M. Cemazar et al., Changed delivery of boron to tumours using electroporation for boron neutron capture therapy with BSH, BR J RADIOL, 73(866), 2000, pp. 195-200
Citations number
23
Categorie Soggetti
Radiology ,Nuclear Medicine & Imaging","Medical Research Diagnosis & Treatment
For effective boron neutron capture therapy (BNCT) it is important that a s
ufficient concentration of boron (B-10) is present in the tumour during irr
adiation. This requirement represents a specific problem. The aim of this s
tudy was to test whether electroporation can be used as a non-specific drug
delivery system to increase the delivery of sodium borocaptate-B-10 (BSH)
into MCF7 (breast carcinoma) and B16F1 (melanoma) tumour cells in vitro and
in B16F1 tumours in vivo. For the in vitro determination of B-10 uptake, t
he cells were incubated in medium containing BSH and exposed to electric pu
lses. Boron levels were determined by inductively coupled plasma atomic emi
ssion spectrometry. In vivo, tumours were exposed to electric pulses 3 min
after intravenous BSH injection. At different times after exposure the B-10
concentration was determined in tumours and in blood. A difference in the
B-10 accumulation in the two cell lines was observed after continuous incub
ation of cells with BSH. No accumulation of B-10 was observed in MCF7 cells
, whereas in B16F1 cells,B-10 accumulated well and reached a plateau within
30 min. Electroporation of these cells resulted in an accumulation of B-10
into MCF7 cells up to the level of B-10 in B16F1 cells. In vivo, the appli
cation of electric pulses increased and prolonged the entrapment of B-10 (B
SH) in the B16F1 melanoma tumours. A sufficient concentration of B-10 was p
resent in the tumour exposed to electric pulses for up to 24 h. Boron was q
uickly washed out from the blood and the level was below the concentrations
in the tumours exposed to electric pulses at 2 h. The results of this stud
y show that electroporation may provide a tool to increase boron concentrat
ion in the cells that have impaired transport of BSH through the plasma mem
brane. Furthermore, prolonged entrapment of BSH in tumours in vivo may, in
addition to electroporation, be caused by the modifying effect of electric
pulses on blood flow.