Department of Bioengineering, The University of Texas at Dallas, Richardson, TX 75080, USA.
EnLiSense LLC, 1813 Audubon Pondway, Allen, TX 75013, USA.
Anal Chim Acta. 2018 Aug 3;1016:29-39. doi: 10.1016/j.aca.2018.02.013. Epub 2018 Feb 14.
We have investigated the role of kosmotropic anionic moieties and chaotropic cationic moieties of room temperature hydrophilic ionic liquids in enhancing the biosensing performance of affinity based immunochemical biosensors in human sweat. Two ionic liquids, 1-butyl-3-methylimidazolium tetrafluoroborate (BMIM[BF]) and choline dihydrogen phosphate (Choline[DHP]) were investigated in this study with Choline[DHP] being more kosmotropic in nature having a more protein stabilizing effect based on the hofmeister series. Non-faradaic interfacial charge transfer has been employed as the mechanism for evaluating the formation and the biosensing of capture probe antibodies in room temperature ionic liquids (RTILs)/aqueous human sweat interface. The charge of the ionic moieties were utilized to form compact electrical double layers around the antibodies for enhancing the stability of the antibody capture probes, which was evaluated through zeta potential measurements. The zeta potential measurements indicated stability of antibodies due to electrostatic repulsion of the RTIL charged moieties encompassing the antibodies, thus preventing any aggregation. Here, we report for the first time of non-faradaic electrochemical impedance spectroscopy equivalent circuit model analysis for analyzing and interpreting affinity based biosensing at hybrid electrode/ionic liquid-aqueous sweat buffer interface guided by the choice of the ionic liquid. Interleukin-6 (IL-6) and cortisol two commonly occurring biomarkers in human sweat were evaluated using this method. The limit of detection (LOD) obtained using both ionic liquids for IL-6 was 0.2 pg mL with cross-reactivity studies indicating better performance of IL-6 detection using Choline[DHP] and no response to cross-reactive molecule. The LOD of 0.1 ng/mL was achieved for cortisol and the cross-reactivity studies indicated that cortisol antibody in BMIM[BF] did not show any signal response to cross-reactive molecules. Furthermore, improved sensitivity and LOD was achieved using ionic liquids as compared to capture probes in aqueous buffer.
我们研究了室温亲水性离子液体中的反离子和抗衡离子对增强基于亲和力的免疫化学生物传感器在人体汗液中生物传感性能的作用。在这项研究中,我们研究了两种离子液体,1-丁基-3-甲基咪唑四氟硼酸盐(BMIM[BF])和磷酸胆碱(Choline[DHP]),根据 Hofmeister 序列,Choline[DHP]的反离子性质更具亲脂性,具有更稳定蛋白质的作用。非 Faradaic 界面电荷转移被用作评估室温离子液体(RTIL)/水性人体汗液界面中捕获探针抗体的形成和生物传感的机制。离子基团的电荷被用于在抗体周围形成紧凑的双电层,以增强抗体捕获探针的稳定性,这通过 zeta 电位测量进行评估。zeta 电位测量表明,由于 RTIL 带电基团的静电排斥作用,抗体处于稳定状态,从而防止了任何聚集。在这里,我们首次报道了非 Faradaic 电化学阻抗谱等效电路模型分析,用于分析和解释基于亲和力的生物传感,该分析和解释由离子液体的选择指导。使用该方法评估了两种常见的人体汗液生物标志物白细胞介素 6(IL-6)和皮质醇。使用两种离子液体获得的 IL-6 的检测限(LOD)均为 0.2 pg/mL,交叉反应研究表明,使用 Choline[DHP]检测 IL-6 的性能更好,对交叉反应分子没有响应。皮质醇的 LOD 为 0.1 ng/mL,交叉反应研究表明,BMIM[BF]中的皮质醇抗体对交叉反应分子没有信号响应。此外,与在水性缓冲液中使用捕获探针相比,离子液体的使用提高了灵敏度和 LOD。