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dc.contributor.authorMcDonald, Rebecca
dc.contributor.authorDanielsson Glende, Øyvind
dc.contributor.authorDale, Ola
dc.contributor.authorStrang, John
dc.date.accessioned2017-06-14T11:05:14Z
dc.date.available2017-06-14T11:05:14Z
dc.date.created2017-06-13T09:07:58Z
dc.date.issued2017
dc.identifier.issn0959-5236
dc.identifier.urihttp://hdl.handle.net/11250/2446018
dc.description.abstractIssues. Non-injectable naloxone formulations are being developed for opioid overdose reversal, but only limited data have been published in the peer-reviewed domain. Through examination of a hitherto-unsearched database, we expand public knowledge of non-injectable formulations, tracing their development and novelty, with the aim to describe and compare their pharmacokinetic properties. Approach. (i) The PatentScope database of the World Intellectual Property Organization was searched for relevant English-language patent applications; (ii) Pharmacokinetic data were extracted, collated and analysed; (iii) PubMed was searched using Boolean search query ‘(nasal OR intranasal OR nose OR buccal OR sublingual) AND naloxone AND pharmacokinetics’. Key Findings. Five hundred and twenty-two PatentScope and 56 PubMed records were identified: three published international patent applications and five peer-reviewed papers were eligible. Pharmacokinetic data were available for intranasal, sublingual, and reference routes. Highly concentrated formulations (10–40 mg mL−1) had been developed and tested. Sublingual bioavailability was very low (1%; relative to intravenous). Non-concentrated intranasal spray (1 mg mL−1; 1 mL per nostril) had low bioavailability (11%). Concentrated intranasal formulations (≥10 mg mL−1) had bioavailability of 21–42% (relative to intravenous) and 26–57% (relative to intramuscular), with peak concentrations (dose-adjusted Cmax = 0.8–1.7 ng mL−1) reached in 19–30 min (tmax). Implications. Exploratory analysis identified intranasal bioavailability as associated positively with dose and negatively with volume. Conclusion. We find consistent direction of development of intranasal sprays to high-concentration, low-volume formulations with bioavailability in the 20–60% range. These have potential to deliver a therapeutic dose in 0.1 mL volume. [McDonald R, Danielsson Glende Ø, Dale O, Strang J. International patent applications for non-injectable naloxone for opioid overdose reversal: Exploratory search and retrieve analysis of the PatentScope database.nb_NO
dc.language.isoengnb_NO
dc.publisherWileynb_NO
dc.titleInternational patent applications for non-injectable naloxone for opioid overdose reversal: Exploratory search and retrieve analysis of the Patent Scope databasenb_NO
dc.typeJournal articlenb_NO
dc.typePeer reviewednb_NO
dc.description.versionacceptedVersionnb_NO
dc.source.journalDrug and Alcohol Reviewnb_NO
dc.identifier.doi10.1111/dar.12571
dc.identifier.cristin1475560
dc.description.localcodeThis is the peer reviewed version of the following article: International patent applications for non-injectable naloxone for opioid overdose reversal: Exploratory search and retrieve analysis of the PatentScope database, which has been published in final form at http://onlinelibrary.wiley.com/doi/10.1111/dar.12571/abstract . This article may be used for non-commercial purposes in accordance with Wiley Terms and Conditions for Self-Archiving. Locked until 08 June 2018 due to copyright restrictionsnb_NO
cristin.unitcode194,65,25,0
cristin.unitnameInstitutt for sirkulasjon og bildediagnostikk
cristin.ispublishedtrue
cristin.fulltextpostprint
cristin.qualitycode1


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