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.

A

To run at

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

A

True

25
Q

What method of absorption is most commonly utilized by drugs at the cellular level?

A

Diffusion through cell membrane — mediated by concentration gradient

26
Q

Describe the solubility of ionized compounds

A

Lower lipid solubility; higher water solubility

Do not easily diffuse across lipid bilayer of membranes

27
Q

Describe solubility of unionized compounds

A

Higher lipid solubility; lower water solubility

Easily diffuse across lipid bilayer

28
Q

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?

A

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
Q

What is the primary difference between carrier-mediated transport and diffusion?

A

Carrier-mediated is an active process that requires ENERGY

30
Q

What method of active transport differs from the rest?

A

Facilitated diffusion - because it does not require energy or proceed against gradients

31
Q

Difference between phase 1 and phase 2 reactions utilized in biotransformation

A

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
Q

Main sites of action of CYP450 enzymes

A

Liver
GI tract
Brain
Kidney

33
Q

Describe first-order kinetics

A

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
Q

Describe zero-order kinetics

A

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
Q

What does “F” represent in pharmacokinetics

A

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
Q

What term is the equivalency factor derived from potency, and represents percentage of a dose that equals the primary serum-assessed drug

A

Salt factor (S)

37
Q

3 items that determine amount of drug absorbed

A

Dose
Bioavailability
Salt factor