Liver and Metabolism 14 Pharmacokinetics 1 – Drug absorption Flashcards

1
Q

what are the 6 rights of prescribing

A
Right patient
Right drug
Right route
Right dose
Right time
Right outcome
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2
Q

what is pharmacokinetics

A

what the body does to the drug

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3
Q

what is pharmacodynamics

A

what the drug does to the body

therapeutic effect

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4
Q

what does pharmacokinetics do

A

Facilitates safe and effective use of medicines
Determines optimal dosage regimen (dose, route, dose interval, duration of treatment)
Predicts potential drug interactions

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5
Q

what makes up pharmacokinetics

A

absorption - Drug transfer from its site of
administration to the systemic circulation (blood)
distribution
metabolism
excretion

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6
Q

Factors that influence enteral absorption

A
Gastrointestinal (GI) motility
Absorptive area
GI blood flow
Drug particle size and formulation
Drug physicochemical properties
Drug binding
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7
Q

routes of drug administration

A

oral
rectal
(sublingual
buccal)

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8
Q

how does solubility effect enteral absorption

A

lipid soluble - non polarised eg NaCl
hydrophilic (polar) - ionised molecules (Na, K)
more lipid soluble - more absorption, more water soluble, less absorption

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9
Q

how does pH affect absorption

A

acidic drugs better absorbed by acidic media (same for basic)
acidic better absorbed by stomach and basic by intestines
better excreted in opposite media (important for poisoning)

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10
Q

routes of drug administration

A
parenteral (injection)
Topical
Transdermal 
Inhalational
Intrathecal
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11
Q

what is ideal dosing

A

between minimum toxic concentration and minimum effective concentration

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12
Q

pharmacokinetic concepts

A
Absorption
First-pass (pre-systemic metabolism)
Bioavailability
Bioequivalence 
Volume of distribution
Cytochrome P450 enzyme system
Half-life
Steady state
Clearance
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13
Q

what is bioavailability

A

Fraction of the administered (oral) dose of a drug that reaches the systemic circulation.
20% OBA needs to be 5x IV dose
Oral AUC/IV AUC

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14
Q

what is first pass (pre-systemic) metabolism

A

metabolism of the drug prior to reaching systemic circulation.
hepatic
smaller it is, the greater the BA

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15
Q

what is bioequivalence

A

Two drugs are considered bioequivalent when there is no significant difference in the rate or extent of bioavailability at the same molar dose and under the same conditions
relevant for different formulas and batches

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