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首页> 外文期刊>European journal of pharmaceutics and biopharmaceutics: official journal of Arbeitsgemeinschaft fuer Pharmazeutische Verfahrenstechnik e.V >Improved in vitro models for preclinical drug and formulation screening focusing on 2D and 3D skin and cornea constructs
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Improved in vitro models for preclinical drug and formulation screening focusing on 2D and 3D skin and cornea constructs

机译:改善了临床前药物和配方筛选的体外模型,重点在2D和3D皮肤和角膜构建体上

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摘要

The present overview deals with current approaches for the improvement of in vitro models for preclinical drug and formulation screening which were elaborated in a joint project at the Center of Pharmaceutical Engineering of the TU Braunschweig. Within this project a special focus was laid on the enhancement of skin and cornea models. For this reason, first, a computation-based approach for in silico modeling of dermal cell proliferation and differentiation was developed. The simulation should for example enhance the understanding of the performed 2D in vitro tests on the antiproliferative effect of hyperforin. A second approach aimed at establishing in vivo-like dynamic conditions in in vitro drug absorption studies in contrast to the commonly used static conditions. The reported Dynamic Micro Tissue Engineering System (DynaMiTES) combines the advantages of in vitro cell culture models and microfluidic systems for the emulation of dynamic drug absorption at different physiological barriers and, later, for the investigation of dynamic culture conditions. Finally, cryopreserved shipping was investigated for a human hemicornea construct. As the implementation of a tissue-engineering laboratory is time-consuming and cost-intensive, commercial availability of advanced 3D human tissue is preferred from a variety of companies. However, for shipping purposes cryopreservation is a challenge to maintain the same quality and performance of the tissue in the laboratory of both, the provider and the customer.
机译:目前概述涉及电流改善临床前药物和配方筛查体外模型的方法,这些筛选在涂布拉旺西格的药物工程中心的联合项目中阐述。在该项目中,特别重点是对皮肤和角膜模型的增强。因此,首先,开发了基于计算的真皮细胞增殖和分化的基于硅模型的计算方法。模拟应该例如增强对所表演的2D体外测试的理解对高纤维蛋白的抗增殖作用。旨在在体外药物吸收研究中建立体内动态条件的第二种方法与常用的静态条件相反。报告的动态微型组织工程系统(Dynamite)结合了体外细胞培养模型和微流体系统的优点,以便在不同生理障碍处仿真动态吸毒,以后,用于调查动态培养条件。最后,研究了用于人的Hemicornea构建体的冷冻保存的运输。由于组织 - 工程实验室的实施是耗时和成本密集的,高级3D人类组织的商业可用性来自各种公司。然而,对于运输目的,冷冻保存是一种挑战,以维持在提供者和客户的实验室中的组织的质量和性能。

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