Nanomedicine: Nanotechnology, Biology and Medicine
Volume 6, Issue 2 , Pages 298-317, April 2010

Chemical power for microscopic robots in capillaries

  • Tad Hogg, PhD

      Affiliations

    • Hewlett-Packard Laboratories, Palo Alto, California, USA
    • Corresponding Author InformationCorresponding author: Hewlett-Packard Laboratories, SCL, 1501 Page Mill MS1139, Palo Alto, CA 94304, USA.
  • ,
  • Robert A. Freitas Jr, JD

      Affiliations

    • Institute for Molecular Manufacturing, Palo Alto, California, USA

Received 5 June 2009; accepted 2 October 2009. published online 16 October 2009.

Abstract 

The power available to microscopic robots (nanorobots) that oxidize bloodstream glucose while aggregated in circumferential rings on capillary walls is evaluated with a numerical model using axial symmetry and time-averaged release of oxygen from passing red blood cells. Robots about 1 μm in size can produce up to several tens of picowatts, in steady state, if they fully use oxygen reaching their surface from the blood plasma. Robots with pumps and tanks for onboard oxygen storage could collect oxygen to support burst power demands two to three orders of magnitude larger. We evaluate effects of oxygen depletion and local heating on surrounding tissue. These results give the power constraints when robots rely entirely on ambient available oxygen and identify aspects of the robot design significantly affecting available power. More generally, our numerical model provides an approach to evaluating robot design choices for nanomedicine treatments in and near capillaries.

From the Clinical Editor

The power available to microscopic robots (nanorobots) that oxidize bloodstream glucose while aggregated in circumferential rings on capillary walls was evaluated in this study. The presented numerical model provides an approach to evaluating robot design choices for nanomedicine treatments in and near capillaries.

Key words: Capillary, Nanomedicine, Nanorobot, Nanorobotics, Numerical model, Oxygen transport, Power

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 R.A.F. acknowledges private grant support for this work from the Life Extension Foundation and the Institute for Molecular Manufacturing. TH acknowledges support from Hewlett-Packard Laboratories.

PII: S1549-9634(09)00190-7

doi:10.1016/j.nano.2009.10.002

Nanomedicine: Nanotechnology, Biology and Medicine
Volume 6, Issue 2 , Pages 298-317, April 2010