Lemos Camila Nunes, de Souza Joel Gonçalves, Simão Patrícia Sper, Lopez Renata Fonseca Vianna
School of Pharmaceutical Sciences of Ribeirão Preto, University of São Paulo, Ribeirão Preto, São Paulo, Brazil.
PLoS One. 2016 Jan 11;11(1):e0145922. doi: 10.1371/journal.pone.0145922. eCollection 2016.
This study examined the potential of iontophoresis in topical photodynamic therapy (PDT) of human invasive squamous cells carcinomas (SCC). SCC was induced in nude BALB/c mice by subcutaneous injection of A431 cells. Tumor penetration and distribution of the photosensitizer tetrasulfonated zinc phthalocyanine (ZnPcS4) was investigated after 10 and 30 min of in vivo iontophoresis of a gel containing ZnPcS4. PDT was performed immediately after iontophoresis using laser at 660 nm with a dose of irradiation of 100 J/cm(2) and irradiance of 48 mW/cm(2) while tumor growth was measured for 30 days. Iontophoresis increased ZnPcS4 penetration into tumors by 6-fold after 30 min when compared with passive delivery. Confocal microscopy analysis showed that ZnPcS4 was homogeneous distributed within deep regions of the tumor after iontophoresis. Irradiation of the tumors immediately after iontophoresis showed reduction in tumor size by more than 2-fold when compared to non-treated tumors. Iontophoretic-PDT treated tumors presented large areas of necrosis. The study concluded that iontophoretic delivery of photosensitizers could be a valuable strategy for topical PDT of invasive SCC.
本研究考察了离子导入法在人浸润性鳞状细胞癌(SCC)局部光动力疗法(PDT)中的潜力。通过皮下注射A431细胞在裸BALB/c小鼠中诱导产生SCC。在含有四磺酸基锌酞菁(ZnPcS4)的凝胶进行10分钟和30分钟的体内离子导入后,研究了光敏剂ZnPcS4的肿瘤渗透和分布情况。离子导入后立即使用波长660nm的激光进行PDT,照射剂量为100J/cm²,辐照度为48mW/cm²,同时测量肿瘤生长30天。与被动给药相比,离子导入30分钟后可使ZnPcS4向肿瘤内的渗透增加6倍。共聚焦显微镜分析表明,离子导入后ZnPcS4在肿瘤深部区域均匀分布。离子导入后立即对肿瘤进行照射,与未治疗的肿瘤相比,肿瘤大小缩小超过2倍。离子导入-PDT治疗的肿瘤出现大面积坏死。该研究得出结论,光敏剂的离子导入给药可能是浸润性SCC局部PDT的一种有价值的策略。