Carlson M, Thompson R D
US Food and Drug Administration, Minneapolis, MN 55401, USA.
J AOAC Int. 2001 May-Jun;84(3):782-8.
A liquid chromatographic (LC) method was developed for the determination of allantoin, uric acid, and indoxyl sulfate in mammalian urine contaminated packaging material including paper bagging, corrugated cardboard, grayboard, and burlap bagging. The procedure involves solvent extraction and isolation of the 3 analytes by reversed-phase LC with ultraviolet detection at 225 nm for allantoin and 286 nm for uric acid and indoxyl sulfate. The composition of authentic mammalian urine such as mouse, rat, cat, dog, and human were also determined with regard to the 3 compounds of interest. A linear concentration range of 0.11-20.4, 0.02-10.0, and 0.04-30.0 microg/mL was obtained for allantoin, uric acid, and indoxyl sulfate, respectively. Limits of detection (LOD) and quantitation (LOQ) were 0.0104 and 0.0345 microg/mL for allantoin; 0.0018 and 0.0060 microg/mL for uric acid; and 0.0049 and 0.0165 microg/mL for indoxyl sulfate, respectively. Interday relative standard deviation values for a mixture of standard allantoin, uric acid, and indoxyl sulfate (n = 5) were 0.97, 0.80, and 0.94%, respectively. Analyte composition for 5 types of authentic mammalian urine varied from 0.19-6.88 mg/mL allantoin; 0.08-0.57 mg/mL uric acid; and 0.03-0.78 mg/mL indoxyl sulfate. Analyte content for 8 samples including 2 samples each for paper, cardboard, grayboard, and burlap bagging each contaminated with mouse or rat urine ranged from <LOD to 4,598 microg/gm allantoin; <LOD to 202 microg/gm uric acid; and 17.5 to 616 microg/gm indoxyl sulfate. Recoveries of allantoin, uric acid, and indoxyl sulfate from 11 fortified samples (4 types) for both mouse and rat urine ranged from 28.2 to 114.1 % for allantoin; 32.6 to 123.4% for uric acid; and 52.6 to 118.2% for indoxyl sulfate.
建立了一种液相色谱(LC)方法,用于测定受哺乳动物尿液污染的包装材料(包括纸袋、瓦楞纸板、灰板和粗麻袋)中的尿囊素、尿酸和硫酸吲哚酚。该方法包括溶剂萃取,并通过反相液相色谱分离这3种分析物,尿囊素在225 nm处、尿酸和硫酸吲哚酚在286 nm处进行紫外检测。还测定了真实的哺乳动物尿液(如小鼠、大鼠、猫、狗和人类尿液)中这3种目标化合物的组成。尿囊素、尿酸和硫酸吲哚酚的线性浓度范围分别为0.11 - 20.4、0.02 - 10.0和0.04 - 30.0μg/mL。尿囊素的检测限(LOD)和定量限(LOQ)分别为0.0104和0.0345μg/mL;尿酸的检测限和定量限分别为0.0018和0.0060μg/mL;硫酸吲哚酚的检测限和定量限分别为0.0049和0.0165μg/mL。标准尿囊素、尿酸和硫酸吲哚酚混合物(n = 5)的日间相对标准偏差值分别为0.97%、0.80%和0.94%。5种真实哺乳动物尿液中分析物的组成分别为:尿囊素0.19 - 6.88 mg/mL;尿酸0.08 - 0.57 mg/mL;硫酸吲哚酚0.03 - 0.78 mg/mL。8个样品(包括分别被小鼠或大鼠尿液污染的纸袋、纸板、灰板和粗麻袋各2个样品)中分析物的含量范围为:尿囊素<检测限至4598μg/g;尿酸<检测限至202μg/g;硫酸吲哚酚17.5至616μg/g。11个加标样品(4种类型)中小鼠和大鼠尿液中尿囊素、尿酸和硫酸吲哚酚的回收率范围为:尿囊素28.2%至114.1%;尿酸32.6%至123.4%;硫酸吲哚酚52.6%至118.2%。