Department of Chemistry, School of Engineering Sciences in Chemistry, Biotechnology and Health, KTH Royal Institute of Technology, 10044 Stockholm, Sweden.
Analyst. 2020 May 7;145(9):3188-3210. doi: 10.1039/d0an00327a. Epub 2020 Apr 2.
The monitoring of ammonium ion concentration has gained the attention of researchers from multiple fields since it is a crucial parameter with respect to environmental and biomedical applications. For example, ammonium is considered to be a quality indicator of natural waters as well as a potential biomarker of an enzymatic byproduct in key physiological reactions. Among the classical analytical methods used for the detection of ammonium ions, potentiometric ion-selective electrodes (ISEs) have attracted special attention in the scientific community because of their advantages such as cost-effectiveness, user-friendly features, and miniaturization ability, which facilitate easy portable measurements. Regarding the analytical performance, the key component of ISEs is the selective receptor, labelled as an ionophore in ISE jargon. Indeed, the preference of an ionophore for ammonium amongst other ions (i.e., selectivity) is a factor that primarily dictates the limit of detection of the electrode when performing measurements in real samples. A careful assessment of the literature for the last 20 years reveals that nonactin is by far the most employed ammonium ionophore to date. Despite the remarkable cross-interference of potassium over the ammonium response of nonactin-based ISEs, analytical applications comprising water quality assessment, clinical tests in biological fluids, and sweat monitoring during sports practice have been successfully researched. Nevertheless, there is evident difficulty in the determination of close-to-micromolar levels of ammonium in real samples with a significant potassium background level (i.e., millimolar concentration). This fact has fostered the search for a large variety of ammonium ionophores over the years, which are critically inspected herein. Overall, we provide an easily readable state of the art accompanied by a comprehensive description of other types of ammonium electrodes, including commercially available units. We conclude that newer breakthroughs are still required in the field to reach the desired analytical applications.
铵离子浓度的监测引起了多个领域研究人员的关注,因为它是环境和生物医学应用中一个至关重要的参数。例如,铵被认为是天然水的质量指标,也是关键生理反应中酶副产物的潜在生物标志物。在用于检测铵离子的经典分析方法中,离子选择性电极 (ISE) 由于其具有成本效益、用户友好的特点和小型化能力等优势,在科学界引起了特别关注,这使得便携式测量变得更加容易。就分析性能而言,ISE 的关键组成部分是选择性受体,在 ISE 术语中称为离子载体。实际上,离子载体对铵的偏好相对于其他离子(即选择性)是决定电极在实际样品测量中检测限的主要因素。对过去 20 年文献的仔细评估表明,非阿霉素迄今为止是最常用的铵离子载体。尽管非阿霉素基 ISE 对钾的铵响应存在显著的交叉干扰,但已成功研究了包括水质评估、生物体液临床测试和运动实践中汗液监测在内的分析应用。然而,在具有显著钾背景水平(即毫摩尔浓度)的实际样品中,确定接近微摩尔级别的铵浓度仍然存在明显的困难。这一事实促使多年来寻找大量不同的铵离子载体,本文对此进行了批判性检查。总的来说,我们提供了一个易于阅读的最新技术状态,并全面描述了其他类型的铵电极,包括市售的单元。我们得出的结论是,该领域仍需要新的突破来实现所需的分析应用。