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用聚合物膜离子选择性电极通过闪光计时电位法测定总钙。

Measurement of total calcium by flash chronopotentiometry at polymer membrane ion-selective electrodes.

作者信息

Gemene Kebede L, Bakker Eric

机构信息

Department of Chemistry, Purdue University, West Lafayette, IN 47907, United States.

出版信息

Anal Chim Acta. 2009 Aug 26;648(2):240-5. doi: 10.1016/j.aca.2009.07.004. Epub 2009 Jul 8.

Abstract

Ionophore-based ion-selective electrodes are widely used for potentiometric electrolyte measurements, in which case they are known to detect the free ion activity. Total ion concentrations cannot be directly assessed by this methodology if the ion is predominantly present in a complexed form. We present here the direct measurement of total calcium using a calcium ion-selective electrode interrogated in a flash chronopotentiometric transduction mode. A high magnitude of cathodic current pulse is applied across a calcium ion-selective membrane containing the ionophore ETH 5234 but void of ion-exchanger to prevent spontaneous extraction. This induces a defined flux of calcium ions from the sample side to the membrane and results in the release of labile bound calcium and a concomitant depletion at the membrane surface at a critical current or time. This is observed as an inflection point on the potential-time curve and the square root of the transition time is linearly related to the total concentration in the sample. It is shown that the responses to solutions of labile calcium complexes of nitrilotriacetic acid (NTA) are in a good agreement with that of the same concentration of calcium chloride in saline solution with this protocol. Initial applications are aimed towards assaying extracellular calcium. Calcium binding to albumin is shown to be inconsequential with sample dilutions typical for clinical assays. Calcium calibration curves in real and artificial dilute serum are finally shown to correspond to that of calcium chloride, suggesting that the methodology is indeed capable of detecting total calcium under these conditions. The present membrane materials allow detection of up to over 0.5mM total calcium in serum, currently requiring such samples to be diluted about 5-fold. The slopes of the square root of time-concentration dependence for the calibrations of free calcium in a background of NaCl and total serum calcium were found to be 3.857 and 3.717 s(1/2)mM(-1), respectively, deviating by just 3.6%. The lower detection limit (3x SD) was calculated as 12 microM.

摘要

基于离子载体的离子选择性电极被广泛用于电位电解质测量,在这种情况下,已知它们能检测游离离子活性。如果离子主要以络合形式存在,则无法通过这种方法直接评估总离子浓度。我们在此展示了使用在闪光计时电位转导模式下询问的钙离子选择性电极直接测量总钙。在含有离子载体ETH 5234但没有离子交换剂以防止自发萃取的钙离子选择性膜上施加高幅度的阴极电流脉冲。这会诱导钙离子从样品侧到膜的特定通量,并导致不稳定结合钙的释放以及在临界电流或时间时膜表面的伴随消耗。这在电位 - 时间曲线上表现为一个拐点,过渡时间的平方根与样品中的总浓度呈线性关系。结果表明,使用该方案,对次氮基三乙酸(NTA)的不稳定钙络合物溶液的响应与盐溶液中相同浓度氯化钙的响应高度一致。初步应用旨在测定细胞外钙。结果表明,对于临床检测典型的样品稀释,钙与白蛋白的结合无关紧要。最终显示,真实和人工稀释血清中的钙校准曲线与氯化钙的校准曲线相对应,这表明该方法确实能够在这些条件下检测总钙。目前的膜材料能够检测血清中高达0.5mM以上的总钙,目前需要将此类样品稀释约5倍。在NaCl背景下游离钙校准和总血清钙校准的时间 - 浓度依赖性平方根的斜率分别为3.857和3.717 s(1/2)mM(-1),偏差仅为3.6%。计算得出的最低检测限(3倍标准差)为12 microM。

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