Lecture 2 barriers to drug deliver Flashcards
Describe bioavailability in drug delivery.
Bioavailability is the rate and extent to which an active agent is absorbed and becomes available at the site of action to elicit a therapeutic response.
what influences bioavailability in drug delivery
It is influenced by absorption, distribution, metabolism, and elimination processes.
What is the concept of relative bioavailability?
Relative bioavailability compares the rate and extent of absorption of two drug formulations (test vs. standard) administered via the same route.
Define absolute bioavailability in pharmacokinetics.
Absolute bioavailability compares the bioavailability of a drug via a specific route of administration with its bioavailability after intravenous (IV) administration.
How is absolute bioavailability calulated
It is calculated as the ratio of the AUC of the route of interest to the AUC after IV administration, always less than 1 if not administered intravenously
How can 100% bioavailability for oral drugs be achieved?
Drug must be completely released into solution in gastrointestinal fluid, remain stable in the solution, pass through the epithelium of the gastrointestinal tract without undergoing first-pass metabolism in the gut wall or liver.
List the barriers to drug delivery.
Barriers to drug delivery include biological (physical) barriers, physicochemical barriers, drug metabolism and elimination processes, patient compliance issues, and immunological barriers.
Explain the physical barriers to drug delivery.
Physical barriers include cell membrane barriers, epithelial barriers with mucus layers and biochemical obstacles like degradative enzymes, hydrophobic membranes with poor absorption of charged molecules, and efflux systems that pump out substances through specific pumps.
Describe passive diffusion in drug delivery.
Passive diffusion involves the movement of drugs down a concentration gradient according to Fick’s law.
What is paracellular drug delivery?
Paracellular drug delivery involves drug molecules moving between adjacent epithelial cells, limited to small hydrophilic molecules.
Define transcellular drug delivery.
Transcellular drug delivery involves drugs moving across epithelial cells, commonly seen with low molecular weight and hydrophobic molecules.
How does carrier-mediated transport work in drug delivery?
Carrier-mediated transport in drug delivery involves active absorption or facilitated diffusion using specialized membrane proteins with specificity for a set of substrates.
Describe facilitated transport in drug delivery.
Facilitated transport in drug delivery works with the concentration gradient passively, such as glucose transporters.
What is endocytosis in drug delivery?
Endocytosis in drug delivery involves the internalization of plasma membrane with the engulfment of extracellular material, including receptor-mediated and adsorptive endocytosis.
Describe the endocytic process in drug delivery.
1) Target molecules bind to receptors in the plasma membrane.
2) Areas coated with ligands form deep pockets in the plasma membrane surface.
3) Pockets pinch off, forming endosomes (coated vesicles).
4) Endosomes fuse with primary lysosomes to form secondary lysosomes.
5) Ligands may be removed and absorbed into the cytoplasm or degraded in acidic lysosomal conditions.
6) The lysosomal and endosomal membranes separate.
7) Endosomes fuse with the plasma membrane, making receptors available for ligand binding again.