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Dynamic in vitro intestinal barrier model coupled to chip-based liquid chromatography mass spectrometry for oral bioavailability studies.
Santbergen, Milou J C; van der Zande, Meike; Gerssen, Arjen; Bouwmeester, Hans; Nielen, Michel W F.
Afiliación
  • Santbergen MJC; Laboratory of Organic Chemistry, Wageningen University, Stippeneng 4, 6708 WE, Wageningen, The Netherlands.
  • van der Zande M; TI-COAST, Science Park 904, 1098 XH, Amsterdam, The Netherlands.
  • Gerssen A; Wageningen Food Safety Research (WFSR), Wageningen University & Research, P.O. Box 230, 6700 AE, Wageningen, The Netherlands.
  • Bouwmeester H; Wageningen Food Safety Research (WFSR), Wageningen University & Research, P.O. Box 230, 6700 AE, Wageningen, The Netherlands.
  • Nielen MWF; Division of Toxicology, Wageningen University, Stippeneng 4, 6708 WE, Wageningen, The Netherlands.
Anal Bioanal Chem ; 412(5): 1111-1122, 2020 Feb.
Article en En | MEDLINE | ID: mdl-31865418
ABSTRACT
In oral bioavailability studies, evaluation of the absorption and transport of drugs and food components across the intestinal barrier is crucial. Advances in the field of organ-on-a-chip technology have resulted in a dynamic gut-on-a-chip model that better mimics the in vivo microenvironment of the intestine. Despite a few recent integration attempts, ensuring a biologically relevant microenvironment while coupling with a fully online detection system still represents a major challenge. Herein, we designed an online technique to measure drug permeability and analyse unknown product formation across an intestinal epithelial layer of Caco-2 and HT29-MTX cells cultured on a flow-through Transwell system, while ensuring the quality and relevance of the biological model. Chip-based ultra-performance liquid chromatography quadrupole time-of-flight mass spectrometry (UPLC-QTOF-MS) was coupled to the dynamic Transwell system via a series of switching valves, thus allowing alternating measurements of the apical and basolateral sides of the in vitro model. Two trap columns were integrated for online sample pre-treatment and compatibility enhancement. Temporal analysis of the intestinal permeability was successfully demonstrated using verapamil as a model drug and ergotamine epimers as a model for natural toxins present in foods. Evidence was obtained that our newly developed dynamic system provided reliable results versus classical static in vitro models, and moreover, for the first time, epimer-specific transport is shown for ergotamine. Finally, initial experiments with the drug granisetron suggest that metabolic activity can be studied as well, thus highlighting the versatility of the bio-integrated online analysis system developed. Graphical abstract.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Cromatografía Liquida / Espectrometría de Masa por Ionización de Electrospray / Espectrometría de Masas en Tándem / Dispositivos Laboratorio en un Chip / Mucosa Intestinal / Modelos Biológicos Límite: Humans Idioma: En Revista: Anal Bioanal Chem Año: 2020 Tipo del documento: Article País de afiliación: Países Bajos

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Cromatografía Liquida / Espectrometría de Masa por Ionización de Electrospray / Espectrometría de Masas en Tándem / Dispositivos Laboratorio en un Chip / Mucosa Intestinal / Modelos Biológicos Límite: Humans Idioma: En Revista: Anal Bioanal Chem Año: 2020 Tipo del documento: Article País de afiliación: Países Bajos