Deck 6: Controlled Drug Delivery
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Deck 6: Controlled Drug Delivery
1
What happens when drugs administered by a conventional dosage form have high rate of absorption and elimination?
A) Drugs are absorbed slowly
B) Drugs have lower Cmax
C) Drugs have longer plasma half life
D) Drugs have shorter duration of action
A) Drugs are absorbed slowly
B) Drugs have lower Cmax
C) Drugs have longer plasma half life
D) Drugs have shorter duration of action
D
2
MTCp is
A) Maximum therapeutic concentration
B) Minimum therapeutic concentration
C) Minimum toxic concentration
D) Maximum toxic concentration
A) Maximum therapeutic concentration
B) Minimum therapeutic concentration
C) Minimum toxic concentration
D) Maximum toxic concentration
C
3
What happens when the rate of drug release equals drug absorption in a controlled drug delivery system?
A) The drug achieves a steady state concentration
B) Results in a flat Cp vs. T profile
C) Maintains constant Cp within in the therapeutic window of the drug
D) All of the above
A) The drug achieves a steady state concentration
B) Results in a flat Cp vs. T profile
C) Maintains constant Cp within in the therapeutic window of the drug
D) All of the above
D
4
What is the primary goal of controlled drug delivery systems?
A) Maintain drug plasma concentration of drugs with narrow therapeutic windows at safe therapeutic levels
B) Reduce dosing frequency
C) Improve patient compliance
D) All of the above
A) Maintain drug plasma concentration of drugs with narrow therapeutic windows at safe therapeutic levels
B) Reduce dosing frequency
C) Improve patient compliance
D) All of the above
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5
What is the rate limiting step for drug absorption in controlled drug delivery systems?
A) Dosage
B) Route of administration
C) Drug release rate
D) Dosing frequency
E) Patient age
A) Dosage
B) Route of administration
C) Drug release rate
D) Dosing frequency
E) Patient age
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6
Which of the following affect drug release rate? More than one answer may be correct.
A) Route of administration
B) Patient weight
C) Polymer degradation
D) Color of dosage form
A) Route of administration
B) Patient weight
C) Polymer degradation
D) Color of dosage form
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7
Drug release rate from a reservoir system depends on: (More than one answer may be correct.)
A) Drug solubility in ethanol
B) Porosity and tortuosity of rate controlling membrane
C) Drug solubility in polymer matrix
D) Osmotic pressure
A) Drug solubility in ethanol
B) Porosity and tortuosity of rate controlling membrane
C) Drug solubility in polymer matrix
D) Osmotic pressure
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8
Which of the following are examples of reservoir system? More than one answer may be correct.
A) Retisert
B) Zoladex
C) Geomatrix
D) Duragesic
A) Retisert
B) Zoladex
C) Geomatrix
D) Duragesic
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9
Which of the following are diffusion controlled drug delivery systems? More than one answer may be correct.
A) Single compartment osmotic pump
B) Monolithic systems
C) Dilacor XR
D) Reservoir systems
E) Mirena
A) Single compartment osmotic pump
B) Monolithic systems
C) Dilacor XR
D) Reservoir systems
E) Mirena
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10
Which of the following is a type of erosion? More than one answer may be correct.
A) Surface erosion
B) Internal erosion
C) Lateral erosion
D) Bulk erosion
A) Surface erosion
B) Internal erosion
C) Lateral erosion
D) Bulk erosion
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11
In erosion controlled systems,the drug is
A) Coated on a polymer matrix
B) Encapsulated in a polymer matrix
C) Released through a rate controlling membrane
D) Dissolved in a polymer
A) Coated on a polymer matrix
B) Encapsulated in a polymer matrix
C) Released through a rate controlling membrane
D) Dissolved in a polymer
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12
During "burst phase"
A) Dosage form bursts
B) Surface bound drug is released
C) Drug is not released
D) None of the above
A) Dosage form bursts
B) Surface bound drug is released
C) Drug is not released
D) None of the above
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13
What is self-healing?
A) Treating oneself without consulting a physician
B) Healing without taking medication
C) Pore closure
D) All of the above
A) Treating oneself without consulting a physician
B) Healing without taking medication
C) Pore closure
D) All of the above
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14
What happens when a swelling controlled system is exposed to aqueous environment?
A) Polymer matrix softens and turns into a gel
B) Swelling propagates outwards radially
C) Polymer chains entangle forming compact matrix
D) The swollen and non-swollen matrices move close to each other
A) Polymer matrix softens and turns into a gel
B) Swelling propagates outwards radially
C) Polymer chains entangle forming compact matrix
D) The swollen and non-swollen matrices move close to each other
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15
The initial drug release in swelling controlled systems follows both fickian and non-fickian kinetics.
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16
Initial drug release from a bulk eroding polymeric matrix depends on
A) Surface pores formed due to water penetration
B) Aqueous solubility of drug encapsulated
C) Size of drug molecules
D) All of the above
A) Surface pores formed due to water penetration
B) Aqueous solubility of drug encapsulated
C) Size of drug molecules
D) All of the above
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17
Viadur is an example for which of the following drug delivery systems?
A) Monolithic release systems
B) Reservoir system
C) Implantable osmotic pump
D) Swellable controlled systems
A) Monolithic release systems
B) Reservoir system
C) Implantable osmotic pump
D) Swellable controlled systems
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18
Briefly explain what happens during the lag phase of release in a bulk eroding system.
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19
Why is surface erosion tough to achieve in erosion controlled systems?
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20
What is the rate-limiting step for drug absorption in controlled drug delivery systems?
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21
What are the major factors that govern the drug release from reservoir systems?
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22
What is an implantable osmotic pump? Briefly explain the release mechanism in 'osmosis controlled systems' with examples.
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23
Explain the mechanism of drug release from monolithic systems.
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24
In surface erosion controlled systems,the rate of erosion remains constant throughout the erosion process.
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25
What is the rate limiting step of drug release from bulk erosion system during initial burst release phase?
A) Drug diffusion through pores
B) Erosion of polymer matrix
C) Polymer chain relaxation
D) Disintegration of eroded matrix
A) Drug diffusion through pores
B) Erosion of polymer matrix
C) Polymer chain relaxation
D) Disintegration of eroded matrix
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26
Fill in the blank: Upon hydration,the polymer chains relax in a swelling controlled drug delivery system because of reduction in the ___ of the polymer.
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27
In a swelling controlled drug delivery system,the swelling begins at the inner layer and radially moves outward as water penetrates the system. (True or False)
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28
Fill in the blank: The moving boundary that separates swollen matrix from nonswollen matrix in a swelling controlled drug delivery system is known as the ____.
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29
Glumetza is a swelling-based gastroretentive formulation of metformin hydrochloride for the treatment of type 2 diabetes. What can be done to maximize the gastric retention and drug bioavailability?
A) Administer tablet on empty stomach
B) Administer tablet with food
C) Administer tablet after meal
A) Administer tablet on empty stomach
B) Administer tablet with food
C) Administer tablet after meal
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30
Fill in the blank: Duros system is an implantable osmotic pump drug delivery system,which contains excess sodium chloride concentration in the engine to maintain osmotic pressure and the subsequent ___ constant.
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31
Fill in the blank: The rate of drug release in an osmotic pump delivery system remains constant as long as there is an ___.
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