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Lanthanide ions hold key to disease screening
14 January 2008
Canadian researchers have devised a way to assess biological samples for the presence of multiple small molecules, which has profound implications for the rapid identification of diseases.
Being able to distinguish diseased cells from healthy ones is vital in the identification of diseases in humans. A rapidly advancing way of doing this is to determine the concentrations of small molecules (biomarkers) present in biological samples, as amounts of these chemicals differ between diseased and healthy cells. Vladimir Baranov and colleagues from the University of Toronto have now developed a sensitive method that, by using lanthanide ions, is able to determine the concentrations of many biomarkers at once. This, they say, will have important applications in clinical diagnostics.

Baranov and colleagues bound 151Eu ions to a polymer chain chemically attached to an antibody, which itself binds to a natural biomarker. Once the unreacted antibody derivative is washed away, the sample is exposed to inductively coupled plasma mass spectrometry. This atomises the entire sample and allows the elemental composition to be determined. In this case, the amount of 151Eu correlates to the amount of biomarker present in the original sample. The number of 151Eu ions within each molecule means that the method is more sensitive to the amount of biomarker than existing techniques, said Baranov.
- Les Ebdon, Vice-Chancellor of the University of Bedfordshire, UK
The importance of this research is emphasised by Les Ebdon, Vice-Chancellor of the University of Bedfordshire, UK, who said 'This exciting study ... promises to advance our abilities to understand and diagnose complex diseases such as leukaemia.'
David Barden
Link to journal article
Development of analytical methods for multiplex bio-assay with inductively coupled plasma mass spectrometry
Olga I. Ornatsky, Robert Kinach, Dmitry R. Bandura, Xudong Lou, Scott D. Tanner, Vladimir I. Baranov, Mark Nitz and Mitchell A. Winnik, J. Anal. At. Spectrom., 2008, 23, 463
DOI: 10.1039/b710510j
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