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IVIVC Assessment of Two Mouse Brain Endothelial Cell Models for Drug Screening.
Puscas, Ina; Bernard-Patrzynski, Florian; Jutras, Martin; Lécuyer, Marc-André; Bourbonnière, Lyne; Prat, Alexandre; Leclair, Grégoire; Roullin, V Gaëlle.
Afiliación
  • Puscas I; Faculty of Pharmacy, Université de Montréal, CP6128 Succursale Centre-ville, Montreal, QC H3C 3J7, Canada.
  • Bernard-Patrzynski F; Faculty of Pharmacy, Université de Montréal, CP6128 Succursale Centre-ville, Montreal, QC H3C 3J7, Canada.
  • Jutras M; Faculty of Pharmacy, Université de Montréal, CP6128 Succursale Centre-ville, Montreal, QC H3C 3J7, Canada.
  • Lécuyer MA; Department of Neuroscience, Faculty of Medicine, Université de Montréal and Centre de Recherc and du CHUM (CRCHUM), Montréal, QC H2X 0A9, Canada.
  • Bourbonnière L; Centre for Biostructural Imaging of Neurodegeneration, Institute for Multiple Sclerosis Research and Neuroimmunology, University Medical Center Göttingen, 37075 Göttingen, Germany.
  • Prat A; Department of Neuroscience, Faculty of Medicine, Université de Montréal and Centre de Recherc and du CHUM (CRCHUM), Montréal, QC H2X 0A9, Canada.
  • Leclair G; Department of Neuroscience, Faculty of Medicine, Université de Montréal and Centre de Recherc and du CHUM (CRCHUM), Montréal, QC H2X 0A9, Canada.
  • Roullin VG; Faculty of Pharmacy, Université de Montréal, CP6128 Succursale Centre-ville, Montreal, QC H3C 3J7, Canada.
Pharmaceutics ; 11(11)2019 Nov 08.
Article en En | MEDLINE | ID: mdl-31717321
Since most preclinical drug permeability assays across the blood-brain barrier (BBB) are still evaluated in rodents, we compared an in vitro mouse primary endothelial cell model to the mouse b.End3 and the acellular parallel artificial membrane permeability assay (PAMPA) models for drug screening purposes. The mRNA expression of key feature membrane proteins of primary and bEnd.3 mouse brain endothelial cells were compared. Transwell® monolayer models were further characterized in terms of tightness and integrity. The in vitro in vivo correlation (IVIVC) was obtained by the correlation of the in vitro permeability data with log BB values obtained in mice for seven drugs. The mouse primary model showed higher monolayer integrity and levels of mRNA expression of BBB tight junction (TJ) proteins and membrane transporters (MBRT), especially for the efflux transporter Pgp. The IVIVC and drug ranking underlined the superiority of the primary model (r2 = 0.765) when compared to the PAMPA-BBB (r2 = 0.391) and bEnd.3 cell line (r2 = 0.019) models. The primary monolayer mouse model came out as a simple and reliable candidate for the prediction of drug permeability across the BBB. This model encompasses a rapid set-up, a fair reproduction of BBB tissue characteristics, and an accurate drug screening.
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Texto completo: 1 Banco de datos: MEDLINE Tipo de estudio: Diagnostic_studies / Prognostic_studies / Screening_studies Idioma: En Revista: Pharmaceutics Año: 2019 Tipo del documento: Article País de afiliación: Canadá

Texto completo: 1 Banco de datos: MEDLINE Tipo de estudio: Diagnostic_studies / Prognostic_studies / Screening_studies Idioma: En Revista: Pharmaceutics Año: 2019 Tipo del documento: Article País de afiliación: Canadá