The development and validation of an analytical method for doxycycline quantification in human plasma - doi:10.5020/18061230.2007.p193
Autor(a) principal: | |
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Data de Publicação: | 2012 |
Outros Autores: | , , , , |
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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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) instacron:UFOR |
instname_str |
Universidade de Fortaleza (Unifor) |
instacron_str |
UFOR |
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) |
repository.mail.fl_str_mv |
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1808844174362935296 |