Lecture 2 Flashcards
Bioavailability
How much free drug there is in your system to exert its effects
Steps of pharmacokinetic
Absorption
Distribution
Metabolism
Excretion
Routes of administration
Inhalation, oral (PO), transdermal (cream, bc, patches), transmucosal,injection
What is the main difference between oral administration and other forms of administrations
Goes through first pass metabolism
Examples of transmucosal
Sublingual/ buccal (between gums and cheeks)
Rectal
Intranasal
Intraocular
Vaginal
Urethral
Different types of injection
Subcutaneous ( under the skin)
Intramuscular
Intravenous
Drugs injected subcutaneously
Vaccines, insulin, growth hormones
Subcutaneous injections are
Slowly released and steady
Intramuscular injections are
Absorbed quicker than subcutaneous but slower than intravenous
Intravenous injections are
Absorbed quickly, accurate
What is cytochrome p450
Family of enzymes responsible for metabolism of many psychoactive drugs
Examples of modification
Induction by repeated use
Inhibition by other drugs or foods
Competition between drugs
What is co-metabolism
When two drugs do not compete to be broken down but will combine and make a new drug
Ex: cocaethylene (alcohol and cocaine)
How can drugs be excreted
Urine, seat, saliva, feces