The effect of biological substrates on the ultrafast excited-state dynamics of zinc phthalocyanine tetrasulfonate in solution

被引:35
作者
Howe, L [1 ]
Zhang, JZ [1 ]
机构
[1] Univ Calif Santa Cruz, Dept Chem & Biochem, Santa Cruz, CA 95064 USA
关键词
D O I
10.1111/j.1751-1097.1998.tb05169.x
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Zinc phthalocyanine tetrasulfonate (ZnPcS4), a potential photosensitizer for photodynamic therapy (PDT), has been studied using femtosecond laser spectroscopy, The excited-state dynamics in water have been found to be fast (<80 ps) and dominated by intermolecular aggregation. Since the proposed mechanism for PDT is energy transfer from the triplet excited state of the photosensitizer to triplet O-2 creating singlet O-2, the short lifetime is expected to be unfavorable for producing singlet O-2, This leads to the suggestion that the presence of biological substrates may have an effect on the excited-state dynamics, To test this hypothesis, the lifetimes of the excited states of ZnPcS4 have been directly measured in the presence of a model membrane, n-hexadecyltrimethylammonium bromide (CTAB). The excited-state dynamics of ZnPcS4 in buffer solutions and with human serum albumin (HSA) have also been measured, The presence of HSA and CTAB increases the excited-state lifetime significantly relative to that observed in water, The longer lifetime of ZnPcS4 in CTAB (>1 ns) indicates that the micellar surface favors monomer formation, By increasing the excited-state lifetime, the surface substantially increases the photosensitizing potential of ZnPcS4.
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页码:90 / 96
页数:7
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