Casalini Tommaso, Perale Giuseppe
Biomaterials Laboratory, Institute for Mechanical Engineering and Materials Technology, SUPSI-University of Applied Sciences and Arts of Southern Switzerland, Via Cantonale 2C, Galleria 2, 6928 Manno, Switzerland.
Institute for Chemical and Bioengineering, Department of Chemistry and Applied Biosciences, ETH Zurich, Vladimir-Prelog-Weg 1-5/10, 8093 Zurich, Switzerland.
Gels. 2019 May 15;5(2):28. doi: 10.3390/gels5020028.
Because of their inherent biocompatibility and tailorable network design, hydrogels meet an increasing interest as biomaterials for the fabrication of controlled drug delivery devices. In this regard, mathematical modeling can highlight release mechanisms and governing phenomena, thus gaining a key role as complementary tool for experimental activity. Starting from the seminal contribution given by Flory-Rehner equation back in 1943 for the determination of matrix structural properties, over more than 70 years, hydrogel modeling has not only taken advantage of new theories and the increasing computational power, but also of the methods offered by computational chemistry, which provide details at the fundamental molecular level. Simulation techniques such as molecular dynamics act as a "computational microscope" and allow for obtaining a new and deeper understanding of the specific interactions between the solute and the polymer, opening new exciting possibilities for an in silico network design at the molecular scale. Moreover, system modeling constitutes an essential step within the "safety by design" paradigm that is becoming one of the new regulatory standard requirements also in the field-controlled release devices. This review aims at providing a summary of the most frequently used modeling approaches (molecular dynamics, coarse-grained models, Brownian dynamics, dissipative particle dynamics, Monte Carlo simulations, and mass conservation equations), which are here classified according to the characteristic length scale. The outcomes and the opportunities of each approach are compared and discussed with selected examples from literature.
由于水凝胶具有固有的生物相容性和可定制的网络设计,作为用于制造可控药物递送装置的生物材料,它们越来越受到关注。在这方面,数学建模可以突出释放机制和控制现象,从而作为实验活动的补充工具发挥关键作用。从1943年Flory-Rehner方程对确定基质结构性质的开创性贡献开始,在70多年的时间里,水凝胶建模不仅利用了新理论和不断提高的计算能力,还利用了计算化学提供的方法,这些方法在基本分子水平上提供细节。分子动力学等模拟技术充当“计算显微镜”,能够对溶质与聚合物之间的特定相互作用有新的、更深入的理解,为分子尺度的计算机模拟网络设计开辟了令人兴奋的新可能性。此外,系统建模是“设计安全”范式中的一个重要步骤,这一范式也正在成为控释装置领域新的监管标准要求之一。本综述旨在总结最常用的建模方法(分子动力学、粗粒化模型、布朗动力学、耗散粒子动力学、蒙特卡罗模拟和质量守恒方程),并根据特征长度尺度对其进行分类。通过文献中的选定实例对每种方法的结果和机会进行了比较和讨论。