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1.
IEEE Trans Neural Syst Rehabil Eng ; 24(9): 971-980, 2016 09.
Article in English | MEDLINE | ID: mdl-26561476

ABSTRACT

Quantitative gait analysis enables clinicians to evaluate patient mobility and to diagnose neuromuscular disorders. The clinical application of gait analysis is currently limited by the high operating costs of gait laboratories. The use of instrumented footwear that performs out of the lab measurements on subjects' walking patterns is a promising way to overcome this limitation. Besides serving as assessment tools, such devices can also act as retraining tools that help regulate a patient's gait with acoustic or vibrotactile stimuli.


Subject(s)
Actigraphy/instrumentation , Micro-Electrical-Mechanical Systems/instrumentation , Monitoring, Ambulatory/instrumentation , Physical Stimulation/instrumentation , Shoes , Walking Speed/physiology , Adult , Equipment Design , Equipment Failure Analysis , Feedback, Sensory/physiology , Female , Humans , Male , Physical Stimulation/methods , Reproducibility of Results , Sensitivity and Specificity , Touch/physiology , Transducers, Pressure
2.
Proc Natl Acad Sci U S A ; 109(33): 13182-7, 2012 Aug 14.
Article in English | MEDLINE | ID: mdl-22847405

ABSTRACT

Bacteria primarily exist in robust, surface-associated communities known as biofilms, ubiquitous in both natural and anthropogenic environments. Mature biofilms resist a wide range of antimicrobial treatments and pose persistent pathogenic threats. Treatment of adherent biofilm is difficult, costly, and, in medical systems such as catheters or implants, frequently impossible. At the same time, strategies for biofilm prevention based on surface chemistry treatments or surface microstructure have been found to only transiently affect initial attachment. Here we report that Slippery Liquid-Infused Porous Surfaces (SLIPS) prevent 99.6% of Pseudomonas aeruginosa biofilm attachment over a 7-d period, as well as Staphylococcus aureus (97.2%) and Escherichia coli (96%), under both static and physiologically realistic flow conditions. In contrast, both polytetrafluoroethylene and a range of nanostructured superhydrophobic surfaces accumulate biofilm within hours. SLIPS show approximately 35 times the reduction of attached biofilm versus best case scenario, state-of-the-art PEGylated surface, and over a far longer timeframe. We screen for and exclude as a factor cytotoxicity of the SLIPS liquid, a fluorinated oil immobilized on a structured substrate. The inability of biofilm to firmly attach to the surface and its effective removal under mild flow conditions (about 1 cm/s) are a result of the unique, nonadhesive, "slippery" character of the smooth liquid interface, which does not degrade over the experimental timeframe. We show that SLIPS-based antibiofilm surfaces are stable in submerged, extreme pH, salinity, and UV environments. They are low-cost, passive, simple to manufacture, and can be formed on arbitrary surfaces. We anticipate that our findings will enable a broad range of antibiofilm solutions in the clinical, industrial, and consumer spaces.


Subject(s)
Biofouling/prevention & control , Solutions/chemistry , Biofilms/drug effects , Escherichia coli/cytology , Escherichia coli/drug effects , Escherichia coli/physiology , Polytetrafluoroethylene/pharmacology , Porosity/drug effects , Pseudomonas aeruginosa/cytology , Pseudomonas aeruginosa/drug effects , Pseudomonas aeruginosa/physiology , Staphylococcus aureus/cytology , Staphylococcus aureus/drug effects , Staphylococcus aureus/physiology , Surface Properties/drug effects
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