Deck 10: Pharmacokinetics and Drug Binding: Understanding Drug Distribution and Transport Across Membranes
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Deck 10: Pharmacokinetics and Drug Binding: Understanding Drug Distribution and Transport Across Membranes
1
……………is located at the sertoli-sertoli cell junction.
A)Blood testis barrier
B)Blood CSF barrier
C)Blood cellular barrier
D)All of the above
A)Blood testis barrier
B)Blood CSF barrier
C)Blood cellular barrier
D)All of the above
Blood testis barrier
2
The Binding Order of drug to tissue is…………………
A)Kidney > Liver > Lungs > Muscle
B)Muscle > Kidney > Lungs > Liver
C)Liver > Kidney > Lungs > Muscle
D)Liver > Lungs > Kidney > Muscle
A)Kidney > Liver > Lungs > Muscle
B)Muscle > Kidney > Lungs > Liver
C)Liver > Kidney > Lungs > Muscle
D)Liver > Lungs > Kidney > Muscle
Liver > Kidney > Lungs > Muscle
3
…………………in lipophilicity increases the extend of binding.
A)Increase
B)Decrease
C)Constant
D)None of the above
A)Increase
B)Decrease
C)Constant
D)None of the above
Increase
4
Protein binding of drugs helps to maintain ……………for absorption of drugs.
A)non sink condition
B)sink condition
C)pKa
D)none of the above
A)non sink condition
B)sink condition
C)pKa
D)none of the above
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5
The loading dose of a drug is based upon the
A)time taken for complete elimination
B)percentage of drug excreted unchanged in urine
C)percentage of drug bound to plasma protein
D)apparent volume of distribution and the desired drug concentration in plasma
A)time taken for complete elimination
B)percentage of drug excreted unchanged in urine
C)percentage of drug bound to plasma protein
D)apparent volume of distribution and the desired drug concentration in plasma
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6
The volume of distribution of drugs is:
A)An expression of total body volume
B)A measure of total fluid volume
C)A relationship between the total amount of drug in the body and the concentration of the drug in the blood
D)Proportional to bioavailability of the drug
A)An expression of total body volume
B)A measure of total fluid volume
C)A relationship between the total amount of drug in the body and the concentration of the drug in the blood
D)Proportional to bioavailability of the drug
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7
The volume of distribution (Vd) relates:
A)Single to a daily dose of an administered drug
B)An administered dose to a body weight
C)An unchanged drug reaching the systemic circulation
D)The amount of a drug in the body to the concentration of a drug in plasma
A)Single to a daily dose of an administered drug
B)An administered dose to a body weight
C)An unchanged drug reaching the systemic circulation
D)The amount of a drug in the body to the concentration of a drug in plasma
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8
Movement of drug across the membrane is called as
A)Symport
B)Antiport
C)Drug transport
D)Absorption
A)Symport
B)Antiport
C)Drug transport
D)Absorption
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9
Which of the following is known as Tamoxifen binding site?
A)Site I
B)Site II
C)Site III
D)Site IV
A)Site I
B)Site II
C)Site III
D)Site IV
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10
Which of the following drug selectively bound to extravascular tissues?
A)Warfarin
B)Diazepam
C)Digitoxin
D)Chloroquin
A)Warfarin
B)Diazepam
C)Digitoxin
D)Chloroquin
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11
Plasma Protein binding …………..the volume of distribution of drugs.
A)increases
B)decreases
C)no change
D)none of the above
A)increases
B)decreases
C)no change
D)none of the above
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12
Following intravenous administration, drugs are distributed fastest to:
A)the skin, kidney, and brain
B)the liver, kidney, and brain
C)the liver, adipose, and brain
D)the liver, kidney, and adipose
A)the skin, kidney, and brain
B)the liver, kidney, and brain
C)the liver, adipose, and brain
D)the liver, kidney, and adipose
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13
…………is the tight junction between sertoli cells.
A)BBB
B)placental barrier
C)blood-testis barrier
D)endothelial barrier
A)BBB
B)placental barrier
C)blood-testis barrier
D)endothelial barrier
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14
Distribution is……………..
A)irreversible process
B)dynamic equilibrium process
C)Both (a) & (b)
D)none of the above
A)irreversible process
B)dynamic equilibrium process
C)Both (a) & (b)
D)none of the above
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15
A drug reverses plasma-protein binding is often referred as……..
A)displacer
B)solvate
C)carrier substance
D)protein hydrolysate
A)displacer
B)solvate
C)carrier substance
D)protein hydrolysate
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16
Primary binding site for albumin is ………………binding site.
A)Warfarin
B)Diazepam
C)Digitoxin
D)Tamoxifen
A)Warfarin
B)Diazepam
C)Digitoxin
D)Tamoxifen
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17
Which of the following strategies are widely used to improve or promote transport of drug to brain?
A)Glycosylation
B)Use of Mannitol
C)Prodrug approach
D)All of the above
A)Glycosylation
B)Use of Mannitol
C)Prodrug approach
D)All of the above
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18
Acidic drug have
A)Low Vd
B)high Vd
C)No Vd
D)none of the above
A)Low Vd
B)high Vd
C)No Vd
D)none of the above
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19
Low molecular weight of drugs have
A)Low Vd
B)high Vd
C)No Vd
D)none of the above
A)Low Vd
B)high Vd
C)No Vd
D)none of the above
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20
Water soluble drugs have
A)Low Vd
B)high Vd
C)No Vd
D)none of the above
A)Low Vd
B)high Vd
C)No Vd
D)none of the above
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21
Lipid soluble drugs have
A)Low Vd
B)high Vd
C)No Vd
D)none of the above
A)Low Vd
B)high Vd
C)No Vd
D)none of the above
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22
Protein binding ……………the distribution of drugs.
A)Decreases
B)Increases
C)No Change
D)none of the above
A)Decreases
B)Increases
C)No Change
D)none of the above
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23
Which one of the following physicochemical property is more important for passive diffusion of drugs from the GIT?
A)Partition coefficient
B)Lipid solubility
C)pH of GIT fluids
D)dissolution constant
A)Partition coefficient
B)Lipid solubility
C)pH of GIT fluids
D)dissolution constant
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24
Drug permeation through BBB can be improved by………..
A)Glycosylation
B)Mannitol
C)Dihydropyridine redox system
D)all of the above
A)Glycosylation
B)Mannitol
C)Dihydropyridine redox system
D)all of the above
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25
Which of the following drug diffuses readily into the brain?
A)Penicillin
B)Thiopental
C)Dopamine
D)all of the above
A)Penicillin
B)Thiopental
C)Dopamine
D)all of the above
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