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Volume of Distribution and Drug Binding

Total questions: 13

Worksheet time: 15mins

Name
Class
Date
1.

A drug with a strong protein binding is likely to?

a)
  1. Be widely distributed

b)
  1. Remain in the plasma compartment

c)
  1. Cross cell membranes easily

d)
  1. Low Vd

2.

Volume of Distribution is used for calculating the (a)   dose of a drug.

3.

What is the major drug-binding protein

a)

Albumin

b)

RBC

c)

Alpha acid Glycoprotein

d)

Albuterol

4.

Which of the following is true about protein-bound drugs?

a)
  1. They are easily excreted

b)
  1. They are pharmacologically active

c)
  1. They cannot cross cell membranes

d)
  1. They have high clearance rates

5.

Volume of distribution is calculated using the

formula:

Vd = (a)   / Plasma Concentration

6.

As VD increases, the dose (Q) of drug required to achieve a particular plasma concentration (Cp) ?

a)

Decreases

b)

Increases

c)

Does not change

d)

NOTA

7.

What type of drug is pharmacologically active and able to cross the cell membrane?

a)

Bound drug

b)

Free drug

c)

Protein-bound drug

8.

The (a)   dose administered after the loading dose that is used to maintain the steady state

9.

A patient receives 800 mg of Drug X, and the plasma concentration after equilibrium is 40 mg/L. What is the volume of distribution (Vd)?

(a)  

10.

If the Vd of Drug Y is 25 L and the desired plasma concentration is 10 mg/L, what dose should be administered?

(a)  

11.

A drug has a Vd of 60 L and a dose of 1200 mg. What is the resulting plasma concentration?

(a)  

12.

Calculate the loading dose for a drug with:

Vd = 45 L

Target concentration = 6 mg/L

Bioavailability = 0.75

(a)  

13.

Determine the maintenance dose for a drug with:

Clearance = 5 L/hr

• Target concentration = 8 mg/L

• Dosing interval = 12 hours

• Bioavailability = 0.8

(a)