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A 7.5 mm diameter of the central cornea was then irradiated with an irradiance of 3 mW/cm (VEGA CBM x-linker, C.S.O, Florence, Italy) for 30 minutes.
An area with 9 mm diameter in the center of the cornea was irradiated with an irradiance of 3.0 mW/cm.
The central cornea was then similarly irradiated with an irradiance of 3 mW/cm (VEGA CBM x-linker, C.S.O, Florence, Italy) for 30 minutes.
The apparatus consisted of 2 double UVA diodes (Roithner Lasertechnik), with overlapping irradiation fields for an irradiance of up to 6 mW/cm [ 6, 15].
The protein was irradiated with NIRW light at an irradiance of 0.2 mW/cm (which is saturating) or kept in green light.
The mixture was irradiated by the UV lamp with an irradiance of 1.1 mW/cm2.
Cells designated for phototoxicity analysis were irradiated for 10 min as indicated above with white light at an irradiance of 16 J/cm/min.
A xenon lamp source (Oriel, USA) with an irradiance of 100 mwasm2 was used to illuminate the solar cell (equivalent to AM1.5 irradiation).
Scleral strips were irradiated with UVA (365 nm, UV-X 1000 system; IROC Innocross AG Co. Ltd., Switzerland) at an irradiance of 3 mW/cm and a distance of 5 cm from the scleral plane.
This may use an irradiance forecast model based on other advanced neural network techniques.
Fibrocapsa japonica was cultured at an irradiance of 35 μmol photons m-2 s-1.
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