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Highly substituted phthalocyanine derivatives as potential photosensitizers for photodynamic therapy of tumors

机译:高度取代的酞菁衍生物可作为潜在的光敏剂用于肿瘤的光动力治疗

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Abstract: An octakis-decyl-substituted Zn(II)-phthalocyanine (ZnODPc) was prepared by chemical synthesis and was shown to possess favorable photophysical properties to act as a photodynamic agent. Intravenous injection of ZnODPc incorporated into Cremophor emulsions (1.2 or 2.4 mg/kg) to Balb/c mice bearing a MS-2 fibrosarcoma resulted in an efficient and selective accumulation of the phthalocyanine in the tumor. Illumination of the ZnODPc-loaded neoplastic lesion at 24 h after injection caused tumor regression as a result of both intracellular and intravascular damage. !11
机译:摘要:用化学合成方法制备了八烷基癸基取代的Zn(II)-酞菁(ZnODPc),具有良好的光物理性质,可以作为光动力剂。向携带MS-2纤维肉瘤的Balb / c小鼠静脉注射掺入Cremophor乳剂(1.2或2.4 mg / kg)的ZnODPc,可在肿瘤中高效,选择性地积累酞菁。注射后24小时照亮ZnODPc的赘生物病变,由于细胞内和血管内损伤,导致肿瘤消退。 !11

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