de With A, Greulich K O
Physikalisch Chemisches Institut, Universität Heidelberg, Germany.
J Photochem Photobiol B. 1995 Sep;30(1):71-6. doi: 10.1016/1011-1344(95)07151-q.
Human lymphocytes from a cell culture were irradiated with laser pulses of an Xe-Cl excimer laser (308 nm) or a dye laser at wavelengths from 312 to 640 nm. After conversion of photoinduced DNA damage into DNA strand breaks the "comet assay" (single-cell gel electrophoresis) was used to determine the number of photons required to induce detectable DNA damage. Between 308 and 450 nm the number of photons necessary for DNA damage increases about 10,000 times from 2.14 x 10(8) to 2.85 x 10(12) photons. Between 308 and 318 nm the number of photons necessary to induce detectable DNA damage is proportional to e0.45 lambda. Between 340 and 450 nm it is proportional to e0.05 lambda. No detectable damage was induced at 540 and 640 nm after irradiation with 9900 kJ m-2. Two-photon effects are unlikely to play a significant role.
用Xe-Cl准分子激光(308纳米)的激光脉冲或波长在312至640纳米之间的染料激光照射细胞培养物中的人类淋巴细胞。在将光诱导的DNA损伤转化为DNA链断裂后,使用“彗星试验”(单细胞凝胶电泳)来确定诱导可检测到的DNA损伤所需的光子数量。在308至450纳米之间,DNA损伤所需的光子数量从2.14×10⁸个光子增加到2.85×10¹²个光子,增加了约10000倍。在308至318纳米之间,诱导可检测到的DNA损伤所需的光子数量与e⁰.⁴⁵λ成正比。在340至450纳米之间,它与e⁰.⁰⁵λ成正比。在用9900 kJ m⁻²照射后,在540和640纳米处未诱导出可检测到的损伤。双光子效应不太可能起重要作用。