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Updated: Nov 6, 2025

A Microfluidic Chip for ICPMS Sample Introduction
Published on: March 5, 2015
Micro-droplet-based calibration for quantitative elemental bioimaging by LA-ICPMS.
Andreas Schweikert1,2, Sarah Theiner3, Debora Wernitznig2
1Institute of Analytical Chemistry, Faculty of Chemistry, University of Vienna, Waehringer Strasse 38, 1090, Vienna, Austria.
A new method uses laser ablation-inductively coupled plasma-time-of-flight mass spectrometry (LA-ICP-TOFMS) with micro-droplet standards for faster, accurate elemental bioimaging. This approach enables high-throughput analysis of metal-based drugs in cancer models.
Area of Science:
- Analytical Chemistry
- Bioimaging
- Mass Spectrometry
Background:
- Quantitative elemental bioimaging is crucial for understanding biological processes and drug distribution.
- Traditional standardization methods can be time-consuming and limit throughput.
- Developing rapid and accurate quantification strategies is essential for advancing bioimaging applications.
Purpose of the Study:
- To evaluate a novel standardization strategy for quantitative elemental bioimaging using laser ablation-inductively coupled plasma-time-of-flight mass spectrometry (LA-ICP-TOFMS).
- To assess the performance of multi-point calibration with gelatin-based micro-droplet standards.
- To demonstrate the application of this method for analyzing metal-based anticancer drugs in complex biological models.
Main Methods:
- Utilized multi-point calibration with precisely deposited gelatin-based micro-droplet standards (400 ± 5 pL).
- Employed laser ablation-inductively coupled plasma-time-of-flight mass spectrometry (LA-ICP-TOFMS) with a low-dispersion setup.
- Achieved high-throughput analysis with pixel acquisition rates exceeding 200 Hz for rapid calibration and imaging.
Main Results:
- Demonstrated precise and accurate quantification of elements including platinum, phosphorus, copper, and zinc.
- Significantly reduced calibration time compared to conventional methods.
- Successfully applied the method to investigate the accumulation of metal-based anticancer drugs in multicellular tumor spheroids.
Conclusions:
- The developed micro-droplet standardization strategy enables high-throughput, quantitative elemental bioimaging comparable to solution-based methods.
- This approach offers a significant advancement for analyzing elemental distributions in biological samples, particularly for drug development and toxicology.
- The method provides a robust tool-set for investigating clinically relevant concentrations of therapeutic agents in complex biological systems.
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