Oral Quick Relief Formulations

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These flashcards cover key vocabulary and concepts related to oral quick relief formulations, emphasizing their characteristics, advantages, and formulation considerations.

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50 Terms

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Oral quick relief formulations

Formulations designed for rapid onset of therapeutic action, often used for acute pain relief.

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Rapid onset of action

The speed at which a drug begins to take effect, typically measured in minutes for oral quick relief formulations.

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First-pass effect

The phenomenon where the concentration of a drug is significantly reduced before it reaches systemic circulation, often due to metabolism in the liver.

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Orodispersible formulations

Formulations that dissolve in saliva and can be swallowed easily, facilitating rapid drug absorption.

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Sublingual dosage forms

Dosage forms placed under the tongue for rapid absorption through the mucosal membranes.

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Superdisintegrants

Materials used in tablet formulations to promote rapid disintegration in contact with moisture.

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Effervescent disintegrant

A substance that produces gas in a liquid, helping a solid formulation quickly dissolve.

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Taste masking

The process of concealing or minimizing unpleasant taste in oral formulations to enhance patient compliance.

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Buccal formulations

Formulations designed to be placed in the buccal cavity (the space between the gums and the inner lining of the cheek) for absorption.

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Mucus

A gelatinous layer that lines the oral cavity, important for drug absorption and protecting the mucosal surface.

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What is the primary clinical need for oral quick relief formulations?

Rapid onset of action for acute pain (e.g. breakthrough pain in arthritis , cancer

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Why do conventional oral dosage forms have a slower onset?
Long GI transit time first-pass metabolism and need for swallowing.
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What are the main oral quick relief formulation options?
Sublingual/Buccal Orodispersible and Dispersible formulations.
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List advantages of sublingual/buccal formulations.

Rapid onset no swallowing required, avoids first-pass metabolism, good bioavailability.

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What are key disadvantages of sublingual/buccal formulations?
Unpleasant taste salivary washout interference with eating/drinking.
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What is a dispersible formulation and its key advantage?
Drug dispersed in water before administration; mitigates swallowing issues.
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How do orodispersible formulations work?
Disperse in the mouth and are swallowed; no need for water; rapid onset.
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How is unpleasant taste managed in quick relief formulations?
Use of flavouring agents sweeteners and other taste-masking excipients.
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Why is moisture-proof packaging important?
Many quick relief formulations are moisture sensitive.
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What surface area is available for oromucosal drug absorption?
~100 cm² (about 60% available for absorption).
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Why is fentanyl well suited for sublingual administration?
Lipophilic bypasses first-pass metabolism good mucosal absorption.
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What is the sublingual bioavailability of fentanyl compared to oral?
Sublingual: 50–65%; Oral:
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What excipients are in Abstral® sublingual tablets?
Mannitol silicified MCC croscarmellose sodium magnesium stearate.
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How are Actiq® lozenges administered?
Sucked and moved around the mouth using an applicator.
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What is the role of oral mucus in drug delivery?
Provides lubrication permeability barrier and supports mucoadhesion.
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Name common effervescent disintegrants.
Carbonate salt bicarbonate salt citric acid.
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What is the Tmax of co-codamol effervescent tablets vs. IR tablets?
20 min vs. ~50 min.
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How quickly should orodispersible tablets disintegrate?
30 seconds – 3 minutes.
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List common superdisintegrants used in oral quick relief formulations.
Crospovidone silicified MCC sodium croscarmellose sodium starch glycolate.
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What is lyophilisation and why is it used?
Freeze-drying to create porous structures for rapid dissolution.
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What is the primary clinical need for oral quick relief formulations?
Rapid onset of action for acute pain (e.g. breakthrough pain in arthritis
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Why do conventional oral dosage forms have a slower onset?
Long GI transit time first-pass metabolism and need for swallowing.
33
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What are the main oral quick relief formulation options?
Sublingual/Buccal Orodispersible and Dispersible formulations.
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List advantages of sublingual/buccal formulations.
Rapid onset
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What are key disadvantages of sublingual/buccal formulations?
Unpleasant taste salivary washout interference with eating/drinking.
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What is a dispersible formulation and its key advantage?
Drug dispersed in water before administration; mitigates swallowing issues.
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How do orodispersible formulations work?
Disperse in the mouth and are swallowed; no need for water; rapid onset.
38
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How is unpleasant taste managed in quick relief formulations?
Use of flavouring agents sweeteners and other taste-masking excipients.
39
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Why is moisture-proof packaging important?
Many quick relief formulations are moisture sensitive.
40
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What surface area is available for oromucosal drug absorption?
~100 cm² (about 60% available for absorption).
41
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Why is fentanyl well suited for sublingual administration?
Lipophilic bypasses first-pass metabolism good mucosal absorption.
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What is the sublingual bioavailability of fentanyl compared to oral?
Sublingual: 50–65%; Oral:
43
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What excipients are in Abstral® sublingual tablets?
Mannitol silicified MCC croscarmellose sodium magnesium stearate.
44
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How are Actiq® lozenges administered?
Sucked and moved around the mouth using an applicator.
45
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What is the role of oral mucus in drug delivery?
Provides lubrication permeability barrier and supports mucoadhesion.
46
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Name common effervescent disintegrants.
Carbonate salt bicarbonate salt citric acid.
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What is the Tmax of co-codamol effervescent tablets vs. IR tablets?
20 min vs. ~50 min.
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How quickly should orodispersible tablets disintegrate?
30 seconds – 3 minutes.
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List common superdisintegrants used in oral quick relief formulations.
Crospovidone silicified MCC sodium croscarmellose sodium starch glycolate.
50
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What is lyophilisation and why is it used?
Freeze-drying to create porous structures for rapid dissolution.