Wu Bingchen, Castagnola Elisa, Cui Xinyan Tracy
Department of Bioengineering, University of Pittsburgh, Pittsburgh, PA 15213, USA.
Center for the Neural Basis of Cognition, Pittsburgh, PA 15213, USA.
Micromachines (Basel). 2023 Jan 27;14(2):323. doi: 10.3390/mi14020323.
The number of people aged 12 years and older using illicit drugs reached 59.3 million in 2020, among which 5.2 million are cocaine users based on the national data. In order to fully understand cocaine addiction and develop effective therapies, a tool is needed to reliably measure real-time cocaine concentration and neural activity in different regions of the brain with high spatial and temporal resolution. Integrated biochemical sensing devices based upon flexible microelectrode arrays (MEA) have emerged as a powerful tool for such purposes; however, MEAs suffer from undesired biofouling and inflammatory reactions, while those with immobilized biologic sensing elements experience additional failures due to biomolecule degradation. Aptasensors are powerful tools for building highly selective sensors for analytes that have been difficult to detect. In this work, DNA aptamer-based electrochemical cocaine sensors were integrated on flexible MEAs and protected with an antifouling zwitterionic poly (sulfobetaine methacrylate) (PSB) coating, in order to prevent sensors from biofouling and degradation by the host tissue. In vitro experiments showed that without the PSB coating, both adsorption of plasma protein albumin and exposure to DNase-1 enzyme have detrimental effects on sensor performance, decreasing signal amplitude and the sensitivity of the sensors. Albumin adsorption caused a 44.4% sensitivity loss, and DNase-1 exposure for 24 hr resulted in a 57.2% sensitivity reduction. The PSB coating successfully protected sensors from albumin fouling and DNase-1 enzyme digestion. In vivo tests showed that the PSB coated MEA aptasensors can detect repeated cocaine infusions in the brain for 3 hrs after implantation without sensitivity degradation. Additionally, the same MEAs can record electrophysiological signals at different tissue depths simultaneously. This novel flexible MEA with integrated cocaine sensors can serve as a valuable tool for understanding the mechanisms of cocaine addiction, while the PSB coating technology can be generalized to improve all implantable devices suffering from biofouling and inflammatory host responses.
2020年,12岁及以上使用非法药物的人数达到5930万,根据全国数据,其中520万是可卡因使用者。为了全面了解可卡因成瘾并开发有效的治疗方法,需要一种工具来以高空间和时间分辨率可靠地测量大脑不同区域的实时可卡因浓度和神经活动。基于柔性微电极阵列(MEA)的集成生化传感装置已成为实现此类目的的强大工具;然而,MEA会遭受不必要的生物污染和炎症反应,而带有固定化生物传感元件的MEA由于生物分子降解会出现额外的故障。适体传感器是构建用于检测难以检测的分析物的高选择性传感器的强大工具。在这项工作中,基于DNA适配体的电化学可卡因传感器集成在柔性MEA上,并用抗污两性离子聚(甲基丙烯酸磺酸甜菜碱)(PSB)涂层进行保护,以防止传感器被宿主组织生物污染和降解。体外实验表明,没有PSB涂层时,血浆蛋白白蛋白的吸附和暴露于DNase-1酶都会对传感器性能产生不利影响,降低传感器的信号幅度和灵敏度。白蛋白吸附导致灵敏度损失44.4%,暴露于DNase-1酶24小时导致灵敏度降低57.2%。PSB涂层成功地保护了传感器免受白蛋白污染和DNase-1酶消化。体内测试表明,PSB涂层的MEA适体传感器在植入后能够检测大脑中重复注入的可卡因达3小时,且灵敏度不会降低。此外,相同的MEA可以同时记录不同组织深度的电生理信号。这种集成了可卡因传感器的新型柔性MEA可作为了解可卡因成瘾机制的有价值工具,而PSB涂层技术可以推广应用于改善所有遭受生物污染和炎症宿主反应的可植入设备。