Cripps D J, Lowe N J, Lerner A B
Br J Dermatol. 1982 Jul;107(1):77-82. doi: 10.1111/j.1365-2133.1982.tb00293.x.
The action spectra for producing minimal phototoxic erythema with topical 0.I% trimethyl psoralen (TMP) and 8-methoxypsoralen (8-MOP) were determined with a double monochromator in the range of 295-380 nm. both psoralens induced photosensitivity in the range of 313-365 nm; TMP was 54% more effective than 8-MOP. There was no difference in the dose needed to produce minimal UV erythema or phototoxic erythema with 8-MOP and TMP at 295 and 305 nm, but at 313 nm with 8-MOP, photosensitivity was enhanced 3.5 times, and with TMP, sensitivity was enhanced 5.5 times. The peak sensitivity with 8-MOP was at 330 nm and for TMP it was 335 nm. No photosensitivity occurred above 380 nm. Results suggest that TMP and 8-MOP are significantly photoreactive at 320-335 nm. Commonly used UV-A light sources show peak emission around 360 nm. If there is a relationship between development of erythema and therapeutic effectiveness than this raises the possibility of alternative UV light sources for phototherapy with psoralens.
使用双单色仪在295 - 380纳米范围内测定了外用0.1%三甲补骨脂素(TMP)和8 - 甲氧基补骨脂素(8 - MOP)产生最小光毒性红斑的作用光谱。两种补骨脂素在313 - 365纳米范围内均能诱导光敏反应;TMP的效果比8 - MOP高54%。在295和305纳米处,产生最小紫外线红斑或光毒性红斑所需的8 - MOP和TMP剂量没有差异,但在313纳米处,8 - MOP的光敏性增强了3.5倍,TMP的敏感性增强了5.5倍。8 - MOP的峰值敏感性在330纳米处,TMP在335纳米处。在380纳米以上未发生光敏反应。结果表明,TMP和8 - MOP在320 - 335纳米处具有显著的光反应性。常用的紫外线A光源的峰值发射在360纳米左右。如果红斑的发展与治疗效果之间存在关联,那么这就增加了使用替代紫外线光源进行补骨脂素光疗的可能性。