1.0 buccal + sublingual formulations

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22 Terms

1
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BUCC + SL formulations are designed for administering drugs via oral mucosa

targeting systemic absorption without involving the GI tract

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these routes bypass first pass metabolism in the liver

ensuring rapid onset and high bioavailability

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BUCC+SL are particularly effective for drugs requiring swift therapeutic action

or those degraded in the GI tract

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BUCC location

between the cheek + gum

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BUCC absorption

enters the bloodstream directly bypassing the digestive system + liver metabolism

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BUCC speed

relatively rapid as the medication is in close contact with the highly vascularised oral mucosa

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SL location

under than tounge

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SL absorption

enters the bloodstream directly bypassing the digestive system + liver metabolism

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SL speed

relatively rapid due to the rich blood supply and thin mucosa membrane under the tounge

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sublingual tablets

facilitates quick disintegration + drug release for rapid action

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buccal tablets

incorporate high molecular weight hydrophilic polymers + gums that form a gel adhering to the site for sustained release

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SL + BUCC tablets generally offer a faster onset of action compared to oral tablets

because the medication is absorbed directly into the bloodstream via the oral mucosa bypassing GI + first pass

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for many buccal medications like prochlorperazine

onset is typically within 30-60 minutes

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sublingual fentanyl provides pain relief

within 5-10 minutes

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advantages of BUCC + SL

  • rapid onset of action

  • bypass of first pass metabolism

  • non invasive

  • ideal for unstable drugs

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rapid onset of action

particularly critical for drugs like GTN during the angina attack

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non invasive

convenient for self administration

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ideal for unstable drugs

protects drugs that are degraded by stomach acid/GI enzymes

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limitations of BUCC + SL

  • taste + irritation

  • limited dose capacity

  • moisture sensitivity

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taste + irritation

drugs may have unpleasant tastes or cause mucosal irritation reducing patient compliance

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limited dose capacity

suitable for drugs with low dose requirements

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moisture sensitivity

some formulations require protection from moisture to maintain stability