DETERMINATION OF SPECIFIC PROTEINS BY THE FIA PRINCIPLE

被引:16
作者
ANDERSEN, I [1 ]
机构
[1] KOMMUNE HOSP COPENHAGEN,DEPT CLIN CHEM,DK-2730 HERLEV,DENMARK
来源
JOURNAL OF AUTOMATIC CHEMISTRY | 1990年 / 12卷 / 02期
关键词
D O I
10.1155/S1463924690000074
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The following analytes have been investigated: urine albumin (u-albumin), plasma-transferrin (p-transferrin), p-haptoglobin, p-IgG, p-IgA, p-IgM, and p-orosomucoid. An unmodified commercial analytical system FIA Star (Tecator) with a two-channel injector (40 μl) was used. The prediluted plasma samples and antibodies are allowed to react for 33 s before the change in turbidity is measured as apeak maximum at 405 nm. The optimal concentrations of calibrators and antibodies have been determined to secure antibody excess. Response time (i.e. delay between aspiration of a sample and presentation of the result in absorption units) is 75 s. Automatic print-out of the absorbance profile and movement of the sample rack further accounted for 21 s per sample, so the throughput is reduced to 75 determinations per 2 h. Results are available within an hour, compared to two-12 days with the present methods (electroimmunoassays). Parallel analyses with established methods/analysers show excellent agreement for u-albumin, p-transferrin and p-haptoglobin. For p-IgG, p-lgA and p-IgM the reaction time of 33 s is insufficient because their relative molecular masses (i.e. the size of the molecules) are so high, 150 000–971 000. Five minutes is a more adequate reaction time, which makes a serial analyser such as FIA Star unsuitable for larger workloads of samples of immunoglobulins. The plasma concentration of Orosomucoid is low, resulting in high sample blanks. It is therefore recommended that the reaction is followed kinetically if a serial analyser is used. © 1990, Taylor & Francis Ltd.
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页码:53 / 59
页数:7
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