建立了一个测定过氧亚硝基阴离子(ONOO-)化学发光的改进体系,测试了某些抗氧化剂清除ONOO-的作用,其体系的组成和启动发光的程序如下:向pH 10.5碳酸缓冲液配的0.01 mol/L浓度NaN3溶液通O3 30 s,取其800 μl原位注入含有100 μl水配样品和100 μl的0.001 mol/L鲁米诺溶液中,启动化学发光(chemiluminescence, CL),立即测定每6秒的脉冲数(CP6S),连续测定10~30次.根据实际需要,选其某一次的CL强度作为评判指标,对比抗氧化剂的活性.该发光体系灵敏、简便、且较稳定,最低可检测限为8.74 μmol/L的ONOO-量,线性范围为8.74~74.04 μmol/L.批内变异系数3.35%(n=10),批间变异系数5.52%(n=10).测得维生素C(Vit.C)、茶多酚(EGCG)、原花菁素、硫脲皆有抑制CL,即清除ONOO-的作用.
An improvement of chemiluminescent system for determination of peroxynitrite anion (ONOO-) has been made. In this system, the effect of some antioxidants for scavenging ONOO- was tested. The constitute of this system and the program of starting were followed as: The ozone (O3) was bubbled through a glass-frit into 10 ml 0.01 mol/L solution of sodium azide in CB(pH 10.5) to generate ONOO-. The 800 μl ozonized solution of azide was injected into a glass tude in situ which contains 100 μl sample and 100 μl luminol solutions to initiate chemiluminescence (CL). The pluses / 6 seconds (CP6S) were determined immediately and continually for 10~30 times. A certain CL intensity (CP6S) was chosen as evaluation index to compare the activity of antioxidants. This chemiluminescent system is sensible, simple and stable. The determination limit was 8.74 μmol/L ONOO-. The linear rang was 8.74~74.04 μmol/L ONOO-. The intra batch and inter batch variation coefficient (CV%) of the analysis were 3.35%(n=10) and 5.52%(n=10) respectively. It was tested that Vit.C, teapolyphenol, procyanidin and thiourea all have effects on scavenging ONOO-.
范小兵,沙大年,梁小凤,韩超,胡天喜.过氧亚硝基-鲁米诺化学发光体系的改进[J].生物化学与生物物理进展,2001,28(2):251-255
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