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
Q

Loading dose

A

Initial higher dose of a drug given at the beginning to rapidly attain high plasma concentration

26
Q

Maintenance dose

A

Rate of drug administration equal to rate of elimination at steady state

27
Q

Therapeutic window

A

The range of drug dosages which can treat disease effectively without having toxic effects

28
Q

potency

A

amount of drug needed to produce a given effect
A function of affinity and efficacy

29
Q

First order kinetics

A

fixed proportion of drug eliminated per unit time
Constant half-life

30
Q

Zero order kinetics

A

Fixed amount of drug eliminated per unit time

31
Q

Hepatic extraction ratio

A

Fraction of drug removed from blood by the liver

32
Q

Eutectic mixture

A

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
Q

Affinity

A

How avidly a drug binds to the receptor

34
Q

Intrinsic activity

A

The magnitude of effect of a drug produced once bound to the receptor

35
Q

Agonist

A

drug that interact with a receptor to increase its activity

36
Q

Inverse agonist

A

Bind receptors and reduce the amount of receptors in the active conformation

37
Q

Antagonist

A

a substance with significant receptor affinity but no intrinsic activity

38
Q

Allosteric modulators

A

Bind at a site distant from the agonist receptor site and alter the binding characteristic of the agonist

39
Q

Poynting effect

A

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
Q

ED95

A

dose of NMB to produce 95% first twitch height reduction in 50% of the population

41
Q

Median effective concentration

A

the concentration of a drug that induces a specified response exactly halfway between baseline and maximum