Synthesis of novel carboranylchlorins with dual application in boron neutron capture therapy (BNCT) and photodynamic therapy (PDT)
Total synthesis of carboranylchlorins 3 and 4, from readily available starting materials, are described and the molecular structures of two key intermediates are presented. Chlorins 3 and 4 show similar spectroscopic behavior but differ considerably in their solubility properties; whereas closo-carboranylchlorin 3 is completely insoluble in water, its nido derivative 4 has good water-solubility. Carboranylchlorin 3 absorbs in the red region of the optical spectrum (at λmax=642nm) six times more strongly than porphyrin 1, and displays a fluorescence emission band at λmax=651nm, upon excitation at 642nm. The water-soluble carboranylchlorin 4 also displays intense absorption and emission bands at λmax=642 and 651nm, respectively, in ethanol solution. It is concluded that carboranylchlorins 3 and 4 have higher promise for the dual application in PDT and BNCT than do comparable porphyrins. © 2004 Elsevier Ltd. All rights reserved.
Publication Source (Journal or Book title)
Applied Radiation and Isotopes
Luguya, R., Fronczek, F., Smith, K., & Vicente, M. (2004). Synthesis of novel carboranylchlorins with dual application in boron neutron capture therapy (BNCT) and photodynamic therapy (PDT). Applied Radiation and Isotopes, 61 (5), 1117-1123. https://doi.org/10.1016/j.apradiso.2004.05.068