Abstract

Platinum-based drugs (cisplatin, carboplatin, and oxaliplatin) are widely used therapeutic agents for cancer treatment. Even though the platinum (Pt)-drugs are routinely used clinically, a clear picture of their distribution within tumor tissues is lacking. The current methods to image the distribution of Pt drugs are limited and do not enable the discrimination of the drug from its metabolites. In this manuscript, we demonstrate a methodology that enables chemical imaging of a Pt drug and its metabolites simultaneously and specifically. Matrix-Assisted Laser Desorption/Ionization (MALDI) Mass Spectrometry Imaging (MSI) is combined with an on-tissue chemical derivatization using diethyldithiocarbamate (DDTC). DDTC abstracts the Pt atom to generate ionizable complexes that can be imaged by MALDI MSI. We demonstrate that Pt drugs and their metabolites can be specifically imaged. This approach was successfully applied to map the penetration and metabolism of oxaliplatin in hyperthermic intraperitoneal chemotherapy (HIPEC)-like treated 3D colorectal tumor mimics. The distribution of cisplatin and carboplatin was mapped in additional 3D tumor mimics. We demonstrate that the approach can also be used to image the distribution of copper ions in cells. This method has the potential to be used to evaluate the penetration and distribution of a wide range of compounds.

Highlights

  • Platinum-based drugs are widely used therapeutic agents for cancer treatment

  • We evaluated the distribution of oxaliplatin in hyperthermic intraperitoneal chemotherapy (HIPEC)-like treated three-dimensional (3D) multicellular tumor spheroids (MCTS)

  • We extend our Matrix-Assisted Laser Desorption/Ionization (MALDI) imaging mass spectrometry (IMS) based analyses to map the distribution of Pt-based drugs, and in particular, the therapeutics oxaliplatin, carboplatin, and cisplatin

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Summary

Introduction

Platinum-based drugs (cisplatin, carboplatin, and oxaliplatin) are widely used therapeutic agents for cancer treatment. We are developing a simple, rapid, and sensitive approach to study the drug response and localization of Pt-based therapeutics within MCTS using DDTC derivatization, followed by MALDI IMS or LC-MS/MS analysis, to better understand and optimize HIPEC treatment. While the Pt(DACH)(Met) complex was detected without DDTC derivatization, no other drug-related species including the intact oxaliplatin molecule, were detected by MALDI in either positive or negative ion mode.

Results
Conclusion

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