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首页> 外文期刊>Molecular pharmaceutics >Experimental Determination of Drug Diffusion Coefficients in Unstirred Aqueous Environments by Temporally Resolved Concentration Measurements
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Experimental Determination of Drug Diffusion Coefficients in Unstirred Aqueous Environments by Temporally Resolved Concentration Measurements

机译:通过时间分辨浓度测量实验测定未经升降含水环境中的药物扩散系数

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The diffusion coefficient (also known as diffusivity) of an active pharmaceutical ingredient (API) is a fundamental physicochemical parameter that affects passive diffusion through biological barriers and, as a consequence, bioavailability and biodistribution. However, this parameter is often neglected, and it is quite difficult to find diffusion coefficients of small molecules of pharmaceutical relevance in the literature. The available methods to measure diffusion coefficients of drugs all suffer from limitations that range from poor sensitivity to high selectivity of the measurements or the need for dedicated instrumentation. In this work, a simple but reliable method based on time-resolved concentration measurements by UV–visible spectroscopy in an unstirred aqueous environment was developed. This method is based on spectroscopic measurement of the variation of the local concentration of a substance during spontaneous migration of molecules, followed by standard mathematical treatment of the data in order to solve Fick’s law of diffusion. This method is extremely sensitive and results in highly reproducible data. The technique was also employed to verify the influence of the environmental characteristics (i.e., ionic strength and presence of complexing agents) on the diffusivity. The method can be employed in any research laboratory equipped with a standard UV–visible spectrophotometer and could become a useful and straightforward tool in order to characterize diffusion coefficients in physiological conditions and help to better understand the drug permeability process.
机译:活性药物成分(API)的扩散系数(也称为扩散性)是通过生物屏障影响被动扩散的基本物理化学参数,结果是生物利用度和生物分布。然而,该参数通常被忽略,并且很难找到文献中的药物相关性的小分子的扩散系数。测量药物扩散系数的可用方法都患有范围从对测量的高选择性的较差或对专用仪器的需要差的限制。在这项工作中,开发了一种简单但可靠的方法,基于UV可见光谱在未经验证的含水环境中的时间分辨浓度测量方法。该方法基于分子自发迁移期间物质局部浓度的变化的光谱测量,其次是数据的标准数学处理,以解决Fick的扩散定律。该方法非常敏感,并导致高度可重复的数据。还采用该技术来验证环境特征(即离子强度和络合剂存在)对扩散率的影响。该方法可以在配备有标准UV可见光度计的任何研究实验室中使用,并且可以成为有用和直接的工具,以表征生理条件下的扩散系数,并有助于更好地理解药物渗透性过程。

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