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基于纸的凝血酶原侧向流动分析方法的开发。

Development of a paper-based lateral flow prothrombin assay.

作者信息

Saidykhan Jerro, Pointon Louise, Cinti Stefano, May Jennifer E, Killard Anthony J

机构信息

Department of Applied Sciences, Centre for Research in Biosciences (CRIB), University of the West of England, Coldharbour Lane, Bristol, BS16 1QY, UK.

North Bristol NHS Trust, Southmead Hospital, Bristol, BS10 5NB, UK.

出版信息

Anal Methods. 2022 Oct 6;14(38):3718-3726. doi: 10.1039/d2ay00965j.

Abstract

Disorders of haemostasis result in both excessive bleeding and clotting and are a major global cause of morbidity and mortality, particularly in the developing world. A small number of simple tests can be used to screen and monitor for such dysfunctions, one of which is the prothrombin time (PT) test and associated International Normalisation Ratio (INR). PT/INR is routine in hospital laboratories in developed countries, and can also be performed using point-of-care instruments. However, neither of these approaches is appropriate in low-resource settings. Significant interest has grown in paper-based devices to form the basis of simple and low-cost assays that may have the potential for application in such environments. This study describes the development of a simple, low-cost, paper-based lateral flow prothrombin assay. The assay employed wax printing on chromatography paper to define test channels, with deposition of thromboplastin reagent and calcium chloride onto the resulting strips. These were placed in a test housing and measurement of the flow rates of deposited plasma samples were performed in triplicate. The flow dynamics of the assay was optimised according to the type of paper substrate used, the nature and quantity of the thromboplastin reagent, the amount of calcium chloride required, and the volume of sample employed. An optimised assay configuration demonstrated a dynamic range of 6 mm between normal and factor-deficient plasmas. The assay showed good correlation with laboratory-based PT assay (Yumizen G200) in artificial plasmas in the 9.8 to 36 s range ( = 0.8112). The assay also demonstrated good dynamic range and correlation in patient plasma samples in comparison with hospital PT, with a range of 9.8 to 45 s ( = 0.7209).

摘要

止血功能障碍会导致出血过多和凝血异常,是全球发病和死亡的主要原因,在发展中国家尤为如此。少量简单的检测可用于筛查和监测此类功能障碍,其中之一是凝血酶原时间(PT)检测及相关的国际标准化比值(INR)。PT/INR在发达国家的医院实验室中是常规检测项目,也可使用即时检测仪器进行检测。然而,这两种方法在资源匮乏地区都不合适。基于纸张的设备引起了人们的极大兴趣,有望成为简单且低成本检测方法的基础,这类检测方法可能适用于此类环境。本研究描述了一种简单、低成本的基于纸张的侧向流动凝血酶原检测方法的开发。该检测方法采用在层析纸上进行蜡印来确定检测通道,将凝血活酶试剂和氯化钙沉积在所得纸条上。将这些纸条置于检测盒中,对沉积的血浆样本的流速进行三次测量。根据所用纸张基质的类型、凝血活酶试剂的性质和数量、所需氯化钙的量以及所用样本的体积,对检测的流动动力学进行了优化。优化后的检测配置在正常血浆和因子缺乏血浆之间显示出6毫米的动态范围。在9.8至36秒范围内的人工血浆中,该检测方法与基于实验室检测(Yumizen G200)的PT检测显示出良好的相关性(r = 0.8112)。与医院的PT检测相比,该检测方法在患者血浆样本中也显示出良好的动态范围和相关性,范围为9.8至45秒(r = 0.7209)。

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