Lee Tae-Rin, Yoo Sung Sic, Yang Jiho
Advanced Institutes of Convergence Technology, Seoul National University, Suwon, 443-270, Republic of Korea.
Department of Computer Science, Technische Universität München, Boltzmannstraße 3, Garching, Germany.
Biomech Model Mechanobiol. 2017 Apr;16(2):497-507. doi: 10.1007/s10237-016-0832-z. Epub 2016 Sep 21.
In microvascular transport, where both blood and drug carriers are involved, plasma skimming has a key role on changing hematocrit level and drug carrier concentration in capillary beds after continuous vessel bifurcation in the microvasculature. While there have been numerous studies on modeling the plasma skimming of blood, previous works lacked in consideration of its interaction with drug carriers. In this paper, a generalized plasma skimming model is suggested to predict the redistributions of both the cells and drug carriers at each bifurcation. In order to examine its applicability, this new model was applied on a single bifurcation system to predict the redistribution of red blood cells and drug carriers. Furthermore, this model was tested at microvascular network level under different plasma skimming conditions for predicting the concentration of drug carriers. Based on these results, the applicability of this generalized plasma skimming model is fully discussed and future works along with the model's limitations are summarized.
在微血管运输中,血液和药物载体都参与其中,在微血管中连续血管分支后,血浆撇取在改变毛细血管床中的血细胞比容水平和药物载体浓度方面起着关键作用。虽然已经有许多关于血液血浆撇取建模的研究,但以前的工作缺乏对其与药物载体相互作用的考虑。本文提出了一个广义血浆撇取模型,以预测每个分支处细胞和药物载体的重新分布。为了检验其适用性,将这个新模型应用于单个分支系统,以预测红细胞和药物载体的重新分布。此外,该模型在不同血浆撇取条件下的微血管网络水平上进行了测试,以预测药物载体的浓度。基于这些结果,充分讨论了这个广义血浆撇取模型的适用性,并总结了未来的工作以及该模型的局限性。