A fiber optic photoacoustic sensor for real-time heparin monitoring

肝素 部分凝血活酶时间 体内 凝血时间激活 血液取样 凝血时间 生物医学工程 全血 医学 药理学 外科 内科学 生物 血小板 生物技术
作者
Jingcheng Zhou,Wonjun Yim,Jiajing Zhou,Zhicheng Jin,Ming Xu,Yash Mantri,Tengyu He,Yong Cheng,Lei Fu,Zhuohong Wu,Tiffany Hancock,William F. Penny,Jesse V. Jokerst
出处
期刊:Biosensors and Bioelectronics [Elsevier BV]
卷期号:196: 113692-113692 被引量:12
标识
DOI:10.1016/j.bios.2021.113692
摘要

Heparin is a common anticoagulant, but heparin overdose is a common intensive care unit (ICU) medication error due to the narrow therapeutic window of heparin. Conventional methods to monitoring heparin suffer from long turnaround time, the need for skilled personnel, and low frequency of sampling. To overcome these issues, we describe here a fiber optic photoacoustic (PA) sensor for real-time heparin monitoring. The proposed sensor was validated with in vitro testing and in a simulated in vivo model using the following samples: (1) phosphate-buffered saline (PBS), (2) spiked human plasma, (3) spiked whole human blood, and (4) clinical samples from patients treated with heparin. Samples were validated by comparing the PA signal to the activated partial thromboplastin time (aPTT) as well as the activated clotting time (ACT). Importantly, the proposed sensor has a short turnaround time (3 min) and a limit of detection of 0.18 U/ml in whole human blood. The PA signal is linear with heparin dose and correlates with the aPTT value (Pearson's r = 0.99). The PA signal from 32 clinical samples collected from eight patients linearly correlated with ACT values (Pearson's r = 0.89, in vitro; Pearson's r = 0.93, simulated in vivo). The PA signal was also validated against the cumulative heparin dose (Pearson's r = 0.94, in vitro; Pearson's r = 0.96, simulated in vivo). This approach could have applications in both in vitro and real-time in vivo heparin monitoring.
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