Development and validation of a rapid turbidimetric assay to determine the potency of cefuroxime sodium in powder for dissolution for injection
Autor(a) principal: | |
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Data de Publicação: | 2014 |
Outros Autores: | , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Institucional da UNESP |
Texto Completo: | http://dx.doi.org/10.3390/pathogens3030656 http://hdl.handle.net/11449/131019 |
Resumo: | The cefuroxime sodium is a second generation cephalosporin indicated for infections caused by Gram-positive and Gram-negative microorganisms. Although this drug is highly studied and researched regarding the antimicrobial activity, pharmacokinetics and pharmacodynamics, there are few studies regarding the development of analytical methodology for this cephalosporin. Thus, research involving analytical methods is essential and highly relevant to optimize its analysis in the pharmaceutical industry and guarantee the quality of the product already sold. This study describes the development and validation of a microbiological assay applying the turbidimetric method for the determination of cefuroxime, using Micrococcus luteus ATCC 9341 as micro-organism test and 3x3 parallel line assay design, with nine tubes for each assay, as recommended by the Brazilian Pharmacopoeia. The developed and validated method showed excellent results of linearity, seletivity, precision and robustness, in the concentration range from 30.0 to 120.0 mg/mL, with 100.21% accuracy and content 99.97% to cefuroxime sodium in injectable pharmaceutical form. |
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Development and validation of a rapid turbidimetric assay to determine the potency of cefuroxime sodium in powder for dissolution for injectionCefuroxime sodiumMicrobiological testingQuality controlValidation and stabilityThe cefuroxime sodium is a second generation cephalosporin indicated for infections caused by Gram-positive and Gram-negative microorganisms. Although this drug is highly studied and researched regarding the antimicrobial activity, pharmacokinetics and pharmacodynamics, there are few studies regarding the development of analytical methodology for this cephalosporin. Thus, research involving analytical methods is essential and highly relevant to optimize its analysis in the pharmaceutical industry and guarantee the quality of the product already sold. This study describes the development and validation of a microbiological assay applying the turbidimetric method for the determination of cefuroxime, using Micrococcus luteus ATCC 9341 as micro-organism test and 3x3 parallel line assay design, with nine tubes for each assay, as recommended by the Brazilian Pharmacopoeia. The developed and validated method showed excellent results of linearity, seletivity, precision and robustness, in the concentration range from 30.0 to 120.0 mg/mL, with 100.21% accuracy and content 99.97% to cefuroxime sodium in injectable pharmaceutical form.Fundação para o Desenvolvimento da UNESP (FUNDUNESP)Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)Faculdade Pitágoras - Campus Poços de Caldas, Av. João Pinheiro, 1046, Poços de Caldas -MG 37701-014, Brazil. danicmvieira@yahoo.com.br.Department of Drugs and Medicines, Faculty of Pharmaceutical Sciences, Universidade Estadual Paulista Júlio de Mesquita Filho, Araraquara14800-901, SP, Brazil. thalitafiuza@uol.com.br.Department of Drugs and Medicines, Faculty of Pharmaceutical Sciences, Universidade Estadual Paulista Júlio de Mesquita Filho, Araraquara14800-901, SP, Brazil. salgadoh@fcfar.unesp.br.Department of Drugs and Medicines, Faculty of Pharmaceutical Sciences, Universidade Estadual Paulista Júlio de Mesquita Filho, Araraquara14800-901, SP, Brazil. thalitafiuza@uol.com.br.Department of Drugs and Medicines, Faculty of Pharmaceutical Sciences, Universidade Estadual Paulista Júlio de Mesquita Filho, Araraquara14800-901, SP, Brazil. salgadoh@fcfar.unesp.br.PathogensFaculdade Pitágoras - Campus Poços de Caldas, Av. João Pinheiro, 1046, Poços de Caldas -MG 37701-014, Brazil. danicmvieira@yahoo.com.br.Universidade Estadual Paulista (Unesp)Vieira, Daniela C. M.Fiuza, Thalita F. M. [UNESP]Salgado, Hérida R. N. [UNESP]2015-12-07T15:30:56Z2015-12-07T15:30:56Z2014info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article656-666application/pdfhttp://dx.doi.org/10.3390/pathogens3030656Pathogens (basel, Switzerland), v. 3, n. 3, p. 656-666, 2014.2076-0817http://hdl.handle.net/11449/13101910.3390/pathogens3030656PMC4243433.pdf25438016PMC4243433PubMedreponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengPathogens (basel, Switzerland)1,421info:eu-repo/semantics/openAccess2024-06-24T13:46:00Zoai:repositorio.unesp.br:11449/131019Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462024-08-05T19:46:47.509170Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false |
