Pharmacology and drugs Flashcards
What is the physicochemical property of a drug that needs to be in blood circulation
Lipophilic
Give an example of a semisynthetic source of drugs
Co- Amoksiklav- Amoksikla and Augmentin
What is the physicochemical property of a drug that does not need to be absorbed and in circulation
Hydrophillic
What role does the Liver play in drug excretion
Metabolism of a drug from a lipophilic state to a water-soluble metabolite
If a drug is hydrophilic what route of administration will get it into the bloodstream
Intravenous administration
What is the major role of hydrophilic drugs administered intravenously
Treating of disorders in circulation(blood and vessels) since hydrophilic drugs won’t easily enter tissues and remain in the bloodstream
Which drugs have a shorter half-life in circulation
Hydrophilic drugs since they do not need to undergo metabolism by the kidney
Xenobiotic
Xenobiotics are chemical substances that are foreign to life
Biliary excretion
When a drug which is heavily lipophilic which is being metabolised by the liver it can dissolve through the gall bladder and excreted through the gi-tract
An example of a lipophilic drug that undergoes biliary excretion
Bilirubin( endogenous bi-product of RBC breakdown) Responsible for the yellow color of urine
What substance is indicated by a yellow stool
Bilirubin
A patient with yellowing in eyes urine and stool indicates an organ malfunction, Which organ is damaged and why is there yellowing in the eyes
A malfunction of the liver which is responsible for lipid metabolism, in this case, Bilirubin metabolism
Bilirubin is a highly lipophilic drug that when not metabolized can find its way into the bloodstream and easily diffuse into tissues leading to the yellowing of the eyes
What is a poison
A drug with a very narrow or no safety dose range
What is the clinical definition of a drug
Chemical substance used to
Prevent
Diagnose or
Treat disease(s)
A drug generally has 3 names
What are they
Chemical name
Generic (non-proprietary) name
Brand (proprietary) name
- What is edrophonium
WHat are the factors that affect pharmacokinetics
Absorption
Distribution
Metabolism
Excretion
What is bioavailabilty
TThe fraction of an administered drug that gets in the bloodstream/plasma in its unchanged form
Which pharmacokinetic factor affects the therapeutic or toxic effect of the drug more
Drug absorption
Is absorption rate directly or inversely proportional to molecular size
Inversely proportional
A weak acidic drug In a strong acidic medi woud be predominantly in its not ionized form which is able to pass through membrane easily and get absorbed however the same weake acid drug in an alkaline medium is predominanty ionized and would not be anle to pass through membranes and would become ion trapped
Orogastric for decontaminating the gi tractfrom toxins or poisons
How does too much peristalsis affect drug absorption
Does not allow enough time to absorb drug
Hepatic encephalopathy
Wjat is the major factor that leadsnto preystematic drug loss
Hepatic metabolic inactivation of drugs
How does the first pass effect affect bioavailability
Reduces the bioavailability