Intro to Pharm, drug discovery and development, routes of administration - Study Guide Flashcards
What is the generic name of a drug?
It comes from the chemical name and can be shorter.
It is also non-prorietary
What is brand name of drugs?
Assigned to the compound by a pharmaceutical company for marketing purposes
What is the chemical name of a drug?
Refers to the specific compound structure that is long and too much to say
What are some examples of nomenclature for a drug?
Chemical name: 2-(diphenylmethoxy)-N,N -dimethylethylamine hydrochloride
Generic name: Diphenhydramine Hydrochloride
Brand names: allergy relief, allermax, diphedryl, ZzzQuil
What is a schedule I substance?
Give some examples!
Drugs with NO accepted medical use with the highest potential for abuse
No medical use - high risk for abuse
Heroin, LSD, weed, MDMA, etc.
What is schedule II substances?
Give examples!
Drugs with high potential for abuse with possible dependece BUT has an accepted medical used through prescriptions
Methylphenidate, methamphetamine, Oxycodone, Morphine, Methadone, Hydropmorphone, Fentanyl, Cocaine, etc.
What is schedule III substances?
Give examples!
Moderate to lower abuse potentional compared to schedule II drugs
Anabolic Steroids, Testosterone, Codeine, Ketamine
What is schedule IV substances?
Lower abuse potential compared to schedule III drugs + lower risk of dependence
Diazepam, Lorazepam, Phenobarb, Propoxyphene, Tramadol
What is schedule V substances?
Give examples!
Lowest abuse potential
Diazepam, Lorazepam, Phenobarb, Propoxyphene, Tramadol
What is Pharmacology?
The study of how chemical agents, both natural and synthetic that affect biological systems.
- has subsystems of pharmacotherapeutics and toxicology
What is pharmokinetics?
What the body does to the drug
What are the categories of pharmacokinetics?
Absorption
Distribution
Metabolism
Excretion
ADME
What is pharmacodynamics?
What the drug does to the body
What does pharmacodynamics depend on?
On the drug receptor and the ability of the drug to bind to the receptors
What is toxicology?
study of effects of chemical, biological and physical agents on humans
What is the difference between pharmacokinetics and pharmcodynamics?
Pharmacokinetics is the body’s response to the drug
Pharmacodynamics is how the drug affects the body
What is absorption affected by?
the bioavailability that depends on the body itself:
- stomach acidity
- gastric emptying
- overall surface area
- GI enzymes
- developmental changes
What does bioavailability depend on?
- the route of administration
- how the drug crosses the membrane barriers (active, passive, faciliated, any special processes)
Where does the drug go and where is it stored?
Where:
- tissue
- blood
- plasma proteins
- subcellular components
Stored:
- fat
- bone
- muscle
- organs
What is the volume of distribution?
ratio of the drug that is concentrated in the plasma
What are the factors that affect distribution?
- the tissue permeability
- blood flow
- how it binds to the plasma protein
- how it binds to the subcellular component
What is the Phase 1 of drug metabolism?
With the use of enzyme CYP450
- it takes a drug and makes it more polar and water solube = easier to be excreted
- it also allow the drug to be properly effective
What is a CYP inductor?
This increases the activity of CYP450 = making the drug less effective
Ex. rifampin and carbamazepine