Deck 9: Pharmacokinetics and Drug Distribution: Understanding Absorption and Transport in the Body

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Question
Which of the following drug is not intended for pulmonary administration?

A)Bronchodilators
B)Antiallergics
C)NSAIDs
D)Anti-inflammatory steroids
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Question
A drug in the concentrated injection is absorbed faster.

A)True
B)False
C)none
D)all
Question
Intramuscular drug absorption is faster than intravascular.

A)True
B)False
C)none
D)all
Question
Several factors such as the thickness of stratum corneum, presence of hair follicles, trauma, hydration of the skin, Grooming, exposure to chemicals determine the passive absorption of drugs from the surface of the skin to below.

A)True
B)False
C)none
D)all
Question
Which process involve alteration of drug distribution

A)Competitive binding
B)Reduced plasma protein level
C)Both
D)None
Question
If drug have very small volume of distribution it is likely that the drug

A)Has short biological half life
B)Does not accumulate in various tissue and organ
C)Not bioavailable
D)will not be effective
Question
If distribution of drug is slower than process of biotransformation and elimination

A)It will cause high blood level of drug
B)It will cause low blood level of drug
C)Cause failure to attain diffusion equilibrium
D)None of the above
Question
If the drug Y bind with plasma albumin with 10 times more affinity than drug X. Which the given statement is true?

A)Apparent volume of distribution of drug X decrease
B)Free concentration of drug X in blood will be increase
C)Apparent volume of distribution of drug Y decrease
D)Toxicity of drug Y increase
Question
The distribution of drugs into the central nervous system (brain) usually depends on:

A)Aqueous diffusion
B)Lipid diffusion
C)Active transport
D)Facilitated tr
Question
Which of the following is most likely to be associated with a high apparent volume of distribution

A)High hepatic extraction ratio
B)Penetration across the blood:brain and blood:testes barriers
C)Extensive binding to plasma protein
D)Extensive binding to tissue constituents
Question
The Initial distribution of drug into the tissue is determined chiefly by

A)Rate of blood flow to tissue
B)Plasma protein binding of drug
C)Affinity for tissue
D)Gastric emptying time
Question
Transfer of drug from plasma to tissue depends on

A)Weight of tissue
B)Blood perfusion rate of tissue
C)Size of tissue
D)All of the above
Question
A hydrophilic medicinal agent has

A)Low ability to penetrate through the cell membrane lipids
B)Easy permeation through the blood-brain barrier
C)Penetrate through membranes by means of endocytosis
D)High reabsorption in renal tubules
Question
Biological barriers include all except:

A)Renal tubules
B)Cell membranes
C)Capillary walls
D)Placenta
Question
Blood Brain Barrier is maximum permeable to

A)Na+
B)C02
C)Cl
D)K+
Question
If a CNS drug is extensively ionized at pH of blood it will

A)Penetrate the blood brain barrier slowly
B)Penetrate the blood brain barrier rapidly
C)Not penetrate blood brain barrier
D)Be eliminated slowly
Question
The rate of drug transport across a cell membrane by lipid diffusion depends on all of the following except

A)Drug size (diffusion constant)
B)Surface area of absorption
C)Lipid partition coefficient
D)Density of tr
Question
The formula to calculate half life (t1/2) is

A)0.693 *Vd / C1
B)0.693 *Cl / Vd
C)0.693 / Cl * Vd
D)0.693 / Cl
Question
The procedure of transporting a drug from the bloodstream to tissues is called as

A)Absorption
B)Dissolution
C)Distribution
D)Elimination
Question
…………..it represents the degree to which a drug is distributed in body tissue rather than

A)Volume of distribution (YD)
B)Effect of distribution
C)Area of distribution
D)None of the above
Question
It is defined as the distribution of a drug between plasma and the rest of the body after oral or parenteral dosing.

A)Volume of distribution (VD)
B)Apparent volume of drug distribution
C)Phagocytosis
D)None of the above
Question
The drugs having molecular size …………..easily cross capillary membrane.

A)<500-600d
B)< 100-200 d
C)<300-600d
D)<90M600d
Question
The concentration of drug in blood or plasma will be comparatively in the GI tract.

A)High
B)Low
C)Very High
D)Very Low
Question
Fat is act as reservoir for……………………… Drugs

A)Highly water soluble
B)Lower lipid soluble
C)Highly lipid soluble.
D)Lower lipid soluble.
Question
Displacement is significant when, the displaced drug is more than protein bound.

A)50%
B)95%
C)10%
D)1%
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Deck 9: Pharmacokinetics and Drug Distribution: Understanding Absorption and Transport in the Body
1
Which of the following drug is not intended for pulmonary administration?

A)Bronchodilators
B)Antiallergics
C)NSAIDs
D)Anti-inflammatory steroids
NSAIDs
2
A drug in the concentrated injection is absorbed faster.

