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Photo-Induced Antitumor Effect of 3,6-Bis(1-methyl-4-vinylpyridinium) Carbazole Diiodide

机译:3,6-双(1-甲基-4-乙烯基吡啶)咔唑二碘化物的光诱导抗肿瘤作用

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摘要

We have applied a fluorescent molecule 3,6-bis(1-methyl-4-vinylpyridinium) carbazole diiodide (BMVC) for tumor targeting and treatment. In this study, we investigated the photo-induced antitumor effect of BMVC. In vitro cell line studies showed that BMVC significantly killed TC-1 tumor cells at light dose greater than 40 J/cm2. The fluorescence of BMVC in the tumor peaked at 3 hours and then gradually decreased to reach the control level after 24 hours. In vivo tumor treatment studies showed BMVC plus light irradiation (iPDT) significantly inhibited the tumor growth. At day 24 after tumor implantation, tumor volume was measured to be 225 ± 79 mm3, 2542 ± 181 mm3, 1533 ± 766 mm3, and 1317 ± 108 mm3 in the iPDT, control, light-only, and BMVC-only groups, respectively. Immunohistochemistry studies showed the microvascular density was significantly lower in the iPDT group. Taken together, our results demonstrated that BMVC may be a potent tumor-specific photosensitizer (PS) for PDT.
机译:我们已将荧光分子3,6-双(1-甲基-4-乙烯基吡啶)咔唑二碘化物(BMVC)用于肿瘤靶向和治疗。在这项研究中,我们研究了BMVC的光诱导抗肿瘤作用。体外细胞系研究表明,BMVC在大于40 J / cm 2 的光剂量下能杀死TC-1肿瘤细胞。肿瘤中BMVC的荧光在3小时达到峰值,然后在24小时后逐渐降低以达到对照水平。体内肿瘤治疗研究表明,BMVC加光照射(iPDT)显着抑制了肿瘤的生长。肿瘤植入后第24天,测得的肿瘤体积为225±79 mm 3 ,2542±181 mm 3 ,1533±766 mm 3 ,和iPDT,对照组,仅光组和仅BMVC组中的1317±108 mm 3 。免疫组织化学研究显示,iPDT组的微血管密度显着降低。两者合计,我们的结果表明BMVC可能是PDT的一种有效的肿瘤特异性光敏剂(PS)。

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