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选择性multitest Coulter达可3.0分析器是评估的指南这场德Instrumentacion de la皇家社会诺拉德Quimica我们和欧洲委员会临床实验室的标准。评价四个步骤进行:分析单位的检查;日常工作的评价;研究的干扰;和评估的实用性。评估包括光度研究。不接受340 nm和420 nm,和不精确的吸光度从0.05到2.00范围从0.06到0.28%在340海里,从0.06到0.08%在420海里。线性显示一些分散在低吸光度PNP型在420 nm和漂移是微不足道的。不精确的吸管输送系统,温度控制系统和清洗系统是令人满意的。在日常工作的情况下,7个分析方法进行了研究:葡萄糖,肌酐,铁、总蛋白质,AST,高山和钙。Within-run不精确范围,在低浓度从0.9% (CV)葡萄糖,为铁7.6%(简历); at medium concentrations, from 0.7% (CV) for total protein to 5.2% (CV) to creatinine; and at high concentrations, it ranged from 0.6% (CV) for glucose to 3.9% (CV) for ALP.Between-run imprecision at low concentrations ranged from 1.4% (CV) for glucose to 15.1% (CV) for iron; at medium concentrations it ranged from 1.2% (CV) for protein to 6.7% (CV) for iron; and at high concentrations the range is from l.2for AST to 5.7% (CV) for iron.No contamination was found in the sample carry-over study. Some contamination was found in the reagent carry-over study (total protein due to iron and calcium reagents). Relative inaccuracy is good for all the constituents assayed. Only LDH (high and low levels) and urate (low level) showed weak and negative interference caused by turbidity, and γ-GT (high level) and amylase, bilirubin and ALP (two levels) showed a negative interference caused by haemolysis.