Adrenaline (epinephrine) microcrystal sublingual tablet formulation: enhanced absorption in a preclinical model. (26th September 2014)

• Record Type: Journal Article
• Authors: Rawas‐Qalaji, Mutasem; Rachid, Ousama; Mendez, Belacryst A.; Losada, Annette; Simons, F. Estelle R.; Simons, Keith J.
• Is Part Of: Journal of pharmacy and pharmacology. Volume 67:Number 1(2015:Jan.)
• Page Start: 20
• Page End: 25
• Publication Date: 2014-09-26
• Subjects: Pharmacy -- Periodicals; Pharmacology -- Periodicals; 615.1
• DOI: 10.1111/jphp.12312
• Languages: English
• ISSNs: 0022-3573

Abstract

<abstract abstract-type="main"> <title>Abstract</title> <sec id="jphp12312-sec-0001" sec-type="section"> <title>Objectives</title> <p>For anaphylaxis treatment in community settings, adrenaline (epinephrine) administration using an auto‐injector in the thigh is universally recommended. Despite this, many people at risk of anaphylaxis in community settings do not carry their prescribed auto‐injectors consistently and hesitate to use them when anaphylaxis occurs.The objective of this research was to study the effect of a substantial reduction in adrenaline (Epi) particle size to a few micrometres (Epi microcrystals (Epi‐MC)) on enhancing adrenaline dissolution and increasing the rate and extent of sublingual absorption from a previously developed rapidly disintegrating sublingual tablet (RDST) formulation in a validated preclinical model.</p> </sec> <sec id="jphp12312-sec-0002" sec-type="section"> <title>Methods</title> <p>The in‐vivo absorption of Epi‐MC 20 mg RDSTs and Epi 40 mg RDSTs was evaluated in rabbits. Epi 0.3 mg intramuscular (IM) injection in the thigh and placebo RDSTs were used as positive and negative controls, respectively.</p> </sec> <sec id="jphp12312-sec-0003" sec-type="section"> <title>Key findings</title> <p>Epi<sub>mean</sub>(standard deviation) area under the plasma concentration vs time curves up to 60 min and C<sub>max</sub> from Epi‐MC 20 mg and Epi 40 mg RDSTs did not differ significantly (<italic>P</italic> > 0.05) from Epi 0.3 mg IM injection. After adrenaline, regardless of route of administration, pharmacokinetic parameters were significantly higher (<italic>P</italic> < 0.05) than after placebo RDSTs administration (reflecting endogenous adrenaline levels).</p> </sec> <sec id="jphp12312-sec-0004" sec-type="section"> <title>Conclusion</title> <p>Epi‐MC RDSTs facilitated a twofold increase in Epi absorption and a 50% reduction in the sublingual dose. This novel sublingual tablet formulation is potentially useful for the first‐aid treatment of anaphylaxis in community settings.</p> </sec> </abstract>