Liquid chromatography-mass spectrometry for the quantitative bioanalysis of anticancer drugs.

Mass Spectrom Rev

Department of Pharmacy & Pharmacology, The Netherlands Cancer Institute/Slotervaart Hospital, Louwesweg 6, 1066 EC Amsterdam, The Netherlands.

Published: November 2005

AI Article Synopsis

  • The monitoring of anticancer drugs is crucial during development and clinical use, traditionally utilizing liquid chromatography (LC) with UV or other detection methods.
  • The combination of LC with mass spectrometry (MS) has significantly improved sensitivity and selectivity, making LC-MS the preferred method for analyzing anticancer agents.
  • Ongoing advancements in mass spectrometry technology and LC optimization suggest a promising future for enhancing bioanalysis capabilities in cancer treatment.

Article Abstract

The monitoring of anticancer drugs in biological fluids and tissues is important during both pre-clinical and clinical development and often in routine clinical use. Traditionally, liquid chromatography (LC) in combination with ultraviolet (UV), fluorescence, or electrochemical detection is employed for this purpose. The successful hyphenation of LC and mass spectrometry (MS), however, has dramatically changed this. MS detection provides better sensitivity and selectivity than UV detection and, in addition, is applicable to a significantly larger group of compounds than fluorescence or electrochemical detection. Therefore, LC-MS has now become the method of first choice for the quantitative bioanalysis of many anticancer agents. There are still, however, a lot of new developments to be expected in this area, such as the introduction of more sensitive and robust mass spectrometers, high-throughput analyses, and further optimization of the coupled LC systems. Many articles have appeared in this field in recent years and are reviewed here. We conclude that LC-MS is an extremely powerful tool for the quantitative analysis of anticancer drugs in biological samples.

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Source
http://dx.doi.org/10.1002/mas.20046DOI Listing

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