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clinical pharmacology
science of drugs and their use in humans
what is a drug?
molecule which has a physiological effect when ingested or otherwise introduced into the body
bioavailibility
the proportion of administered drug which reaches systemic circulation unchanged and is thus available for distribution to site of action
intravenous injection
achieves 100% bioavailibilty
all of drug dose reaches systemic circulation unchanged
rapid and powerful action
incovenient for long term therapy
subcutaneous injection
consistent absorption from small volumes
uptake into bloodstream via absorption across capillary walls
intramuscular injection
access to large blood flow in muscles of upper arm
route is reliable and can be suitable for certain irritant drugs
good for depot preparations (longer lasting drug release)
rapid absorption and good for larger volumes compared with SC injections (common for vaccinations)OR
oral routes
very common, safe, convenient
always less than 100% bioavailability achieved
exposure to pH, enzymes and microbial activity in gut
exposure to first pass metabolism
absorption can depend on rates of GI transit
requires patient compliance
mucosal routes
routes:
sublingual, buccal
nasal
vaginal, rectal
achieves rapid transit to systemic circulation
avoids first pass metabolism
drug stability (pH in mouth is neutral compared to acidic in stomach)
inhalation route
aerosols: for airway disease
lipid soluble anaesthetics: rapid absorption
avoids first pass metabolism
transdermal route
outer skin layer in fluences rate of absorption
low input rates can aid long term use
topical route
especially for dermatology
e.g- steroid cremas for skin conditions
pharmacokinetics
what the body does to the drug
study of drug movements within the body
pharmacodynamics
what drug does to the body
study of drug effects and mechanisms of action
ADME criteria
Absorption
Distribution
Metabolism
Excretion