替代体外和体内试验:从细胞附着到组织再生的计算模型。

Hao Huang, Chao-Zong Liu, Teng Yi, Maryam Tamaddon, Shan-Shan Yuan, Zhen-Yun Shi, Zi-Yu Liu
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引用次数: 1

摘要

为了获得最佳的骨科植入物或再生医学产品,需要进行反复试验分析,研究合适的产品材料、结构、力学性能等。从体内试验到临床试验的整个过程既昂贵又耗时。计算模型被看作是产品开发的一种有用的分析工具。综述了一系列模拟组织工程从细胞附着到组织再生过程的模型。具有挑战性的是模拟组织工程过程的模型是单独开发的。从细胞到组织的再生,取出缺损后需进行血液注射;使细胞分散并附着在支架上;增殖、迁移和分化;直到最后一部分——成为成熟的组织。本文对组织工程过程的相关模型进行了综述,旨在为研究人员建立一个成熟的组织工程全过程模型提供契机。本文重点介绍了组织工程中细胞粘附、营养转运和细胞增殖、分化和迁移的模型分析方法。在细胞粘附模型中,最准确的方法之一是使用离散相模型来控制细胞的运动,使用Stanton-Rutland模型来模拟细胞的粘附。在养分运移模型中,数值模型与流体体积模型和物种运移模型的耦合更适合于养分运移过程的预测。对于细胞的增殖、分化和迁移,采用随机游走算法的有限元法是最先进的模拟方法之一。大多数模型分析方法需要进一步的实验来验证其准确性和有效性。由于缺乏检测营养物质扩散速率的技术,在凝血领域的模型分析方法研究尤其少。因此,组织工程全过程模型方法的研究还有很多工作要做。在未来,数值模型将被视为研究组织工程产品生物性能的最佳方法,也可以优化组织工程产品的参数和材料类型。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Substitution for In Vitro and In Vivo Tests: Computational Models from Cell Attachment to Tissue Regeneration.

To get an optimal product of orthopaedic implant or regenerative medicine needs to follow trial-and-error analyses to investigate suitable product's material, structure, mechanical properites etc. The whole process from in vivo tests to clinical trials is expensive and time-consuming. Computational model is seen as a useful analysis tool to make the product development. A series of models for simulating tissue engineering process from cell attachment to tissue regeneration are reviewed. The challenging is that models for simulating tissue engineering processes are developed separately. From cell to tissue regeneration, it would go through blood injection after moving out the defect; to cell disperse and attach on the scaffold; to proliferation, migration and differentiation; and to the final part-becoming mature tissues. This paper reviewed models that related to tissue engineering process, aiming to provide an opportunity for researchers to develop a mature model for whole tissue engineering process. This article focuses on the model analysis methods of cell adhesion, nutrient transport and cell proliferation, differentiation and migration in tissue engineering. In cell adhesion model, one of the most accurate method is to use discrete phase model to govern cell movement and use Stanton-Rutland model for simulating cell attachment. As for nutrient transport model, numerical model coupling with volume of fluid model and species transport model together is suitable for predicting nutrient transport process. For cell proliferation, differentiation and migration, finite element method with random-walk algorithm is one the most advanced way to simulate these processes. Most of the model analysis methods require further experiments to verify the accuracy and effectiveness. Due to the lack of technology to detect the rate of nutrient diffusion, there are especially few researches on model analysis methods in the area of blood coagulation. Therefore, there is still a lot of work to be done in the research of the whole process model method of tissue engineering. In the future, the numerical model would be seen as an optimal way to investigate tissue engineering products bioperformance and also enable to optimize the parameters and material types of the tissue engineering products.

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