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34 Cards in this Set
- Front
- Back
Drug administration phase
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The drug administration phase describes the method by which a drug dose is made available to the body
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Drug Dose form
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Physical state of the drug in association with non-drug compenents.
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Route of administration
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POrtal or entry for the drug into the body
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Enteral Drug route
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Drugs intended to be absorbed in the GI tract
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Parenteral
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Intravenous, intramuscular, subcutanously
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Transdermal
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Absorbed percutanously
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Devices for inhaled administration of drugs
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1_vaporizer
2)Atomizer 3)Nebulizer, small or large 4)Metered dose inhaler, with/without spacer 5)Dry Powder inhaler 6)Ultrasonic nebulizer |
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Pharmacokinetic Phase
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Pharmacokinetic Phase of drug action describes the time course and deposition of a drug in the body, based on its absorption, metabolism, and elimination
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Definition of Absorption
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1)The process by which a drug gets introduced to the body in a way it can be distributed
2)Involves the ability (or inability) of a drug to cross different barriers (cell membranes, lipid membranes, etc). |
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Distribution
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1)Process by which a drug is transported to its sites of action, eliminated, and stored
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Distribution Continued
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1)Intended distribution may be systemic or local
2)To be effective, a drug must deliver a high enough concentration at an intended site |
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Metabolism of a drug
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Complex Processes that cause the biotransformation or metabolism of a drug
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Where is the main site of drug metabolism
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In the liver
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Elimination phase
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1)Primary site for the excretion of drugs is the kidneys
2)Maintenance dose-dose needed to equal the rate of elimination to maintain a steady concentration of the drug |
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Critical threshold
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The minimum of drug concentration needed for a therapeutic effect
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L/T ratio
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Lung availability versus total systemic availability
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Factors increasing the L/T ratio with inhaled drugs
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1)Efficient delivery devices
2)Inhaled drugs with a high first pass metabolism 3)Use of a resovoir device |
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Pharmacodynamic phase
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Describes the mechanisms of drug action by which a drug molecule causes its effects on the body
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Structure/Activity relations in the pharmacodynamic phase
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Relationship between a drug's chemical structure and its clinical effect or activity
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Nature and type of drug receptors
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1)Most receptors are proteins or polypeptides whose shape and electric charge provide a match to the drug's corresponding shape and charge.
2)Receptor proteins can be found on the cell's surface and within the cell 3)Resultant complex molecular mechanism translates, or, even better, tranduces a signal into an intracellular sequence that controls cell function |
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Types of transmembrane signalling
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1)Lipid soluble drugs cross the cell membranes and act on intracellular receptors
2)Drug attaches to an extracellular portion of a protein receptor which projects into the cell's protoplasm 3)Ion channels 4)Second messenger system |
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G protein signalling
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Drug attaches to a transmembrane receptor that is coupled to an intracellular enzyme by a g protein
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Examples of drugs that use g-protein signalling
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Beta-adrenergic agents, and acetycholine at parasympathetic nerve endings
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Dose-response relations
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1)Response of a drug is proportional to the drug concentration, As drug concentration increases, the numbers of receptors increase, and the drug effect also increases up to a maximal point
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ED 50
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The dose that produces 50 percent of teh maximal effect
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Agonist
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Drug or chemical that binds to a corresponding receptor (has affinity)and initiates an cellular response (has efficacy)
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Antagonist
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Drug or chemical that is able to bind to a receptor, but causes no response.
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ED50 gives information about___
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Potency. Two drugs could have differential maixmal responses, but similar potency.
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ED 50 inflection point
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At the steepest part of the curve(the ED50), minor changes in the dose have the greatest effect.
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Corticosteriods___
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Change transcription of DNA.
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Steroids____
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Reduce inflammation, work on the innermost layer of the epithelial cells
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Beta one receptors
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Are in the heart
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First Pass effect
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The meds that get absorbed in the stomach. Will cause a systemic effect.
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Fours phases of the pharmacokinetic phase
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1)Absorption
2)Metabolism 3)Elimination 4)Distribution |