Ar. Young et al., THE UVR WAVELENGTH DEPENDENCE FOR LOMEFLOXACIN PHOTOSENSITIZATION OF HUMAN SKIN, Journal of photochemistry and photobiology.B, Biology, 32(3), 1996, pp. 165-170
Lomefloxacin is a new fluoroquinolone with effective broad-spectrum an
timicrobial activity. However, in common with other structurally relat
ed drugs, skin photosensitization reactions have been reported. The wa
velength dependence for such photosensitization has been investigated
on the previously unexposed buttock skin of 12 normal healthy human vo
lunteers of skin types I and II. Using geometric root 2 dose increment
s, baseline 24 h minimal erythema doses were assessed at 300, 320, 330
, 340, 350 and 360 nm, and with broad-band UVA. In addition, dose-resp
onse curves were constructed for erythema as measured by a reflectance
device. Subjects received single daily oral doses of 400 mg lomefloxa
cin at specified times for 4 days. At 2 h after the final dose, new ar
eas of buttock skin were irradiated to assess changes in minimal eryth
ema dose and erythema dose-response. Convolution of the erythema actio
n spectra obtained pre- and on-drug with a terrestrial solar spectrum
showed that, although the UVA sensitivity on-drug was enhanced, most o
f the erythemally effective solar energy was still in the UVB region.
An action spectrum derived for lomefloxacin skin photosensitization sh
owed peak activity at 320 nm, the same spectral region as that for max
imal absorption of the drug. There was no evidence of skin photosensit
ization at 300 nm.