Chapter 2 - Pharmacokinetics, Pharmacodynamics, and Pharmacogenetics Flashcards
drugs administered ________ there is no disintegration process, which occurs when a drug becomes a solution that can cross the illogic membrane
parenterally
which drugs are already in solution, which is the form necessary for absorption in the gastrointestinal tract
liquid suspension
these tablets resist disintegration in the acidic environment of the stomach and disintegrate when they reach the small intestine
enteric coated
Will acidic drugs enhance the absorption of enteric coated tablets? What slows the absorption rate?
No. high fat food.
what must be given parentally because they re destroy in the small intestine by digestive enzymes?
Insulin, growth hormones, and other protein based drugs
this types of tissue has fewer blood vessels, so absorption is slower
subcutaneous
Why is insulin injected subcutaneously
because it is desirable to have it absorb slowly
what do water soluble drugs require to pass through the GI membrane
carrier enzyme or protein
high fat foods are useful for that that are?
lipid soluble
food can stimulate the production of gastric acid, so medications requiring an acidic environment would be given with?
a meal
drugs given ________ absorb faster in muscles that the more blood vessels such as the deltoid
IM
Drugs that undergo ______________ are absorbed into the portal vein from the intestinal lumen and go through the liver where they are either unchanged or are metabolized to an inactive or a more active form
first-pass metabolism
what kind of drugs have less bioavailability because a lower percentage of the drug reaches the systemic circulation?
Oral
refers to the process by which cells carry a solute across a membrane
Pinocytosis
describes a rapid decrease in response to drugs that occurs when tolerance develops quickly
Tachyphylaxis
Drugs that are highly _______ bind with albumin and other proteins, leaving less free drug in circulation
protein bound
If a patient is low in _________, the drug is not bound, and there is more free drug to cause drug effects. There would be increased absorption, increased interactions with other drugs, and increased toxicity
albumin
Two drugs that are highly ______ will compete for protein binding sites, leaving more free drug in circulation and an increased risk of adverse effects as well as increased bioavalibility, inquired drug effects, and increased drug interactions.
protein bound
LIver diseases such as cirrhosis and hepatitis alter drug?
metabolism
When the drug metabolism rate is decreased what happens
excess drug accumulation can occur and lead to toxicity
Steady state levels occur at how many half lives?
3-5
A druge with a longer half life should be given at longer___________ to avoid drug toxicity
intervals