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DRUG ABSORPTION - Coggle Diagram
DRUG ABSORPTION
permeability
types of drug transport
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paracellular absorption
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total surface area of paracellular spaces is extremely low, the overall contribution of paracellular diffusion in the drug absorption process is limited
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the permeability of a drug at the absorption site into the systemic circulation is intimately related to the molecular structure and properties of the drug and to the physical and biochemical properties of the cell membrane
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ex vivo experiments
everted gut sac
why evert
to expose the mucosal surface to the dissolution media and the serosal surface to media inside the perfusion apparatus
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based on assumptions that membrane permeability of drugs is not species-dependent, since the composition of plasma membrane of intestinal epithelial cells is similar across the species
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small intestine
for most drugs, the optimum site for drug absorption after oral administration is the upper portion of the small intestine or
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the unique anatomy of the duodenum provides an immense surface area for the drug to be absorbed efficiently
the large surface area of the duodenum is due to the presence of valvelike folds in the mucus membrane on which are small projectons known as villi
these villi contain even smaller projections known as microvilli, forming a brush border
in addition, the duodenal region is highly perfused with a network of capillaries
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