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Method for Determination of Polyethylene Glycol Molecular Weight

机译:聚乙二醇分子量的测定方法

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A method utilizing competitive adsorption between polyethylene glycols (PEGs) and labeled protein to nanoparticles was developed for the determination of PEG molecular weight (MW) in a microtiter plate format. Two mix-and-measure systems, time-resolved luminescence resonance energy transfer (TR-LRET) with donor europium(III) polystyrene nanoparticles and acceptor-labeled protein and quenching with quencher gold nanoparticles and fluorescently labeled protein were compared for their performance. MW is estimated from the PEG MW dependent changes in the competitive adsorption properties, which are presented as the luminescence signal vs PEG mass concentration. The curves obtained with the TR-LRET system overlapped for PEGs larger than 400 g/mol providing no information on MW. Distinctly different curves were obtained with the quenching system enabling the assessment of PEG MW within a broad dynamic range. The data was processed with and without prior knowledge of the PEG concentration to measure PEGs over a MW range from 62 to 35 000 g/mol. The demonstration of the measurement independent of the PEG concentration suggests that the estimation of MW is possible with quenching nanoparticle system for neutrally charged and relatively hydrophilic polymeric molecules widening the applicability of the simple and cost-effective nanoparticle-based methods.
机译:开发了一种利用聚乙二醇(PEG)和标记的蛋白质之间竞争性吸附到纳米粒子的方法,用于测定微量滴定板形式的PEG分子量(MW)。比较了两种混合测量系统,时间分辨的发光共振能量转移(TR-LRET)与施主euro(III)聚苯乙烯纳米粒子和受体标记的蛋白质以及淬灭剂金纳米粒子和荧光标记的蛋白质淬灭的性能。分子量是根据竞争吸附特性中PEG MW依赖的变化估算的,这些变化表示为发光信号与PEG质量浓度的关系。对于大于400 g / mol的PEG,使用TR-LRET系统获得的曲线重叠,没有提供有关MW的信息。通过淬灭系统获得了截然不同的曲线,从而可以在较宽的动态范围内评估PEG MW。在有或没有PEG浓度的先验知识的情况下处理数据,以测量分子量范围为62至35000 g / mol的PEG。与PEG浓度无关的测量结果表明,对于中性电荷和相对亲水的聚合物分子,用猝灭纳米颗粒系统估算分子量是可能的,从而拓宽了简单且经济高效的基于纳米颗粒的方法的适用范围。

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