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使用基于栓塞的微流控系统对抗凝剂阿加曲班进行芯片上滴定,并测定全血或血浆中的凝血时间。

On-chip titration of an anticoagulant argatroban and determination of the clotting time within whole blood or plasma using a plug-based microfluidic system.

作者信息

Song Helen, Li Hung-Wing, Munson Matthew S, Van Ha Thuong G, Ismagilov Rustem F

机构信息

Department of Chemistry and Institute for Biophysical Dynamics, University of Chicago, 5735 South Ellis Avenue, Chicago, Illinois 60637, USA.

出版信息

Anal Chem. 2006 Jul 15;78(14):4839-49. doi: 10.1021/ac0601718.

Abstract

This paper describes extending plug-based microfluidics to handling complex biological fluids such as blood, solving the problem of injecting additional reagents into plugs, and applying this system to measuring of clotting time in small volumes of whole blood and plasma. Plugs are droplets transported through microchannels by fluorocarbon fluids. A plug-based microfluidic system was developed to titrate an anticoagulant (argatroban) into blood samples and to measure the clotting time using the activated partial thromboplastin time (APTT) test. To carry out these experiments, the following techniques were developed for a plug-based system: (i) using Teflon AF coating on the microchannel wall to enable formation of plugs containing blood and transport of the solid fibrin clots within plugs, (ii) using a hydrophilic glass capillary to enable reliable merging of a reagent from an aqueous stream into plugs, (iii) using bright-field microscopy to detect the formation of a fibrin clot within plugs and using fluorescent microscopy to detect the production of thrombin using a fluorogenic substrate, and (iv) titration of argatroban (0-1.5 microg/mL) into plugs and measurement of the resulting APTTs at room temperature (23 degrees C) and physiological temperature (37 degrees C). APTT measurements were conducted with normal pooled plasma (platelet-poor plasma) and with donor's blood samples (both whole blood and platelet-rich plasma). APTT values and APTT ratios measured by the plug-based microfluidic device were compared to the results from a clinical laboratory at 37 degrees C. APTT obtained from the on-chip assay were about double those from the clinical laboratory but the APTT ratios from these two methods agreed well with each other.

摘要

本文描述了将基于微滴的微流控技术扩展至处理诸如血液等复杂生物流体,解决向微滴中注入额外试剂的问题,并将该系统应用于测量少量全血和血浆的凝血时间。微滴是由氟碳流体通过微通道输送的液滴。开发了一种基于微滴的微流控系统,用于将抗凝剂(阿加曲班)滴定到血液样本中,并使用活化部分凝血活酶时间(APTT)试验测量凝血时间。为了进行这些实验,针对基于微滴的系统开发了以下技术:(i)在微通道壁上使用聚四氟乙烯AF涂层,以形成包含血液的微滴并使微滴内的固体纤维蛋白凝块得以运输;(ii)使用亲水玻璃毛细管,使试剂能从水流可靠地合并到微滴中;(iii)使用明场显微镜检测微滴内纤维蛋白凝块的形成,并使用荧光显微镜通过荧光底物检测凝血酶的产生;(iv)在室温(23℃)和生理温度(37℃)下将阿加曲班(0 - 1.5μg/mL)滴定到微滴中,并测量由此产生的APTT值。使用正常混合血浆(少血小板血浆)和供体血液样本(全血和富血小板血浆)进行APTT测量。将基于微滴的微流控装置测量的APTT值和APTT比值与临床实验室在37℃下的结果进行比较。芯片检测获得的APTT约为临床实验室结果的两倍,但这两种方法的APTT比值彼此吻合良好。

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