Hansson Kenny M, Johansen Knut, Wetterö Jonas, Klenkar Goran, Benesch Johan, Lundström Ingemar, Lindahl Tomas L, Tengvall Pentti
Division of Applied Physics, Department of Physics, Chemistry and Biology, Linköping University, SE-581 83 Linköping, Sweden.
Biosens Bioelectron. 2007 Sep 30;23(2):261-8. doi: 10.1016/j.bios.2007.04.009. Epub 2007 May 4.
A surface plasmon resonance (SPR) based flow chamber device was designed for real time detection of blood coagulation and platelet adhesion in platelet rich plasma (PRP) and whole blood. The system allowed the detection of surface interactions throughout the 6mm length of the flow chamber. After deposition of thromboplastin onto a section of the sensor surface near the inlet of the flow chamber, coagulation was detected downstream of this position corresponding to a SPR signal of 7 to 8 mRIU (7 to 8 ng/mm2). A nonmodified control surface induced coagulation 3.5 times slower. Platelet adhesion to gold and fibrinogen coated surfaces in the magnitude of 1.25 and 1.66 mRIU was also shown with platelets in buffer, respectively. SPR responses obtained with PRP and whole blood on surfaces that were methylated or coated with von Willebrand factor (vWF), fibrinogen, or collagen, coincided well with platelet adhesion as observed with fluorescence microscopy in parallel experiments. The present SPR detection equipped flow chamber system is a promising tool for studies on coagulation events and blood cell adhesion under physiological flow conditions, and allows monitoring of short-range surface processes in whole blood.
设计了一种基于表面等离子体共振(SPR)的流动腔装置,用于实时检测富血小板血浆(PRP)和全血中的血液凝固和血小板黏附。该系统能够检测整个6mm长的流动腔内的表面相互作用。在将凝血活酶沉积到流动腔入口附近的传感器表面部分后,在该位置下游检测到凝血,对应于7至8 mRIU(7至8 ng/mm2)的SPR信号。未修饰的对照表面诱导凝血的速度慢3.5倍。在缓冲液中的血小板对涂有金和纤维蛋白原的表面的黏附量分别为1.25和1.66 mRIU。在平行实验中,用甲基化或涂有血管性血友病因子(vWF)、纤维蛋白原或胶原蛋白的表面上的PRP和全血获得的SPR响应与荧光显微镜观察到的血小板黏附情况非常吻合。目前配备SPR检测的流动腔系统是研究生理流动条件下凝血事件和血细胞黏附的有前途的工具,并允许监测全血中的短程表面过程。