TY - JOUR
T1 - Hyperthermic sensitization by the radical initiator 2,2'azobis (2-amidinopropane) dihydrochloride (AAPH). I. In vitro studies
AU - Krishna, M. C.
AU - Dewhirst, M. W.
AU - Friedman, H. S.
AU - Cook, J. A.
AU - Degraff, W.
AU - Samuni, A.
AU - Russo, A.
AU - Mitchell, J. B.
PY - 1994
Y1 - 1994
N2 - AAPH (2,2'azobis-(2-amidinopropane dihydrochloride)) is a water-soluble, heat-labile azo compound which undergoes thermal decomposition to produce carbon-centred free radicals. These carbon-centred radicals might be directly cytotoxic or may react with oxygen to produce potentially cytotoxic alkoxyl and peroxyl radicals. The rate of free radical production as a result of AAPH thermal decomposition increases with increasing temperature. We have evaluated the efficacy of AAPH as a heat sensitizer for Chinese hamster V79 cells by the clonogenic assay. AAPH (50 mM) was not cytotoxic to V79 cells at 37°C for exposures up to 3 h. In contrast, AAPH (50 mM) was found to markedly sensitize cells exposed to 42, 43 and 45°C. For a 75 min exposure to 42°C alone, cell survival was reduced to 9×10-1; however, a 75 min exposure at 42°C + AAPH resulted in survival of 5.5×10-4. For 43 and 45.5°C heating, cell survival was potentiated by AAPH at the 1% survival level by 4.1 and 1.4-fold, respectively. AAPH was also found to sensitize both hypoxic cells and thermotolerant cells. These findings would encourage in vivo evaluation of AAPH (or analogues) as a temperature-dependent heat sensitizer. AAPH represents a new class of heat sensitizers which may have use in unravelling the mechanism(s) of heat killing and may have utility in local hyperthermia treatment.
AB - AAPH (2,2'azobis-(2-amidinopropane dihydrochloride)) is a water-soluble, heat-labile azo compound which undergoes thermal decomposition to produce carbon-centred free radicals. These carbon-centred radicals might be directly cytotoxic or may react with oxygen to produce potentially cytotoxic alkoxyl and peroxyl radicals. The rate of free radical production as a result of AAPH thermal decomposition increases with increasing temperature. We have evaluated the efficacy of AAPH as a heat sensitizer for Chinese hamster V79 cells by the clonogenic assay. AAPH (50 mM) was not cytotoxic to V79 cells at 37°C for exposures up to 3 h. In contrast, AAPH (50 mM) was found to markedly sensitize cells exposed to 42, 43 and 45°C. For a 75 min exposure to 42°C alone, cell survival was reduced to 9×10-1; however, a 75 min exposure at 42°C + AAPH resulted in survival of 5.5×10-4. For 43 and 45.5°C heating, cell survival was potentiated by AAPH at the 1% survival level by 4.1 and 1.4-fold, respectively. AAPH was also found to sensitize both hypoxic cells and thermotolerant cells. These findings would encourage in vivo evaluation of AAPH (or analogues) as a temperature-dependent heat sensitizer. AAPH represents a new class of heat sensitizers which may have use in unravelling the mechanism(s) of heat killing and may have utility in local hyperthermia treatment.
UR - http://www.scopus.com/inward/record.url?scp=0028331459&partnerID=8YFLogxK
U2 - 10.3109/02656739409009348
DO - 10.3109/02656739409009348
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C2 - 8064185
AN - SCOPUS:0028331459
SN - 0265-6736
VL - 10
SP - 271
EP - 281
JO - International Journal of Hyperthermia
JF - International Journal of Hyperthermia
IS - 2
ER -