Lecture 6 Flashcards
Absorption
Review of Absorption Factors
- Smaller particles cross membranes more easily
- Nonionized particles can cross membranes
- Lipophilic particles can cross membranes
Via passive diffusion
Endocytosis + Exocytosis
Other methods of entering and exiting a cell
Endocytosis
- Can be leveraged for particle-based drug delivery
- Phagocytosis and micropinocytosis = non-specific
- Calveolar, clathrin-mediated, and receptor-mediated endocytosis are generally selective at varying degrees
Is tissue one cell?
No. It is several cells that differ in structure and properties. These different properties can affect drug absorption
Ex: Continuous (skin), fenestrated (kidney), or discontinuous (liver) junctions
Diffusion Overview
- Not inhibited
- Equilibrium
- Determined by charge and lipophilicity rather than structure
- Not highly cell-type specific
Transporter-Mediated Overview
- Saturable based on number of transporters available
- Can be inhibited
- May be structure specific/selective
- Greater cell type specificity
Total absorption =
Sum of all different uptake mechanisms
Drug Ionization
- Another major factor in drug update
- Acid absorbed in acid, base absorbed in base
- Ratio of unionized:ionized influences rate of absorption and also distribution and elimination
- Can leads to ion trapping
Surface Area
- Also matters in connection with absorption
- Weak acids are readily absorbed in stomach, BUT intestines have a larger surface area than the stomach
- This increase in surface area compensates for the unfavorable unionized:ionized ratio
Absorption
Movement of a drug from its site of administration into the bloodstream
Tmax
Time to reach Cmax
Cmax
The peak plasma concentration of a drug after administration.
AUC
The integral of the concentration-time curve (after a single dose or in steady state).
Endocytosis
A process by which the plasma membrane folds inward to bring substances into the cell.
Exocytosis
A process by which vessicle contents are released from the cell following membrane fusion