Pharmacology Flashcards

1
Q

Half-life

A

Time taken for the concentration of a drug to decrease by half

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2
Q

Volume of distribution

A

The apparent volume a drug disperses into at steady state to produce the observed concentration

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3
Q

Clearance

A

Amount of plasma cleared of drug per unit time. The units are the same as flow, in L/min

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4
Q

Hepatic clearance

A

Volume of blood cleared of drug, by the liver, per unit time.

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5
Q

First-order kinetics

A

Rate of reaction is dependent on the concentration of reactant, mostly used in the concept of elimination, when a constant % of drug is eliminated per unit time

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6
Q

Zero-order process

A

Rate of reaction is independent of the concentration of reactant. Constant amount of drug eliminated per unit time

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7
Q

Bioavailability

A

The % of drug reaching the systemic circulation, expressed as a fraction of the same amount of drug given IV

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8
Q

What is hepatic extraction ratio

A

Fraction of substance removed from blood flowing through the liver during a single pass.

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9
Q

Context-sensitive half time

A

Time taken for the plasma concentration to fall by 50% after the cessation of drug infusion, with the context being the duration of infusion

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10
Q

Ke0

A

Rate constant of drug elimination from the effect site.
Main determinant of the time to peak effect from a bolus of drug.

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11
Q

T1/2 Ke0

A

Value which describes the time taken to achieve 50% effect-site concentration when the plasma levels are maintained at steady state

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12
Q

Purpose of TCI?

A

Achieve and maintain a predetermined target concentration of said drug, rapidly, and without overshooting

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13
Q

Bristol method

A

Achieve plasma [propofol] of 3 microg/ml
Loading 1mg/kg
Immediate infusion at 10mg/kg/hr for 10 mins
then 8mg/kg/hr for 10 mins
then 6mg/kg/hr for 10mins

Plus N2O

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14
Q

Typical remifentanil infusion targets?

A

plasma target
4ng/ml, or 0.2ug/kg/min infusion

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15
Q

Drug

A

Any compound that affects a biochemical or physiological effect in the body

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16
Q

mechanisms of drug effects

A

Physicochemical: mannitol, chelating agents
Receptor interaction
Enzyme activity alteration

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17
Q

Ligand

A

Substance that binds to a specific site of a receptor

18
Q

Receptor

A

A protein containing a ligand binding site to bring about a response

19
Q

Dissociation constant

A

Concentration of a ligand required to cause 50% receptor occupancy

20
Q

Law of mass action

A

rate of chemical reaction is proportional to product of concentration of reactants

21
Q

Solution

A

A homogenous mixture to intimately combined to be distinguishable by looking

22
Q

Suspension

A

A heterogenous mixture where particles eventually settle out

23
Q

Emulsion

A

A stable suspension of small globules of 1 liquid in a second liquid

24
Q

Emulsifier

A

A surface-active agent that promotes the formation of an emulsion

25
Loading dose
Initial higher dose of a drug given at the beginning to rapidly attain high plasma concentration
26
Maintenance dose
Rate of drug administration equal to rate of elimination at steady state
27
Therapeutic window
The range of drug dosages which can treat disease effectively without having toxic effects
28
potency
amount of drug needed to produce a given effect A function of affinity and efficacy
29
First order kinetics
fixed proportion of drug eliminated per unit time Constant half-life
30
Zero order kinetics
Fixed amount of drug eliminated per unit time
31
Hepatic extraction ratio
Fraction of drug removed from blood by the liver
32
Eutectic mixture
mixture of 2 compounds in fixed proportions which behave with a single set of physical characteristics. EMLA has a lower melting point than the individual substances
33
Affinity
How avidly a drug binds to the receptor
34
Intrinsic activity
The magnitude of effect of a drug produced once bound to the receptor
35
Agonist
drug that interact with a receptor to increase its activity
36
Inverse agonist
Bind receptors and reduce the amount of receptors in the active conformation
37
Antagonist
a substance with significant receptor affinity but no intrinsic activity
38
Allosteric modulators
Bind at a site distant from the agonist receptor site and alter the binding characteristic of the agonist
39
Poynting effect
Mixture of 2 gases has a different set of physicochemical properties than the individual components. i.e bubbling O2 through N2O lowers the critical temp to -7 degrees
40
ED95
dose of NMB to produce 95% first twitch height reduction in 50% of the population
41
Median effective concentration
the concentration of a drug that induces a specified response exactly halfway between baseline and maximum