Pharmacokinetics 2 Flashcards
P-glycoprotein Efflux Pump
- Active Transport of drugs
- Blood-Brain Barrier
- Secretes drug back into lumen of capillary
- Keeps drug concentrations / exposure in CNS low
- Intestines
- Secretes absorbed drug back into the lumen of intestine
- Decreases drug absorption
- Liver
- Secretes drug into bile canaliculus
- Active Biliary Secretion
- Enhances drug elimination
- Kidneys
- Renal excretion
- Blood-Brain Barrier
P-glycoprotein Efflux Pump:
Limiting effects
Some drugs act as p-gp inhibitors decreasing the rate of drug efflux
- Ketaconazole
- concurrent administration with cyclosporine increases the oral absorption of cyclosporine
Some dogs have mutations of the gene encoding the p-gp, resulting in decreased expression of functional p-gp
- Ivermecting and loperamide toxicity in some dogs
- increased penetration to the brain
- Decreases drug elimination
- increases drug absorption
P-glycoprotein Efflux Pump:
Deficiency
- Increased penetration of drugs into the CNS
- Ivermectin, Loperamide
- Decreased elimination of drugs
- Biliary secretion - vincristine
- Renal excretion
- May also be linked to decreased metabolism
- Increased oral absorption of drugs
- Digoxin - Cardiac Disease treatment
P-Glycoprotein Deficiency
- Homozygous Normal
- Lowest toxicity
- Ivermectin toxicity > 2mg/kg
- Heterozygous Mutation
- Increased toxicity
- Ivermectin Toxic dose ~0.3mg/kg
- Homozygous Mutation
- Highest toxicity
- Ivermectin toxic dose ~0.12mg/kg
- Heartworm prevention dose: 0.006mg/kg is safe
Acid
Proton Donor (H+)
Base
Proton acceptor
Amphoteric
Capable of acting as an acid and base
pKa
pH at which 50% of the drug is ionized
Ionized compounds have poor lipid solubility
pKa does not predict if a compound is an acid or base
pH
-log(h+)
can change
Drug Ionization
Unionized drug is more lipid soluble and more capable of diffusion through cell membranes
Ionized drug movement across anatomic membranes is restricted due to a positive or negative charge and poor lipid solubility
Henderson-Hasslbalch Equation
- Weak Acid
- ionized form favored when fluid pH > drug pKa
- Unionized form favored when fluid pH < drug pKa
- “acid-acid” an acid in a more acidic environment favors the unionized form and diffusion
- Weak Base
- Ionized form favored when fluid pH < drug pKa
- Unionized form favored when fluid pH > drug pKa
- “base-base” a base in a more basic environment favors the unionized form and diffusion
Ion trapping
differential drug accumulation in tissue compartments with different pH’s due to drug ionization and poor ability of ionized drug to diffuse across lipid membranes