Characterization of the nicotine uptake and safety of Nordic spirit tobacco-free oral nicotine pouches: A randomized cross-over study.

IF 3.5 3区 医学 Q2 NEUROSCIENCES Psychopharmacology Pub Date : 2024-11-23 DOI:10.1007/s00213-024-06721-7
Karine Renard, Daisuke Nishihara, Johan Nilsson, Sylvain Larroque, Javier Martinez, Lesley Giles
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Abstract

Rationale: Given the nascency of tobacco-free oral nicotine pouches (NPs) and the heterogeneity of commercially available NP brands, there is a need for scientific evaluation of different NP formulations. Nordic Spirit, novel NPs are distinguished by their unique composition.

Objectives: To characterize blood nicotine delivery, pharmacokinetics (PK), subjective and physiological effects and to monitor safety of three Nordic Spirit NPs (6 mg, 9 mg and 11.2 mg/pouch) compared with LD tobacco snus (11.2 mg/pouch) and Nicorette® gum (4 mg/unit) following single 30 min use.

Methods: This was a randomized, open-label, ten-sequence, single-use, cross-over clinical study with 30 healthy adult Swedish snus users.

Results: Peak nicotine concentrations (Cmax) ranged from 10.92 to 17.32 ng/mL for the three Nordic Spirit NPs, with a trend toward dose proportionality, and 8.18 ng/mL and 9.23 ng/mL for the LD snus and Nicorette® gum comparators, respectively. Peak concentration for Nordic Spirit NPs was reached (Tmax) after 30 to 38 min, and after 45 min for LD snus and Nicorette® gum. No notable safety concerns were observed after single use for any of the study products.

Conclusions: Delivery of nicotine from the three Nordic Spirit NPs appeared to be nicotine content-dependent, based on Cmax and AUC. The amount of nicotine extracted showed positive correlation with the reported Cmax and AUC. For Nordic Spirit NPs, Tmax was immediately after end of use. The characteristics of Nordic Spirit NPs were found to be favourable for profiling NP nicotine delivery and safety in human use, and for further product development. ISRCTN registry study no. ISRCTN75583947.

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北欧精神无烟尼古丁口服小袋的尼古丁吸收特征和安全性:随机交叉研究
理由鉴于无烟口服尼古丁袋(NPs)的诞生以及市售 NPs 品牌的多样性,有必要对不同的 NP 配方进行科学评估。北欧精神、新型 NP 因其独特的成分而与众不同:与低密度烟草鼻烟(11.2毫克/袋)和尼古丁口香糖(4毫克/单位)相比,三种Nordic Spirit NPs(6毫克、9毫克和11.2毫克/袋)在单次使用30分钟后的血液尼古丁输送、药代动力学(PK)、主观和生理效应的特征,并监测其安全性:这是一项随机、开放标签、十序列、一次性、交叉临床研究,研究对象为 30 名瑞典健康成年鼻烟使用者:结果:三种Nordic Spirit NPs的尼古丁峰值浓度(Cmax)介于10.92至17.32纳克/毫升之间,呈剂量比例趋势;LD snus和Nicorette®口香糖的尼古丁峰值浓度(Cmax)分别为8.18纳克/毫升和9.23纳克/毫升。Nordic Spirit NPs在30至38分钟后达到峰值浓度(Tmax),LD snus和Nicorette®口香糖则在45分钟后达到峰值浓度(Tmax)。任何一种研究产品在一次性使用后都没有发现明显的安全问题:根据Cmax和AUC,三种Nordic Spirit NPs的尼古丁释放量似乎与尼古丁含量有关。尼古丁提取量与报告的Cmax和AUC呈正相关。对于 Nordic Spirit NPs 而言,Tmax 在使用结束后立即达到。研究发现,Nordic Spirit NPs的特性有利于分析NP尼古丁在人体使用中的输送和安全性,也有利于进一步的产品开发。ISRCTN 登记研究编号ISRCTN75583947。
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来源期刊
Psychopharmacology
Psychopharmacology 医学-精神病学
CiteScore
7.10
自引率
5.90%
发文量
257
审稿时长
2-4 weeks
期刊介绍: Official Journal of the European Behavioural Pharmacology Society (EBPS) Psychopharmacology is an international journal that covers the broad topic of elucidating mechanisms by which drugs affect behavior. The scope of the journal encompasses the following fields: Human Psychopharmacology: Experimental This section includes manuscripts describing the effects of drugs on mood, behavior, cognition and physiology in humans. The journal encourages submissions that involve brain imaging, genetics, neuroendocrinology, and developmental topics. Usually manuscripts in this section describe studies conducted under controlled conditions, but occasionally descriptive or observational studies are also considered. Human Psychopharmacology: Clinical and Translational This section comprises studies addressing the broad intersection of drugs and psychiatric illness. This includes not only clinical trials and studies of drug usage and metabolism, drug surveillance, and pharmacoepidemiology, but also work utilizing the entire range of clinically relevant methodologies, including neuroimaging, pharmacogenetics, cognitive science, biomarkers, and others. Work directed toward the translation of preclinical to clinical knowledge is especially encouraged. The key feature of submissions to this section is that they involve a focus on clinical aspects. Preclinical psychopharmacology: Behavioral and Neural This section considers reports on the effects of compounds with defined chemical structures on any aspect of behavior, in particular when correlated with neurochemical effects, in species other than humans. Manuscripts containing neuroscientific techniques in combination with behavior are welcome. We encourage reports of studies that provide insight into the mechanisms of drug action, at the behavioral and molecular levels. Preclinical Psychopharmacology: Translational This section considers manuscripts that enhance the confidence in a central mechanism that could be of therapeutic value for psychiatric or neurological patients, using disease-relevant preclinical models and tests, or that report on preclinical manipulations and challenges that have the potential to be translated to the clinic. Studies aiming at the refinement of preclinical models based upon clinical findings (back-translation) will also be considered. The journal particularly encourages submissions that integrate measures of target tissue exposure, activity on the molecular target and/or modulation of the targeted biochemical pathways. Preclinical Psychopharmacology: Molecular, Genetic and Epigenetic This section focuses on the molecular and cellular actions of neuropharmacological agents / drugs, and the identification / validation of drug targets affecting the CNS in health and disease. We particularly encourage studies that provide insight into the mechanisms of drug action at the molecular level. Manuscripts containing evidence for genetic or epigenetic effects on neurochemistry or behavior are welcome.
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