Tanak Ambalika S, Muthukumar Sriram, Krishnan Subramaniam, Schully Kevin L, Clark Danielle V, Prasad Shalini
Department of Bioengineering, The University of Texas at Dallas, TX, USA.
EnLiSense LLC, 1813 Audubon Pond Way, Allen, TX, 75013, USA.
Biosens Bioelectron. 2021 Jan 1;171:112726. doi: 10.1016/j.bios.2020.112726. Epub 2020 Oct 19.
The implementation of endotype-driven effective intervention strategies is now considered as an essential component for sepsis management. Rapid screening and frequent monitoring of immune responses are critical for evidence-based informed decisions in the early hours of patient arrival. Current technologies focus on pathogen identification that lack rapid testing of the patient immune response, impeding clinicians from providing appropriate sepsis treatment. Herein, we demonstrate a first-of-its-kind novel point-of-care device that uses a unique approach by directly monitoring a panel of five cytokine biomarkers (IL-6, IL-8, IL-10, TRAIL & IP-10), that is attributed as a sign of the body's host immune response to sepsis. The developed point-of-care device encompasses a disposable sensor cartridge attached to an electrochemical reader. High sensitivity is achieved owing to the unique sensor design with an array of nanofilm semiconducting/metal electrode interface, functionalized with specific capture probes to measure target biomarkers simultaneously using non-faradaic electrochemical impedance spectroscopy. The sensor has a detection limit of ~1 pg/mL and provides results in less than five minutes from a single drop of undiluted plasma sample. Furthermore, the sensor demonstrates an excellent correlation (Pearson's r > 0.90) with the reference method for a total n = 40 clinical samples, and the sensor's performance is ~30 times faster compared to the standard reference technique. We have demonstrated the sensor's effectiveness to enhance diagnosis with a mechanistic biomarker-guided approach that can help disease endotypying for effective clinical management of sepsis at the patient bedside.
内型驱动的有效干预策略的实施现在被认为是脓毒症管理的重要组成部分。对免疫反应进行快速筛查和频繁监测对于患者入院早期基于证据的明智决策至关重要。当前技术侧重于病原体识别,缺乏对患者免疫反应的快速检测,这阻碍了临床医生提供适当的脓毒症治疗。在此,我们展示了一种首创的新型即时检测设备,该设备采用独特方法,直接监测一组五种细胞因子生物标志物(IL-6、IL-8、IL-10、TRAIL和IP-10),这些生物标志物被视为身体对脓毒症宿主免疫反应的标志。所开发的即时检测设备包括一个连接到电化学读取器的一次性传感器盒。由于独特的传感器设计,具有纳米薄膜半导体/金属电极界面阵列,并通过特定的捕获探针进行功能化,以使用非法拉第电化学阻抗谱同时测量目标生物标志物,从而实现了高灵敏度。该传感器的检测限约为1 pg/mL,从一滴未稀释的血浆样品中可在不到五分钟内得出结果。此外,对于总共n = 40份临床样品,该传感器与参考方法显示出极好的相关性(皮尔逊r>0.90),并且该传感器的性能比标准参考技术快约30倍。我们已经证明了该传感器通过机械生物标志物引导方法增强诊断的有效性,该方法有助于在患者床边对脓毒症进行疾病内型分类以实现有效的临床管理。