Photosensitized oxidation of hypoxanthine and xanthine by aluminum phthalocyanine tetrasulfonate. Role of the alkylating quinone 2,5-dichloro-diaziridinyl-1,4-benzoquinone.
Photosensitized oxidation of hypoxanthine and xanthine by aluminum phthalocyanine tetrasulfonate. Role of the alkylating quinone 2,5-dichloro-diaziridinyl-1,4-benzoquinone.
复制标题
酞菁四磺酸铝光敏氧化次黄嘌呤和黄嘌呤。
DOI:
10.1111/j.1751-1097.2008.00389.x
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发表时间:
2008
影响因子:
3.3
通讯作者:
Kumar,Ajay
中科院分区:
文献类型:
--
作者:
Alegria,AntonioE;Inostroza,Yaritza;Kumar,Ajay
Photoirradiation of nitrogen‐saturated aqueous solutions containing aluminum phthalocyanine tetrasulfonate (AlPcS4) at 675 nm in the presence of 2,5‐dichloro‐diaziridinyl‐1,4‐benzoquinone (AZDClQ) and hypoxanthine (HX) produces the oxidized HX derivatives, xanthine (X) and uric acid (UA). Concentrations of the AZDClQ semiquinone, X and UA increase at the expense of HX with an increase in irradiation time. Almost negligible decomposition of HX, as well as very low amounts of X, are detected if photolysis occurs under identical conditions but in the absence of AZDClQ. Addition of calf‐thymus DNA produces quinone‐DNA covalent adducts after photolysis of anaerobic samples containing quinone, DNA and AlPcS4, in the presence or absence of HX and at pH 5.5. However, larger amounts of quinone‐DNA adducts are detected if HX is present. The results presented here could have applications in the photodynamic treatment of hypoxic tissues such as solid tumors, under conditions of high HX concentration, where Type‐I pathways could be more important than singlet oxygen generation.