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用于无增塑剂荧光离子光极微球传感器的聚合尼罗蓝衍生物

Polymerized Nile Blue derivatives for plasticizer-free fluorescent ion optode microsphere sensors.

作者信息

Ngeontae Wittaya, Xu Chao, Ye Nan, Wygladacz Katarzyna, Aeungmaitrepirom Wanlapa, Tuntulani Thawatchai, Bakker Eric

机构信息

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

出版信息

Anal Chim Acta. 2007 Sep 5;599(1):124-33. doi: 10.1016/j.aca.2007.07.058. Epub 2007 Aug 1.

Abstract

Lipophilic H+-selective fluorophores such as Nile Blue derivatives are widely used in ISE-based pH sensors and bulk optodes, and are commonly dissolved in a plasticized matrix such as PVC. Unfortunately, leaching of the active sensing ingredients and plasticizer from the matrix dictates the lifetime of the sensors and hampers their applications in vivo, especially with miniaturized particle based sensors. We find that classical copolymerization of Nile Blue derivatives containing an acrylic side group gives rise to multiple reaction products with different spectral and H+-binding properties, making this approach unsuitable for the development of reliable sensor materials. This limitation was overcome by grafting Nile Blue to a self-plasticized poly(n-butyl acrylate) matrix via an urea or amide linkage between the Nile Blue base structure and the polymer. Optode leaching experiments into methanol confirmed the successful covalent attachment of the two chromoionophores to the polymer matrix. Both polymerized Nile Blue derivatives have satisfactory pH response and appropriate optical properties that are suitable for use in ion-selective electrodes and optodes. Plasticizer-free Na+-selective microsphere sensors using the polymerized chromoionophores were fabricated under mild conditions with an in-house sonic microparticle generator for the measurement of sodium activities at physiological pH. The measuring range for sodium was found as 10(-1)-10(-4) M and 1-10(-3) M, for Nile Blue derivatives linked via urea and amide functionalities, respectively, at physiological pH. The observed ion-exchange constants of the plasticizer-free microsphere were log K(exch) = -5.6 and log K(exch) = -6.5 for the same two systems, respectively. Compared with earlier Na+-selective bulk optodes, the fabricated optical sensing microbeads reported here have agreeable selectivity patterns, reasonably fast response times, and more appropriate measuring ranges for determination of Na+ activity at physiological pH in undiluted blood samples.

摘要

亲脂性H⁺选择性荧光团,如尼罗蓝衍生物,广泛应用于基于离子选择性电极(ISE)的pH传感器和整体光极中,通常溶解在诸如聚氯乙烯(PVC)之类的增塑基质中。不幸的是,活性传感成分和增塑剂从基质中的浸出决定了传感器的寿命,并阻碍了它们在体内的应用,特别是对于基于微型颗粒的传感器。我们发现,含有丙烯酸侧基的尼罗蓝衍生物的经典共聚会产生具有不同光谱和H⁺结合特性的多种反应产物,使得这种方法不适用于开发可靠的传感器材料。通过尼罗蓝碱基结构与聚合物之间的脲或酰胺键将尼罗蓝接枝到自增塑的聚(丙烯酸正丁酯)基质上,克服了这一限制。将光极浸入甲醇中的实验证实了两种发色离子载体成功地共价连接到聚合物基质上。两种聚合的尼罗蓝衍生物都具有令人满意的pH响应和适合用于离子选择性电极和光极的光学性质。使用聚合发色离子载体的无增塑剂Na⁺选择性微球传感器在温和条件下用自制的声波微粒发生器制造,用于在生理pH下测量钠活度。在生理pH下,发现通过脲和酰胺官能团连接的尼罗蓝衍生物的钠测量范围分别为10⁻¹ - 10⁻⁴ M和1 - 10⁻³ M。对于相同的两个系统,无增塑剂微球的观察到的离子交换常数分别为log K(exch) = -5.6和log K(exch) = -6.5。与早期的Na⁺选择性整体光极相比,本文报道的制造的光学传感微珠具有良好的选择性模式、合理快速的响应时间以及更适合在未稀释血液样本中生理pH下测定Na⁺活度的测量范围。

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