Week 4 Flashcards

1
Q

A suspension is defined as a [Select all that apply]
solid dispersed in an immiscible liquid
liquid dispersed in an immiscible liquid
solid dispersed in a gas or volatile propellant
liquid dispersed in a gas or volatile propellant

A

solid dispersed in an immiscible liquid

solid dispersed in a gas or volatile propellant

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2
Q

Suspensions can be characterized based on______________. [Select all that apply]
their dispersion medium
the size of the dispersed particles
the viscosity of the external phase
the route of administration
the electrokinetic nature of the dispersed particles

A

their dispersion medium
the size of the dispersed particles
the route of administration
the electrokinetic nature of the dispersed particles

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3
Q

The zeta potential is optimized in a ______ suspension

A

flocculated

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4
Q

Colloidal suspensions have dispersed phase sizes that are?

A

less than 1 um

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5
Q

The dominant force in flocculated suspensions is _____ due to the _____ size of the flocs

A

gravity; larger

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6
Q

T/F Ready to use suspensions have drugs with low chemical stability.

A

false

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7
Q

T/F Suspensions can mask the bitter taste of drugs better than solutions.

A

true

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8
Q

A lipophilic drug delivered in a suspension requires ________ external phase of the formulation

A

aqueous-based

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9
Q
Which excipient in a suspension dosage form will promote the formation of flocs?
Preservative 
Wetting agent 
Particulate hydrocolloid 
Thickening agent
A

Particulate hydrocolloid

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10
Q

The purpose of a wetting agent in a suspension is to?

A

reduce interfacial tension

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11
Q

Which type of electrokinetic suspension will form a loose fluffy sediment that will re-disperse easily? [Select all that apply]
Deflocculated suspension
Flocculated suspension
Flocculated suspension in a structured vehicle
Deflocculated suspension in a structured vehicle

A

Flocculated suspension

Flocculated suspension in a structured vehicle

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12
Q

The incorporation of a structured vehicle in a suspension enhances its stability by?

A

reducing the rate of settling

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13
Q
Irreversible physical stability issues with suspensions include\_\_\_\_\_\_\_\_\_\_\_. [Select all that apply]
flocculation 
caking 
crystallization 
coalescence
A

caking and crystallization

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14
Q

T/F Suspensions are prone to chemical instabilities and cannot be used with chemically unstable drugs

A

false

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15
Q

T/F Coarse suspensions can be administered parenterally by the IV route

A

false

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16
Q
Drug S is available as an aqueous suspension. Drug S has a MW of 512 Da and a log Ko/w of 1.  What will be the rate-limiting step for Drug S in this dosage form?
Diffusion coefficient 
Partition coefficient 
Dissolution rate 
Permeability constant
A

Dissolution rate

17
Q

A semisolid is defined as a:
solid dispersed in an immiscible liquid.
liquid dispersed in an immiscible liquid.
solid dissolved in a miscible liquid.
neither a solid nor a liquid dosage form.

A

neither a solid nor a liquid dosage form.

18
Q

Semisolid inserts for rectal, vaginal or urethal drug delivery are called?

A

suppositories

19
Q
Ointment bases include\_\_\_\_\_\_\_\_\_\_\_\_\_. [Select all that apply] 
hydrocarbon 
water-removable 
gels 
pastes
A

hydrocarbon

water-removable

20
Q
Semisolid bases that can be used to incorporate drugs that hydrolyze are \_\_\_\_\_\_. [Select all that apply]
gels 
water-soluble 
absorption 
water-removable 
hydrocarbon
A

absorption

hydrocarbon

21
Q
Which of the following bases can pull water and irritate the mucosa.?
Hydrocarbon 
Water-soluble 
Gel 
Pastes
A

Water-soluble

22
Q
Semisolid base(s) that are occlusive include. [Select all that apply]
hydrocarbon 
anhydrous 
water-removable 
water-soluble 
gel
A

hydrocarbon

anhydrous

23
Q
Which semisolid dosage forms can only be used for the oral cavity? 
lozenges 
creams 
lotions 
ointments
24
Q

T/F Ideal drug candidates for semisolid preparation are large, hydrophilic molecules.

25
``` What type of a base would you recommend for a patient with dry skin? Hydrocarbon Water-removable Gel Paste ```
Hydrocarbon
26
``` What type of an excipient would you incorporate in a semisolid formulation for a patient with serous discharge or secretion? Preservative Humectant Astringent Emollient ```
Astringent
27
``` What type of a base would you recommend for the fast release of a hydrophilic drug? Hydrocarbon Water-removable Gel Paste ```
Hydrocarbon
28
What type of formulation would you recommend for chronic use to minimize the number of times an ointment needs to be applied? Drug suspended in the base. Drug dissolved in the base. Either drug suspended or dissolved. in the base
Drug suspended in the base.
29
``` The purpose of a levigating agent in a semisolid is to_________________ reduce interfacial tension increase viscosity optimize the zeta potential reduce the particle size ```
reduce the particle size
30
``` Which type of semisolid preparation will experience bleeding issues? [Select all that apply] Ointments with hydrocarbon bases Ointments with absorption bases Ointments with water-removable bases Ointments with water-washable bases Semisolids with gel bases ```
Ointments with absorption bases | Ointments with water-removable bases
31
``` Drying of the semisolid preparation will most likely be seen in which of the following semisolids bases? [Select all that apply] Hydrocarbon base. Gel base. Absorption base. Water-slouble base. ```
Gel base.
32
T/F Semisolid preparations applied to various regions in the body are intended for local effect.
false
33
``` Drug T has a MW of 290 Da, log Ko/w of 2.5. It is available as Drug T suspension in a hydrocarbon base, and Drug T dissolved in a gel base. What will be the rate-limiting step for Drug T in the hydrocarbon base? Diffusion coefficient. Partition coefficient. Dissolution rate. Permeability constant. ```
Partition coefficient.