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火焰原子吸收光谱法同时测定尿液中钾和钠 被引量:5

Simultaneous Determination of K and Na in Urine with FAAS
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摘要 采用原子吸收光谱仪同时测定了尿液中钾和钠的含量,并确立了测定钾和钠的优惠条件。加入氯化铯可消除电离干扰,当稀释比例达到1:1000时,可以消除尿基质的干扰。钾和钠的检测限分别为0.0049mg/L和0.0040mg/L,测定范围分别为0.2-5.0mg/L和0.2-3.0mg/L,方法回收率分别为99.6%-108.7%和99.2%-101.3%,变异系数分别为0.56%-1.08%和0A1%-0.82%。结果表明该方法准确、灵敏度高、简便快速。 The simultaneous determination of potassium (K) and sodium (Na) content in urine was established using the atomic absorption spectrometer. The optimized working conditions were ascertained. In order to remove the disturbance of ionization, cesium chloride was added. The disturbance of urinary substrate could be avoided after the urines were diluted to 1:100. The detection limit of K and Na was 0.004 9 mg/L and 0.004 0 mg/L, determination range was 0.2-5.0 mg/L and 0.2-3.0 mg/L, the recovery was 99.6%-108.7% and 99.2%-101.3%, the RSD was 0.56%-1.08%, and 0.41%-0.82%, respectively. The results showed that the method was accurate, sensitive and simple.
出处 《精细化工中间体》 CAS 2008年第5期68-70,共3页 Fine Chemical Intermediates
关键词 火焰原子吸收光谱法 尿液 atomic absorption spectrometer potassium sodium urine
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  • 1彭会然,王建清,孙艳.ICP—AES法直接测定卤水中11种杂质元素[J].中国井矿盐,1995,26(3):34-36. 被引量:5
  • 2水质分析大全编写组.水质分析大全[M].重庆:科学技术文献出版社重庆分社,1989.3.
  • 3National Committee tor Clinical Laboratory Standards. Evaluation of Precision Performance of Clinical Chemistry Devices: Tentatixe Guideline[ S]. 2nd ed. Document EP5-A.Wayne, Pa, NCCLS, 1999.
  • 4National Committee for Clinical Laboratory Standards. Method Comparison and Bias Estimation Using Patient Samples: Approved Guideline [ S ]. Document EP9- A. Wayne, Pa, NCCLS, 1995.
  • 5Buttner J, Borth R, Boutwell JH, et al. ( IFCC Committee on Standards): Provisional recommendations on quality control ill Clinical: general principles and terminology [ J ]. Clin Chem, 1976, 22 (2) : 532- 539.
  • 6National Committee for Clinical Laboratory Standards. Evaluation of the Linearity of Quantitative Analytical Methods: Proposed Guideline[S]. Document EP6-P. Wayne, Pa, NCCLS, 1986.
  • 7庄俊华,黄宪章,翟培军.医学实验室质量体系文件编写指南[M].人民卫生出版社,2005.192-195.
  • 8Clinical Laboratory Improvements Amendments of 1988. Final Rule. Laboratory Requirements [ J ]. Fed Regist, 1992, 57(40) :7002-7186
  • 9Reference Samples/Reference Materials. Geel, Belgium, Institute for Reference Materials and Measurements [S]. European Commission, Joint Research enter, 1996.
  • 10Fraser CG. Biological variation in clinical chemistry an update : collated data, 1988-1991 [ J ]. Arch Pathol Lab Med, 1992,116 ( 9 ) : 916-923.

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