TY - JOUR
T1 - Carboranyl-porphyrazines and derivatives for boron neutron capture therapy
T2 - From synthesis to in vitro tests
AU - Pietrangeli, Daniela
AU - Rosa, Angela
AU - Ristori, Sandra
AU - Salvati, Anna
AU - Altieri, Saverio
AU - Ricciardi, Giampaolo
PY - 2013/8
Y1 - 2013/8
N2 - The recent advances in the synthesis of highly boronated porphyrazines and tetrabenzoporphyrazines (phthalocyanines) are reviewed, together with an analysis of their relevant physical and chemical properties. It is also shown how liposomes of variable lipid formulation and polarity can be efficiently loaded with carboranyl-porphyrazines, opening a perspective to the use of these supramolecular adducts as boron carriers for application in boron neutron capture therapy (BNCT). In particular, the remarkable chemical and structural stability of the loaded liposomal vectors, evaluated through state-of-art physicochemical techniques, suggests that the carboranyl-porphyrazine/liposome adducts can effectively and selectively enter the membrane of cancerous cells. This has been explicitly checked by in vitro tests on model colon carcinoma cell cultures, showing that carboranyl-porphyrazines are incorporated in the cancerous cells at a high ratio, especially if liposome carriers with a cationic formulation are used. This behavior, together with the observed very low toxicity, makes polycarboranyl-porphyrazines suited for application in BNCT. (c) 2013 Elsevier B.V. All rights reserved.
AB - The recent advances in the synthesis of highly boronated porphyrazines and tetrabenzoporphyrazines (phthalocyanines) are reviewed, together with an analysis of their relevant physical and chemical properties. It is also shown how liposomes of variable lipid formulation and polarity can be efficiently loaded with carboranyl-porphyrazines, opening a perspective to the use of these supramolecular adducts as boron carriers for application in boron neutron capture therapy (BNCT). In particular, the remarkable chemical and structural stability of the loaded liposomal vectors, evaluated through state-of-art physicochemical techniques, suggests that the carboranyl-porphyrazine/liposome adducts can effectively and selectively enter the membrane of cancerous cells. This has been explicitly checked by in vitro tests on model colon carcinoma cell cultures, showing that carboranyl-porphyrazines are incorporated in the cancerous cells at a high ratio, especially if liposome carriers with a cationic formulation are used. This behavior, together with the observed very low toxicity, makes polycarboranyl-porphyrazines suited for application in BNCT. (c) 2013 Elsevier B.V. All rights reserved.
KW - Carboranyl-porphyrazines
KW - BNCT
KW - Carboranyl-phthalocyanines
KW - Liposomes
KW - SANS
KW - SAXS
KW - APPENDED PYRIDINE RINGS
KW - METAL-ION BINDING
KW - PHOTODYNAMIC THERAPY
KW - GENE DELIVERY
KW - PHOTOTHERMAL SENSITIZATION
KW - PHOTOPHYSICAL PROPERTIES
KW - UNILAMELLAR LIPOSOMES
KW - CATIONIC LIPOSOMES
KW - DRUG-DELIVERY
KW - PALLADIUM(II) COMPLEX
U2 - 10.1016/j.ccr.2013.03.035
DO - 10.1016/j.ccr.2013.03.035
M3 - Review article
SN - 0010-8545
VL - 257
SP - 2213
EP - 2231
JO - Coordination Chemistry Reviews
JF - Coordination Chemistry Reviews
IS - 15-16
ER -