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国际非注射用纳洛酮治疗阿片类药物过量逆转的专利申请:对 PatentScope 数据库的探索性检索和提取分析。

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

机构信息

National Addiction Centre, Institute of Psychiatry, Psychology and Neuroscience, King's College London, London, UK.

Department of Circulation and Medical Imaging, NTNU-The Norwegian University of Science and Technology, Trondheim, Norway.

出版信息

Drug Alcohol Rev. 2018 Feb;37(2):205-215. doi: 10.1111/dar.12571. Epub 2017 Jun 8.

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 ) had been developed and tested. Sublingual bioavailability was very low (1%; relative to intravenous). Non-concentrated intranasal spray (1 mg mL ; 1 mL per nostril) had low bioavailability (11%). Concentrated intranasal formulations (≥10 mg mL ) had bioavailability of 21-42% (relative to intravenous) and 26-57% (relative to intramuscular), with peak concentrations (dose-adjusted C  = 0.8-1.7 ng mL ) reached in 19-30 min (t ).

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. Drug Alcohol Rev 2017;00:000-000].

摘要

问题

正在开发非注射用纳洛酮制剂以逆转阿片类药物过量,但在同行评审领域仅发表了有限的数据。通过检查一个迄今为止尚未搜索过的数据库,我们扩展了公众对非注射制剂的认识,追溯它们的开发和新颖性,目的是描述和比较它们的药代动力学特性。

方法

(i)在世界知识产权组织的 PatentScope 数据库中搜索相关的英文专利申请;(ii)提取、整理和分析药代动力学数据;(iii)使用布尔搜索查询“(鼻内 OR 鼻腔内 OR 鼻 OR 颊 OR 舌下) AND 纳洛酮 AND 药代动力学”在 PubMed 中搜索。

主要发现

共确定了 522 项 PatentScope 和 56 项 PubMed 记录:有 3 项已发表的国际专利申请和 5 篇同行评议论文符合条件。可获得鼻腔内、舌下和参考途径的药代动力学数据。已开发和测试了高浓度制剂(10-40mg/mL)。舌下生物利用度非常低(1%;相对于静脉内)。非浓缩鼻腔喷雾剂(1mg/mL;每鼻孔 1mL)的生物利用度低(11%)。浓度为 10mg/mL 及以上的鼻腔内制剂的生物利用度为 21-42%(相对于静脉内)和 26-57%(相对于肌内),达峰浓度(剂量调整后 C = 0.8-1.7ng/mL)在 19-30min(t )达到。

意义

探索性分析发现,鼻腔内生物利用度与剂量呈正相关,与体积呈负相关。

结论

我们发现鼻腔喷雾剂的发展方向一致,朝着高浓度、低体积的制剂发展,生物利用度在 20-60%范围内。这些制剂有可能在 0.1mL 体积内输送治疗剂量。[McDonald R, Danielsson Glende Ø, Dale O, Strang J. 非注射用纳洛酮治疗阿片类药物过量逆转的国际专利申请:对 PatentScope 数据库的探索性搜索和检索分析。药物和酒精审查 2017;00:000-000]。

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