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Closed-loop control of circulating drug levels in live animals

Nature Biomedical Engineering volume 1, Article number: 0070 (2017) Cite this article

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Abstract

Current methods of drug dosing rely on physical parameters (such as sex, age and weight) that do not account for genetic and physiological differences among individual patients. These differences can greatly affect how drugs are processed in the body and can result in ineffective underdosing or toxic overdosing. Here, we describe a generalizable closed-loop system consisting of a biosensor, controller and infusion pump, and a model of drug pharmacokinetics that continuously monitors and adjusts the concentration of a given drug in the body. As proof of concept, we demonstrate that the system can maintain the concentration of doxorubicin—a widely used chemotherapy drug—in live rabbits and rats at any desired set point and in real time, while automatically compensating for large pharmacokinetic differences among individual animals and stabilizing dramatic perturbations arising from acute drug–drug interactions. The feedback-loop system opens up the possibility of tightly controlled, patient-specific dosing of chemotherapeutics and other drugs within narrow therapeutic windows.

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Figure 1: Closed-loop control of in vivo drug levels with real-time biosensing.
Figure 2: Closed-loop feedback control of Dox in vivo.
Figure 3: Closed-loop control of plasma drug levels in animals with varying PK.
Figure 4: Closed-loop infusion during acute drug–drug interactions.
Figure 5: Closed-loop feedback control of Dox in live, anaesthetized Sprague–Dawley rats.

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Acknowledgements

We are grateful for the financial support of the Garland Initiative, Army Research Office (W911NF-10-2-0114, W911QY-15-C-0026) and the W. M. Keck Foundation Medical Research Program. We thank B. Eisenhower, D. Hoggarth, J. Somerson, D. Mamerow, A. Pressman, G. Marcus, S. Hall, M. Eisenstein, M. Nakamoto, K. Plaxco and F. Doyle for helpful discussions. We also thank A. Griffin, R. Wynn, and M. Garcia at the UCSB Animal Resource Center for their technical expertise and assistance with the animal studies.

Author information

Author notes

  1. P. L. Mage

    Present address: Department of Electrical Engineering, Stanford University, Stanford, California, 94305, USA

  2. B. S. Ferguson

    Present address: Aptitude Medical Systems, Inc., Santa Barbara, California, 93105, USA

Authors and Affiliations

  1. Department of Materials, University of California, Santa Barbara, 93106, California, USA

    P. L. Mage & H. T. Soh

  2. Institute for Collaborative Biotechnologies, University of California, Santa Barbara, 93106, California, USA

    B. S. Ferguson, D. Maliniak, K. L Ploense, T. E. Kippin & H. T. Soh

  3. Department of Psychological and Brain Sciences, University of California, Santa Barbara, 93106, California, USA

    K. L Ploense & T. E. Kippin

  4. Neuroscience Research Institute, University of California, Santa Barbara, 93106, California, USA

    T. E. Kippin

  5. Department of Molecular, Cellular and Developmental Biology, University of California, Santa Barbara, 93106, California, USA

    T. E. Kippin

  6. Department of Electrical Engineering, Stanford University, Stanford, 94305, California, USA

    H. T. Soh

  7. Department of Radiology, Stanford University, Stanford, 94305, California, USA

    H. T. Soh

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Contributions

B.S.F. and H.T.S. conceived of the project. P.L.M. and B.S.F. designed the experiments, fabricated the sensors and created the control and simulation software. P.L.M. directed the animal studies, performed the controller simulations and analysed the data. D.M. and K.L.P. performed all animal procedures in the studies. T.E.K. assisted in design of, provided supervision for, and wrote the protocols for the animal studies. P.L.M. and H.T.S wrote and edited the manuscript. All authors discussed the results and commented on the manuscript.

Corresponding author

Correspondence to H. T. Soh.

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Mage, P., Ferguson, B., Maliniak, D. et al. Closed-loop control of circulating drug levels in live animals. Nat Biomed Eng 1, 0070 (2017). https://doi.org/10.1038/s41551-017-0070

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