[超高效液相色谱法同时测定电子烟油中的五种吲哚/吲唑酰胺类合成大麻素]。

IF 1.2 4区 化学 Q4 CHEMISTRY, ANALYTICAL 色谱 Pub Date : 2023-07-01 DOI:10.3724/SP.J.1123.2022.10014
Zhe Yang, Jian-Xia Lyu, Yi-di Wu, Li-Wei Jiang, Dong-Mei Li
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The proposed method successfully quantified the five SCs in electronic cigarette oil via the external standard method. The samples were extracted using methanol, and the target analytes were separated on a Waters ACQUITY UPLC CSH C18 column (100 mm×2.1 mm, 1.7 μm) at column temperature of 35 ℃ and flow rate of 0.3 mL/min. The injection volume was 1 μL. The mobile phase consisted of acetonitrile and ultrapure water, and gradient elution was employed. The detection wavelengths were 290 and 302 nm. The five SCs were completely separated within 10 min under optimized conditions and showed good linear relationships between 1-100 mg/L, with correlation coefficients (<i>r</i><sup>2</sup>) of up to 0.9999. The limits of detection (LOD) and quantification (LOQ) were 0.2 and 0.6 mg/L, respectively. Precision was determined using standard solutions of the five SCs at mass concentrations of 1, 10, and 100 mg/L. The intra-day precision (<i>n</i>=6) was <1.5%, and the inter-day precision (<i>n</i>=6) was <2.2%. Accuracy was determined by spiking electronic cigarette oil with low (2 mg/L), moderate (10 mg/L), and high (50 mg/L) levels of the five SCs, with six replicates per determination. The recoveries of the five SCs were 95.5%-101.9%, and their relative standard deviations (RSDs, <i>n</i>=6) were 0.2%-1.5%, with accuracies ranging from -4.5% to 1.9%. The proposed method showed good performance when applied to the analysis of real samples. It is accurate, rapid, sensitive, and effective for the determination of five indole/indazole amide-based SCs in electronic cigarette oil. 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引用次数: 0

摘要

合成大麻素(SC)被认为是当今滥用最广泛的新型精神活性物质,其药效比天然大麻强得多,而且功效更强。通过在一个芳香环系统中添加卤素、烷基或烷氧基等取代基,或改变烷基链的长度,可以开发出新的合成大麻素。继所谓的第一代 SC 出现之后,进一步的发展导致了第八代吲哚/吲唑酰胺基 SC 的出现。鉴于所有 SC 于 2021 年 7 月 1 日被列为受控物质,用于检测这些物质的技术必须迅速改进。由于 SC 种类繁多、化学成分多样且更新速度快,确定和识别新的 SC 具有挑战性。近年来,人们发现了几种吲哚/吲唑酰胺类 SC,但对这些化合物的系统研究仍然有限。因此,开发快速、灵敏、准确的定量方法来测定新型 SC 具有重要意义。与高效液相色谱(HPLC)相比,超高效液相色谱(UPLC)具有更高的分辨率、更好的分离效率和更快的分析速度,因此可以满足对缉获物中吲哚/吲唑酰胺类 SC 的定量分析需求。N-(1-甲氧基-3,3-二甲基-1-氧代丁-2-基)-1-(5-氟戊基)-1H-吲哚-3-甲酰胺 (5F-MDMB-PICA)、甲基-3、3-二甲基-2-(1-(戊-4-烯-1-基)-1H-吲唑-3-甲酰胺基)丁酸酯(MDMB-4en-PINACA)和 N-(金刚烷-1-基)-1-(4-氟丁基)-1H-吲唑-3-甲酰胺(4F-ABUTINACA);近年来,在缉获的材料中检测到这些 SC 的频率越来越高。该方法对流动相、洗脱梯度、柱温、检测波长等影响分离和检测性能的主要因素进行了优化。通过外标法成功定量了电子烟油中的5种SCs。样品经甲醇提取后,采用Waters ACQUITY UPLC CSH C18色谱柱(100 mm×2.1 mm, 1.7 μm)分离,柱温35 ℃,流速0.3 mL/min。进样量为 1 μL。流动相为乙腈和超纯水,梯度洗脱。检测波长为 290 和 302 nm。在优化的条件下,5种SC在10分钟内完全分离,并在1-100 mg/L之间呈现良好的线性关系,相关系数(r2)高达0.9999。检测限(LOD)和定量限(LOQ)分别为 0.2 mg/L 和 0.6 mg/L。使用质量浓度为 1、10 和 100 mg/L 的五种 SC 标准溶液测定了精密度。日内精密度(n=6)为0.2%-1.5%,准确度为-4.5%-1.9%。该方法在实际样品分析中表现出良好的性能。该方法准确、快速、灵敏、有效,可用于电子烟油中 5 种吲哚/吲唑酰胺类 SCs 的检测。因此,该方法满足了实际测定的要求,并为采用超高效液相色谱法测定具有相似结构的SCs提供了参考。
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[Simultaneous determination of five indole/indazole amide-based synthetic cannabinoids in electronic cigarette oil by ultra performance liquid chromatography].

