摘要
木犀草素在0.04mol/L B~R(pH4.00)缓冲溶液中于+0.478V(vs.SCE)和+0.450V(vs.SCE)有一对氧化还原峰。当向该溶液中加入DNA分子后,通过比较电化学参数转移系数α和表观电子传递速率常数κs的变化,可知木犀草素嵌入DNA碱基对间形成了非电活性的超分子化合物从而使得峰电位正移,峰电流下降;通过二者的紫外吸收光谱对其嵌入作用进行了验证。研究发现木犀草素的氧化峰电流,Ipa与DNA质量浓度在2~12mg/L的范围内基本呈线性关系,线性回归方程为Ipa(10^-5 A)=8.68—0.322ρDNA(mg/L),相关系数r为0.989;建立了定量检测DNA的方法。并求得木犀草素和DNA嵌入作用的结合常数β=3.02×10^11,结合数m=2。
A pair of voltmmetric peaks for the redox reaction of luteolin in the B - R buffer solution was found with the anodic peak potential of + 0. 478 V (vs. SCE ) and the cathodic peak potential of +0. 450 V(vs. SCE). After the addition of DNA, the peak current decreased due to the intercalation of luteolin with DNA by forming an electrochemical inactive supramolecular complex DNA - 2Lu. The electrochemical parameters such as charge coefficient α and standard electron transfer rate constant κs in the absence and presence of DNA were estimated. The combination number m of the interaction of 2 and the combine constant β of 3.02 × 10H were also calculated, and the results were confirmed by ultraviolet -visible spectra. The oxidation peak current showed a linear relationship with the DNA concentration in the range of 2 -12 mg/L, and the linear regression equation was Ipa (10^-5 A) = 8.68 - 0. 322ρDNA (mg/L) with the correlation coefficient of 0. 989. Based on this, a new voltammetric method for the determination of DNA was established.
出处
《分析测试学报》
CAS
CSCD
北大核心
2008年第1期79-83,共5页
Journal of Instrumental Analysis
基金
河南省创新人才基金资助项目(0421002300)
河南省杰出人才基金资助项目(0512001400)