期刊文献+

总胆红素氧化酶法检测系统的性能评价 被引量:3

Evaluation on the performance of total bilirubin oxidase assay system performance
下载PDF
导出
摘要 目的评价氧化酶法测定血清总胆红素(TBil)的性能。方法用氧化酶法测定血清TBil,探讨氧化酶法的精密度、线性、分析灵敏度、抗干扰性和回收率,并与改良J-G法进行比较。结果 TBil的高、低浓度样本批内CV分别为0.38%、0.78%,日间CV分别为1.78%、2.73%;平均回收率为101.2%;分析灵敏度为1.23μmol/L;线性范围为1.23~574.40μmol/L;2种方法相关性良好,直线回归方程为Y=1.105X-1.11,r=0.998。血红蛋白、维生素C和脂肪乳分别为4.8 g/L、500 mg/L和5%时对氧化酶法测定血清TBil不产生干扰。结论氧化酶法具有良好的精密度、线性范围和抗干扰能力,与改良J-G法具有很好的一致性,适用于临床常规检测。 Objective To evaluate the performance of serum total bilirubin(TBil) determination by oxidase method.Methods Serum TBil was determined by oxidase method,and the method′s precision,linearity,analytical sensitivity,anti-interference ability and recovery rate were evaluated.The method was compared with the modified J-G method.Results The within-run coefficients of variation(CV) of high and low TBil concentration samples were 0.38% and 0.78% respectively.The day to day CV of high and low TBil concentration samples were 1.78% and 2.73% respectively.The average recovery rate was 101.2%.The analytical sensitivity was 1.23 μmol/L,and the linear range was from 1.23 to 574.4 μmol/L.There was a good correlation between the 2 methods,and the linear regression equation was Y = 1.105X-1.11(r=0.998).There was no interference when hemoglobin,vitamin C and fat emulsion were 4.8 g/L,500 mg/L and 5% for serum TBil oxidase.Conclusions Oxidase method has good precision,linear range and anti-interference ability and has a good consistency with the modified J-G method.It is suitable for routine clinical testing.
出处 《检验医学》 CAS 北大核心 2011年第12期811-813,共3页 Laboratory Medicine
关键词 总胆红素 氧化酶法 分析灵敏度 Total bilirubin Oxidase method Analytical sensitivity
  • 相关文献

参考文献10

  • 1叶应妩,王毓三,申子瑜主编..全国临床检验操作规程 第3版[M].南京:东南大学出版社,2006:1034.
  • 2Perry B, Doumas BT, Buffone G, et al. Measurement of total bilirubin by use of bilirubin oxidase [ J ]. Clin Chem, 1986,32(2) :329-332. 被引量:1
  • 3Doumas BT ,Eckfeldt JH. Errors in measurement of total bilirubin: a perennial problem [ J ]. Clin Chem, 1996,42(6 Pt 1 ) :845-848. 被引量:1
  • 4Jendrassik L, Grof P. Vereinfachte photometrische methoden zur bestimmung des blutbilirubins [ J ]. Biochem Ztschr, 1938,297( 1 ) :81-89. 被引量:1
  • 5National Committee for Clinical Laboratory Standands. Evaluation of the liuearity of quantitative measurement procedures : a statistical approach ; approved guideline [S]. EP6-A,NCCLS,2003. 被引量:1
  • 6冯仁丰主编..临床检验质量管理技术基础[M].上海:上海科学技术文献出版社,2007:428.
  • 7Clinical Laboratory Standands Institute. Interference testing in clinical chemistry; proposed guideline[S]. EP7-A2,CLSI,2005. 被引量:1
  • 8National Committee for Clinical Laboratory Standands. Method comparison and bias estimation using patient samples-approved guideline [ S ]. EP9-A2, NCCLS, 2002. 被引量:1
  • 9Schwertner HA. Association of smoking and low serum bilirubin antioxidant concentrations [ J ]. Atherosclerosis, 1998,136 ( 2 ) : 383-387. 被引量:1
  • 10Wu TW, Fung KP, Wu J, et al. Antioxidation of human low density lipoprotein by unconjugated and conjugated bilirubins [ J ]. Biochem Pharmacol, 1996, 51(6) : 859-862. 被引量:1

同被引文献31

  • 1王治国,李小鹏,武平原.临床检验室内质量控制数据实验室间比对[J].中华检验医学杂志,2004,27(10):701-702. 被引量:42
  • 2姜翠云,温庆祥.血清淀粉酶同工酶测定对胰腺疾病的诊断意义[J].上海医学检验杂志,1996,11(1):33-34. 被引量:3
  • 3周雷,韩继光,黄昆,黄侠春,周宗正.急性非结石性胆囊炎18例诊治分析[J].实用全科医学,2007,5(10):914-915. 被引量:4
  • 4International Standard Organization. In Vitro diagnostic medical de-vices measurement of quantities in biological samples- metrologicaltraceability of values assigned to calibrators and control materials[S].IS017511,ISC),2003. 被引量:1
  • 5Basil T. Doumas, Poon Pat Kwork-cheung,Billy W. Perry, et al.Candidate reference method for determination of total bilirubin in se-rum: development and validation [ J ]. Clinical Chemistry, 1985 ,31(11),1779-1789. 被引量:1
  • 6National Committee for Clinical Laboratory Standards. Method com-parison and bias estimation using patient samples ; approved guide-line [S ] . EP9-A2,NCCLS ,2002. 被引量:1
  • 7中华人民共和国卫生部.临床生物化学检验常规项目分析质量指标[S]. WS/T403,MoH,2012. 被引量:1
  • 8Joint Committee for Guides in Metrology. Evaluation of measurementdata- Guide to the expression of uncertainty in measurement ( GUM)[S]. JCGM 100,JCGM,2008. 被引量:1
  • 9A Focus for Analytical Chemistry in Europe/Cooperation on Interna- tional Traceability in Analytical Chemistry. Quantifying uncertainty in analytical measurement(QUAM) [ S]. Guide CG4 ,EURACHEM/ CITAC, 2000. 被引量:1
  • 10International Standard Organization. Medical laboratories- Particularrequirements for quality and competence[ S]. ISO 15189 ,ISO,2007. 被引量:1

引证文献3

二级引证文献13

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部