Ullmann U, Kühne F W
Infection. 1984 May-Jun;12(3):225-9. doi: 10.1007/BF01640911.
The first non-metallic oxygen carrier, tetrachlorodecaoxide (TCDO), showed in vitro antibacterial activity among aerobic and anaerobic bacteria. The lethal dose for Escherichia coli, for example, was 150 micrograms/ml whereas 15 micrograms/ml reduced the bacterial amount after a latent period of two hours, but regrowth started after four hours. The bactericidal effect of TCDO, however, was dose-dependent and species-specific. This suggests that some aerobic bacterial species might not be able to produce sufficient amounts of protecting enzymes like catalase or superoxide dismutase. The computer controlled measurement of chemiluminescence was used as a model for the phagocytic activity. With isolated human granulocytes and opsonized zymosan as antigen no increase in peak counts per minute was observed compared with controls without TCDO. However, with human whole blood, positive effects were seen using TCDO together with zymosan as well as specific and non-specific opsonized Klebsiella pneumoniae K 17. It seems that whole blood possesses additional, but as yet unknown biocatalysers to split TCDO into oxygen and chloride.
首个非金属氧载体——十氧化四氯(TCDO),在需氧菌和厌氧菌中均展现出体外抗菌活性。例如,大肠杆菌的致死剂量为150微克/毫升,而15微克/毫升在两小时的潜伏期后可减少细菌数量,但四小时后细菌又开始重新生长。然而,TCDO的杀菌效果具有剂量依赖性和物种特异性。这表明一些需氧细菌物种可能无法产生足够量的如过氧化氢酶或超氧化物歧化酶等保护酶。化学发光的计算机控制测量被用作吞噬活性的模型。以分离的人粒细胞和经调理的酵母聚糖作为抗原,与未添加TCDO的对照组相比,每分钟的峰值计数未见增加。然而,对于人全血,使用TCDO与酵母聚糖以及特异性和非特异性调理的肺炎克雷伯菌K17一起时可观察到积极效果。似乎全血拥有额外的但尚未知晓的生物催化剂,可将TCDO分解为氧气和氯化物。