Pharmacokinetics Concepts Flashcards

1
Q

1kg = ? Lbs

A

1 kg = 2.2 lbs

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2
Q

How many mLs in:

1 tsp

1 tbsp

1 oz

A

1 tsp = 5 mL

1 tbsp = 15 mL

1 oz = 30 mL

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3
Q

How many mLs in:

1 qt

1 pint

1 gallon

A

1 qt = 946 mL

1 pint = 473 mL

1 gallon = 3.79 L (4 quarts or 8 pints)

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4
Q

“Qam” dosing

A

Every morning

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5
Q

“Qpm” dosing

A

Every evening

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6
Q

“Qhs” dosing

A

Every night at bedtime

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7
Q

“Ac” dosing

A

Before meals

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8
Q

“Pc” dosing

A

After meals

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9
Q

Administer od

A

Right eye

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10
Q

Administer os

A

Left eye

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11
Q

Administer ou

A

Both eyes

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12
Q

Administer ad

A

R ear

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13
Q

Administer as

A

L ear

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14
Q

Administer au

A

Both ears

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15
Q

“Gtt”

A

Drops

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16
Q

U.d.

A

As directed

17
Q

T.r.a.

18
Q

K.v.o

A

Keep vein open

19
Q

CaCl lactated ringer

A

20mg/100mL

20
Q

KCl lactated ringer

A

30mg/100mL

21
Q

NaCl lactated ringer

A

600mg/100ml

22
Q

sodium lactate - lactated ringer

A

310mg/100mL

23
Q

In terms of drug distribution, what does “alpha” represent?

A

The unbound fraction (%)

Aka the active drug

24
Q

T/F: drugs that have low protein binding are less affected by drug-drug interactions

25
What method of absorption is most commonly utilized by drugs at the cellular level?
Diffusion through cell membrane — mediated by concentration gradient
26
Describe the solubility of ionized compounds
Lower lipid solubility; higher water solubility Do not easily diffuse across lipid bilayer of membranes
27
Describe solubility of unionized compounds
Higher lipid solubility; lower water solubility Easily diffuse across lipid bilayer
28
2 important areas of the body where pH varies and commonly impacts ionization status are GI tract and kidneys. What does this mean for highly ionized drugs in these areas?
Highly ionized drugs do NOT readily get absorbed into GI tract or re-absorbed from renal tubules back into systemic circulation Highly ionized drugs are ELIMINATED
29
What is the primary difference between carrier-mediated transport and diffusion?
Carrier-mediated is an active process that requires ENERGY
30
What method of active transport differs from the rest?
Facilitated diffusion - because it does not require energy or proceed against gradients
31
Difference between phase 1 and phase 2 reactions utilized in biotransformation
Phase 1 = formation of new or modified functional group or cleavage of chemical-groups (e.g., oxidation, reduction, hydrolysis) — typically CYP450 enzymes Phase 2 = involve conjugation (covalent linkages; glucuronidation, sulfation, acetylation) with an endogenous substance (e.g., glucuronic acid, sulfate, glycine,etc.)
32
Main sites of action of CYP450 enzymes
Liver GI tract Brain Kidney
33
Describe first-order kinetics
Rate of elimination is proportional to plasma concentration (Cp) Aka amount of drug removed per unit time will vary proportionately with Cp The percentage of total amount of change in the Cp remains constant over time
34
Describe zero-order kinetics
Rate of elmination is not proportional to Cp — amount of drug removed per unit time stays the same over time The percentage of total amount of change in Cp is NOT constant over time
35
What does “F” represent in pharmacokinetics
Bioavailability represents fraction of a dose that enters circulation — always considered F=1 for IV route Note that it does not describe rate of absorption
36
What term is the equivalency factor derived from potency, and represents percentage of a dose that equals the primary serum-assessed drug
Salt factor (S)
37
3 items that determine amount of drug absorbed
Dose Bioavailability Salt factor