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盐析辅助液液萃取法结合超高效液相色谱-串联质谱法测定口服传统烟草制品和新型烟草制品中的尼古丁

Salting-Out-Assisted Liquid-Liquid Extraction Method for the Determination of Nicotine from Oral Traditional and Innovative Tobacco Products Using UPLC-MS/MS.

作者信息

Aldeek Fadi, Lopez Vanessa, Miller John H

机构信息

Altria Client Services LLC, 601 East Jackson Street, Richmond, Virginia 23219, United States.

出版信息

ACS Omega. 2023 Aug 16;8(34):31256-31264. doi: 10.1021/acsomega.3c03474. eCollection 2023 Aug 29.

Abstract

In this study, we developed and validated a novel method that allows for the extraction and quantitation of nicotine from a variety of commercially available oral tobacco products including loose and pouched traditional moist smokeless tobacco products, and oral tobacco-derived nicotine (OTDN) lozenges, gums, and pouches. The method employed an extraction technique consisting of salting-out assisted liquid-liquid extraction using sodium hydroxide and acetonitrile in conjunction with ultra-high pressure liquid chromatography coupled to mass spectrometry. Accurate quantitation was obtained using nicotine methyl- isotopically labeled internal standard. Chromatographic separation of nicotine and nicotine methyl- internal standard was achieved using a Waters Acquity C18 column (50 mm × 2.1 mm i.d., 2.5 μm) with 10 mM ammonium acetate buffer (pH = 10) and acetonitrile as mobile phase A and B, respectively. Using a gradient elution and a flow rate of 0.4 mL/min for 5 min runtime, nicotine eluted at 1.74 min. The method was validated according to ICH guidelines for all the sample types with an accuracy for nicotine within 89-109%. Repeatability and intermediate precision were both estimated to be ≤7% relative standard deviation (% RSD). This method is applicable for a wide range of traditional moist smokeless and OTDN tobacco products.

摘要

在本研究中,我们开发并验证了一种新方法,该方法可从多种市售口腔烟草制品中提取并定量尼古丁,这些制品包括散装和袋装的传统湿无烟烟草制品,以及口腔烟草衍生尼古丁(OTDN)含片、口香糖和袋装产品。该方法采用一种提取技术,包括使用氢氧化钠和乙腈进行盐析辅助液液萃取,并结合超高压液相色谱与质谱联用。使用尼古丁甲基同位素标记内标物实现了准确的定量。尼古丁和尼古丁甲基内标物的色谱分离是使用沃特世 Acquity C18 柱(50 mm × 2.1 mm 内径,2.5 μm),以 10 mM 醋酸铵缓冲液(pH = 10)和乙腈分别作为流动相 A 和 B 来实现的。采用梯度洗脱,流速为 0.4 mL/min,运行时间为 5 min,尼古丁在 1.74 min 洗脱。该方法根据国际协调会议(ICH)指南对所有样品类型进行了验证,尼古丁的准确度在 89 - 109% 范围内。重复性和中间精密度的相对标准偏差(% RSD)均估计≤7%。该方法适用于广泛的传统湿无烟和 OTDN 烟草制品。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1873/10468829/1cccad17e3f4/ao3c03474_0002.jpg

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