In Vivo Glucose Sensing 2009
DOI: 10.1002/9780470567319.ch7
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Transdermal Microfluidic Continuous Monitoring Systems

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Cited by 4 publications
(4 citation statements)
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“…The impressive success of the noninvasive biosensing GlucoWatch (Cygnus) system is because it relies on reverse iontophoresis. Since the cells membrane is negatively charged, the commented device cycles a ∼0.5 mA cm −2 DC between two gel swabs on the skin [ 65 ]. Abundant Na + ions into the ISF (~ 140 mM) are moved electrophoretically to the cathode, while anions are electrorepulsed, e.g., Cl − , ascorbate, urate [ 65 ].…”
Section: Sweat Gland Physiology and Web's Sweat Samplingmentioning
confidence: 99%
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“…The impressive success of the noninvasive biosensing GlucoWatch (Cygnus) system is because it relies on reverse iontophoresis. Since the cells membrane is negatively charged, the commented device cycles a ∼0.5 mA cm −2 DC between two gel swabs on the skin [ 65 ]. Abundant Na + ions into the ISF (~ 140 mM) are moved electrophoretically to the cathode, while anions are electrorepulsed, e.g., Cl − , ascorbate, urate [ 65 ].…”
Section: Sweat Gland Physiology and Web's Sweat Samplingmentioning
confidence: 99%
“…Since the cells membrane is negatively charged, the commented device cycles a ∼0.5 mA cm −2 DC between two gel swabs on the skin [ 65 ]. Abundant Na + ions into the ISF (~ 140 mM) are moved electrophoretically to the cathode, while anions are electrorepulsed, e.g., Cl − , ascorbate, urate [ 65 ]. Cations present at sweat ducts and hair follicles pass through the paracellular spaces among cells, while neutral molecules like glucose and others get out to the skin surface at a rate proportional to the applied potential, e.g., 15–150 nL of ISF at 0.3 mA by 3 min [ 65 ].…”
Section: Sweat Gland Physiology and Web's Sweat Samplingmentioning
confidence: 99%
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“…One region of the optical spectrum with untapped potential for continuous measurement of physiological information is the short-wavelength infrared (SWIR), 3 , 4 which typically incorporates 900 to 1700 nm light. In this region, there are key absorption peaks for biological molecules, such as glucose, urea, triacetin, and water 3 , 5 , 6 . However, changes in these peaks cannot easily be isolated using traditional broad light-emitting diodes (LEDs) and a single photodiode, causing them to become confounding variables for one another.…”
Section: Introductionmentioning
confidence: 99%