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Modeling and Simulation as a Tool to Assess Voriconazole Exposure in the Central Nervous System.
Staudt, Keli Jaqueline; Dias, Bruna Bernar; Alves, Izabel Almeida; Lelièvre, Bénédicte; Bouchara, Jean-Philippe; de Araújo, Bibiana Verlindo.
Afiliação
  • Staudt KJ; Pharmaceutical Sciences Graduate Program, Federal University of Rio Grande do Sul-UFRGS, Porto Alegre 90610-000, Brazil.
  • Dias BB; Pharmaceutical Sciences Graduate Program, Federal University of Rio Grande do Sul-UFRGS, Porto Alegre 90610-000, Brazil.
  • Alves IA; Faculty of Pharmacy, Federal University of Bahia-UFBA, Salvador 40170-115, Brazil.
  • Lelièvre B; University of Angers-University of Brest, IRF (Infections Respiratoires Fongiques), SFR ICAT 4208, CEDEX 9, 49933 Angers, France.
  • Bouchara JP; University of Angers-University of Brest, IRF (Infections Respiratoires Fongiques), SFR ICAT 4208, CEDEX 9, 49933 Angers, France.
  • de Araújo BV; Pharmaceutical Sciences Graduate Program, Federal University of Rio Grande do Sul-UFRGS, Porto Alegre 90610-000, Brazil.
Pharmaceutics ; 15(7)2023 Jun 21.
Article em En | MEDLINE | ID: mdl-37513968
Voriconazole is a triazole antifungal used empirically for the treatment of complicated meningitis associated with Cryptococcus neoformans. Biopsy studies show that the drug exhibits adequate brain penetration although levels of cerebral spinal fluid (CSF) are highly variable. Considering that CSF is one of the main surrogates for CNS exposure, the present work proposed the building of a population pharmacokinetic modeling (popPK) model able to describing the exposure achieved by voriconazole in the plasma, interstitial cerebral fluid and CSF of healthy and infected rats. The developed popPK model was described by four compartments, including total plasma, free brain and total CSF concentrations. The following PK parameters were determined: Km = 4.76 mg/L, Vmax = 1.06 mg/h, Q1 = 2.69 L, Qin = 0.81 h-1 and Qout = 0.63 h-1. Infection was a covariate in the Michaelis-Menten constant (Km) and intercompartmental clearance from the brain tissue compartment to central compartment (Qout). Simulations performed with the popPK model to determine the probability of reaching the therapeutic target of fAUC > MIC showed that VRC has sufficient tissue exposure in the interstitial fluid and in the CSF for the treatment of fungal infections in these tissues at prevalent minimum inhibitory concentrations.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Prognostic_studies Idioma: En Revista: Pharmaceutics Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Brasil País de publicação: Suíça

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Prognostic_studies Idioma: En Revista: Pharmaceutics Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Brasil País de publicação: Suíça