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首页> 外文期刊>Drug and alcohol review >International patent applications for non‐injectable naloxone for opioid overdose reversal: Exploratory search and retrieve analysis of the PatentScope database
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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。非注射型纳洛酮制剂正在研发中,用于阿片类药物过量逆转,但同行评审领域仅发表了有限的数据。通过检查一个迄今尚未检索的数据库,我们扩大了非注射制剂的公共知识,追踪其发展和新颖性,旨在描述和比较其药代动力学特性。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(鼻或鼻内或鼻或颊或舌下)和纳洛酮和药代动力学搜索PubMed。关键发现。共鉴定出522份PatentScope和56份PubMed记录:三份已发表的国际专利申请和五份同行评审的论文符合资格。可获得鼻内、舌下和参考途径的药代动力学数据。已经开发并测试了高浓度配方(10-40毫克/毫升)。舌下生物利用度非常低(1%,相对于静脉注射)。非浓缩鼻内喷雾剂(1?mg?mL?1;每个鼻孔1?mL)的生物利用度较低(11%)。浓缩鼻内制剂(≥10?mg?毫升?1)生物利用度为21–42%(相对于静脉注射)和26–57%(相对于肌肉注射),峰值浓度(经剂量调整的C最大值=0.8–1.7纳克毫升)在19–30分钟内达到?最小值(t最大值)。启示。探索性分析发现,鼻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,鼻腔喷雾剂向高浓度、低容量剂型发展的方向是一致的,生物利用度在20-60%之间。这些药物有可能提供0.1%的治疗剂量?毫升体积。[McDonald R,Danielsson Glende?,Dale O,Strang J.阿片类药物过量逆转非注射性纳洛酮的国际专利申请:PatentScope数据库的探索性搜索和检索分析。药物酒精版本2017;00:000-000]

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