Teri Devin, Aly Noor A, Dodds James N, Zhang Jian, Thiessen Paul A, Bolton Evan E, Joseph Kara M, Williams Antony J, Schymanski Emma L, Rusyn Ivan, Baker Erin S
Department of Veterinary Physiology and Pharmacology, Texas A&M University, College Station, Texas 77843, USA.
Department of Chemistry, University of North Carolina, Chapel Hill, North Carolina 27599, USA.
bioRxiv. 2025 Feb 27:2025.02.22.639656. doi: 10.1101/2025.02.22.639656.
As our health is affected by the xenobiotic chemicals we are exposed to, it is important to rapidly assess these molecules both in the environment and our bodies. Targeted analytical methods coupling either gas or liquid chromatography with mass spectrometry (GC-MS or LC-MS) are commonly utilized in current exposure assessments. While these methods are accepted as the gold standard for exposure analyses, they often require multiple sample preparation steps and more than 30 minutes per sample. This throughput limitation is a critical gap for exposure assessments and has resulted in an evolving interest in using ion mobility spectrometry and MS (IMS-MS) for non-targeted studies. IMS-MS is a unique technique due to its rapid analytical capabilities (millisecond scanning) and detection of a wide range of chemicals based on unique collision cross section (CCS) and mass-to-charge () values. To increase the availability of IMS-MS information for exposure studies, here we utilized drift tube IMS-MS to evaluate 4,685 xenobiotic chemical standards from the Environmental Protection Agency Toxicity Forecaster (ToxCast) program including pesticides, industrial chemicals, pharmaceuticals, consumer products, and per- and polyfluoroalkyl substances (PFAS). In the analyses, 3,993 [M+H], [M+Na], [M-H] and [M+] ion types were observed with high confidence and reproducibility (≤1% error intra-laboratory and ≤2% inter-laboratory) from 2,140 unique chemicals. These values were then assembled into an openly available multidimensional database and uploaded to PubChem to enable rapid IMS-MS suspect screening for a wide range of environmental contaminants, faster response time in environmental exposure assessments, and assessments of xenobiotic-disease connections.
由于我们的健康会受到所接触的外源性化学物质的影响,因此快速评估环境和我们体内的这些分子非常重要。目前的暴露评估中通常采用将气相色谱或液相色谱与质谱联用的靶向分析方法(气相色谱-质谱联用或液相色谱-质谱联用)。虽然这些方法被公认为暴露分析的金标准,但它们通常需要多个样品制备步骤,每个样品耗时超过30分钟。这种通量限制是暴露评估中的一个关键差距,并且导致人们越来越关注使用离子迁移谱和质谱联用(IMS-MS)进行非靶向研究。IMS-MS是一种独特的技术,因为它具有快速分析能力(毫秒级扫描),并且能够基于独特的碰撞截面(CCS)和质荷比()值检测多种化学物质。为了增加用于暴露研究的IMS-MS信息的可用性,我们在此利用漂移管IMS-MS评估了来自美国环境保护局毒性预测(ToxCast)计划的4685种外源性化学标准品,包括农药、工业化学品、药品、消费品以及全氟和多氟烷基物质(PFAS)。在分析中,从2140种独特的化学物质中高置信度且可重复地(实验室内误差≤1%,实验室间误差≤2%)观察到3993种[M+H]、[M+Na]、[M-H]和[M+]离子类型。然后将这些值组装成一个公开可用的多维数据库,并上传到PubChem,以实现对多种环境污染物的快速IMS-MS可疑物筛选、环境暴露评估中更快的响应时间以及外源性物质与疾病关联的评估。