A cellulose-based photoacoustic sensor to measure heparin concentration and activity in human blood samples

被引:28
作者
Jeevarathinam, Ananthakrishnan Soundaram [1 ]
Pai, Navin [1 ]
Huang, Kevin [1 ]
Hariri, Ali [1 ]
Wang, Junxin [1 ]
Bai, Yuting [1 ]
Wang, Lu [1 ]
Hancock, Tiffany [4 ]
Keys, Stanley [4 ]
Penny, William [4 ]
Jokerst, Jesse V. [1 ,2 ,3 ]
机构
[1] Univ Calif San Diego, Dept NanoEngn, La Jolla, CA 92093 USA
[2] Univ Calif San Diego, Mat Sci Program, La Jolla, CA 92093 USA
[3] Univ Calif San Diego, Dept Radiol, La Jolla, CA 92093 USA
[4] VA Healthcare Syst, Cardiol Unit, La Jolla, CA 92161 USA
基金
美国国家卫生研究院;
关键词
Heparin sensing; Photoacoustic imaging; Ultrasound; Anticoagulation therapy; Cellulose based sensor; PARTIAL THROMBOPLASTIN TIME; CHONDROITIN SULFATE CONTAMINANT; ACTIVATED CLOTTING TIME; UNFRACTIONATED HEPARIN; BLUE; SYSTEM; PROBES; ASSAY;
D O I
10.1016/j.bios.2018.11.052
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
Heparin is an indispensable drug in anticoagulation therapy but with a narrow therapeutic window, which dictates regular testing and dose adjustment. However, current monitoring tools have a long turnaround time or are operator intensive. In this work, we describe a cellulose-based photoacoustic sensor for heparin. The sensors have a turnaround time of 6 min for whole blood samples and 3 min for plasma samples regardless of heparin concentration. These sensors have a limit of detection of 0.28 U/ml] heparin in human plasma and 0.29 U/ml in whole blood with a linear response (Pearson's r = 0.99) from 0 to 2 U/ml heparin in plasma and blood samples. The relative standard deviation was < 12.5% in plasma and < 17.5% in whole blood. This approach was validated with heparin-spiked whole human blood and had a linear correlation with the activated partial thromboplastin time (aPTT) (r = 0.99). We then studied 16 sets of clinical samples these had a linear correlation with the activated clotting time (ACT) (Pearson's r = 0.86, P < 0.0001). The photoacoustic signal was also validated against the cumulative heparin dose (Pearson's r = 0.71, P < 0.0001). This approach could have applications in bed-side heparin assays for continuous heparin monitoring.
引用
收藏
页码:831 / 837
页数:7
相关论文
共 54 条
  • [1] Effect of freezing method and storage at-20 °C and-70 °C on prothrombin time, aPTT and plasma fibrinogen levels
    Alesci, Sonja
    Borggrefe, Martin
    Dempfle, Carl-Erik
    [J]. THROMBOSIS RESEARCH, 2009, 124 (01) : 121 - 126
  • [2] Electrochemical heparin sensing at liquid/liquid interfaces and polymeric membranes
    Amemiya, Shigeru
    Kim, Yushin
    Ishimatsu, Ryoichi
    Kabagambe, Benjamin
    [J]. ANALYTICAL AND BIOANALYTICAL CHEMISTRY, 2011, 399 (02) : 571 - 579
  • [3] [Anonymous], 1989, Lancet, V2, P182
  • [4] [Anonymous], THROMB J
  • [5] [Anonymous], ANGEW CHEM INT ED EN
  • [6] [Anonymous], J BIOPHOTONICS
  • [7] [Anonymous], C SPIE BIOS SPIE
  • [8] Guidelines on the use and monitoring of heparin
    Baglin, T
    Barrowcliffe, TW
    Cohen, A
    Greaves, M
    [J]. BRITISH JOURNAL OF HAEMATOLOGY, 2006, 133 (01) : 19 - 34
  • [9] Anticoagulation and pediatric extracorporeal membrane oxygenation: Impact of activated clotting time and heparin dose on survival
    Baird, Christopher W.
    Zurakowski, David
    Robinson, Barbara
    Gandhi, Sanjiv
    Burdis-Koch, Leighann
    Tamblyn, Joseph
    Munoz, Ricardo
    Fortich, Karol
    Pigula, Frank A.
    [J]. ANNALS OF THORACIC SURGERY, 2007, 83 (03) : 912 - 920
  • [10] Therapeutic monitoring of unfractionated heparin - trials and tribulations
    Baluwala, Israfil
    Favaloro, Emmanuel J.
    Pasalic, Leonardo
    [J]. EXPERT REVIEW OF HEMATOLOGY, 2017, 10 (07) : 595 - 605