Synthetic cannabinoids (SCs), which are considered some of the most widely abused new psychoactive substances available today, are much more potent than natural cannabis and display greater efficacy. New SCs can be developed by adding substituents such as halogen, alkyl, or alkoxy groups to one of the aromatic ring systems, or by changing the length of the alkyl chain. Following the emergence of the so-called first-generation SCs, further developments have led to eighth-generation indole/indazole amide-based SCs. Given that all SCs were listed as controlled substances on July 1, 2021, the technologies used to detect these substances must be quickly improved. Due to the sheer number of SCs, the chemical diversity and the fast update speed, it is challenging to determine and identify the new SCs. In recent years, several types of indole/indazole amide-based SCs have been seized, but systematic research on these compounds remains limited. Therefore, developing rapid, sensitive, and accurate quantitative methods to determine new SCs are of great importance. Compared with high performance liquid chromatography (HPLC), ultra performance liquid chromatography (UPLC) shows higher resolution, better separation efficiency, and faster analysis speeds; thus, it can meet the demand for the quantitative analysis of indole/indazole amide-based SCs in seized materials. In this study, a UPLC method was developed for the simultaneous determination of five indole/indazole amide-based SCs, including N-(1-amino-3,3-dimethyl-1-oxobutan-2-yl)-1-butyl-1H-indazole-3-carboxamide (ADB-BUTINACA), methyl 2-(1-(4-fluorobutyl)-1H-indole-3-carboxamido)-3,3-dimethylbutanoate (4F-MDMB-BUTICA), N-(1-methoxy-3,3-dimethyl-1-oxobutan-2-yl)-1-(5-fluoropentyl)-1H-indole-3-carboxamide (5F-MDMB-PICA), methyl 3,3-dimethyl-2-(1-(pent-4-en-1-yl)-1H-indazole-3-carboxamido)butanoate (MDMB-4en-PINACA), and N-(adamantan-1-yl)-1-(4-fluorobutyl)-1H-indazole-3-carboxamide (4F-ABUTINACA) in electronic cigarette oil; these SCs have been detected with increasing frequency in seized materials in recent years. The main factors influencing the separation and detection performance of the proposed method, including the mobile phase, elution gradient, column temperature, and detection wavelength, were optimized. The proposed method successfully quantified the five SCs in electronic cigarette oil via the external standard method. The samples were extracted using methanol, and the target analytes were separated on a Waters ACQUITY UPLC CSH C18 column (100 mm×2.1 mm, 1.7 μm) at column temperature of 35 ℃ and flow rate of 0.3 mL/min. The injection volume was 1 μL. The mobile phase consisted of acetonitrile and ultrapure water, and gradient elution was employed. The detection wavelengths were 290 and 302 nm. The five SCs were completely separated within 10 min under optimized conditions and showed good linear relationships between 1-100 mg/L, with correlation coefficients (r2) of up to 0.9999. The limits of detection (LOD) and quantification (LOQ) were 0.2 and 0.6 mg/L, respectively. Precision was determined using standard solutions of the five SCs at mass concentrations of 1, 10, and 100 mg/L. The intra-day precision (n=6) was <1.5%, and the inter-day precision (n=6) was <2.2%. Accuracy was determined by spiking electronic cigarette oil with low (2 mg/L), moderate (10 mg/L), and high (50 mg/L) levels of the five SCs, with six replicates per determination. The recoveries of the five SCs were 95.5%-101.9%, and their relative standard deviations (RSDs, n=6) were 0.2%-1.5%, with accuracies ranging from -4.5% to 1.9%. The proposed method showed good performance when applied to the analysis of real samples. It is accurate, rapid, sensitive, and effective for the determination of five indole/indazole amide-based SCs in electronic cigarette oil. Thus, it satisfies the requirements for practical determination and provides a reference for the determination of SCs with similar structures by UPLC.

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来源期刊
色谱
色谱 CHEMISTRY, ANALYTICAL-
CiteScore
1.30
自引率
42.90%
发文量
7198
期刊介绍: "Chinese Journal of Chromatography" mainly reports the basic research results of chromatography, important application results of chromatography and its interdisciplinary subjects and their progress, including the application of new methods, new technologies, and new instruments in various fields, the research and development of chromatography instruments and components, instrument analysis teaching research, etc. It is suitable for researchers engaged in chromatography basic and application technology research in scientific research institutes, master and doctoral students in chromatography and related disciplines, grassroots researchers in the field of analysis and testing, and relevant personnel in chromatography instrument development and operation units. The journal has columns such as special planning, focus, perspective, research express, research paper, monograph and review, micro review, technology and application, and teaching research.
期刊最新文献
[Off-line comprehensive two-dimensional countercurrent chromatography-liquid chromatography separation of Curcuma volatile oil]. [Advances in synthesis methods and applications of microporous organic networks for sample preparation]. [Application progress of on-line sample preparation techniques coupled with liquid chromatography-mass spectrometry system in the detection of food hazards]. [Chiral capillary gas chromatography for the separation of the enantiomers of 4-chloromethyl-2,2-dimethyl-1,3-dioxolane]. [Determination of 14 β-agonists in animal meat by ultra high performance liquid chromatography-tandem mass spectrometry].
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