Yi Hang, Wang Alexander, Wang Christopher, Chong Jared, Ma Chungyiu, Bramlage Luke, Ludwig Bryan, Yang Zifeng
Department of Mechanical and Materials Engineering, Wright State University, 3640 Colonel Glenn Hwy., Dayton, OH 45435, USA.
Centerville High School, 500 E Franklin St, Centerville, OH 45459, USA.
Bioengineering (Basel). 2025 Jul 12;12(7):758. doi: 10.3390/bioengineering12070758.
Blood analogs are widely employed in in vitro experiments such as particle image velocity (PIV) to secure hemodynamics, assisting pathophysiological diagnoses of neurovascular and cardiovascular diseases, as well as pre-surgical planning and intraoperative orientation. To obtain accurate physical parameters, which are critical for diagnosis and treatment, blood analogs should exhibit realistic non-Newtonian shear-thinning features. In this study, two types of blood analogs working under room temperature (293.15 K) were created to mimic the steady-state shear-thinning features of blood over a temperature range of 295 to 312 K and a shear range of 1~250 s at a hematocrit of ~40%. Type I was a general-purpose analog composed of deionized (DI) water and xanthan gum (XG) powder, while Type II was specially designed for PIV tests, incorporating DI water, XG, and fluorescent microspheres. By minimizing the root mean square deviation between generated blood analogs and an established viscosity model, formulas for both blood analogs were successfully derived for the designated temperatures. The results showed that both blood analogs could replicate the shear-thinning viscosities of real blood, with the averaged relative discrepancy < 5%. Additionally, a strong linear correlation was observed between body temperature and XG concentration in both blood analogs (coefficient of determination > 0.96): for Type I, 295-312 K correlates with 140-520 ppm, and for Type II, 295-315 K correlates with 200-560 ppm. This work bridges the gap between idealized steady-state non-Newtonian viscosity models of blood and the complexities of real-world physiological conditions, offering a versatile platform for advancing particle image velocimetry tests and hemodynamics modeling, optimizing therapeutic interventions, and enhancing biomedical technologies in temperature-sensitive environments.
血液模拟物广泛应用于体外实验,如粒子图像测速(PIV)以确保血流动力学,辅助神经血管和心血管疾病的病理生理诊断,以及术前规划和术中定位。为了获得对诊断和治疗至关重要的准确物理参数,血液模拟物应呈现出现实的非牛顿剪切变稀特性。在本研究中,制备了两种在室温(293.15 K)下工作的血液模拟物,以模拟血细胞比容约为40%时,在295至312 K的温度范围和1~250 s的剪切范围内血液的稳态剪切变稀特性。I型是由去离子(DI)水和黄原胶(XG)粉末组成的通用模拟物,而II型是专门为PIV测试设计的,包含去离子水、XG和荧光微球。通过最小化生成的血液模拟物与既定粘度模型之间的均方根偏差,成功推导出了两种血液模拟物在指定温度下的公式。结果表明,两种血液模拟物都能复制真实血液的剪切变稀粘度,平均相对差异<5%。此外,在两种血液模拟物中均观察到体温与XG浓度之间存在很强的线性相关性(决定系数>0.96):对于I型,295 - 312 K与140 - 520 ppm相关,对于II型,295 - 315 K与200 - 560 ppm相关。这项工作弥合了血液理想化稳态非牛顿粘度模型与现实世界生理条件复杂性之间的差距,为推进粒子图像测速测试和血流动力学建模、优化治疗干预以及增强温度敏感环境中的生物医学技术提供了一个通用平台。