Center for Nanotechnology and Nanotoxicology, T.H. Chan School of Public Health, Harvard University, Boston, MA, USA.
Environmental Occupational Health Sciences Institute, School of Public Health, Rutgers University, New Brunswick, NJ, USA.
Crit Rev Toxicol. 2022 Mar;52(3):188-220. doi: 10.1080/10408444.2022.2082918. Epub 2022 Jul 13.
"E-Cigarette (e-cig) Vaping-Associated Acute Lung Injury" (EVALI) has been linked to vitamin-E-acetate (VEA) and Δ-9-tetrahydrocannabinol (THC), due to their presence in patients' e-cigs and biological samples. Lacking standardized methodologies for patients' data collection and comprehensive physicochemical/toxicological studies using real-world-vapor exposures, very little data are available, thus the underlying pathophysiological mechanism of EVALI is still unknown. This review aims to provide a comprehensive and critical appraisal of existing literature on clinical/epidemiological features and physicochemical-toxicological characterization of vaping emissions associated with EVALI. The literature review of 161 medical case reports revealed that the predominant demographic pattern was healthy white male, adolescent, or young adult, vaping illicit/informal THC-containing e-cigs. The main histopathologic pattern consisted of diffuse alveolar damage with bilateral ground-glass-opacities at chest radiograph/CT, and increased number of macrophages or neutrophils and foamy-macrophages in the bronchoalveolar lavage. The chemical analysis of THC/VEA e-cig vapors showed a chemical difference between THC/VEA and the single THC or VEA. The chemical characterization of vapors from counterfeit THC-based e-cigs or in-house-prepared e-liquids using either cannabidiol (CBD), VEA, or medium-chain triglycerides (MCT), identified many toxicants, such as carbonyls, volatile organic compounds, terpenes, silicon compounds, hydrocarbons, heavy metals, pesticides and various industrial/manufacturing/automotive-related chemicals. There is very scarce published toxicological data on emissions from THC/VEA e-liquids. However, CBD, MCT, and VEA emissions exert varying degrees of cytotoxicity, inflammation, and lung damage, depending on puffing topography and cell line. Major knowledge gaps were identified, including the need for more systematic-standardized epidemiological surveys, comprehensive physicochemical characterization of real-world e-cig emissions, and mechanistic studies linking emission properties to specific toxicological outcomes.
电子烟相关急性肺损伤(EVALI)与维生素 E 醋酸酯(VEA)和 Δ-9-四氢大麻酚(THC)有关,因为它们存在于患者的电子烟和生物样本中。由于缺乏患者数据收集的标准化方法和使用真实蒸汽暴露进行全面的物理化学/毒理学研究,因此可用的数据非常少,因此 EVALI 的潜在病理生理机制尚不清楚。本综述旨在全面、批判性地评估与 EVALI 相关的电子烟蒸汽排放的临床/流行病学特征和物理化学/毒理学特征的现有文献。对 161 份医学病例报告的文献回顾表明,主要的人口统计学模式是健康的白人男性、青少年或年轻成年人,吸食非法/非正式含有 THC 的电子烟。主要的组织病理学模式包括弥漫性肺泡损伤,胸部 X 线/CT 显示双侧磨玻璃影,支气管肺泡灌洗液中巨噬细胞或中性粒细胞和泡沫状巨噬细胞增多。THC/VEA 电子烟蒸汽的化学分析显示 THC/VEA 与单一 THC 或 VEA 之间存在化学差异。使用大麻二酚(CBD)、VEA 或中链甘油三酯(MCT)对假冒 THC 电子烟或自制电子烟液蒸汽进行化学特征分析,鉴定出许多有毒物质,如羰基化合物、挥发性有机化合物、萜烯、硅化合物、碳氢化合物、重金属、农药和各种工业/制造/汽车相关化学品。关于 THC/VEA 电子烟液排放的毒理学数据非常少。然而,CBD、MCT 和 VEA 的排放会根据抽吸模式和细胞系的不同,表现出不同程度的细胞毒性、炎症和肺损伤。还确定了许多知识空白,包括需要进行更系统、标准化的流行病学调查、对真实世界电子烟排放的全面物理化学特征进行描述,以及将排放特性与特定毒理学结果联系起来的机制研究。