PAMPA—a drug absorption in vitro model: 11. Matching the in vivo unstirred water layer thickness by individual-well stirring in microtitre plates
Many plate-based in vitro assays of membrane permeability (e.g., Caco-2, MDCK, PAMPA) of sparingly soluble candidate molecules report permeability of water, and not of the intended membrane barrier. This is so because the unstirred water layer on both sides of the membrane barrier is rate limiting f...
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Veröffentlicht in: | European journal of pharmaceutical sciences 2004-08, Vol.22 (5), p.365-374 |
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Sprache: | eng |
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Zusammenfassung: | Many plate-based in vitro assays of membrane permeability (e.g., Caco-2, MDCK, PAMPA) of sparingly soluble candidate molecules report permeability of water, and not of the intended membrane barrier. This is so because the unstirred water layer on both sides of the membrane barrier is rate limiting for these highly permeable molecules. The thickness of this water layer can be 1500–4000
μm in unstirred assays. Under in vivo conditions, however, the unstirred water layer is believed to be 30–100
μm thick. Lightly stirred in vitro assays, using plate shakers, cannot lower the thickness of the water layer to match that found in vivo. In this study, 55 lipophilic drugs were employed to characterize the effect of stirring in parallel artificial membrane permeability assay (PAMPA). Highly efficient individual-well magnetic stirring at speeds greater than 110
rpm has been demonstrated to lower the unstirred water layer thickness to the in vivo range. Stirring at 622
rpm has lowered the layer thickness to 13
μm in some cases, which had not been previously achieved for plate-based permeability assays. With diminished water layer contribution at 622
rpm, for example, the effective permeability of progesterone is 2754 × 10
−6
cm/s. The new stirring apparatus used in this study is not only suitable for PAMPA, but can also be used in Caco-2 assays. Because of the diminished resistance of the thinner water layer, the stirred PAMPA permeation time has decreased from the usual 15
h to about 15
min for lipophilic compounds. |
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ISSN: | 0928-0987 1879-0720 |
DOI: | 10.1016/j.ejps.2004.04.009 |