Department of Pharmacology and Molecular Sciences , Johns Hopkins School of Medicine , Baltimore , Maryland 21205 , United States.
ACS Sens. 2019 Oct 25;4(10):2832-2837. doi: 10.1021/acssensors.9b01616. Epub 2019 Oct 15.
The electrochemical aptamer-based (E-AB) sensing platform appears to be a convenient (rapid, single-step, and calibration-free) and modular approach to measure concentrations of specific molecules (irrespective of their chemical reactivity) directly in blood and even in situ in the living body. Given these attributes, the platform may thus provide significant opportunities to render therapeutic drug monitoring (the clinical practice in which dosing is adjusted in response to plasma drug measurements) as frequent and convenient as the measurement of blood sugar has become for diabetics. The ability to measure arbitrary molecules in the body in real time could even enable closed-loop feedback control over plasma drug levels in a manner analogous to the recently commercialized controlled blood sugar systems. As initial exploration of this, we describe here the selection of an aptamer against vancomycin, a narrow therapeutic window antibiotic for which therapeutic monitoring is a critical part of the standard of care, and its adaptation into an electrochemical aptamer-based (E-AB) sensor. Using this sensor, we then demonstrate: (i) rapid (seconds) and convenient (single-step and calibration-free) measurement of plasma vancomycin in finger-prick-scale samples of whole blood, (ii) high-precision measurement of subject-specific vancomycin pharmacokinetics (in a rat animal model), and (iii) high-precision, closed-loop feedback control over plasma levels of the drug (in a rat animal model). The ability to not only track (with continuous-glucose-monitor-like measurement frequency and convenience) but also actively control plasma drug levels provides an unprecedented route toward improving therapeutic drug monitoring and, more generally, the personalized, high-precision delivery of pharmacological interventions.
电化学适体(E-AB)传感平台似乎是一种便捷(快速、单步、无需校准)且模块化的方法,可以直接在血液中测量特定分子的浓度(无论其化学反应性如何),甚至可以在活体中进行原位测量。鉴于这些特性,该平台可能为治疗药物监测(根据血浆药物测量结果调整剂量的临床实践)提供重要机会,使其像糖尿病患者测量血糖一样频繁和方便。实时测量体内任意分子的能力甚至可以实现对血浆药物水平的闭环反馈控制,类似于最近商业化的血糖控制系统。作为对此的初步探索,我们在这里描述了针对万古霉素的适体选择,万古霉素是一种治疗窗狭窄的抗生素,其治疗监测是标准护理的重要组成部分,并将其改编为电化学适体(E-AB)传感器。然后,我们使用该传感器演示了:(i)在手指穿刺全血样本中快速(秒级)和方便(单步且无需校准)测量血浆万古霉素,(ii)高精度测量个体特有的万古霉素药代动力学(在大鼠动物模型中),以及(iii)高精度、闭环反馈控制药物的血浆水平(在大鼠动物模型中)。不仅能够跟踪(具有类似于连续葡萄糖监测的测量频率和便利性)而且能够主动控制血浆药物水平的能力为改善治疗药物监测以及更普遍地为个性化、高精度的药物干预提供了一条前所未有的途径。