Numerical characterization of a tomographic system for online dose measurements in Boron Neutron Capture Therapy

2007 ◽  
Author(s):  
D. M. Minsky ◽  
A. A. Valda ◽  
A. A. Burlon ◽  
A. J. Kreiner ◽  
H. Somacal
2005 ◽  
Vol 32 (12) ◽  
pp. 3729-3736 ◽  
Author(s):  
P. J. Binns ◽  
K. J. Riley ◽  
O. K. Harling ◽  
W. S. Kiger ◽  
P. M. Munck af Rosenschöld ◽  
...  

2010 ◽  
Author(s):  
Alejandro A. Burlon ◽  
Santiago Girola ◽  
Alejandro A. Valda ◽  
Daniel M. Minsky ◽  
Andrés J. Kreiner ◽  
...  

2008 ◽  
Vol 6 (2) ◽  
pp. 154-160
Author(s):  
Afaf Genady ◽  
Mohamed El-Zaria ◽  
Detlef Gabel

AbstractDerivatives of purine, adenine, guanine, and 2,6-diaminopurine linked to the azanonaborane (B8N cluster) have been prepared, for possible use as powerful agents for boron neutron capture therapy (BNCT). The synthesis was carried out via a ligand exchange reaction. The exo-NH2R group of the azanonaborane of the type [(RH2N)B8H11NHR] can be exchanged by one hetero-nitrogen atom of the pyrimidine ring, and except for guanine, also by an N atom of the imidazole ring. The identity of the products was confirmed by NMR, elemental analysis, IR, and mass spectrometry. No reaction was found to occur with caffeine and theophylline under the same reaction conditions.


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