Peter F, Strunc G
Clin Chem. 1984 Jun;30(6):893-5.
In this method for quantitative determination of mercury in blood, urine, and hair, the specimen is first digested in a mixture of solid potassium permanganate and concentrated sulfuric acid. Excess oxidizing agent is reduced by hydroxylamine hydrochloride. The mercury liberated with stannous chloride is quantified by measuring its absorbance at 254 nm. This method shortens digestion time considerably and ensures accurate and reproducible results. Reagents must be free of mercury contamination; every new lot must be checked before use. This system can reliably accommodate as many as 30 specimens per hour and is suitable for use in laboratories that analyze a large number of biological specimens for total mercury.
在这种用于定量测定血液、尿液和毛发中汞含量的方法中,首先将样品在固体高锰酸钾和浓硫酸的混合物中进行消化。过量的氧化剂用盐酸羟胺还原。用氯化亚锡释放出的汞通过测量其在254nm处的吸光度进行定量。该方法大大缩短了消化时间,并确保了结果的准确和可重复性。试剂必须无汞污染;每一批新试剂在使用前都必须进行检查。该系统每小时可可靠地处理多达30个样品,适用于对大量生物样品进行总汞分析的实验室。