Yslas Edith Inés, Milla Laura Natalia, Romanini Silvia, Durantini Edgardo Néstor, Bertuzzi Mabel, Rivarola Viviana Alicia
Departments of Molecular Biology ; Chemistry, and.
Exp Ther Med. 2010 Jul;1(4):713-718. doi: 10.3892/etm_00000110. Epub 2010 Jul 1.
In the present study, a comparative photodynamic therapy (PDT) study was performed using the phthalocyanine derivatives, ZnPc(OCH(3))(4) and ZnPc(CF(3))(4), in a mouse tumor model, under identical experimental procedures. We studied the ablation of tumors induced by PDT. The end-point was to compare the photodynamic efficacy of ZnPc(OCH(3))(4) and ZnPc(CF(3))(4). ZnPc(OCH(3))(4) and ZnPc(CF(3))(4) were administered intraperitoneally at a dose of 0.2 mg/kg body weight. The injections of drugs were carried out in Balb/c mice bearing subcutaneously inoculated LM2 mouse mammary adenocarcinoma. Histological examination and serum biochemical parameters were used to evaluate hepatic and renal toxicity and function. Phototherapeutic studies were achieved employing a light intensity of 210 J/cm(2). After PDT, tumoral regression analyses were carried out, and the degree of tumor cell death was measured utilizing the vital stain Evan's blue. In this pilot study, we revealed that the cytotoxic effect of ZnPc(OCH(3))(4) after PDT led to a higher success rate compared to ZnPc(CF(3))(4)-PDT when both were intraperitoneally injectioned. Both phthalocynanine derivatives were able to induce ablation in the tumors. In summary, these results demonstrate the feasibility of ZnPc(OCH(3))(4)- or ZnPc(CF(3))(4)-PDT and its potential as a treatment for small tumors.
在本研究中,在相同的实验程序下,使用酞菁衍生物ZnPc(OCH(3))(4)和ZnPc(CF(3))(4)在小鼠肿瘤模型中进行了比较光动力疗法(PDT)研究。我们研究了PDT诱导的肿瘤消融情况。终点是比较ZnPc(OCH(3))(4)和ZnPc(CF(3))(4)的光动力疗效。以0.2mg/kg体重的剂量腹腔注射ZnPc(OCH(3))(4)和ZnPc(CF(3))(4)。在皮下接种了LM2小鼠乳腺腺癌的Balb/c小鼠中进行药物注射。采用组织学检查和血清生化参数来评估肝毒性和肾毒性以及肝肾功能。采用210J/cm(2)的光强度进行光治疗研究。PDT后,进行肿瘤消退分析,并使用活性染料伊文思蓝测量肿瘤细胞死亡程度。在这项初步研究中,我们发现,当两者均腹腔注射时,与ZnPc(CF(3))(4)-PDT相比,ZnPc(OCH(3))(4)在PDT后的细胞毒性作用导致更高的成功率。两种酞菁衍生物都能够诱导肿瘤消融。总之,这些结果证明了ZnPc(OCH(3))(4)-或ZnPc(CF(3))(4)-PDT的可行性及其作为小肿瘤治疗方法的潜力。