scholarly journals Side-by-Side Comparison of DNA Damage Induced by Low-Energy Electrons and High-Energy Photons with Solid TpTpT Trinucleotide

2013 ◽  
Vol 117 (35) ◽  
pp. 10122-10131 ◽  
Author(s):  
Yeunsoo Park ◽  
Anita R. Peoples ◽  
Guru S. Madugundu ◽  
Léon Sanche ◽  
J. Richard Wagner
2014 ◽  
Vol 10 (S313) ◽  
pp. 97-98
Author(s):  
Kenji Yoshida

AbstractSymmetric and triangle-shaped flux variability in X-ray and gamma-ray light curves is observed from many blazars. We derived the X-ray spectrum changing in time by using a kinetic equation of high energy electrons. Giving linearly changing the injection of low energy electrons into accelerating and emitting region, we obtained the preliminary results that represent the characteristic X-ray variability of the linear flux increase with hardening in the rise phase and the linear decrease with softening in the decay phase.


2001 ◽  
Vol 7 (S2) ◽  
pp. 268-269
Author(s):  
J.C.H. Spence ◽  
U. Weierstall ◽  
J. Fries

Recent experiments with X-rays and high energy electrons have shown that image recovery from diffracted intensities is possible for non-periodic objects using iterative algorithms. Application of these methods to biological molecules raises the crucial problem of radiation damage, which may be quantified by Q = ΔE σi/σe, the amount of energy deposited by inelastic events per elastic event. Neutrons, helium atoms and low energy electrons below most ionization thresholds produce the smallest values of Q (see for TMV imaged at 60 eV). For neutrons (λ = 10-2Å, and deuterated, 15N-abelled molecules) Q is ∼3000 times smaller (∼50 times for λ = 1.8Å) than for electrons (80- 500keV) and about 4x 106 times smaller than for soft X-rays (1.5Å). Since σe for neutrons is about 105 times smaller than for electrons (and about 10 times smaller than for soft X-rays), a 105 times higher neutron dose is required to obtain the same S/N in a phase contrast image compared with electrons, if other noise sources are absent.


2011 ◽  
Vol 175 (2) ◽  
pp. 240-246 ◽  
Author(s):  
Yeunsoo Park ◽  
Zejun Li ◽  
Pierre Cloutier ◽  
Léon Sanche ◽  
J. Richard Wagner

2010 ◽  
Vol 22 (8) ◽  
pp. 084006 ◽  
Author(s):  
Mahesh Rajappan ◽  
Lin L Zhu ◽  
Jizhou Wang ◽  
Graeme Gardner ◽  
Kevin Bu ◽  
...  

2004 ◽  
Vol 93 (1) ◽  
Author(s):  
R. Cimino ◽  
I. R. Collins ◽  
M. A. Furman ◽  
M. Pivi ◽  
F. Ruggiero ◽  
...  

2021 ◽  
Vol 22 (16) ◽  
pp. 8984
Author(s):  
Maicol Cipriani ◽  
Styrmir Svavarsson ◽  
Filipe Ferreira da Silva ◽  
Hang Lu ◽  
Lisa McElwee-White ◽  
...  

Platinum coordination complexes have found wide applications as chemotherapeutic anticancer drugs in synchronous combination with radiation (chemoradiation) as well as precursors in focused electron beam induced deposition (FEBID) for nano-scale fabrication. In both applications, low-energy electrons (LEE) play an important role with regard to the fragmentation pathways. In the former case, the high-energy radiation applied creates an abundance of reactive photo- and secondary electrons that determine the reaction paths of the respective radiation sensitizers. In the latter case, low-energy secondary electrons determine the deposition chemistry. In this contribution, we present a combined experimental and theoretical study on the role of LEE interactions in the fragmentation of the Pt(II) coordination compound cis-PtBr2(CO)2. We discuss our results in conjunction with the widely used cancer therapeutic Pt(II) coordination compound cis-Pt(NH3)2Cl2 (cisplatin) and the carbonyl analog Pt(CO)2Cl2, and we show that efficient CO loss through dissociative electron attachment dominates the reactivity of these carbonyl complexes with low-energy electrons, while halogen loss through DEA dominates the reactivity of cis-Pt(NH3)2Cl2.


2020 ◽  
Vol 65 (4) ◽  
pp. 045007 ◽  
Author(s):  
Stefanos Margis ◽  
Maria Magouni ◽  
Ioanna Kyriakou ◽  
Alexandros G Georgakilas ◽  
Sebastien Incerti ◽  
...  

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