30,007 research outputs found
Distributed Control of Microscopic Robots in Biomedical Applications
Current developments in molecular electronics, motors and chemical sensors
could enable constructing large numbers of devices able to sense, compute and
act in micron-scale environments. Such microscopic machines, of sizes
comparable to bacteria, could simultaneously monitor entire populations of
cells individually in vivo. This paper reviews plausible capabilities for
microscopic robots and the physical constraints due to operation in fluids at
low Reynolds number, diffusion-limited sensing and thermal noise from Brownian
motion. Simple distributed controls are then presented in the context of
prototypical biomedical tasks, which require control decisions on millisecond
time scales. The resulting behaviors illustrate trade-offs among speed,
accuracy and resource use. A specific example is monitoring for patterns of
chemicals in a flowing fluid released at chemically distinctive sites.
Information collected from a large number of such devices allows estimating
properties of cell-sized chemical sources in a macroscopic volume. The
microscopic devices moving with the fluid flow in small blood vessels can
detect chemicals released by tissues in response to localized injury or
infection. We find the devices can readily discriminate a single cell-sized
chemical source from the background chemical concentration, providing
high-resolution sensing in both time and space. By contrast, such a source
would be difficult to distinguish from background when diluted throughout the
blood volume as obtained with a blood sample
Using Surface-Motions for Locomotion of Microscopic Robots in Viscous Fluids
Microscopic robots could perform tasks with high spatial precision, such as
acting in biological tissues on the scale of individual cells, provided they
can reach precise locations. This paper evaluates the feasibility of in vivo
locomotion for micron-size robots. Two appealing methods rely only on surface
motions: steady tangential motion and small amplitude oscillations. These
methods contrast with common microorganism propulsion based on flagella or
cilia, which are more likely to damage nearby cells if used by robots made of
stiff materials. The power potentially available to robots in tissue supports
speeds ranging from one to hundreds of microns per second, over the range of
viscosities found in biological tissue. We discuss design trade-offs among
propulsion method, speed, power, shear forces and robot shape, and relate those
choices to robot task requirements. This study shows that realizing such
locomotion requires substantial improvements in fabrication capabilities and
material properties over current technology.Comment: 14 figures and two Quicktime animations of the locomotion methods
described in the paper, each showing one period of the motion over a time of
0.5 milliseconds; version 2 has minor clarifications and corrected typo
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