Department of Chemistry, University of Toronto, 80 St. George Street, Toronto, ON, Canada M5S 3H6.
Chem Soc Rev. 2012 Sep 7;41(17):5599-612. doi: 10.1039/c2cs35170f. Epub 2012 Jul 6.
Upon contact with bodily fluids/tissues, exogenous materials spontaneously develop a layer of proteins on their surface. In the case of biomedical implants and equipment, biological processes with deleterious effects may ensue. For biosensing platforms, it is synonymous with an overwhelming background signal that prevents the detection/quantification of target analytes present in considerably lower concentrations. To address this ubiquitous problem, tremendous efforts have been dedicated over the years to engineer protein-resistant coatings. There is now extensive literature available on stealth organic adlayers able to minimize fouling down to a few ng cm(-2), however from technologically irrelevant single-protein buffered solutions. Unfortunately, few coatings have been reported to present such level of performance when exposed to highly complex proteinaceous, real-world media such as blood serum and plasma, even diluted. Herein, we concisely review the surface chemistry developed to date to minimize fouling from these considerably more challenging blood-based fluids. Adsorption dynamics is also discussed.
当与体液/组织接触时,外源性材料会在其表面自发形成一层蛋白质。对于生物医学植入物和设备,可能会产生有害影响的生物过程。对于生物传感平台,这意味着背景信号压倒性强,从而阻止了对浓度明显较低的目标分析物的检测/定量。为了解决这个普遍存在的问题,多年来人们致力于开发抗蛋白质涂层。现在已经有大量关于能够将污染减少到几个纳克/平方厘米的隐形有机覆盖层的文献,但这些文献都来自于技术上不相关的单蛋白缓冲溶液。不幸的是,当暴露于高度复杂的蛋白质真实介质(如血清和血浆,甚至是稀释的)时,很少有报道称涂层能达到如此水平的性能。在此,我们简明地回顾了迄今为止为了最大限度地减少这些更具挑战性的基于血液的流体污染而开发的表面化学。还讨论了吸附动力学。