CPC A61N 5/0613 (2013.01) [A61N 5/0601 (2013.01); A61N 5/0603 (2013.01); A61N 5/0624 (2013.01); H01L 27/15 (2013.01); A61N 2005/0611 (2013.01); A61N 2005/0626 (2013.01); A61N 2005/0647 (2013.01); A61N 2005/0652 (2013.01); A61N 2005/0653 (2013.01); A61N 2005/0661 (2013.01); A61N 2005/0662 (2013.01); A61N 2005/0663 (2013.01)] | 22 Claims |
1. A method comprising:
providing a first dose of light to mammalian tissue that induces a first biological effect for a first pathogen, the first dose of light being administered during a first time window, and an intensity of light of the first dose decreases to a reduced non-zero value during the first time window; and
providing a second dose of light to the mammalian tissue that induces a second biological effect, the second dose of light being administered during a second time window that is different than the first time window, wherein the second time window overlaps with a portion of the first time window, and wherein the first dose differs from the second dose by at least one of the following:
the first dose comprises a first peak wavelength in a range from 400 nanometers (nm) to 490 nm, the second dose comprises a second peak wavelength in a range from 500 nm to 900 nm or in a range from 320 nm to 400 nm, and the first peak wavelength is different than the second peak wavelength; or
the first dose comprises a first radiant flux in a range from 5 milliwatts per square centimeter (mW/cm2) to 10 mW/cm2, the second dose comprises a second radiant flux in a range from 10 mW/cm2 to 60 mW/cm2, and the second dose is different than the first dose.
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