230.2007.p193
title The development and validation of an analytical method for doxycycline quantification in human plasma - doi:10.5020/18061230.2007.p193
spellingShingle The development and validation of an analytical method for doxycycline quantification in human plasma - doi:10.5020/18061230.2007.p193
Aguiar, Geysa
Doxiciclina
Cromatografia Líquida
Plasma
Estudos de Validação.
title_short The development and validation of an analytical method for doxycycline quantification in human plasma - doi:10.5020/18061230.2007.p193
title_full The development and validation of an analytical method for doxycycline quantification in human plasma - doi:10.5020/18061230.2007.p193
title_fullStr The development and validation of an analytical method for doxycycline quantification in human plasma - doi:10.5020/18061230.2007.p193
title_full_unstemmed The development and validation of an analytical method for doxycycline quantification in human plasma - doi:10.5020/18061230.2007.p193
title_sort The development and validation of an analytical method for doxycycline quantification in human plasma - doi:10.5020/18061230.2007.p193
author Aguiar, Geysa
author_facet Aguiar, Geysa
Kano, Eunice Kazue
Rolim, Clarice Madalena Bueno
Serra, Cristina Helena dos Reis
Ferraz, Humberto Gomes
Porta, Valentina
author_role author
author2 Kano, Eunice Kazue
Rolim, Clarice Madalena Bueno
Serra, Cristina Helena dos Reis
Ferraz, Humberto Gomes
Porta, Valentina
author2_role author
author
author
author
author
dc.contributor.author.fl_str_mv Aguiar, Geysa
Kano, Eunice Kazue
Rolim, Clarice Madalena Bueno
Serra, Cristina Helena dos Reis
Ferraz, Humberto Gomes
Porta, Valentina
dc.subject.por.fl_str_mv Doxiciclina
Cromatografia Líquida
Plasma
Estudos de Validação.
topic Doxiciclina
Cromatografia Líquida
Plasma
Estudos de Validação.
description The aim of this study was to develop and validate a simple, quick and sensitive assay for determination of doxycycline concentration in human plasma by High Performance Liquid Chromatography (HPLC). Doxycycline and Oxytetracycline (internal standard) were extracted from 0,5 mL human plasma into ethyl acetate. The HPLC system was operated isocratically at controlled temperature (30°C) with reversed phase Phenomenex Luna C8 column (150 mm x 4.6mm i.d.; 4 ?m particle size) and using a mobile phase consisting in water: acetonitrile: tetrahydrofuran (80:15:5 v/v/v) adjusted to pH 2.5, at a flow rate of 1.0 mL/min. Detection was achieved with a UV detector at 357 nm. Method validation investigated parameters such as the sensitivity, linearity (r2= 0.9946), precision, accuracy, recovery and stability. The limit of quantification was 0,25 ?g/mL. Under the assay conditions, doxycycline and oxytetracycline had retention times of 7,5 and 2,4 minutes, respectively. No interferences with endogenous compounds or with anticoagulant were observed. The mean recovery of doxycycline was 84.57%, and 80.73% for the intern standard at working concentration (20?g/mL). The method showed to be precise and accurate both for analyses held in a same day (intra-day) as in different days (inter-days). A good stability of doxycycline and oxytetracycline was observed during extraction and analysis, when stored over a fourmonth period at -20°C, on the auto sample during 24 hours and to 3 freeze-thaw cycles. The present method is suitable for sensitive, precise and accurate determination of doxycycline concentrations in human plasma, within the limits established for this type of analyses
publishDate 2012
dc.date.none.fl_str_mv 2012-01-04
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv https://ojs.unifor.br/RBPS/article/view/1025
10.5020/1025
url https://ojs.unifor.br/RBPS/article/view/1025
identifier_str_mv 10.5020/1025
dc.language.iso.fl_str_mv por
language por
dc.relation.none.fl_str_mv https://ojs.unifor.br/RBPS/article/view/1025/2185
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv application/pdf
dc.publisher.none.fl_str_mv Universidade de Fortaleza
publisher.none.fl_str_mv Universidade de Fortaleza
dc.source.none.fl_str_mv Brazilian Journal in Health Promotion; Vol. 20 No. 3 (2007); 193-198
Revista Brasileña en Promoción de la Salud; Vol. 20 Núm. 3 (2007); 193-198
Revista Brasileira em Promoção da Saúde; v. 20 n. 3 (2007); 193-198
1806-1230
reponame:Revista Brasileira em Promoção da Saúde
instname:Universidade de Fortaleza (Unifor)
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instname_str Universidade de Fortaleza (Unifor)
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institution UFOR
reponame_str Revista Brasileira em Promoção da Saúde
collection Revista Brasileira em Promoção da Saúde
repository.name.fl_str_mv Revista Brasileira em Promoção da Saúde - Universidade de Fortaleza (Unifor)
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