Intro To Pharm Flashcards
(25 cards)
Pharmacokinetics
Absorption, Distribution, Metabolism, Excretion
Pharmacodynamics
Drug-receptor interactions to produce an effect
Pharmaceutical phase
Dissociation into molecules for bioavailability
Parenteral route
Anything involving a needle
Issues with oral admin
Irritation
Destruction by acid/enzymes
Complex formation in GI tract
First pass effect
Sublingual admin issues
Bad taste
Rectal admin issues
Inconvenience leading to lack of compliance
SubQ/IM admin issues
Irritation
Variable blood flow leading to variable absorption
IV admin issues
Sterility required
Not for self medication
Intraarterial (IA) admin issues
Danger of hemorrhage
Intraspinal admin issues
Difficult technique
Are ionized or non-ionized drugs more lipid soluble?
Non-ionized. Includes groups like quaternary ammonia groups
Factors affecting absorption from all sites
Blood flow
Surface area
Cell layers
Drug concentration gradient
Three tissues with highest vascularity
- Brain
- Liver
- Kidneys
Factors affecting distribution of drug
- Vascularity
- Ease of drug crossing membrane barriers (pKa, pH, gradients)
- Polarity of drug
- Plasma protein binding
Effect of plasma protein binding
- Non linear response in drug after plasma protein saturation reached
- Drug competition on plasma proteins leading to drug-drug interactions
Blood brain barrier characteristics
- Tight junctions between endothelial cells of capillaries
- Molecules enter through passive diffusion of cell membranes or active transport
- Fat soluble>water soluble drugs
Therapeutic index
TD50/ED50
OR
LD50/ED50
Smaller # = worse drug (<30)
Competitive antagonists
Increase ED50, reversible
Non-competitive antagonists
Decrease Emax due to inactivation of receptors
Are receptor selective or specific drugs more common?
Receptor selective drugs more common
Side effects sources
Chemical properties of drug
Drug that interacts w/multiple receptor types
Drug that acts on receptor subtype present in multiple tissues
Drug that acts with single receptor type but multiple subtypes
Termination of drug mechanisms (3)
Redistribution
Biotransformation
Excretion
Common sites of drug-drug interaction?
CYPs
Plasma proteins