RELATIVE BIOAVAILABILITY OF TWO FORMULATIONS CONTAINING 40MG OF PANTOPRAZOLE UNDER FASTING AND POSTPRANDIAL CONDITIONS (Atena Editora)

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Autor(es): dc.contributor.authorSantos, Alessandra Ferreira dos-
Autor(es): dc.contributor.authorFrancisco, Quevellin Alves dos Santos-
Autor(es): dc.contributor.authorCorrea, Carlos Eduardo Melo-
Autor(es): dc.contributor.authorCoelho, Edvaldo Capobiango-
Data de aceite: dc.date.accessioned2022-01-26T15:41:49Z-
Data de disponibilização: dc.date.available2022-01-26T15:41:49Z-
Data de envio: dc.date.issued2022-01-17-
Fonte: dc.identifier.urihttp://educapes.capes.gov.br/handle/capes/645188-
Resumo: dc.description.abstractThe aim of this study was to evaluate the bioequivalence between two formulations of delayed-release tablets containing 40 mg of pantoprazole. The products were administered to healthy volunteers as a single dose under fasting (2x2 inbred; n=48) and postprandial (2x4 fully replicated inbred; n=80) conditions with washout of 7 days. Plasma pantoprazole concentrations were determined by ultra-performance liquid chromatography coupled with tandem mass spectrometry. After logarithmic transformation of the experimentally found plasma concentrations, the pharmacokinetic parameters used in the bioequivalence calculation were obtained: Cmax e ASC0-t. The 90% confidence interval for the ratios of the geometric means between the test drug and the reference drug, for the parameters Cmax e ASC0-t, are comprised in the IC 90% between 80%-125%. It is concluded that the formulations are bioequivalent, in terms of speed and extent of absorption of the active in the body, in both conditions studied, therefore interchangeable.pt_BR
Idioma: dc.language.isoenpt_BR
Palavras-chave: dc.subjectBIOEQUIVALENCEpt_BR
Título: dc.titleRELATIVE BIOAVAILABILITY OF TWO FORMULATIONS CONTAINING 40MG OF PANTOPRAZOLE UNDER FASTING AND POSTPRANDIAL CONDITIONS (Atena Editora)pt_BR
Tipo de arquivo: dc.typelivro digitalpt_BR
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