Diffusive Transport in the Vitreous Humor: Experimental and Analytical Studies.

IF 1.9
Journal of heat transfer Pub Date : 2019-05-01 Epub Date: 2019-04-01 DOI:10.1115/1.4042297
Anita Penkova, Rex Moats, Mark S Humayun, Scott Fraser, Satwindar Singh Sadhal
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引用次数: 4

Abstract

In relation to intravitreal drug delivery, predictive mathematical models for drug transport are being developed, and to effectively implement these for retinal delivery, the information on biophysical properties of various ocular tissues is fundamentally important. It is therefore necessary to accurately measure the diffusion coefficient of drugs and drug surrogates in the vitreous humor. In this review, we present the studies conducted by various researchers on such measurements over the last several decades. These include imaging techniques (fluorescence and magnetic resonance imaging (MRI)) that make use of introducing a contrast agent or a labeled drug into the vitreous and tracking its diffusive movement at various time points. A predictive model for the same initial conditions when matched with the experimental measurements provides the diffusion coefficient, leading to results for various molecules ranging in size from approximately 0.1 to 160 kDa. For real drugs, the effectiveness of this system depends on the successful labeling of the drugs with suitable contrast agents such as fluorescein and gadolinium or manganese so that fluorescence or MR imagining could be conducted. Besides this technique, some work has been carried out using the diffusion apparatus for measuring permeation of a drug across an excised vitreous body from a donor chamber to the receptor by sampling assays from the chambers at various time intervals. This has the advantage of not requiring labeling but is otherwise more disruptive to the vitreous. Some success with nanoparticles has been achieved using dynamic light scattering (DLS), and presently, radioactive labeling is being explored.

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玻璃体内弥漫性转运:实验与分析研究。
关于玻璃体内给药,药物运输的预测数学模型正在开发中,为了有效地实现这些视网膜给药,各种眼部组织的生物物理特性信息是至关重要的。因此,有必要准确测定药物和药物替代物在玻璃体内的扩散系数。在这篇综述中,我们介绍了在过去的几十年里由不同的研究人员对这些测量进行的研究。这些包括成像技术(荧光和磁共振成像(MRI)),利用将造影剂或标记药物引入玻璃体并在不同时间点跟踪其扩散运动。当与实验测量相匹配时,相同初始条件下的预测模型提供了扩散系数,导致大小从大约0.1到160 kDa的各种分子的结果。对于真正的药物,该系统的有效性取决于用合适的造影剂(如荧光素、钆或锰)成功标记药物,以便进行荧光或MR成像。除了这项技术之外,一些工作已经使用扩散装置进行了,通过在不同的时间间隔从腔室取样分析,测量药物穿过切除的玻璃体从供体腔室到受体的渗透。这样做的优点是不需要标记,但对玻璃体的破坏更大。利用动态光散射(DLS)技术在纳米颗粒上取得了一些成功,目前,放射性标记正在探索中。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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