Week 1 Flashcards
Differentiate between the 2 phases of drug action
- Pharmacokinetics
- Pharmacodynamics
What is Pharmacokinetics?
The process of drug movement throughout the body and is composed of 4 processes
What are the 4 processess of Pharmacokinetics?
ADME
- Absorption
- Distribution
- Metabolism
- Excretion
What is drug absorption?
The movement of drugs into the blood stream and occurs as one of three main transport routes
What are the three main transport routes of drug absorption?
APP
- Active transport
- Passive transport
- Pinocytosis
What is active transport?
transport that requires a carrier such as a protein to move against the concentration gradient
requires energy
What is Passive transport?
Transport that occurs by either diffusion or facilitated diffusion
What is diffusion?
When drugs move across the cell membrane to an area of lower concentration
What is facilitated diffusion?
When a drug relies on a carrier to move from an area of lower concentration
What is Pinocytosis?
A process in which the cells carry a drug across their membrane by engulfing the drug particles in a vesicle
Where do most oral meds become absorbed?
Across the mucosal lining of the small intestines
What is the first pass effect?
When the drug concentration is greatly reduced by the liver prior it the drug being absorbed into the blood stream
What is the Bio-availability of a drug?
The percentage of an administered drug available for activity
What two main factors effect bioavailability?
Absorption and First-pass effect
What are some factors that can affect absorption?
poor Circulation-can lover absorption
Hunger, Pain, Stress, Fasting, Food, pH-Can increase or decrease absorption depending on condition especially when they affect gastric emptying
What are factors that can alter bioavailability of a drug?
- Drug form
- Route of administration
- Gastric and mucosal motility
- Presence of food in stomach
- Decreased liver functionincreases bioavail
What is Drug Distribution?
The movement of a drug from the bloodstream to the body tissues
What three main factors influence drug distribution?
- Rate of blood flow to tissue
- Drug affinity to tissue
- Protein Binding
What are free drugs?
Drugs that remain unbound to proteins and cause a pharmacological response
What is drug metabolism?
The process which the body chemically changes drugs into a form that can be excreted
What is the main site of drug metabolism?
the liver
Why are patients with impaired liver disease at higher risk for drug toxicity?
Because if the liver is impaired it can not metabolize the drugs efficiency which will lead to an excess buildup of free drugs in the system leading to toxicity
What is Drug half life?
The amount of time it takes for X amount of drug to be reduced by half in the body.
What factors affect drug half-life?
- The amount of drug initially given
- The amount of drug remaining in the system at the next dose
- rate of metabolism
- rate of excretion
Why do drugs with long half-life’s sometimes need a loading dose?
Because drugs with long half-life’s tend to take longer to reach a therapeutic level in the system and if the patient needs the effect of the therapeutic action faster than the standard dose will allow, a larger loading dose is given and subsequent doses are given to maintain the level of available drugs in the system
What is drug excretion?
The elimination of the drug and its metabolites from the body
What is the main site of drug excretion?
The kidneys
What are the three types of conditions that can effect excretion?
_Pre-renal-reduced blood flow
_Intra-renal-altered GFR, secretion and reabsorption
_Post-renal- Urinary obstruction
What is Pharmacodynamics?
The study of the effects of drugs on the body