Pharm exam I misc q's Flashcards

0
Q

Phase I metabolism involves primarily what chemical reactions?

A

Oxidation, reduction, and hydrolysis

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1
Q

The driving forces for diffusional distribution into a tissue are what?

A

relative solubility, conc gradient, rate of blood flow

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2
Q

Enzyme CP-450 requires what to become active?

A

an electron donor (from NAD-coenzymes formed from naicin)and molecular O2

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3
Q

Under low conditions of Partial Pressure O2, enzyme CP-450 does what?

A

transfers electron to a substrate rather than to oxygen (insufficient amount of O2 to compete for electrons) This can lead to certain toxic build up.

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4
Q

Drugs that rely on the Oxidation pathway can lead to what?

A

Toxicity

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5
Q

What is conjugation?

A

another metabolism method that uses CP-450 to render substance inactive and water soluble therefore available for elimination.

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6
Q

If decreased enzyme activity interferes with conjugation what can happen?

A

the drug is prone to toxicity (risk of hyperbilirubinemia in neonates)

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7
Q

Does Hydrolysis use microsomal enzymes CP-450 for metabolism?

A

No

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8
Q

What is the Phase II metabolic pathway?

A

Conjugation

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9
Q

Where does hydrolysis often work to metabolize drugs?

A

often at ester bonds

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10
Q

Does enzyme induction affect non-microsomal metabolism?

A

No its activity is genetically determined.

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11
Q

How is volume of distribution proportional to protein binding?

A

inversely

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12
Q

What is pKa?

A

the pH at which a drug is 50% ionized and 50% unionized

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13
Q

A drug is a weak acid if it forms a salt with what?

A

a positive ion ie. Na+, K+, Ca+, Mg+

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14
Q

A drug is a weak base if it forms a salt with what?

A

A negative ion ie. Cl-, SO4-,

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15
Q

Small changes in pH does what in ionization?

A

cause large changes in ionization (example if you take an acid that is 50% ionized and add 2 pH points more basic it becomes 90% ionized)

16
Q

Are local anesthetics weak acids or weak bases?

A

Weak bases

17
Q

If a drugs pKa is close to bloods pH will it work faster or slower?

A

faster ex drug with pka= 7.9 and blood pH= 7.45 will work faster than drug with pKa=8.16 in blood with pH=7.45

18
Q

What is important to note about circumventricular organs?:

A

areas where the BBB is weak (ex area postrema= vomit center)

19
Q

Are NMBD lipid soluble?

A

No they are poorly lipid soluble and remain in blood longer but take their action after leaving central compartment.

20
Q

What determines rate of metabolism?

A
  1. concentration of drug at site of metabolism (hepatic blood flow)
  2. Intrinsic rate of the metabolic process
21
Q

First order kinetics are what?

A

metabolic enzymes not saturated and amount of drug metabolized is proportional to drug concentration

22
Q

What is zero order kinetics?

A

metabolic enzymes are saturated and can only metabolize constant amount of drugs per unit of time.

23
Q

What is MAC?

A

(Minimum aveolar concentration) the inspired concentration at 1 atm that prevents skeletal muscle movement in response to painful stimuli in 50% of patients

24
Q

When inspired gas concentration = expired gas concentration what is this called?

A

equilibrium and anesthesia can be anticipated (O&J pg. 164)

25
Q

Uptake of an inhaled gas is the product of what 3 things?

A

Uptake= Cardiac Output x concentration gradient (alveolar to venous partial pressure difference) x blood-to-gas solubility.
* If any of these = 0 as in cardiac arrest, no concentration gradient, or agent is insoluble in blood than uptake is impossible