To study primary DNA damge in human blood lymphocytes exposed to 2450 MHz radiofrequency radiation.
Frequency | 2.45 GHz |
---|---|
Type | |
Charakteristic | |
Exposure duration | continuous for 2 h |
Modulation type | pulsed |
---|---|
Pulse width | 10 µs |
Duty cycle | 10 % |
Repetition frequency | 10 kHz |
Exposure source |
|
---|---|
Distance between exposed object and exposure source | 1.75 m |
Chamber | The anechoic room of 5.2 x 3.35 x 3.35 m was maintained at 22 ± 1°C. A Plexiglas (0.6-cm thick) box with two compartments and outside dimensions of 24.5 x 21.0 x 3.7 cm was placed in a tightly fitting pressed-foam box of 27 x 22 x 7 cm which was positioned directly under the horn antenna. |
Setup | Four T-25 tissue culture flasks were positioned in the open upper compartment of 1.2 cm height, three of them containing 6 ml of whole blood, the fourth one being used for temperature monitoring. The compartment was filled with warm water up to the height of the medium in the flasks. The closed lower compartment was circulated with warm water to maintain the liquid in the flasks at 37°C. |
Sham exposure | A sham exposure was conducted. |
Additional info | The pressed-foam box for simultaneous sham exposure was placed at the far end of the anechoic room away from the horn. Control samples were incubated for 2 h minus 5 min and in the end exposed to 50 cGy of ionizing radiation from a 137Cs γ-ray source at a dose rate of 1.008 cGy/min. |
No evidence for induction of DNA single-strand breaks and alkali-labile lesions in human blood lymphocytes exposed to pulsed-wave 2450 MHz radiofrequencey radiation was found, either immediately or at 4h after exposure.
This website uses cookies to provide you the best browsing experience. By continuing to use this website you accept our use of cookies.