Electrochemical Aptamer-Based Sensors for Improved Therapeutic Drug Monitoring and High-Precision, Feedback-Controlled Drug Delivery

被引:160
|
作者
Dauphin-Ducharme, Philippe [1 ,2 ]
Yang, Kyungae [6 ]
Arroyo-Curras, Netzahualcoyotl [8 ]
Ploense, Kyle L. [1 ,2 ]
Zhang, Yameng [6 ]
Gerson, Julian [3 ,4 ,5 ]
Kurnik, Martin [1 ,2 ]
Kippin, Tod E. [3 ,4 ,5 ]
Stojanovic, Milan N. [6 ,7 ]
Plaxco, Kevin W. [1 ,2 ]
机构
[1] Univ Calif Santa Barbara, Dept Chem & Biochem, Santa Barbara, CA 93106 USA
[2] Univ Calif Santa Barbara, Ctr Bioengn, Santa Barbara, CA 93106 USA
[3] Univ Calif Santa Barbara, Dept Psychol & Brain Sci, Santa Barbara, CA 93106 USA
[4] Univ Calif Santa Barbara, Dept Mol Cellular & Dev Biol, Santa Barbara, CA 93106 USA
[5] Univ Calif Santa Barbara, Neurosci Res Inst, Santa Barbara, CA 93106 USA
[6] Columbia Univ, Ctr Innovat Diagnost & Therapeut Approaches, Dept Med, New York, NY 10032 USA
[7] Columbia Univ, Dept Biomed Engn & Syst Biol, New York, NY 10032 USA
[8] Johns Hopkins Univ, Sch Med, Dept Pharmacol & Mol Sci, Baltimore, MD 21205 USA
基金
加拿大自然科学与工程研究理事会; 美国国家卫生研究院;
关键词
vancomycin; therapeutic drug monitoring; controlled drug delivery; square-wave voltammetry; DNA aptamer; electrochemical DNA biosensor; IN-VITRO SELECTION; MOLECULAR MEASUREMENTS; LIQUID-CHROMATOGRAPHY; HPLC METHOD; VANCOMYCIN; PHARMACOKINETICS; IMMUNOASSAYS; PLASMA;
D O I
10.1021/acssensors.9b01616
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
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.
引用
收藏
页码:2832 / 2837
页数:11
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