Guo J A, Mo P S, Li G X
National Center for Clinical Laboratory, Beijing, People's Republic of China.
Appl Biochem Biotechnol. 1990 Jan;23(1):15-24. doi: 10.1007/BF02942049.
Glucose oxidase (GOD) and Horseradish peroxidase (HRP) were covalently coupled to alkylamine controlled pore glass by means of glutaraldehyde. About 700-800 U/g of immobilized GOD and 300-400 U/g of immobilized HRP were obtained. Some factors of affecting enzyme immobilization were discussed. The immobilized enzymes were packed into a plastic tube and used in flow-injection analysis (FIA) for glucose in serum. A good linearity range was observed for this immobilized enzyme system at 20 mg/mL to 1000 mg/dL D-glucose, the recovery was 95.4-103.5%, the within-batch imprecision was 0.8-2.2%, and the between-batch imprecision was 2.2-4.2%. More than 100 samples were measured within an hour. One enzyme column with five units of immobilized GOD and HRP, applied for 50 assays/d, has been used for more than 2 mo.
葡萄糖氧化酶(GOD)和辣根过氧化物酶(HRP)通过戊二醛共价偶联到烷基胺控制孔径玻璃上。获得了约700 - 800 U/g的固定化GOD和300 - 400 U/g的固定化HRP。讨论了影响酶固定化的一些因素。将固定化酶装入塑料管中,用于血清中葡萄糖的流动注射分析(FIA)。该固定化酶系统在20 mg/mL至1000 mg/dL D - 葡萄糖范围内观察到良好的线性范围,回收率为95.4 - 103.5%,批内不精密度为0.8 - 2.2%,批间不精密度为2.2 - 4.2%。一小时内可测量100多个样品。一个含有五个单位固定化GOD和HRP的酶柱,每天用于50次测定,已使用超过2个月。