Deck 6: Exploring Drug Formulation and Delivery: Membrane Permeability, Tablet Disintegration, and Excipient Selection

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Question
Which part of the membrane is responsible for the relative impermeability of polar molecules in and out of the cell?

A)Polar head
B)Hydrophobic head
C)Hydrophobic core
D)Non polar head
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Question
What helps in the passing of inorganic ions?

A)Ion channels
B)Voltage gated channels
C)Aqueous filled pores
D)Diffusion
Question
The cell membrane is ___________

A)Impermeable
B)Semipermeable
C)Permeable
D)Permeable to only gases
Question
What is the most important characteristic of a drug to be absorbed after oral administration?

A)Dissolved in HCL
B)Dissolved in alkaline solution
C)Can pass through the cell membrane
D)Form aggregate and settle down
Question
Cell membrane can pass easily Oxygen and Carbon dioxide.

A)False
B)True
C)none
D)all
Question
Which one of these is an example of Enteral Route?

A)Skin
B)IV
C)Gastrointestinal
D)Inhalation
Question
Gastrointestinal route is an example of which of the major drug delivery routes?

A)The enteral route
B)The parenteral route
C)The topical route
D)The intravenous route
Question
Which form of drug formulation has disintegration time?

A)Injections
B)Syrups
C)Capsules and Tablets
D)Only tablets
Question
Which tablets have longer Disintegration time?

A)Single coated tablets
B)Uncoated tablets
C)Sugar-coated tablets
D)Capsules
Question
Disintegration time is directly proportional to the amount of binder present in the tablet.

A)True
B)False
C)none
D)all
Question
Which of the following is not a form of excipients?

A)Paracetamol
B)Disintegrants
C)Lubricants
D)Binders
Question
Which of the following is not a limitation granulation?

A)Formation of crystal bridge by the presence of liquid
B)The liquid may act as a medium for affecting chemical reactions such as hydrolysis
C)Increase the cost due to more additional processing
D)The drying step may harm the thermolabile drugs
Question
The agglomerative phase of the communication method grinds the drug in a ball mill for a long time to affect spontaneous agglomeration. But results showed tablets produced are softer.

A)True
B)False
C)none
D)all
Question
Which of these is not a characteristic of tablet formulation by Agglomerative phase of the communication process?

A)Tablets are stronger
B)Usage of more binding agent
C)Rapid dissolution
D)Increase in internal surface area of the granules
Question
What does the graph of Rate of Drug dissolution v/s Compression force with this type of curve interpret?

A)Tight binding of the molecules in drug
B)Deformation of the drug particles into smaller particles
C)The influence of compression force on the dissolution rate is difficult
D)Both tight bonding and deformation of the drug molecules
Question
What does the graph of Rate of Drug dissolution v/s Compression force with this type of curve interpret?

A)Tight binding of the molecules in drug
B)Deformation of the drug particles into smaller particles
C)The influence of compression force on the dissolution rate is difficult
D)Both tight bonding and deformation of the drug molecules
Question
Capsules with bigger particles and intense packing have poor drug release and dissolution rate due to an increase in the pore size.

A)True
B)False
C)none
D)all
Question
Which one of them is not a common form of excipients of drug manufacturing?

A)Diluents
B)Binders
C)Sweeteners
D)Essential oils
Question
Vehicles are the solvent system for the liquefied drug. Which one of them is not an example of a kind of vehicle?

A)Aqueous vehicle
B)Non-aqueous water-miscible vehicles
C)Non-aqueous water immiscible vehicles
D)A salt solution of the drug
Question
Which one of the following will be an example of organic diluents?

A)Starch
B)Dicalcium phosphate
C)Tetracycline
D)Tween 80
Question
What is the function of a granulating agent in drug formulation?

A)Promote cohesive compacts
B)Added if the required dosage is inadequate so that necessary bulk can be produced
C)Tablets can disintegrate easily
D)Used as solubilizer
Question
What is the full form of PVP and what is its function in drug formation?

A)Polyvinyl propylene, diluent
B)Polyvinyl pyrrolidine, solubilizing agent
C)Polyvinyl propylene, buffering agent
D)Polyvinyl pyrrolidine, Binding agent
Question
Which one of the following sentences depicts the function of Disintegrants correctly?

A)These agents help in holding the powders together to form granules
B)These agents overcome the cohesive strength of the tablets and help in dissolution
C)These agents help in the flow of granules and reduce friction between particles
D)Added when the required dosage is inadequate
Question
A large amount of binders tends to increase the hardness of tablets.

A)True
B)False
C)none
D)all
Question
An example of lubricants will be __________

A)PVP
B)Carbowaxes
C)CMC
D)Tetracycline
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Deck 6: Exploring Drug Formulation and Delivery: Membrane Permeability, Tablet Disintegration, and Excipient Selection
1
Which part of the membrane is responsible for the relative impermeability of polar molecules in and out of the cell?

A)Polar head
B)Hydrophobic head
C)Hydrophobic core
D)Non polar head
Hydrophobic core
2
What helps in the passing of inorganic ions?

