Pharm midterm Flashcards

1
Q

What is the Vd?

A

Amount of drug/ desired plasma concentration

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2
Q

What does Vd assume?

A

Cannot undergo biotransformation till its fully absorbed

Drug distributes instantaneously

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3
Q

What happens if a Vd exceeds TBW? (>42L) ?

A

Considered lipophilic

Needs higher dose to achieve given plasma concentration

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4
Q

What happens if the Vd is less than TBW? <42L

A

Considered to be hydrophilic

Does not go into fat

Need less drug

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5
Q

What is drug clearance proportinal to?

A

Blood flow to organ

Extraction ratio

Drug dose

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6
Q

What is drug clearance inversely proportional to?

A

Half-life

Drug concentration

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7
Q

What is steady state?

A

Rate of Administration = Rate of elimination

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8
Q

What is the alpha distribution phase?

A

Drugs going from the plasma to the tissues?

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8
Q

How many half lives to achieve steady state?

A

5

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9
Q

What is the beta phase?

A

Drugs going from the tissues to reenter the plasma

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10
Q

What is context sensitive half time?

A

** Does not consider time

Time required for the plasma to decline by 50%

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11
Q

What happens to the context sensitive half time of fentanyl when it is given for an extended period?

A

Takes longer to eliminate because of the buildup in peripheral compartments

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12
Q

*** What two factors determine the amount of ionization?

A

pH of the solution
pKa of the drug

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13
Q

*** WHAT HAPPENS WHEN PKA AND PH ARE THE SAME??

A

50% OF THE DRUG IS IONIZED AND 50% IS UNIONIZED

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14
Q

What drugs are more likely to undergo renal elimination ? Liver?

A

Renal - ionized
Liver - unionized

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15
Q

What are weak bases usually paried with?

A

With a negative ion,

Chloride or sulfate

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16
Q

What are weak acids usually paired with?

A

Positive ion such as Na, Ca, Mag

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17
Q

What are 3 main plasma proteins?

A

Albumin
a1-acid glycoprotein
Beta globulin

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18
Q

What conditions reduce serum albumin?

A

Liver and Renal disease
Old age
Malnutrition
Pregnancy

19
Q

What conditions decrease
a1-acid glycoprotein?

A

Neonates
Pregnancy

20
Q

If a drug is 98% bound and is reduced to 96% bound, what is the change?

A

100%

21
Q

***A drug is drug is cleared from the body at a rate proportional to plasma concentration, what model is this?

A

First order

Constant rate of fraction is eliminated per time

22
Q

What is zero order?

A

Drug is eliminated independent of plasma drug concentration

**Ex: 5mg every hour regardless of how much is in the body

22
Q

What drugs undergo zero order??

A
23
Q

What is a phase 2 reaction?

A

Adds a highly polar water substrate

CAN GO STRAIGHT TO PHASE 2

Glucuronic acid
Glycine
Acetic acid
Sulfuric acid
Methyl group

24
Q

What is enterohepatic circulation? Ex:?

A

Drugs secreted in bile are reabsorbed

Valium
Warfarin

25
Q

What is the extraction ratio?

A

How much of the drug is delivered and cleared by the organ

26
Q

ER of 1.0 means? ER of 0.5 means?

A

1.0 - Removes 100% of delivered drug

.5 - Removes 50% of delivered drug

27
Q

Which drugs are metabolized by pseudocholinesterase?

A

Succ, mivacurium
Tetracaine, Procaine, Benzocaine

28
Q

One drug that is biotransformed by alkaline phosphatase hydrolysis?

A

Fospropofol

29
Q

What is potency and how is it measured?

A

Dose required to achieve clinical effect

30
Q

Risk factors for propofol infusion syndrome?

A

4mg/kg.hr
Duration > 48 hours
Adults > children
Sepsis
Cerebral injury
Inadequate O2

31
Q

S+S of propfol infusion syndrome?

A

Brady
Asystole

Rhabdo
Metabolic acidosis
Renal failure
HLD
Fatty liver

32
Q

How do halogenated anesthetics produce immobility?

A

Ventral and Dorsal horn

33
Q

How do halogenated anesthetics produce unconsciousness?

A

Cerebral Cortex
Thalamus
RAS

34
Q

How do halogenated anesthetics produce amnesia?

A

Hippocampus
Amygdala

35
Q

How do halogenated anesthetics produce autonomic modulation?

A

Pons
Medulla

36
Q

What is CMRO2 a function of?

A

Electrical activity 60%
Cellular homeostasis 40%

Once isoelectric, cannot reduce any further

37
Q

How do gasses effect evoked potentials?

A

Visual - most sensitive
Brainstem - most resistant

SSEP and MEP are between

38
Q

Highest and lowest bioavailibility?

A

IV

Lowest - intrathecal

39
Q

What type of nerve is blocked first?

A

B
C
A

40
Q

What is a differential blockade?

A

Lower doses spare motor function, as dosage increases, motor is blocked

41
Q

What state are sodium channels unable to be bound to?

A

Resting

42
Q

What subunit do local’s bind to?

A

Alpha

43
Q

Three parts to local molecule?

A

Benzene ring- lipophilic

Intermediate chain- class, metabolism, allergy

Tertiary amine - hydrophilic

44
Q

How are the two classes of locals metabolized?

A

Esters- pseudocholinesterase
Amide- hepatic

*exception is cocaine - uses both for metabolism