This study was performed to examine whether radiofrequency fields characteristic of mobile phones at non-thermal levels can induce apoptosis in murine neuroblastoma cells in both proliferating and differentiated states.
The positive controls were X-ray (4 Gy) treated cells.
The complete detail of the exposure apparatus, the signal profile, the exposure geometry and dosimetry have been described in [Schuderer et al., 2004].
Frequency | 935 MHz |
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Type | |
Charakteristic |
|
Exposure duration | continuous for 24 h |
Exposure source |
|
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Chamber | Two identical waveguide cavities were placed in a tissue culture incubator maintained at 37°C with a humidified atmosphere of 5% CO2 in air. They were randomly assigned for RF or sham exposure. Good exposure and environmental control was achieved using field sensors, air temperature sensors, and an optimised airflow system. |
Setup | Cells were seeded into 35-mm Petri dishes in 3 ml of growth medium 24 h before any treatment and were placed inside the waveguides one hour before exposure. A specially designed holder allowed eight 35-mm Petri dishes to be placed accurately inside each chamber. |
Sham exposure | A sham exposure was conducted. |
Frequency | 935 MHz |
---|---|
Type | |
Charakteristic |
|
Exposure duration | continuous for 24 h |
Exposure source |
|
---|---|
Sham exposure | A sham exposure was conducted. |
Frequency | 935 MHz |
---|---|
Type | |
Charakteristic |
|
Exposure duration | continuous for 24 h |
Modulation type | CW |
---|
Exposure source |
|
---|---|
Sham exposure | A sham exposure was conducted. |
No statistically significant differences in apoptosis levels were found between the exposed and sham-exposed murine neuroblastoma cells neither in proliferating nor in differentiated state using the three assays at any time point post-radiofrequency irradiation.
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