Short Term Caco-2/TC7 Cell Culture : Comparison between of Conventional 21-d and a Commercially Available 3-d System(Biopharmacy)
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概要
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The Caco-2 cell model is a valuable tool for studying intestinal biotransformation of xenobiotics and to evaluate the potential of human intestinal absorption of new compounds. These properties were evaluated with Caco-2/TC7 cells in accelerated conditions to reduce maturation lag time from 21-d to 3-d in order to increase time and labor efficiency. Transmission electron and fluorescent microscopy were used for morphological characterization. Alkaline phosphatase and lactate dehydrogenase activities were assessed within time. Cytochrome P450 expression was studied by RT-PCR. Apparent permeabilities of a set of passively absorbed molecules across Caco-2/TC7 cell monolayers were determined to evaluate potential of both systems for prediction of human intestinal absorption. Microscopic images revealed that cells under both conditions differentiated as enterocyte-like cells but did so heterogeneously in the 3-d model. TEER values have shown that the 3-d model is a leakier cell system with higher mannitol Papp (cm/s). Biochemical characterization (hydrolase activities, CYP450 expression) suggested that the 3-d model was at a lower maturation level than the 21-d model. Carrier-mediated uptake of L-Phe was lower in the 3-d model suggesting that this model has limited application for mechanistic studies. Reasonable correlation was obtained between the two models (r^2=0.88, p>0.01) for 11 passively absorbed compounds with high potential of rank ordering of compounds. Although results suggested that the 3-d cells are under-differentiated, they could be usable to estimate the oral absorption of passively absorbed compounds.
- 公益社団法人日本薬学会の論文
- 2004-12-01
著者
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Arnaud Philippe
Service Commun De Microscopie Electronique Faculte Des Sciences Pharmaceutiques Et Biologiques Unive
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Provot Gerard
Laboratoire Glaxosmithkline New Chemical Entity Unit
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VIOLANTE Georges
Laboratoire de Pharmacie Galenique, UPRES EA 2498, Faculte des Sciences Pharmaceutiques et Biologiqu
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ZERROUK Naima
Laboratoire de Pharmacie Galenique, UPRES EA 2498, Faculte des Sciences Pharmaceutiques et Biologiqu
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RICHARD Isabelle
Laboratoire GlaxoSmithKline, New Chemical Entity Unit
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FRENDO Jean-Louis
Developpement humain, croissance et differenciation, INSERM U427, Faculte des Sciences Pharmaceutiqu
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ZHIRI Azzedine
Laboratoire GlaxoSmithKline, New Chemical Entity Unit
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LI-KHUAN Rene
Service commun de microscopie electronique, Faculte des Sciences Pharmaceutiques et Biologiques, Uni
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TRICOTTET Viviane
Service commun de microscopie electronique, Faculte des Sciences Pharmaceutiques et Biologiques, Uni
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CHAUMEIL Jean-Claude
Laboratoire de Pharmacie Galenique, UPRES EA 2498, Faculte des Sciences Pharmaceutiques et Biologiqu
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Chaumeil Jean-claude
Laboratoire De Pharmacie Galenique Ea 2498 Universite Paris Descartes:unite Recherche Et Developpeme
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Li-khuan Rene
Service Commun De Microscopie Electronique Faculte Des Sciences Pharmaceutiques Et Biologiques Unive
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Zerrouk Naima
Laboratoire De Pharmacie Galenique Upres Ea 2498 Faculte Des Sciences Pharmaceutiques Et Biologiques
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Zhiri Azzedine
Laboratoire Glaxosmithkline New Chemical Entity Unit
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Violante Georges
Laboratoire De Pharmacie Galenique Upres Ea 2498 Faculte Des Sciences Pharmaceutiques Et Biologiques
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Richard Isabelle
Laboratoire Glaxosmithkline New Chemical Entity Unit
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Tricottet Viviane
Service Commun De Microscopie Electronique Faculte Des Sciences Pharmaceutiques Et Biologiques Unive
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Frendo Jean-louis
Developpement Humain Croissance Et Differenciation Inserm U427 Faculte Des Sciences Pharmaceutiques
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Chaumeil Jean-claude
Unite Rech. Et Developpement Galenique Agence Generale Des Equipements Et Produits De Sante
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Richard Isabelle
Laboratoire D'epidemiologie Ergonomie Et Sante Au Travail University Of Angers
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Da Violante
Laboratoire de Pharmacie Galenique, UPRES EA 2498, Faculte des Sciences Pharmaceutiques et Biologiques, Universite Rene Descartes
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Zerrouk Naima
Laboratoire de Pharmacie Galénique, Faculté des Sciences Pharmaceutiques et Biologiques, UPRESS EA 2498, Université René Descartes
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