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AAPS PharmSciTech ; 22(3): 84, 2021 Mar 01.
Artigo em Inglês | MEDLINE | ID: mdl-33649887

RESUMO

Prediction of performance of traditional, reformulated, and novel oral formulations in adults and pediatrics is of great importance. This study was conducted to assess solubility of celecoxib in age-appropriate fasted- and fed-state gastric and intestinal biorelevant media, classify celecoxib into biopharmaceutical classification system (BCS), and assess the effects of age-related developmental changes in the composition and volume of gastrointestinal fluids on the solubility and performance of oral formulations containing celecoxib. Solubility of celecoxib was assessed at 37°C in the pH range specified by the BCS-based criteria in 13 age-appropriate biorelevant media reflective of the gastric and proximal small intestinal environment in both fasted and fed states in adults and different pediatric subpopulations. A validated HPLC-UV method was used to quantify celecoxib. Experimental and computational molecular descriptors and in vivo pharmacokinetic data were used to assign the permeability class of celecoxib. Celecoxib belonged to BCS class 2. The pediatric to adult solubility ratios were outside the 80-125% boundaries in 3 and borderline in 1 biorelevant media. Significant age-related variability could be predicted for oral formulations containing celecoxib intended for pediatric use. Findings of this study indicated that the criteria used in the adult BCS might not be directly applied to pediatric subpopulations.


Assuntos
Produtos Biológicos/classificação , Produtos Biológicos/farmacocinética , Celecoxib/classificação , Celecoxib/farmacocinética , Jejum/metabolismo , Absorção Gastrointestinal/fisiologia , Administração Oral , Adulto , Anti-Inflamatórios não Esteroides/classificação , Anti-Inflamatórios não Esteroides/farmacocinética , Líquidos Corporais/química , Líquidos Corporais/metabolismo , Criança , Pré-Escolar , Avaliação Pré-Clínica de Medicamentos/métodos , Previsões , Absorção Gastrointestinal/efeitos dos fármacos , Humanos , Lactente , Recém-Nascido , Permeabilidade , Solubilidade
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