Division of Laboratory Sciences, Tobacco and Volatiles Branch, Centers for Disease Control and Prevention, Atlanta, GA, 30341, USA.
Rapid Commun Mass Spectrom. 2020 Oct 15;34(19):e8879. doi: 10.1002/rcm.8879.
Over 2800 e-cigarette, or vaping, product use-associated lung injury (EVALI) cases were reported to the Centers for Disease Control and Prevention (CDC) during August 2019 to February 2020. Bronchoalveolar lavage (BAL) fluid samples from 51 EVALI and 99 non-EVALI cases were analyzed for toxicants including terpenes. We describe a novel method to measure selected terpenes in BAL fluid by gas chromatography/tandem mass spectrometry (GC/MS/MS).
α-Pinene, β-pinene, β-myrcene, 3-carene, and limonene were measured in BAL fluid specimens by headspace solid-phase microextraction/gas chromatography/tandem mass spectrometry. We created and characterized BAL fluid pools from non-EVALI individuals to determine assay accuracy, precision, linearity, limits of detection, and analytical specificity. All measurements were conducted in accordance with the CDC's Division of Laboratory Sciences rigorous method validation procedures.
Matrix validation experiments showed that calibration curves in BAL fluid and saline had similar slopes, with differences of less than 7%. The assay precision ranged from 2.52% to 5.30%. In addition, the limits of detection for the five analytes ranged from 1.80 to 16.8 ng/L, and the linearity was confirmed with R values >0.99.
We developed and validated a method to quantify selected terpenes in BAL fluid specimens using GC/MS/MS. The assay provided accurate and precise analyses of EVALI and non-EVALI BAL fluid specimens in support of CDC's EVALI response. This method is applicable to the determination of a broad range of terpenes in BAL fluid specimens.
2019 年 8 月至 2020 年 2 月期间,疾病控制与预防中心(CDC)报告了超过 2800 例与电子烟或蒸气相关的肺损伤(EVALI)病例。对 51 例 EVALI 和 99 例非 EVALI 病例的支气管肺泡灌洗液(BAL)样本进行了毒理学分析,包括萜烯。我们描述了一种通过气相色谱/串联质谱(GC/MS/MS)测量 BAL 液中选定萜烯的新方法。
通过顶空固相微萃取/气相色谱/串联质谱法测量 BAL 液标本中的α-蒎烯、β-蒎烯、β-月桂烯、3-蒈烯和柠檬烯。我们创建并表征了来自非 EVALI 个体的 BAL 液池,以确定测定的准确性、精密度、线性、检测限和分析特异性。所有测量均按照疾病预防控制中心实验室科学司严格的方法验证程序进行。
基质验证实验表明,BAL 液和生理盐水的校准曲线斜率相似,差异小于 7%。测定精密度范围为 2.52%至 5.30%。此外,五种分析物的检测限范围为 1.80 至 16.8ng/L,线性关系通过 R 值>0.99 得到证实。
我们开发并验证了一种使用 GC/MS/MS 定量 BAL 液标本中选定萜烯的方法。该测定法为支持疾病预防控制中心 EVALI 应对措施提供了 EVALI 和非 EVALI BAL 液标本的准确和精确分析。该方法适用于测定 BAL 液标本中广泛范围的萜烯。