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基质辅助激光解吸电离质谱成像技术中内标法定量检测单球体伊立替康

Quantification of Irinotecan in Single Spheroids Using Internal Standards by MALDI Mass Spectrometry Imaging.

机构信息

Department of Chemistry and Biochemistry, The Ohio State University, Columbus, Ohio 43210, United States.

Comprehensive Cancer Center, The Ohio State University, Columbus, Ohio 43210, United States.

出版信息

Anal Chem. 2023 Jun 20;95(24):9227-9236. doi: 10.1021/acs.analchem.3c00699. Epub 2023 Jun 7.

Abstract

Matrix-assisted laser desorption/ionization mass spectrometry imaging (MALDI-MSI) has been used to visualize molecular distributions in various biological samples. While it has succeeded in localizing molecules ranging from metabolites to peptides, quantitative MSI (qMSI) has remained challenging, especially in small biological samples like spheroids. Spheroids are a three-dimensional cellular model system that replicate the chemical microenvironments of tumors. This cellular model has played an important role in evaluating the penetration of drugs to better understand the efficacy of clinical chemotherapy. Therefore, we aim to optimize a method to quantify the distribution of therapeutics in a single spheroid using MALDI-MSI. Studies were performed with the therapeutic irinotecan (IR). The calibration curve showed a linear relationship with a limit of detection (LOD) of 0.058 ng/mm and value at 0.9643. Spheroids treated with IR for different lengths of time were imaged using the optimized method to quantify the drug concentration during the penetration process. With a dosing concentration of 20.6 μM, the concentration of IR at 48 h of treatment was 16.90 μM within a single spheroid. Furthermore, spheroids were divided into different layers by spatial segmentation to be quantified separately. This MALDI-qMSI method is amenable to a wide range of drugs as well as their metabolites. The quantification results show great potential to extend this method to other small biological samples such as organoids for patient derived therapies.

摘要

基质辅助激光解吸电离质谱成像(MALDI-MSI)已被用于可视化各种生物样本中的分子分布。虽然它已经成功定位了从代谢物到肽的分子,但定量 MALDI-MSI(qMSI)仍然具有挑战性,尤其是在像球体这样的小生物样本中。球体是一种三维细胞模型系统,可复制肿瘤的化学微环境。这种细胞模型在评估药物渗透以更好地了解临床化疗效果方面发挥了重要作用。因此,我们旨在优化一种使用 MALDI-MSI 对单个球体中的治疗剂分布进行定量的方法。研究使用治疗剂伊立替康(IR)进行。校准曲线呈线性关系,检测限(LOD)为 0.058 ng/mm, 值为 0.9643。用优化的方法对不同时间处理 IR 的球体进行成像,以定量穿透过程中的药物浓度。在 20.6 μM 的给药浓度下,在 48 小时的治疗中,单个球体中的 IR 浓度为 16.90 μM。此外,通过空间分割将球体分为不同的层进行单独定量。这种 MALDI-qMSI 方法适用于广泛的药物及其代谢物。定量结果表明,该方法有很大的潜力扩展到其他小的生物样本,如用于患者衍生疗法的类器官。

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