Literature DB >> 21542416

Caco-2 cells, biopharmaceutics classification system (BCS) and biowaiver.

Libuse Smetanová1, Vĕra Stĕtinová, Zbynek Svoboda, Jaroslav Kvetina.   

Abstract

Almost all orally administered drugs are absorbed across the intestinal mucosa. The Caco-2 monolayers are used as an in vitro model to predict drug absorption in humans and to explore mechanism of drug absorption. The Caco-2 cells are derived from a human colon adenocarcinoma and spontaneously differentiate to form confluent monolayer of polarized cells structurally and functionally resembling the small intestinal epithelium. For studying drug permeability, Caco-2 cells are seeded onto the Transwell inserts with semipermeable membrane and grown to late confluence (21 days). After determination of cell viability, the integrity of monolayer is checked by phenol red permeability and by 14C-mannitol permeability. The transport from apical to basolateral (AP-BL) and basolateral to apical (BL-AP) is studied by adding the diluted drug on the apical or basolateral side and withdrawing the samples from the opposite compartment, respectively, for HPLC analysis or liquid scintillation spectrometry. Ca2+ -free transport medium is used to determine paracellular component of the drug transport. On the basis of permeability and solubility, drugs can be categorized into four classes of Biopharmaceutics Classification System (BCS). For certain drugs, the BCS-based biowaiver approach can be used which enables to reduce in vivo bioequivalence studies.

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Year:  2011        PMID: 21542416

Source DB:  PubMed          Journal:  Acta Medica (Hradec Kralove)        ISSN: 1211-4286


  15 in total

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4.  Molecular analysis and anticancer properties of two identified isolates, Fusarium solani and Emericella nidulans isolated from Wady El-Natron soil in Egypt against Caco-2 (ATCC) cell line.

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5.  Characterization of in vitro ADME properties of diosgenin and dioscin from Dioscorea villosa.

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6.  Zanamivir oral delivery: enhanced plasma and lung bioavailability in rats.

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7.  Lipo-endomorphin-1 derivatives with systemic activity against neuropathic pain without producing constipation.

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8.  Assessment of Cr(VI)-induced cytotoxicity and genotoxicity using high content analysis.

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9.  Absorption and metabolism characteristics of rutin in Caco-2 cells.

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Review 10.  Lipid- and sugar-modified endomorphins: novel targets for the treatment of neuropathic pain.

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