Issue 6, 2014

Recent progress of ICP-MS in the development of metal-based drugs and diagnostic agents

Abstract

Drug discovery and development is a long, expensive, and multiplex process, most of the steps (if not all of them) are unfeasible without use of different analytical techniques. In the case of metal-based drugs, their preclinical development and clinical testing increasingly rely on ICP-MS, having no-match analytical features in this seemingly ‘killer’ application. Applied with the standalone or combined (hyphenated) setup, the method allows robust, sensitive, and precise determinations of drug-comprising metals as well as specific and often multielemental detection of the biomolecular metabolic forms. This analytical information is invaluable for the assessment of drug-like properties, metabolite fingerprinting and profiling, monitoring the drug–biomolecule interactions, cellular uptake and pharmacokinetic studies, etc. but above all, for a better understanding of a drug's mechanisms of delivery and action. This review is mainly focused on the emerging role and current challenges of ICP-MS-based methodology in the field. Consistently with the title matter, special emphasis is placed on investigational metal-containing compounds that not only exhibit certain pharmacological or diagnostic properties but also hold promise of being advanced to (or already entered) clinical studies. It also provides a brief outlook of how the potential of ICP-MS is to be exploited in the future so as to accelerate the metallodrug development and reduce the enormous accompanying costs.

Graphical abstract: Recent progress of ICP-MS in the development of metal-based drugs and diagnostic agents

Supplementary files

Article information

Article type
Critical Review
Submitted
16 Dec 2013
Accepted
27 Feb 2014
First published
27 Feb 2014

J. Anal. At. Spectrom., 2014,29, 1058-1072

Author version available

Recent progress of ICP-MS in the development of metal-based drugs and diagnostic agents

A. R. Timerbaev, J. Anal. At. Spectrom., 2014, 29, 1058 DOI: 10.1039/C3JA50394A

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