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出 处:《中国卫生检验杂志》2008年第9期1838-1841,共4页Chinese Journal of Health Laboratory Technology
摘 要:目的:建立精确有效、简便快速的同位素标记法用于实验室移液器容量的比对与校准,实现移液器准确度与精确度的有效监控。方法:以125I标记溶液为示踪材料,以放射性γ计数仪为设备,以测定CPM值为观察指标,用已通过重量分析法检定的移液器为标准,其他待检移液器容量通过放射性同位素溶液吸样测定CPM与之比较进行方法学评价。结果:放射性同位素法检测批内精密度在0.88%~1.08%之间;平均回收率98.83%;CPM值与125I浓度梯度及容量之间关系的回归方程分别为:Y=23879X-388.4(r2=0.9992)和Y=572.18X-175.83(r2=0.9994)呈正相关;标准移液器与待检移液器的容量平行试验结果良好。结论:放射性同位素125I标记进行移液器容量比对与校准技术,方法灵敏、精确、简便,可适用于临床实验室。Objective:To establish the sensitivity,efficiency,convenient,and rapid radioisotopic iodine-125-labeled method for volumes checking and calibration,which monitoring the accuracy and precision for the contains of pipettes.Methods:We employs an ^125I solution and experiment instrument for evaluation the new method.The delivery volume of one pipette is checked by gravimetric analysis.Than the remaining anticipate pipettes are compared by dispensing ^125I solution.Measuring the counts per minute(CPM) and calculate the mean,SD and CV% to ensure that the accuracy and precision were within or outside the acceptable range.Results:The inter-assay imprecision were 0.88%-1.08%.The average rate of spiking recovery was 98.83%.The regression equation for a linear curve between CPM and gradient dilution concentrations of ^125I or volumes were:Y=23879X-388.4(r^2=0.9992)and Y=572.18X-175.83(r^2=0.9994)revealed positively correlated.Paralleled comparative analysis of the certified pipette and the anticipate pipettes were performed good.Conclusion:We presented a novel radioactive ^125I-labeled methodology,which combines highly sensitivity,accuracy,simplicity.This approach could be used for clinical laboratory.
关 键 词:移液器 容量 比对与校准 放射性同位素法125碘标记 每分钟脉冲数计数
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