Pogue B W, Momma T, Wu H C, Hasan T
Department of Dermatology, Massachusetts General Hospital, Boston 02114, USA.
Br J Cancer. 1999 May;80(3-4):344-51. doi: 10.1038/sj.bjc.6690361.
High intensity pulsed-laser light can be used to excite absorbing molecules to transient states in large proportions. The laser-induced spectral changes can be characterized by transient changes in light propagation; through the tissue provided the excited states of these molecules have altered absorption spectra. Characterization of these transient changes may then be used to exploit new mechanisms in photosensitization and/or to optimize photobiological effects. In this study, transmittance and reflectance were measured as a function of laser pulse energy, from tissue-simulating media as well as in rat muscle and liver slices, both with and without the photosensitizer benzoporphyrin derivative monoacid (BPD-MA) present. There was a transient decrease in absorption from the photosensitizer at peak pulse irradiance in the range of 100-1000 W cm(-2). The depth of photodynamic treatment-induced tissue necrosis was measured in a subcutaneous prostate cancer model in Copenhagen rats. A comparison between continuous wave irradiation and pulsed irradiation with the same average incident irradiance showed no statistically significant difference in the depth of necrosis at 48 h after irradiation. These results indicate that photosensitizer population-state changes are measurable in tissues and may provide a method for measuring triplet-state properties of photosensitizer in vivo, but for BPD-MA at clinically used concentrations these changes do not significantly affect the depth of photodynamically-induced tissue damage.
高强度脉冲激光可用于将大量吸收分子激发到瞬态。激光诱导的光谱变化可通过光传播的瞬态变化来表征;前提是这些分子的激发态改变了吸收光谱,且光通过组织。对这些瞬态变化的表征随后可用于探索光致敏的新机制和/或优化光生物学效应。在本研究中,测量了透射率和反射率作为激光脉冲能量的函数,测量对象包括组织模拟介质以及大鼠肌肉和肝脏切片,测量时分别加入和不加入光敏剂苯并卟啉衍生物单酸(BPD-MA)。在100 - 1000 W cm(-2)范围内的峰值脉冲辐照下,光敏剂的吸收出现了瞬态下降。在哥本哈根大鼠的皮下前列腺癌模型中测量了光动力治疗诱导的组织坏死深度。在相同平均入射辐照度下,连续波照射与脉冲照射之间的比较表明,照射后48小时坏死深度没有统计学上的显著差异。这些结果表明,光敏剂群体状态变化在组织中是可测量的,并且可能提供一种在体内测量光敏剂三重态性质的方法,但对于临床使用浓度的BPD-MA,这些变化不会显著影响光动力诱导的组织损伤深度。