Prencipe L, Fossati P, Vanzetti G
Quad Sclavo Diagn. 1978 Sep;15(3):382-94.
We describe a direct colorimetric method for the enzymatic assay of uric acid. 50 microliters serum aliquots are incubated for 30 min with a diluted hexacyanoferrate solution, to remove interference by non-specific reducing agents. Uric acid is then oxidized to allantoin in the presence of uricase (Aspergillus flavus), with the simultaneous production of hydrogen peroxide; this is measured by a modified Emerson-Trinder reaction, in which phenol has been replaced by sulphonated 2,4-dichlorophenol, a more sensitive chromogen. The method gives linear results up to 20 mg of uric acid/100 ml.
我们描述了一种用于尿酸酶法测定的直接比色法。取50微升血清等分试样,与稀释的高铁氰化物溶液孵育30分钟,以消除非特异性还原剂的干扰。然后在尿酸酶(黄曲霉)存在的情况下,尿酸被氧化为尿囊素,同时产生过氧化氢;通过改良的Emerson-Trinder反应测定过氧化氢,其中苯酚已被磺化的2,4-二氯苯酚取代,后者是一种更灵敏的显色剂。该方法在尿酸含量高达20mg/100ml时给出线性结果。