2019
DOI: 10.1002/bem.22223
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Millimeter‐Wave Heating in In Vitro Studies: Effect of Convection in Continuous and Pulse‐Modulated Regimes

Abstract: Shallow penetration of millimeter waves (MMW) and non-uniform illumination in in vitro experiments result in a non-uniform distribution of the specific absorption rate (SAR). These SAR gradients trigger convective currents in liquids affecting transient and steady-state temperature distributions. We analyzed the effect of convection on temperature dynamics during MMW exposure in continuous-wave (CW) and pulsed-wave (PW) amplitude-modulated regimes using microthermocouples. Temperature rise kinetics are charact… Show more

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Cited by 7 publications
(14 citation statements)
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References 59 publications
(68 reference statements)
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“…The exposure system used in this study is presented in Fig. 1 and described in detail in [24]. A WR15 waveguide (WG) aperture antenna, operating at 58.4 GHz, was used to drive the MMW radiation toward one well of the 12-well tissue culture plate set 5 mm from it (inset of Fig.…”
Section: Methodsmentioning
confidence: 99%
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“…The exposure system used in this study is presented in Fig. 1 and described in detail in [24]. A WR15 waveguide (WG) aperture antenna, operating at 58.4 GHz, was used to drive the MMW radiation toward one well of the 12-well tissue culture plate set 5 mm from it (inset of Fig.…”
Section: Methodsmentioning
confidence: 99%
“…Temperature measurements and cell exposures were performed in separate experiments to avoid possible cellular damage or contamination as well as local increase of SAR in the cell monolayer due to the presence of the µTC (see sections A and B of Results). Indeed, the presence of the cells induces an approximatively 1% drop of the incoming energy absorbed by the culture medium [30], that affects only slightly the temperature dynamics [24] (differences < 1% compared to measurements with cells). Temperature measurements were repeated 4 times to ensure reproducibility.…”
Section: B Microscale Temperature Measurementsmentioning
confidence: 95%
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“…The cells were exposed in the corresponding culture medium supplemented with 10 mM 4-(2-hydroxyethyl)-1-piperazineethanesulfonic acid (HEPES) for primary keratinocyte cultures and 4.6 mM HEPES for HaCaT cells for 3 h. For each experiment 4 ml of medium was used. Note that the volume does not influence either the SAR or the IPD [Orlacchio et al, 2019]. Two exposure conditions (unexposed [Sham] and MMW-exposed [Expo]) were used under the same cell culture conditions.…”
Section: Exposure System and Experimental Setupmentioning
confidence: 99%