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通过声凝块分析定量和优化洗涤人血小板的凝块回缩。

Quantification and optimization of clot retraction in washed human platelets by Sonoclot coagulation analysis.

机构信息

Department of Zoology, School of Biological Sciences, Central University of Punjab, Bathinda, India.

出版信息

Int J Lab Hematol. 2022 Feb;44(1):177-185. doi: 10.1111/ijlh.13710. Epub 2021 Oct 5.

DOI:10.1111/ijlh.13710
PMID:34609044
Abstract

INTRODUCTION

Clot retraction is a pivotal process for haemostasis, where platelets develop a contractile force in fibrin meshwork and lead to the increased rigidity of clot. The pathophysiological alteration in contractile forces generated by the platelet-fibrin meshwork can lead to haemostatic disorders. Regardless of its utter significance, clot retraction remains a limited understood process owing to lack of quantification methodology. Sonoclot analysis is a point-of-care technique used in clinical laboratories for whole blood analysis that provides in vitro qualitative as well as quantitative assessment of coagulation process from initial fibrin formation to clot retraction.

METHODS

Human washed platelets were isolated by differential centrifugation method and analysed via optical imaging, microscopy and Sonoclot analysis using 1-2 × 10 /mL of washed platelets, 1 U/mL of thrombin, 1 mg/mL of fibrinogen and 1 mM of calcium chloride.

RESULTS

In this study, we demonstrate the novelty of this instrument in the quantitative evaluation of clot retraction in washed platelets and attempted to optimize the reference range of Sonoclot parameters including ACT - 87.3 ± 20.997, CR - 16.23 ± 3.538 and PF - 3.57 ± 0.629, (n = 10).

DISCUSSION

Sonoclot analysis provides a simple and quantitative method to better understand in vitro clot retraction and its modulation by retraction components including platelet count, fibrinogen and platelet-fibrin interaction compared with existing conventional methods. Sonoclot may prove to be a valuable tool in thrombus biology research to understand fundamental basis of blood clot retraction.

摘要

简介

血栓收缩是止血的关键过程,在此过程中血小板在纤维蛋白网中产生收缩力,导致血栓的刚性增加。血小板-纤维蛋白网产生的收缩力的病理生理改变可导致止血障碍。尽管其意义重大,但由于缺乏定量方法,血栓收缩仍然是一个有限的理解过程。Sonoclot 分析是一种用于临床实验室的即时检测技术,用于分析全血,可从初始纤维蛋白形成到血栓收缩对凝血过程进行体外定性和定量评估。

方法

通过差速离心法分离人洗涤血小板,并通过光学成像、显微镜和 Sonoclot 分析进行分析,使用 1-2×10 /mL 洗涤血小板、1U/mL 凝血酶、1mg/mL 纤维蛋白原和 1mM 氯化钙。

结果

在这项研究中,我们展示了该仪器在定量评估洗涤血小板血栓收缩方面的新颖性,并尝试优化 Sonoclot 参数的参考范围,包括 ACT-87.3±20.997、CR-16.23±3.538 和 PF-3.57±0.629(n=10)。

讨论

Sonoclot 分析提供了一种简单和定量的方法,可以更好地了解体外血栓收缩及其通过收缩成分的调节,包括血小板计数、纤维蛋白原和血小板-纤维蛋白相互作用,与现有的常规方法相比。Sonoclot 可能成为血栓生物学研究的有用工具,以了解血液血栓收缩的基本原理。

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