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International patent applications for non‐injectable naloxone for opioid overdose reversal: Exploratory search and retrieve analysis of the PatentScope database

机译:用于阿片类药物过量的非注射纳洛酮的国际专利申请过量逆转:PatentScope数据库的探索性搜索和检索分析

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Abstract Issues. 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 C max ?=?0.8–1.7?ng?mL ?1 ) reached in 19–30?min (t max ). 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 ?, Dale O, Strang J. International patent applications for non‐injectable naloxone for opioid overdose reversal: Exploratory search and retrieve analysis of the PatentScope database. Drug Alcohol Rev 2017;00:000‐000]
机译:抽象问题。正在为阿片类药物过量逆转开发未注射的纳洛酮制剂,但在同行评审域中只公布了有限的数据。通过审查迄今为止的数据库,我们扩大了公众对非可注射配方的知识,追踪其发展和新颖性,目的是描述和比较其药代动力学性质。方法。 (i)搜查了世界知识产权组织的Patentscope数据库,以获取相关的英语专利申请; (ii)提取,整理和分析药代动力学数据; (iii)使用布尔搜索查询'(鼻腔或鼻腔或鼻子或舌下或舌下)和纳洛酮和药代动力学进行搜查。主要发现。确定了五百二十二个Patentscope和56个PubMed记录:三个公布的国际专利申请和五篇审查的文件有资格。药代动力学数据可用于鼻内,舌下和参考路线。已经开发并测试了高度浓缩的制剂(10-40?mg?1)。舌下生物利用度非常低(1%;相对于静脉管)。非浓缩的鼻内喷雾(1?mg?mlα1;每鼻肌)的生物利用度(11%)。浓缩的鼻内配方(≥10·mg?ml = 1)的生物利用度为21-42%(相对于静脉内)和26-57%(相对于肌肉内),具有峰浓度(剂量调节的C max?= 0.8- 1.7?ng?ml?1)在19-30〜30?min(t max)达到。含义。探索性分析鉴定鼻内生物利用度与剂量正相关,对体积负相关。结论。我们发现一致的鼻内喷雾剂的发展方向,在20-60%范围内具有生物利用度的高浓度,低容量配方。这些有可能在0.1×ml体积中递送治疗剂量。 [麦当劳·丹尼尔斯逊格伦德吗?,Dale O,斯特朗J.非注射纳洛酮的国际专利申请OpioID过量逆转:PatontCope数据库的探索性搜索和检索分析。药物酒精Rev 2017; 00:000-000]

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