Mo(Ⅵ)-邻硝基苯基荧光酮配合物光谱探针测定蛋白质  被引量:2

Determination of micro amount of protein with o-Nitrophenylfluorone-Molybdenum(Ⅵ) as a spectroscopic probe

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作  者:周兴军[1] 敖登高娃[1] 黄臻臻[1] 

机构地区:[1]内蒙古大学化学化工学院,呼和浩特010021

出  处:《分析试验室》2007年第8期25-28,共4页Chinese Journal of Analysis Laboratory

基  金:内蒙古教育厅基金(NJ05040)项目资助

摘  要:研究了Mo(Ⅵ)-邻硝基苯基荧光酮(o-NPF)配合物与蛋白质的相互作用及光谱性质。提出了以Mo(Ⅵ)-邻硝基苯基荧光酮配合物作为光谱探针测定微量蛋白质的方法。结果表明,在pH为2.2的HAc-NaAc缓冲介质中,乳化剂OP存在下,o-NPF-Mo(Ⅵ)在40℃加热10 min后与蛋白质形成稳定的复合物,最大吸收波长红移至587 nm。蛋白质质量浓度在0-10 mg/L范围内符合比尔定律,复合物的表观摩尔吸光系数为3.53×10^6L·mol^-1·cm^-1。该方法具有很高的灵敏度和选择性,可直接用于人尿、新生牛血清中蛋白质的测定,回收率分别为93%和99%。The interaction and spectral charactenstics of o-Nitmphenylfluomne-Molybdenum( Ⅵ ) and protein was studied. A novel method for the determination of protein using o-NPF-Mo( Ⅵ ) complex as a spectroscopic probe was developed. In the buffer medium of HCl-NaAc at pH 2.2 and in the presence of p-octylpolyethylenther(OP), o-NPF-Mo ( Ⅵ) complex combines protein at 40 ℃ for 10 min to form a stable compound, which results in change of absorption spectrum of o-NPF-Mo( Ⅵ ) complex and increase of the absorption peak value at 587 nm. Beer's law was obeyed in the range of 0 - 10 mg/L for protein. The molar absorptivity of the complex at 587 nm was 3.53 - 10^6 L/(mol·cm). The method has high sensitivity as well as high selectivity. It could be used to determine protein in human urine, binvine serum and the recoveries were between 93 % and 99%.

关 键 词:蛋白质 Mo(Ⅵ)-邻硝基苯基荧光酮 光谱探针 

分 类 号:O657.39[理学—分析化学]

 

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