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| Caco-2-Zellpermeabilitätsassay× | Liposomale Wirkstofffreisetzung× | |
|---|---|---|
| Fachgebiet | Pharmakologie | Pharmakologie |
| Familie | Process / pipeline | Process / pipeline |
| Entstehungsjahr≠ | 1989 | 1965 |
| Urheber≠ | Ingrid Hidalgo | Alec Bangham |
| Typ≠ | absorption screening | formulation technology |
| Wegweisende Quelle≠ | Hidalgo, I. J., Raub, T. J., & Borchardt, R. T. (1989). Characterization of the human colon carcinoma cell line (Caco-2) as a model system for intestinal epithelial permeability. Gastroenterology, 96(3), 736-749. DOI ↗ | Bangham, A. D., Standish, M. M., & Watkins, J. C. (1965). Diffusion of univalent ions across the lamellae of swollen phospholipid films and the determination of membrane potential. Journal of Molecular Biology, 13(1), 238-252. DOI ↗ |
| Aliasnamen | Caco-2 assay, intestinal permeability, ADME screening | liposomal formulation, vesicular delivery, lipid nanoparticles |
| Verwandt | 3 | 3 |
| Zusammenfassung≠ | The Caco-2 assay is an in vitro model system using human colon carcinoma cell monolayers to screen drug intestinal permeability. Developed by Hidalgo and colleagues in 1989, Caco-2 cells differentiate into an epithelial barrier resembling intestinal mucosa, enabling rapid assessment of drug absorption potential and identification of transporter-mediated transport. | Liposomal encapsulation is a formulation technique using lipid bilayer vesicles (liposomes) to enclose drugs, improving bioavailability, reducing toxicity, and enabling targeted delivery. Developed by Alec Bangham in 1965, liposomes are now standard in pharmaceutical development, with several FDA-approved liposomal drugs on the market. |
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