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石墨炉原子吸收光谱法测定非转铁蛋白结合铁的灵敏方法。

Sensitive method for nontransferrin-bound iron quantification by graphite furnace atomic absorption spectrometry.

作者信息

Jakeman A, Thompson T, McHattie J, Lehotay D C

机构信息

Saskatchewan Provincial Health Laboratory, 3211 Albert Street, S4S 5W6, Regina, Saskatchewan, Canada.

出版信息

Clin Biochem. 2001 Feb;34(1):43-7. doi: 10.1016/s0009-9120(00)00194-6.

Abstract

OBJECTIVE

To establish a sensitive method for measuring nontransferrin-bound iron (NTBI) in serum samples using graphite furnace atomic absorption spectrometry (GFAAS).

DESIGN AND METHODS

Nontransferrin-bound iron (NTBI) was chelated using nitrilotriacetic acid (NTA) and then ultrafiltered according to the method employed by Singh et al. [1]. Serum ultrafiltrates were diluted eightfold with distilled water. NTBI from the Fe-NTA complex present in the serum ultrafiltrate was measured using GFAAS.

RESULTS

Nontransferrin-bound iron (NTBI) and other parameters were measured in seven patients diagnosed with hereditary hemochromatosis by liver biopsy. Total serum iron, NTBI and transferrin saturation values (ranging from 87% to 90%) were elevated for three of the seven hemochromatosis patients tested before therapeutic phlebotomy. Six of the seven hemochromatosis patients had undergone phlebotomy and revealed normal total serum iron, NTBI and transferrin saturation values. Nine test subjects (not diagnosed with hemochromatosis) with abnormally high total serum iron and/or ferritin concentrations exhibited normal NTBI values (< or =0.14 micromol/L to 0.29 micromol/L). The detection limit was 0.1 micromol/L for a 25 microL injection volume.

CONCLUSIONS

The GFAAS method presented here provides a sensitive assay to quantitate NTBI in serum samples. The method developed is 4 to 5 times more sensitive than the only other GFAAS method [2] and more than an order of magnitude more sensitive than other colorimetric methods [1,3]. Improvement in sensitivity over the other GFAAS method [2] may be accounted for by differences in sample preparation between this method and that of Nielsen et al. [2]. Serum ultrafiltrates in this study were diluted eightfold with distilled water and mixed with a magnesium nitrate matrix modifier before GFAAS analysis. NTBI results obtained from this study indicate that the plasma iron pool in hemochromatosis patients awaiting phlebotomy increases to a level at which transferrin's ability to bind iron becomes exhausted and elevated NTBI levels appear in the serum. NTBI can mediate the production of reactive oxygen species and may cause organ damage associated with iron overload.

摘要

目的

建立一种使用石墨炉原子吸收光谱法(GFAAS)测定血清样本中非转铁蛋白结合铁(NTBI)的灵敏方法。

设计与方法

采用次氮基三乙酸(NTA)螯合非转铁蛋白结合铁(NTBI),然后按照Singh等人[1]采用的方法进行超滤。血清超滤液用蒸馏水稀释八倍。使用GFAAS测定血清超滤液中Fe-NTA复合物中的NTBI。

结果

对7例经肝活检诊断为遗传性血色素沉着症的患者测定了非转铁蛋白结合铁(NTBI)及其他参数。在7例血色素沉着症患者中,有3例在进行治疗性放血前,血清总铁、NTBI和转铁蛋白饱和度值(范围为87%至90%)升高。7例血色素沉着症患者中有6例接受了放血治疗,其血清总铁、NTBI和转铁蛋白饱和度值均正常。9名血清总铁和/或铁蛋白浓度异常高的受试者(未诊断为血色素沉着症)NTBI值正常(≤0.14微摩尔/升至0.29微摩尔/升)。进样体积为25微升时,检测限为0.1微摩尔/升。

结论

本文介绍的GFAAS方法为定量血清样本中的NTBI提供了一种灵敏的检测方法。所开发的方法比唯一的另一种GFAAS方法[2]灵敏4至5倍,比其他比色法[1,3]灵敏超过一个数量级。与另一种GFAAS方法[2]相比,灵敏度的提高可能是由于本方法与Nielsen等人[2]的方法在样品制备上存在差异。本研究中的血清超滤液用蒸馏水稀释八倍,并在GFAAS分析前与硝酸镁基体改进剂混合。本研究获得的NTBI结果表明,等待放血治疗的血色素沉着症患者血浆铁池增加到转铁蛋白结合铁的能力耗尽且血清中NTBI水平升高的程度。NTBI可介导活性氧的产生,并可能导致与铁过载相关的器官损伤。

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