dc.title.none.fl_str_mv |
Development and validation of a rapid turbidimetric assay to determine the potency of cefuroxime sodium in powder for dissolution for injection |
title |
Development and validation of a rapid turbidimetric assay to determine the potency of cefuroxime sodium in powder for dissolution for injection |
spellingShingle |
Development and validation of a rapid turbidimetric assay to determine the potency of cefuroxime sodium in powder for dissolution for injection Vieira, Daniela C. M. Cefuroxime sodium Microbiological testing Quality control Validation and stability |
title_short |
Development and validation of a rapid turbidimetric assay to determine the potency of cefuroxime sodium in powder for dissolution for injection |
title_full |
Development and validation of a rapid turbidimetric assay to determine the potency of cefuroxime sodium in powder for dissolution for injection |
title_fullStr |
Development and validation of a rapid turbidimetric assay to determine the potency of cefuroxime sodium in powder for dissolution for injection |
title_full_unstemmed |
Development and validation of a rapid turbidimetric assay to determine the potency of cefuroxime sodium in powder for dissolution for injection |
title_sort |
Development and validation of a rapid turbidimetric assay to determine the potency of cefuroxime sodium in powder for dissolution for injection |
author |
Vieira, Daniela C. M. |
author_facet |
Vieira, Daniela C. M. Fiuza, Thalita F. M. [UNESP] Salgado, Hérida R. N. [UNESP] |
author_role |
author |
author2 |
Fiuza, Thalita F. M. [UNESP] Salgado, Hérida R. N. [UNESP] |
author2_role |
author author |
dc.contributor.none.fl_str_mv |
Faculdade Pitágoras - Campus Poços de Caldas, Av. João Pinheiro, 1046, Poços de Caldas -MG 37701-014, Brazil. danicmvieira@yahoo.com.br. Universidade Estadual Paulista (Unesp) |
dc.contributor.author.fl_str_mv |
Vieira, Daniela C. M. Fiuza, Thalita F. M. [UNESP] Salgado, Hérida R. N. [UNESP] |
dc.subject.por.fl_str_mv |
Cefuroxime sodium Microbiological testing Quality control Validation and stability |
topic |
Cefuroxime sodium Microbiological testing Quality control Validation and stability |
description |
The cefuroxime sodium is a second generation cephalosporin indicated for infections caused by Gram-positive and Gram-negative microorganisms. Although this drug is highly studied and researched regarding the antimicrobial activity, pharmacokinetics and pharmacodynamics, there are few studies regarding the development of analytical methodology for this cephalosporin. Thus, research involving analytical methods is essential and highly relevant to optimize its analysis in the pharmaceutical industry and guarantee the quality of the product already sold. This study describes the development and validation of a microbiological assay applying the turbidimetric method for the determination of cefuroxime, using Micrococcus luteus ATCC 9341 as micro-organism test and 3x3 parallel line assay design, with nine tubes for each assay, as recommended by the Brazilian Pharmacopoeia. The developed and validated method showed excellent results of linearity, seletivity, precision and robustness, in the concentration range from 30.0 to 120.0 mg/mL, with 100.21% accuracy and content 99.97% to cefuroxime sodium in injectable pharmaceutical form. |
publishDate |
2014 |
dc.date.none.fl_str_mv |
2014 2015-12-07T15:30:56Z 2015-12-07T15:30:56Z |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
http://dx.doi.org/10.3390/pathogens3030656 Pathogens (basel, Switzerland), v. 3, n. 3, p. 656-666, 2014. 2076-0817 http://hdl.handle.net/11449/131019 10.3390/pathogens3030656 PMC4243433.pdf 25438016 PMC4243433 |
url |
http://dx.doi.org/10.3390/pathogens3030656 http://hdl.handle.net/11449/131019 |
identifier_str_mv |
Pathogens (basel, Switzerland), v. 3, n. 3, p. 656-666, 2014. 2076-0817 10.3390/pathogens3030656 PMC4243433.pdf 25438016 PMC4243433 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
Pathogens (basel, Switzerland) 1,421 |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
656-666 application/pdf |
dc.publisher.none.fl_str_mv |
Pathogens |
publisher.none.fl_str_mv |
Pathogens |
dc.source.none.fl_str_mv |
PubMed reponame:Repositório Institucional da UNESP instname:Universidade Estadual Paulista (UNESP) instacron:UNESP |
instname_str |
Universidade Estadual Paulista (UNESP) |
instacron_str |
UNESP |
institution |
UNESP |
reponame_str |
Repositório Institucional da UNESP |
collection |
Repositório Institucional da UNESP |
repository.name.fl_str_mv |
Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP) |
repository.mail.fl_str_mv |
|
_version_ |
1808129117431791616 |