Nitazene test strips: a laboratory evaluation.

IF 4 2区 社会学 Q1 SUBSTANCE ABUSE
Liam M De Vrieze, Christophe P Stove, Marthe M Vandeputte
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引用次数: 0

Abstract

Background: 2-Benzylbenzimidazole 'nitazene' opioids pose a growing threat to public health. Nitazene analogues are increasingly found mixed with or (mis)sold as heroin and in falsified (non-)opioid medications, posing a great risk of intoxication in users (un)knowingly exposed to these potent opioids. Lateral flow immunoassay nitazene test strips (NTS; BTNX Rapid Response™) became commercially available in Q1 2024, with the aim to enable rapid detection of nitazene analogues in drug samples. As only limited independent data is available on the performance of these strips, this lab-based study aimed at evaluating their potential for drug checking applications.

Methods: Following dilution of drug standards in water, the NTS readouts were analyzed independently by two individuals and by ImageJ. The limit of detection for isotonitazene was determined using two manufacturing lots of NTS. Cross-reactivity with 32 other nitazene analogues was evaluated. Six sourced drug samples were tested to explore the ability of NTS to detect the presence of a nitazene analogue in authentic samples.

Results: The limits of detection for isotonitazene were 2000 or 3000 ng/mL, depending on the lot. Twenty-four of the 33 tested nitazene analogues cross-reacted with the NTS at concentrations ≤ 9000 ng/mL. Structural analysis indicated that either substitution or removal of the 5-nitro group, or lengthening the linker between the two aromatic rings, generally hampered detection. All six authentic drug samples consistently tested positive, with no observed false negatives.

Conclusions: This study provides a better understanding of the potential of NTS for drug checking purposes. Our findings indicate that NTS can theoretically alert to the presence of most nitazene analogues that have emerged on recreational drug markets. However, 'desnitazenes' (lacking the 5-nitro group) may yield false negative results due to low cross-reactivity. Although factors like specificity, lot-to-lot variability, nitazene analogue content in drug samples, solubility, and different testing conditions should be considered, our study results indicate that, at least under the conditions evaluated here (using reference standards and sourced powders), NTS are capable of detecting the presence of a wide range of nitazene analogues. Hence, NTS may alert users of the presence of nitazene analogues in drug samples.

硝氮试纸:实验室评估。
背景:2-苄基苯并咪唑 "硝氮烯 "类阿片对公众健康构成了日益严重的威胁。越来越多的硝氮类似物被发现混入海洛因或作为海洛因(误)出售,也越来越多地出现在伪造的(非)阿片类药物中,这给有意接触这些强效阿片类药物的使用者带来了极大的中毒风险。侧流免疫测定硝氮烯试纸(NTS;BTNX Rapid Response™)于 2024 年第一季度上市,旨在快速检测药物样本中的硝氮烯类似物。由于有关这些试纸条性能的独立数据有限,本实验室研究旨在评估其在药物检测应用中的潜力:方法:将药物标准品在水中稀释后,由两个人独立用 ImageJ 对 NTS 读数进行分析。使用两个生产批次的 NTS 确定了异烟肼的检测限。评估了与其他 32 种硝氮类似物的交叉反应。测试了六个来源药物样品,以探索 NTS 检测真实样品中是否存在硝氮类似物的能力:根据批次的不同,异烟肼的检测限为 2000 或 3000 纳克/毫升。所检测的 33 种硝氮类似物中有 24 种与 NTS 发生了交叉反应,浓度≤ 9000 ng/mL。结构分析表明,无论是取代或去除 5-硝基,还是加长两个芳香环之间的连接物,通常都会妨碍检测。所有六种真药样本的检测结果均为阳性,未发现假阴性:这项研究让我们更好地了解了 NTS 在药物检查方面的潜力。我们的研究结果表明,理论上 NTS 可以检测出娱乐性毒品市场上出现的大多数硝氮类似物。不过,"去硝基苯类"(缺少 5-硝基)可能会因交叉反应性低而产生假阴性结果。尽管需要考虑特异性、批次间的差异、药物样本中硝氮类似物的含量、溶解度和不同检测条件等因素,但我们的研究结果表明,至少在本文评估的条件下(使用参考标准和来源粉末),NTS 能够检测出多种硝氮类似物。因此,NTS 可以提醒用户药物样本中存在硝氮类似物。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Harm Reduction Journal
Harm Reduction Journal Medicine-Public Health, Environmental and Occupational Health
CiteScore
5.90
自引率
9.10%
发文量
126
审稿时长
26 weeks
期刊介绍: Harm Reduction Journal is an Open Access, peer-reviewed, online journal whose focus is on the prevalent patterns of psychoactive drug use, the public policies meant to control them, and the search for effective methods of reducing the adverse medical, public health, and social consequences associated with both drugs and drug policies. We define "harm reduction" as "policies and programs which aim to reduce the health, social, and economic costs of legal and illegal psychoactive drug use without necessarily reducing drug consumption". We are especially interested in studies of the evolving patterns of drug use around the world, their implications for the spread of HIV/AIDS and other blood-borne pathogens.
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