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48 Cards in this Set

  • Front
  • Back

Factors that influence drug concentration

1. Absorption


2. Distribution


3. Biotransformation


4. Elimination

Transport physiology

Transport categories are based on whether energy is required to move a substance across the body's compartments:


1. Active transport


2. Passive transport

Active transport

Requires energy to move a substance from an area of low concentration go an area of high concentration

Mitochondria produce

ATP

ATP breaks down to

ADP producing biochemical energy



This energy is used to facilitate the movement of ions "up" the concentration gradient

Passive transport

Movement of a substance without the use of energy from an area of high concentration to an area of low concentration

Three processes of passive transport

1. Diffusion


2. Osmosis


3. Filtration

Drug absorption

The process of movement of a drug from the site of application into the specific target

Factors that affect the rate of drug absorption

1. Drug solubility


2. Drug concentration


3. Drug pH


4. Site of absorption


5. Absorbing surface area


6. Circulatory status


7. Bioavailability (the amount of medication in systemic circulation)

Drug solubility

The tendency of a drug to dissolve

Drug concentration

Drugs given in high concentration are more quickly absorbed than those in low concentration


•Drugs administered by more than one rout may have various concentrations

Drug pH

Acid vs basic (alkaline)


•Acidic drugs are more rapidly absorbed in acidic environments (stomach)


•Basic drugs are more rapidly absorbed in alkaline environments (kidneys)

Site of absorption

Site of absorption affects the rate of absorption

Absorbing surface area

Drugs are absorbed more quickly from large surface areas

Blood supply to the site of absorption

Different body tissues and organs have varied degrees of blood supply

Bioavailability

The amount of drug that is still active after it reaches its target tissue

Distribution

The process whereby a drug is transported from the site of absorption to the site of action

Factors that affect distribution

1. Cardiovascular function


2. Regional blood flow


3. Drug storage reservoirs


4. Physiological barriers

Distribution - Cardiovascular function

Impared cardiovascular function results in slower and unpredictable drug distribution with decreased perfusion and drug delivery

Distribution - regional blood flow

Regional as well as systemic blood flow can impact drug distribution by causing the drug to not reach all parts of the intended target

Distribution - physiological barriers

Two main barriers:


blood-brain barrier/blood-cerebrospinal barriers are tightly packed cell membranes that restrict damaging drugs and toxins. Only non protein bound, highly lipid soluble drugs can cross the barriers of the CNS

Biotransformation

Once in the body, a drug is metabolized or broken down into different chemicals (metabolites)


1. Makes it into a more or less active metabolite


2. Makes it more water soluble (to facilitate eliminafion)


Biotransformation usually occurs in the liver but can also occur in the kidneys, lungs, GI tract

Biotransformation: Hepatic "first-pass" metabolism

The first-pass metabolism or presystemic metabolism is the phenomenon which occurs whenever the drug administered orally, enters the liver and suffers extensive biotransformation to such an extent that bioavailability is drastically reduced, thus showing subtherapeutic action


The first-pass metabolism or presystemic metabolism is the phenomenon which occurs whenever the drug administered orally, enters the liver and suffers extensive biotransformation to such an extent that bioavailability is drastically reduced, thus showing subtherapeutic action

Elimination

Movement of a drug, or its metabolites from tissues back into circulation and circulation to the organs of excretion

Drug half-life

The time required for the total amount of a drug in the body to diminish by half

Predictable responses

Anticipate responses beyond the desired effect

Iatrogenic responses

An adverse condition inadvertently induced in a patient by the treatment given

Therapeutic threshold

Is the minimum concentration necessary for a drug to produce it's desired effect

Autonomic nervous system

Part of the PNS which controls the body's autamatic or involuntary functions such as:


•BP


•Cardiac function


•Bladder


•Temperature

Neurochemical transmission

Process of chemical signaling between cells


•Synthesis of chemical signals


•Signals are stored in nerve terminal


•Signals released from the nerve ending


•Signal is bound to a receptor

The vagus nerve is the what cranial nerve?

10th (Cranial nerve X)

Acetylcholine

Is the neurotransmitter that initiates PNS responses (enables vagal nerve stimulation)

Parasympathetic Nervous system

Decreases HR (normal HR)


•Bronchoconstriction


•Increased GI smooth muscle activity


•Digestive enzymes


•Pupillary constriction (normal pupils)


•Salvation


•Hypotension (normal bp)


•Urine production

Sympathetic nervous system

Dry mouth


•Tachycardia


•Increased myocardial contractility


•Hypertension


•Dialated pupils


•Shunting of blood to vital organs/muscles


•Bronchodilation


•Increased sweat glands secretion


•Converts glycogen to glucose

Anticholinergic drugs block what?

PNS influence

Cholinergic drugs mimic what?

PNS influence

Cholinergic (PNS)

Neurons and effector organs activated by acetylcholine are called cholinergic

Adrenergic (SNS)

Neuronal and effector organs are activated by norepinephrine/epinephrine are called adrenergic

Adrenergic drugs cause ..

Adrenaline effects in the body

Antiadreneric drugs...

Block the effects of adrenaline like drugs

Epinephrine is a what agonist?

Alpha and beta

Alpha 1

Receptor stimulation causes artery and venous constriction

Alpha 2

Receptor stimulation blocks norepinephrine release

Beta 1

Receptor stimulation causes increased force and contractility of the heart

Beta 2

Receptor stimulation causes bronchodilation in the lungs

Sympathomimetics

Mimic sympathetic stimulation

Agonist

Drug that bunds to a receptor and causes it to initiate the expected response

Antagonist

Drug binds to a site but do not cause the expected response