Masiá F, Alumá A, Biosca C, Easamajó M T, Antoja F, Galimany R
Servei d'Anàlisis Clíniques Hospital Universitari 'Germans Trias Pujol' Carretera de Canyet Badalona s/n 08916 Spain.
J Automat Chem. 1993;15(4):127-32. doi: 10.1155/S1463924693000161.
This paper reports an evaluation of the IL-Phoenix Chemistry/Electrolyte Analyser; the evaluation was carried out in accordance with internationally recognized guidelines. The evaluation was performed in three steps: evaluation in routine conditions; assessment of interferences; and study of practicability. Seven constituents were studied under routine working conditions. Within-run imprecision rangedfrom 0.6% (CV) for chloride to 3.1% (CV) for glucose. Between-run imprecision ranged from 0.9% for sodium to 6.0% (CV) for urea. Sample-related carryover was not significant. The relative inaccuracy was acceptable; drift was negligible; linearity was agreed with the range showed by the supplier. Haemoglobin produced negative interferences with sodium and chloride. Turbidity interfered negatively with sodium, chloride, potassium and total calcium, andpositively with glucose. Bilirubin showed a negative interference with sodium, chloride and creatinine.
本文报道了对IL-菲尼克斯化学/电解质分析仪的评估;该评估是按照国际认可的指南进行的。评估分三个步骤进行:常规条件下的评估;干扰评估;实用性研究。在常规工作条件下对七种成分进行了研究。批内不精密度范围为:氯化物为0.6%(变异系数),葡萄糖为3.1%(变异系数)。批间不精密度范围为:钠为0.9%,尿素为6.0%(变异系数)。与样品相关的残留不显著。相对误差可接受;漂移可忽略不计;线性符合供应商给出的范围。血红蛋白对钠和氯化物产生负干扰。浊度对钠、氯化物、钾和总钙产生负干扰,对葡萄糖产生正干扰。胆红素对钠、氯化物和肌酐表现出负干扰。