详细信息
A novel urinary oxalate determination method via a catalase model compound with oxalate oxidase ( SCI-EXPANDED收录)
文献类型:期刊文献
英文题名:A novel urinary oxalate determination method via a catalase model compound with oxalate oxidase
作者:Zuo, Guanke[2];Jiang, Xiaojun[2];Liu, Hui[2];Zhang, Jingyan[1,2]
机构:[1]E China Univ Sci & Technol, State Key Lab Bioreactor Engn, Shanghai 200237, Peoples R China;[2]E China Univ Sci & Technol, Sch Pharm, Dept Pharmaceut Sci, Shanghai 200237, Peoples R China
年份:2010
卷号:2
期号:3
起止页码:254
外文期刊名:ANALYTICAL METHODS
收录:;WOS:【SCI-EXPANDED(收录号:WOS:000276805900007)】;
基金:The authors gratefully acknowledge the National Science Foundation (No 20671034) and Shanghai Pujiang Scholarship Program (No 06PJ14030) for financial support
语种:英文
摘要:This work describes a novel method of urinary oxalate determination based on a catalase model compound MnL(H2O)(2)(ClO4)(2) (L = bis(2-pyridylmethyl)ammo)propionic acid) Urinary oxalate is first decomposed by the oxalate oxidase into carbon dioxide and hydrogen peroxide. The later is then disproportionated into water and oxygen by the catalase model compound forming a color compound, which can be spectrophotometrically monitored The oxalate concentration of the sample is quantified according to the UV-vis absorbance of the formed color compound This model compound method maintains the specificity and sensitivity of the conventional enzymatic assay It has several advantages over the traditional enzymatic method, including low cost, simplicity, large linear range, and adjustable assay time The model compound method showed a very good linearity in the range of 0 002-20 mmol L-1 oxalate, with a detection limit of 2 mu mol L-1 oxalate The mean urinary oxalate determined by this method was 28.6 mu g mL (1), standard deviation (SD) was 1 07 mu g mL(-1), and variation coefficient (CV) is less than 4% The results are consistent with that acquired from the enzymatic and HPLC methods The model compound method also showed that the model compounds of the corresponding enzymes can be an alternative to the enzymes, thus the cost of the methods or assays using the enzymes can be greatly decreased
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