4.7 Article

Micro-droplet-based calibration for quantitative elemental bioimaging by LA-ICPMS

期刊

ANALYTICAL AND BIOANALYTICAL CHEMISTRY
卷 414, 期 1, 页码 485-495

出版社

SPRINGER HEIDELBERG
DOI: 10.1007/s00216-021-03357-w

关键词

Laser ablation; Mass spectrometry; ICP-MS; Quantification strategy; Bioimaging

资金

  1. University of Vienna

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A novel standardization strategy for quantitative elemental bioimaging was evaluated in this study, showing promising results with multi-element quantification using micro-droplet standards. The high-throughput analysis enabled the establishment of imaging measurement sequences with quality control and standardization samples, providing an important experimental method for future research.
In this work, a novel standardization strategy for quantitative elemental bioimaging is evaluated. More specifically, multi-element quantification by laser ablation-inductively coupled plasma-time-of-flight mass spectrometry (LA-ICP-TOFMS) is performed by multi-point calibration using gelatin-based micro-droplet standards and validated using in-house produced reference materials. Fully automated deposition of micro-droplets by micro-spotting ensured precise standard volumes of 400 +/- 5 pL resulting in droplet sizes of around 200 mu m in diameter. The small dimensions of the micro-droplet standards and the use of a low-dispersion laser ablation setup reduced the analysis time required for calibration by LA-ICPMS significantly. Therefore, as a key advance, high-throughput analysis (pixel acquisition rates of more than 200 Hz) enabled to establish imaging measurement sequences with quality control- and standardization samples comparable to solution-based quantification exercises by ICP-MS. Analytical figures of merit such as limit of detection, precision, and accuracy of the calibration approach were assessed for platinum and for elements with biological key functions from the lower mass range (phosphorus, copper, and zinc). As a proof-of-concept application, the tool-set was employed to investigate the accumulation of metal-based anticancer drugs in multicellular tumor spheroid models at clinically relevant concentrations.

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