A)Ion channels
B)Voltage gated channels
C)Aqueous filled pores
D)Diffusion
Aqueous filled pores
3
The cell membrane is ___________

A)Impermeable
B)Semipermeable
C)Permeable
D)Permeable to only gases
Permeable
4
What is the most important characteristic of a drug to be absorbed after oral administration?

A)Dissolved in HCL
B)Dissolved in alkaline solution
C)Can pass through the cell membrane
D)Form aggregate and settle down
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5
Cell membrane can pass easily Oxygen and Carbon dioxide.

A)False
B)True
C)none
D)all
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6
Which one of these is an example of Enteral Route?

A)Skin
B)IV
C)Gastrointestinal
D)Inhalation
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7
Gastrointestinal route is an example of which of the major drug delivery routes?

A)The enteral route
B)The parenteral route
C)The topical route
D)The intravenous route
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8
Which form of drug formulation has disintegration time?

A)Injections
B)Syrups
C)Capsules and Tablets
D)Only tablets
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9
Which tablets have longer Disintegration time?

A)Single coated tablets
B)Uncoated tablets
C)Sugar-coated tablets
D)Capsules
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10
Disintegration time is directly proportional to the amount of binder present in the tablet.

A)True
B)False
C)none
D)all
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11
Which of the following is not a form of excipients?

A)Paracetamol
B)Disintegrants
C)Lubricants
D)Binders
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k this deck
12
Which of the following is not a limitation granulation?

A)Formation of crystal bridge by the presence of liquid
B)The liquid may act as a medium for affecting chemical reactions such as hydrolysis
C)Increase the cost due to more additional processing
D)The drying step may harm the thermolabile drugs
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13
The agglomerative phase of the communication method grinds the drug in a ball mill for a long time to affect spontaneous agglomeration. But results showed tablets produced are softer.

A)True
B)False
C)none
D)all
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k this deck
14
Which of these is not a characteristic of tablet formulation by Agglomerative phase of the communication process?

A)Tablets are stronger
B)Usage of more binding agent
C)Rapid dissolution
D)Increase in internal surface area of the granules
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k this deck
15
What does the graph of Rate of Drug dissolution v/s Compression force with this type of curve interpret?

A)Tight binding of the molecules in drug
B)Deformation of the drug particles into smaller particles
C)The influence of compression force on the dissolution rate is difficult
D)Both tight bonding and deformation of the drug molecules
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Unlock Deck
k this deck
16
What does the graph of Rate of Drug dissolution v/s Compression force with this type of curve interpret?

A)Tight binding of the molecules in drug
B)Deformation of the drug particles into smaller particles
C)The influence of compression force on the dissolution rate is difficult
D)Both tight bonding and deformation of the drug molecules
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Unlock Deck
k this deck
17
Capsules with bigger particles and intense packing have poor drug release and dissolution rate due to an increase in the pore size.

A)True
B)False
C)none
D)all
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Unlock Deck
k this deck
18
Which one of them is not a common form of excipients of drug manufacturing?

A)Diluents
B)Binders
C)Sweeteners
D)Essential oils
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Unlock for access to all 25 flashcards in this deck.
Unlock Deck
k this deck
19
Vehicles are the solvent system for the liquefied drug. Which one of them is not an example of a kind of vehicle?

A)Aqueous vehicle
B)Non-aqueous water-miscible vehicles
C)Non-aqueous water immiscible vehicles
D)A salt solution of the drug
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Unlock Deck
k this deck
20
Which one of the following will be an example of organic diluents?

A)Starch
B)Dicalcium phosphate
C)Tetracycline
D)Tween 80
Unlock Deck
Unlock for access to all 25 flashcards in this deck.
Unlock Deck
k this deck
21
What is the function of a granulating agent in drug formulation?

A)Promote cohesive compacts
B)Added if the required dosage is inadequate so that necessary bulk can be produced
C)Tablets can disintegrate easily
D)Used as solubilizer
Unlock Deck
Unlock for access to all 25 flashcards in this deck.
Unlock Deck
k this deck
22
What is the full form of PVP and what is its function in drug formation?

A)Polyvinyl propylene, diluent
B)Polyvinyl pyrrolidine, solubilizing agent
C)Polyvinyl propylene, buffering agent
D)Polyvinyl pyrrolidine, Binding agent
Unlock Deck
Unlock for access to all 25 flashcards in this deck.
Unlock Deck
k this deck
23
Which one of the following sentences depicts the function of Disintegrants correctly?

A)These agents help in holding the powders together to form granules
B)These agents overcome the cohesive strength of the tablets and help in dissolution
C)These agents help in the flow of granules and reduce friction between particles
D)Added when the required dosage is inadequate
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Unlock Deck
k this deck
24
A large amount of binders tends to increase the hardness of tablets.

A)True
B)False
C)none
D)all
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Unlock Deck
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25
An example of lubricants will be __________

A)PVP
B)Carbowaxes
C)CMC
D)Tetracycline
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Unlock Deck
k this deck
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