Gerth K
Anal Biochem. 1985 Feb 1;144(2):432-5. doi: 10.1016/0003-2697(85)90137-x.
The method described comprises the transformation of ammonium into ammonia, the rapid and gentle liberation of the ammonia followed by the measurement of the nitrogen in a Dohrmann nitrogen analyzer. Untreated biological samples (1-50 microliters) were pipetted onto magnesium oxide tablets at 130 degrees C and the ammonia liberated was transferred by a continuous stream of nitrogen carrier gas into the nitrogen analyzer. There the ammonia was determined by oxidative pyrolysis and subsequent chemiluminescence measurement of the excited NO2. The result could be read in nanograms ammonia nitrogen within 6.5 min. Apart from volatile amines, which are usually negligible in biological samples, the method was specific for ammonia because under the given conditions of volatilization the labile groups of glutamine and asparagine did not interfere. The assay was sensitive in the range of 1.5-150 nmol ammonia and suitable for the routine analysis of small samples.
所述方法包括将铵转化为氨,快速温和地释放氨,然后在杜尔曼氮分析仪中测定氮。将未处理的生物样品(1 - 50微升)移液到130℃的氧化镁片剂上,释放出的氨通过连续的氮载气气流转移到氮分析仪中。在那里,通过氧化热解和随后对激发态NO2的化学发光测量来测定氨。结果可在6.5分钟内以纳克氨氮读出。除了挥发性胺类(在生物样品中通常可忽略不计)外,该方法对氨具有特异性,因为在给定的挥发条件下,谷氨酰胺和天冬酰胺的不稳定基团不会产生干扰。该测定法在1.5 - 150纳摩尔氨的范围内敏感,适用于小样品的常规分析。