Wackers Gideon, Cornelis Peter, Putzeys Tristan, Peeters Marloes, Tack Jan, Troost Freddy, Doll Theodor, Verhaert Nicolas, Wagner Patrick
Laboratory for Soft Matter and Biophysics, KU Leuven, Celestijnenlaan 200D, Leuven B-3001, Belgium.
Research Group Experimental Oto-rhino-laryngology, KU Leuven, O&N II, Herestraat 49, Leuven B-3001, Belgium.
ACS Sens. 2021 Jan 22;6(1):100-110. doi: 10.1021/acssensors.0c01844. Epub 2020 Dec 18.
In this article, we report on the development of a catheter-based, biomimetic sensor as a step toward a minimally invasive diagnostic instrument in the context of functional bowel disorders. Histamine is a key mediator in allergic and inflammatory processes in the small intestines; however, it is a challenge to determine histamine levels at the duodenal mucosa, and classical bioreceptors are unsuitable for use in the digestive medium of bowel fluid. Therefore, we have developed molecularly imprinted polypyrrole coatings for impedimetric sensing electrodes, which enable the quantification of histamine in nondiluted, human bowel fluid in a broad concentration range from 25 nM to 1 μM. The electrodes show negligible cross-sensitivity to histidine as a competitor molecule and, for comparison, we also evaluated the response of nonimprinted and taurine-imprinted polypyrrole to histamine. Furthermore, using equivalent-circuit modeling, we found that the molecular recognition of histamine by polypyrrole primarily increases the resistive component of the electrode-liquid interface while capacitive effects are negligible. The sensor, integrated into a catheter, measures differentially to correct for nonspecific adsorption effects in the complex matrix of bowel fluids, and a single triggering frequency is sufficient to determine histamine concentrations. Together, these features are beneficial for real-time diagnostic tests.
在本文中,我们报告了一种基于导管的仿生传感器的研发情况,这是朝着功能性肠道疾病的微创诊断仪器迈出的一步。组胺是小肠过敏和炎症过程中的关键介质;然而,测定十二指肠黏膜处的组胺水平具有挑战性,并且传统生物受体不适用于肠液的消化介质。因此,我们为阻抗传感电极开发了分子印迹聚吡咯涂层,能够在25 nM至1 μM的宽浓度范围内对未稀释的人体肠液中的组胺进行定量。该电极对作为竞争分子的组氨酸表现出可忽略不计的交叉敏感性,并且作为比较,我们还评估了非印迹和牛磺酸印迹聚吡咯对组胺的响应。此外,通过等效电路建模,我们发现聚吡咯对组胺的分子识别主要增加了电极 - 液体界面的电阻分量,而电容效应可忽略不计。集成在导管中的传感器进行差分测量以校正肠液复杂基质中的非特异性吸附效应,并且单一触发频率足以确定组胺浓度。这些特性共同有利于实时诊断测试。