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血液的被动高频微流变特性。

Passive high-frequency microrheology of blood.

机构信息

CREOL, The College of Optics and Photonics, University of Central Florida, 4304 Scorpius, Orlando, Florida, 32816, USA.

Pediatric Cardiothoracic Surgery, The Heart Center, Arnold Palmer Hospital for Children, Orlando, Florida, USA.

出版信息

Soft Matter. 2022 Mar 23;18(12):2452-2461. doi: 10.1039/d1sm01726h.

Abstract

Indicative of various pathologies, blood properties are under intense scrutiny. The hemorheological characteristics are traditionally gauged by bulk, low-frequency indicators that average out critical information about the complex, multi-scale, and multi-component structure. In particular, one cannot discriminate between the erythrocytes contribution to global rheology and the impact of plasma. Nevertheless, in their fast stochastic movement, before they encounter each other, the erythrocytes probe the subtle viscoelasticity of their protein-rich environment. Thus, if these short time scales can be resolved experimentally, the plasma properties could be determined without having to separate the blood components; the blood is practically testing itself. This microrheological description of blood plasma provides a direct link between the composition of whole blood and its coagulability status. We present a parametric model for the viscoelasticity of plasma, which is probed by the erythrocytes over frequency ranges of kilohertz in a picoliter-sized volume. The model is validated both , using artificial hemo-systems where the composition is controlled, as well as on whole blood where continuous measurements provide real-time information. We also discuss the possibility of using this passive microrheology as an assay for clinically relevant situations where the blood clotting condition must be observed and managed continuously for diagnosis or during therapeutic procedures at different stages of hemostatic and thrombotic processes.

摘要

血液特性是各种病理的指示物,目前受到了深入研究。传统上,血液流变学特性是通过大容量、低频指标来测量的,这些指标平均了关于复杂、多尺度和多组分结构的关键信息。特别是,人们无法区分红细胞对整体流变学的贡献和血浆的影响。然而,在它们快速随机运动过程中,在它们相遇之前,红细胞会探测到富含蛋白质的环境的微妙粘弹性。因此,如果这些短时间尺度可以在实验中得到解决,就可以在不分离血液成分的情况下确定血浆特性;血液实际上是在自我检测。这种对血浆的微观流变学描述提供了全血组成与其凝血状态之间的直接联系。我们提出了一个用于探测红细胞在皮升级别、千赫兹频率范围内的血浆粘弹性的参数模型。该模型通过控制组成的人工血液系统以及全血进行了验证,全血的连续测量提供了实时信息。我们还讨论了将这种被动微观流变学用作分析临床相关情况的可能性,这些情况必须持续观察和管理血液凝固条件,以进行诊断或在止血和血栓形成过程的不同阶段进行治疗。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a7d4/8941587/7252eeb8b40a/d1sm01726h-f1.jpg

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