Pharmacokinetics 2 Flashcards
intravenous injection: what? speed?
drug injected into vein. rapid distribution and onset of action.
intravenous injection: method requires? should not cause? cons?
skill to find vein and special drug solutions that are sterile. shouldn’t cause direct damage to veins or pain. greater risk or overall costs.
intravenous injection: drug given in what two ways?
rapid as a bolus = push. continuous infusion = drip.
subcutaneous injection: what? speed?
drug injected below skin close to capillaries. absorption speed fairly rapid but depends on blood flow, not really faster than oral route.
subcutaneous injection: how to limit absorption ? have to limit volume? common route for?
addition of vasoconstrictors helps prolong local action. limit volume to reduce swelling and pain. insulin, heparin, allergy tests
intramuscular route: drug injected where? volume? __ route prevents?
into skeletal muscle; can accommodate larger volume. Z route prevents leakage
intramuscular injection: speed? what affects rate?
may not be faster than oral. muscle activity and blood flow affects rate
intramuscular injection: poor route for?
obese patients because site may be fatty
drug administration by inhalation: speed? why?
drug absorbed rapidly through lungs: high surface area and high blood flow, rapid distribution (lung to heart to body)
inhalation: common route for?
general anesthetics, nicotine, cocaine, poison gases
inhalation: drug in what form?
gas, vapor or fine powder.
drug administration via skin: aka? most chemicals crossing skin?
topical; through or across layers of dermis but most chemicals won’t cross intact skin
common drugs in transdermal patches. 3 pros?
estrogen, nicotine, scopolamine, nitroglycerin, fentanyl. easy, continuous and stable.
drugs distribute evenly? redistribution effects?
rarely distribute evenly in body: redistribution may limit duration of action, may prolong time drug remains in the body
drugs partition according to? (4)
special membrane barriers, solubility of drug in fat/tissue. degree of ionization of drug. plasma protein binding.