Jori G
Department of Biology, University of Padova, Italy.
J Photochem Photobiol B. 1996 Nov;36(2):87-93. doi: 10.1016/s1011-1344(96)07352-6.
While Photofrin, the photosensitizer currently in clinical use for photodynamic therapy (PDT) of tumours, has been shown to be both efficacious and safe in the treatment of a variety of human cancers, its chemical heterogeneity and low absorbance in the phototherapeutically useful wavelength range (600-850 nm) make the development of new photosensitizers with improved characteristics desirable. A suitable manipulation of the molecular structure of porphyrins offers several interesting possibilities for controlling the optical and photophysical properties of the photosensitizer, as well as its biodistribution between tumour and peritumoural tissues or at the subtissular and subcellular level. The achievement of these goals may also be facilitated by the association of the photosensitizer with selected delivery systems, opening the way to a qualitative and quantitative improvement of PDT.
虽然目前用于肿瘤光动力疗法(PDT)的光敏剂卟吩姆钠已被证明在治疗多种人类癌症方面既有效又安全,但其化学异质性以及在光治疗有效波长范围(600 - 850纳米)内的低吸光度使得开发具有改进特性的新型光敏剂成为必要。对卟啉分子结构进行适当操作,为控制光敏剂的光学和光物理性质以及其在肿瘤与瘤周组织之间或在组织和亚细胞水平的生物分布提供了多种有趣的可能性。将光敏剂与选定的递送系统相结合也可能有助于实现这些目标,为光动力疗法的定性和定量改进开辟道路。