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用离子选择电极测定血浆中的氟化物:临床实验室的一种简化方法。

Fluoride determination in plasma by ion selective electrodes: a simplified method for the clinical laboratory.

作者信息

Fuchs C, Dorn D, Fuchs C A, Henning H V, McIntosh C, Scheler F, Stennart M

出版信息

Clin Chim Acta. 1975 Apr 16;60(2):157-67. doi: 10.1016/0009-8981(75)90121-7.

Abstract

A potentiometric method for the determination of fluoride (F-) in serum and plasma is proposed; it is based on a combination of the single-known-addition method and the electrode slope-by-dilution method. This procedure provides reliable results in extremely low measuring ranges down to 2.5 mug/l, where the electrode slope deviates markedly from Nernstian behaviour. In this method no electrode calibration is required and only one standard is necessary. 1 ml of plasma is sufficient for one analysis. Apart from a 5% enrichment of all samples with a concentrated total ionic strength adjustment buffer, no further preparation of the sample is required. The simplicity of the various pipetting and analytical steps, and also of the evaluation of the readings, may render this method highly suitable for the clinical laboratory. Investigations into the accuracy and precision of the method produced satisfactory results. The recovery in plasma amounted to 99.7%, even in the low measuring ranges. The discrimination capacity of the method amounts to 0.1 mug/l. With the apparatus and experimental procedures described, 18 plasma analyses per day can be performed even at low F- concentrations with which longer electrode stabilization periods are required. Storage of the plasma samples frozen at --20 degrees C for up to 8 weeks exerts no effect on the F- concentration. Problems of sample contamination and other disturbances are discussed. Determinations of normal values in 20 test subjects resulted in a mean value of 10.4 plus or minus 4.01 mug/l (Mean plus or minus S.D.). The modal value amounted to 9.5 mug/l, and the range was between 5.9 and 18.8 mug/l. The F- content of the drinking water supplied to this group of persons amounted to 180 mug/l. The importance of the method has been illustrated using a clinico-nephrological study as an example.

摘要

提出了一种测定血清和血浆中氟离子(F-)的电位分析法;该方法基于单次已知添加法和电极斜率稀释法的结合。在低至2.5μg/l的极低测量范围内,该程序能提供可靠结果,此时电极斜率明显偏离能斯特行为。此方法无需电极校准,仅需一种标准溶液。1ml血浆足以进行一次分析。除了用浓缩的总离子强度调节缓冲液对所有样品进行5%的富集外,无需对样品进行进一步处理。各种移液和分析步骤以及读数评估的简单性,可能使该方法非常适合临床实验室。对该方法的准确性和精密度的研究产生了令人满意的结果。即使在低测量范围内,血浆中的回收率也达到了99.7%。该方法的鉴别能力为0.1μg/l。使用所述仪器和实验程序,即使在需要较长电极稳定期的低F-浓度下,每天也可进行18次血浆分析。将血浆样品在-20℃冷冻保存长达8周对F-浓度无影响。讨论了样品污染和其他干扰问题。对20名受试者的正常值测定结果为平均值10.4±4.01μg/l(平均值±标准差)。众数为9.5μg/l,范围在5.9至18.8μg/l之间。该组人员饮用的水中F-含量为180μg/l。以一项临床肾脏病学研究为例说明了该方法的重要性。

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