SYNTHESIS AND TUMOR-PHOTOBIOLOGICAL ACTIVITIES OF MESO-TETRASUBSTITUTED PHENYL PORPHINES / 第二军医大学学报

The preparation of 7 meso-tetrasubstituted phenyl porphines and the photosensitizing effects and tumor-photobiological activities of 4 of these compounds in cell-free system are presented here.It has been shown by the data in determination of the ability of compounds Ⅰ1_4 to sensitize photooxidation of NADPH in D2O under the illumination _of He-Ne laser that the ability to generate active oxygen species of them was much higher than those of YHpD and PsD-007.But they were weak in photoinactivation for the cultured human tongue squamocell cancer cells TCA-8113 in vitro.However, they were effective, in some degree, in the photo-localization and photodynamic therapy of sarcoma Si80 in mice.Severe delayed phototoxic reaction occurred in the mice administered these compounds.Porphines with halogen atoms in their molecules (compounds Ⅱ1_3) could not be excited and were non-fluorescent.This suggests that there was possibly a quenching effect of ha'ogen atoms on porphine fluorescence.

Studies on Separation and Identification of the Components as well as the Tu- mor-photobiological Activities of the Major Components of Photocarcinorin / 第二军医大学学报

The chemical composition, separation and identification of the components as well as the tumor photobiological activities of the major components of the new tumor-photochemodiagnostic and photochemotherapeutic agent photocarcinorin (PsD-007) were represented in this paper. It has been shown by the results of HPLC analysis in combination with spectroscopic determinations that PsD-007 is composed of 7 different porphyrins: MHD, DMD, MVD, AHD, HVD, Hp and Pp. The experimental results show that MHD, DMD and MVD are the major tumor photobiologically active components of PsD-007.