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• W1983111851 endingPage "1003" @default.
• W1983111851 startingPage "997" @default.
• W1983111851 abstract "In designing effective therapeutic strategies, novel drugs must exhibit favorable pharmacokinetic properties. The physicochemical characteristics of a drug, such as pKa, molecular weight, solubility and lipophilicity, will influence the way the drug partitions from the aqueous phase into membranes, and thus, will influence its ability to cross cellular barriers, such as the lining of the gastrointestinal tract and the blood–brain barrier. Physicochemical characteristics also influence the degree to which a drug is able to cross a barrier layer, and the route by which it does this; whether transcellular (across the cells)-by diffusion, carrier-mediated transport or transcytosis-or paracellular-by diffusing through the tight junctions between the cells. The in vitro model systems that are currently employed to screen the permeation characteristics of a drug often represent a compromise between high throughput with low predictive potential and low throughput with high predictive potential. Here, we will examine the way in which in vitro cellular permeability assays are often performed and the assumptions that are implied but sometimes forgotten, and we will make simple suggestions for improving the methodological techniques and mathematical equations used to determine drug permeability." @default.
• W1983111851 created "2016-06-24" @default.
• W1983111851 creator A5050129474 @default.
• W1983111851 creator A5078166589 @default.
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• W1983111851 date "2003-11-01" @default.
• W1983111851 modified "2023-10-03" @default.
• W1983111851 title "In vitro trans-monolayer permeability calculations: often forgotten assumptions" @default.
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• W1983111851 doi "https://doi.org/10.1016/s1359-6446(03)02873-3" @default.
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• W1983111851 hasPublicationYear "2003" @default.
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