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Combined kinetic osmometry and pyrometric microcalorimetry on protein solutions: Setup and data evaluation

机译:蛋白质溶液的动态渗透压和高温微热分析相结合:设置和数据评估

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摘要

A novel principle to measure simultaneously the equilibrium solvent vapour pressure (solvent activity) and the solvent heat of evaporation of aqueous macromolecular (protein) solutions is presented. These measurements are based on the simultaneous recording and evaluation of both the course of the sample mass and sample temperature during the sample evaporation. A setup is described where the mass and the temperature of the sample are continuously measured by weighing and contactless pyrometry, respectively. The sample in the mu l-range is stored in a container placed within a box where temperature and relative humidity is stabilized up to 10(-2) K and 10(-1)%, respectively. The incoming data reflect the effect of the continuously increasing solute concentration (changing at a ratio of about 2:1 up to 3: 1) provided that, in practice, the solvent only evaporates. The protein concentration-dependent part mu((s,P))(A) and h(A)((s,P)) of the solvent chemical potential and the solvent molecular enthalpy, respectively, can be simultaneously determined (the latter for the first time). For appropriate protein concentrations, the second-order and third-order contributions in solute concentrations can be determined by a regression analysis. The data evaluation utilizes reference measurements on the pure solvent and upstream measurements on the solution of the precipitant only. Supported by FE simulations, a prodecure to minimize statistical errors and to eliminate systematic errors is derived and applied. For conditions of an ordinary laboratory, the equipment described enables a measurement of h(A)((s,P))/k(B)T and mu((s,P))(A)/k(B)T with an absolute accuracy <= 10(-1) and <= 10(-3), respectively (k(B): Boltzmann constant; T. temperature). We present measurements on aqueous solutions of Insulin Glargine (Hoe901) with ammonium sulfate as main precipitant component to demonstrate basic steps of the data evaluation procedure and the use of our measuring method. (C) 2007 Elsevier B.V. All rights reserved.
机译:提出了一种新的原理,可以同时测量大分子(蛋白质)水溶液的平衡溶剂蒸气压(溶剂活性)和溶剂蒸发热。这些测量是基于同时记录和评估样品蒸发过程中样品质量和样品温度的过程。描述了一种设置,其中分别通过称重和非接触式高温测定法连续测量样品的质量和温度。多范围的样品存储在一个放置在盒子中的容器中,温度和相对湿度分别稳定在10(-2)K和10(-1)%。输入的数据反映了不断增加的溶质浓度(以约2:1的比例变化至最大3:1的比例)的效果,但前提是实际上仅蒸发溶剂。可以同时确定溶剂化学势和溶剂分子焓的蛋白质浓度依赖性部分mu((s,P))(A)和h(A)((s,P))(后者用于第一次)。对于适当的蛋白质浓度,可以通过回归分析确定溶质浓度的二阶和三阶贡献。数据评估仅使用纯溶剂的参考测量值,仅使用沉淀剂溶液的上游测量值。在有限元仿真的支持下,推导并应用了将统计误差降至最低并消除系统误差的程序。对于普通实验室的条件,所描述的设备能够用以下方法测量h(A)((s,P))/ k(B)T和mu((s,P))(A)/ k(B)T绝对精度分别为<= 10(-1)和<= 10(-3)(k(B):玻尔兹曼常数;温度)。我们介绍了以硫酸铵为主要沉淀成分的甘精胰岛素(Hoe901)水溶液的测量结果,以证明数据评估程序的基本步骤以及我们的测量方法的使用。 (C)2007 Elsevier B.V.保留所有权利。

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