Oral solid dosage forms Flashcards

(19 cards)

1
Q

How do effervescent tablets work

A

Acid base reaction to produce carbon dioxide

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2
Q

Advantages of effervescent tablets

A

Mask drug taste, drug in solution prior to ingestion, faster onset of action, easier to swallow

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3
Q

Ingredients of effervescent tablets

A

Active ingredients, buffering agent, soluble organic acid, alkali metal carbonate salt, water soluble binders, water soluble lubricants, artificial and natural sweeteners, flavouring agents, surfactants

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4
Q

How should effervescent tablets be packaged

A

Tightly closed containers, moisture proof, dry air added when sealed, heavy gauge foil to minimise risk of holes

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5
Q

Testing of effervescent tablets

A

Hardness, friability, disintegration, dissolution

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6
Q

What are lozenges

A

Solid preparations designed to dissolve or disintegrate slowly in the mouth, keep drug in contact with oral cavity for extended period

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7
Q

What is the compression of lozenges

A

Compressed harder than normal tablets so they dissolve/disintegrate slowly

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8
Q

What excipients do hard lozenges not usually have

A

Disintegrants and preservatives

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9
Q

Base of soft lozenges

A

Gelatin or PEG

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10
Q

Roles of acacia in soft lozenges

A

Adds texture and smoothness

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11
Q

Roles of silica gel

A

Suspending agent- reduce drug settling during cooling process

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12
Q

What are orodisperisble tablets

A

Uncoated tablets intended to be placed in the mouth where they disperse rapidly before being swallowed

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13
Q

How long should it take orodispersible tablets to disintegrate

A

3 minutes

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14
Q

Advantages of orodispersible tablets

A

No need for water, good for swallowing difficulties, sometimes see improved bioavailability

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15
Q

Limitations of orodispersible tablets

A

Get balance between mechanical strength and rapid disintegration, taste masking problems, high drug loading

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16
Q

Manufacturing techniques for orodispersible tablets

A

Disintegrant addition, freeze drying/lyophilisation, cotton candy process, sublimation, moulding compression

17
Q

Locations for transmucosal drug delivery

A

Oral cavity (mucosal membranes), sublingual (place drug under tongue), buccal (place drug between teeth and cheek)

18
Q

Why is transmucosal drug delivery used

A

Absorption from oral mucosa avoids 1st pass metabolism

19
Q

Limitations/disadvantages of transmucosal drug delivery

A

Short residence time, small absorption area, taste sensing organ, inadequate permeability for some molecules