scholarly journals Electron paramagnetic resonance and mass spectrometry: Useful tools to detect ultraviolet light induced skin lesions on a molecular basis – A short review

2006 ◽  
Vol 20 (1) ◽  
pp. 1-17 ◽  
Author(s):  
Ulrike Hochkirch ◽  
Werner Herrmann ◽  
Reinhard Stößer ◽  
Hans-Hubert Borchert ◽  
Michael W. Linscheid

Ultraviolet radiation is considered responsible for sunburning, premature skin aging, and cancerogenesis through the production of free radical species. Therefore, the favoured possibility for direct detection of unpaired electrons – electron paramagnetic resonance spectroscopy – is predestinated for detection and structural and dynamic analysis of this kind of molecules. However, many of UV induced radicals in skin have a short lifetime at ambient conditions and possibilities for stabilisation or transformation into definite para- or diamagnetic products have to be found. On the other hand, diamagnetic products, potentially also originated by reporter molecules, which are not detectable by EPR, are target molecules for mass spectrometric analysis. In this review, potentials and limitations of both spectroscopic methods are reviewed, and the effect of ultraviolet radiation on human skin is discussed in particular. Suitable combinations of both techniques result in detailed information about photoproducts and processes taking place within skin during and after irradiation. The literature is viewed from a recent perspective; historical aspects were not in the scope of this paper.

2020 ◽  
Vol 6 (22) ◽  
pp. eaaz8244
Author(s):  
Fei Kong ◽  
Pengju Zhao ◽  
Pei Yu ◽  
Zhuoyang Qin ◽  
Zhehua Huang ◽  
...  

Electron paramagnetic resonance (EPR) spectroscopy is among the most important analytical tools in physics, chemistry, and biology. The emergence of nitrogen-vacancy (NV) centers in diamond, serving as an atomic-sized magnetometer, has promoted this technique to single-spin level, even under ambient conditions. Despite the enormous progress in spatial resolution, the current megahertz spectral resolution is still insufficient to resolve key heterogeneous molecular information. A major challenge is the short coherence times of the sample electron spins. Here, we address this challenge by using a magnetic noise–insensitive transition between states of different symmetry. We demonstrate a 27-fold narrower spectrum of single substitutional nitrogen (P1) centers in diamond with a linewidth of several kilohertz, and then some weak couplings can be resolved. Those results show both spatial and spectral advances of NV center–based EPR and provide a route toward analytical (EPR) spectroscopy at the single-molecule level.


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