To detect DNA single-strand breaks in lymphoblastoid cells exposed for short (2 and 3h) and long (21h) periods to pulsed signals at cellular telephones frequencies (813.5625 MHz and 836.55 MHz).
The studies were perfomed at low SAR to look for athermal radiofrequency radiation effects.
Exposure | Parameters |
---|---|
Exposure 1:
813.5625 MHz
Modulation type:
pulsed
Exposure duration:
intermittent 20 min on/off for 2, 3 and 21 hours
|
|
Exposure 2:
836.55 MHz
Modulation type:
pulsed
Exposure duration:
intermittent 20 min on/off for 2, 3 and 21 hours
|
Frequency | 813.5625 MHz |
---|---|
Type | |
Charakteristic |
|
Exposure duration | intermittent 20 min on/off for 2, 3 and 21 hours |
Modulation type | pulsed |
---|---|
Pulse width | 15 ms |
Repetition frequency | 22.22 Hz |
Additional info |
iDEN: time-domain multiplexing in which each second is broken down into a series of about 22 frames, each of 45 ms duration. Each frame is divided into three 15 ms slots. This results in RF carrier bursts of 15 ms duration, repeating at 45 ms intervals, at the mobile phone and the head of the user. The brief amplitude training pulse included at the leading edge of each slot is transmitted once every 200 frames (i.e. every 9 s) at 10 times the slot average power. |
Exposure source | |
---|---|
Chamber | Two TEM cells of 18 x 18 x 9 cm (both above and below the septum) were housed in a single incubator. They were each powered (exposed) or unpowered (sham). |
Setup | One 60-mm Petri dish with 5 ml of medium was placed on a 1.5 cm platform of styrene plastic which was placed centrally along the longitudinal axis on the septum in a region of reasonably uniform E-field normal to the dish. |
Additional info | The exposure pattern resulted in total exposure durations of 1, 1.67 and 10.67, respectively. There was no detectable rise in temperature at any power density used in these experiments. The ambient 60 Hz magnetic field outside the TEM cells was 0.13 ± 0.02 µT rms and 0.20 ± 0.04 µT rms. |
Frequency | 836.55 MHz |
---|---|
Type | |
Charakteristic |
|
Exposure duration | intermittent 20 min on/off for 2, 3 and 21 hours |
The results indicate that exposure of the cells to two different radiofrequency signals under athermal conditions altered the amount of DNA single-strand breaks. Exposure of cells to the iDEN signal (SAR of 2.4 µW/g, 2 or 21h) significantly decreased DNA damage and exposure at an SAR of 24 µW/g (2 or 21h) significantly increased DNA damage. Exposure of cells to the TDMA signal (SAR of 2.6 µW/g, 2 or 21h) and exposure at an SAR of 26 µW/g for 2h significantly decreased DNA damage.
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