A)True
B)False
C)none
D)all
True
3
Intramuscular drug absorption is faster than intravascular.

A)True
B)False
C)none
D)all
False
4
Several factors such as the thickness of stratum corneum, presence of hair follicles, trauma, hydration of the skin, Grooming, exposure to chemicals determine the passive absorption of drugs from the surface of the skin to below.

A)True
B)False
C)none
D)all
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k this deck
5
Which process involve alteration of drug distribution

A)Competitive binding
B)Reduced plasma protein level
C)Both
D)None
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Unlock Deck
k this deck
6
If drug have very small volume of distribution it is likely that the drug

A)Has short biological half life
B)Does not accumulate in various tissue and organ
C)Not bioavailable
D)will not be effective
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k this deck
7
If distribution of drug is slower than process of biotransformation and elimination

A)It will cause high blood level of drug
B)It will cause low blood level of drug
C)Cause failure to attain diffusion equilibrium
D)None of the above
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k this deck
8
If the drug Y bind with plasma albumin with 10 times more affinity than drug X. Which the given statement is true?

A)Apparent volume of distribution of drug X decrease
B)Free concentration of drug X in blood will be increase
C)Apparent volume of distribution of drug Y decrease
D)Toxicity of drug Y increase
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9
The distribution of drugs into the central nervous system (brain) usually depends on:

A)Aqueous diffusion
B)Lipid diffusion
C)Active transport
D)Facilitated tr
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k this deck
10
Which of the following is most likely to be associated with a high apparent volume of distribution

A)High hepatic extraction ratio
B)Penetration across the blood:brain and blood:testes barriers
C)Extensive binding to plasma protein
D)Extensive binding to tissue constituents
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Unlock Deck
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11
The Initial distribution of drug into the tissue is determined chiefly by

A)Rate of blood flow to tissue
B)Plasma protein binding of drug
C)Affinity for tissue
D)Gastric emptying time
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k this deck
12
Transfer of drug from plasma to tissue depends on

A)Weight of tissue
B)Blood perfusion rate of tissue
C)Size of tissue
D)All of the above
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k this deck
13
A hydrophilic medicinal agent has

A)Low ability to penetrate through the cell membrane lipids
B)Easy permeation through the blood-brain barrier
C)Penetrate through membranes by means of endocytosis
D)High reabsorption in renal tubules
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k this deck
14
Biological barriers include all except:

A)Renal tubules
B)Cell membranes
C)Capillary walls
D)Placenta
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Unlock Deck
k this deck
15
Blood Brain Barrier is maximum permeable to

A)Na+
B)C02
C)Cl
D)K+
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k this deck
16
If a CNS drug is extensively ionized at pH of blood it will

A)Penetrate the blood brain barrier slowly
B)Penetrate the blood brain barrier rapidly
C)Not penetrate blood brain barrier
D)Be eliminated slowly
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Unlock Deck
k this deck
17
The rate of drug transport across a cell membrane by lipid diffusion depends on all of the following except

A)Drug size (diffusion constant)
B)Surface area of absorption
C)Lipid partition coefficient
D)Density of tr
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Unlock for access to all 25 flashcards in this deck.
Unlock Deck
k this deck
18
The formula to calculate half life (t1/2) is

A)0.693 *Vd / C1
B)0.693 *Cl / Vd
C)0.693 / Cl * Vd
D)0.693 / Cl
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Unlock Deck
k this deck
19
The procedure of transporting a drug from the bloodstream to tissues is called as

A)Absorption
B)Dissolution
C)Distribution
D)Elimination
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Unlock Deck
k this deck
20
…………..it represents the degree to which a drug is distributed in body tissue rather than

A)Volume of distribution (YD)
B)Effect of distribution
C)Area of distribution
D)None of the above
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Unlock for access to all 25 flashcards in this deck.
Unlock Deck
k this deck
21
It is defined as the distribution of a drug between plasma and the rest of the body after oral or parenteral dosing.

A)Volume of distribution (VD)
B)Apparent volume of drug distribution
C)Phagocytosis
D)None of the above
Unlock Deck
Unlock for access to all 25 flashcards in this deck.
Unlock Deck
k this deck
22
The drugs having molecular size …………..easily cross capillary membrane.

A)<500-600d
B)< 100-200 d
C)<300-600d
D)<90M600d
Unlock Deck
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Unlock Deck
k this deck
23
The concentration of drug in blood or plasma will be comparatively in the GI tract.

A)High
B)Low
C)Very High
D)Very Low
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Unlock Deck
k this deck
24
Fat is act as reservoir for……………………… Drugs

A)Highly water soluble
B)Lower lipid soluble
C)Highly lipid soluble.
D)Lower lipid soluble.
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Unlock Deck
k this deck
25
Displacement is significant when, the displaced drug is more than protein bound.

A)50%
B)95%
C)10%
D)1%
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k this deck
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Unlock for access to all 25 flashcards in this deck.