首页> 外文期刊>The Journal of Urology >Whole bladder photodynamic therapy for orthotopic superficial bladder cancer in rats: a study of intravenous and intravesical administration of photosensitizers.
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Whole bladder photodynamic therapy for orthotopic superficial bladder cancer in rats: a study of intravenous and intravesical administration of photosensitizers.

机译:对大鼠原位浅表性膀胱癌的全膀胱光动力疗法:光敏剂静脉内和膀胱内给药的研究。

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PURPOSE: Photodynamic therapy after intravenous injection of Photofrin (QLT Phototherapeutics, Vancouver, British Columbia, Canada) results in a contracted bladder and skin photosensitivity, which limits its clinical application. In an attempt to overcome these limitations photodynamic therapy after intravesical instillation of Photofrin or 5-aminolevulinic acid (ALA) in an orthotopic rat bladder tumor model was explored and compared with intravenous Photofrin for photodynamic therapy efficacy and phototoxicity. MATERIALS AND METHODS: At 2 weeks after bladder implantation of 1.5 x 10(6) AY-27 tumor cells animals were randomly grouped. Photofrin was administered (5 mg./kg. intravenously and 2 mg./ml. intravesically). The ALA concentration for intravesical instillation was 300 mM. Whole bladder photodynamic therapy with graded doses of light (lambda = 630 nm.) was performed 4 hours after drug administration. Tumor control and complications were evaluated. RESULTS: Photodynamic therapy with intravenous Photofrin plus 100 J./cm.(2) light resulted in severe bladder damage. Of 10 rats 6 died and 2 of the 10 that received 50 J./cm.(2) died. There were no photodynamic therapy related deaths in groups receiving intravesical instillation of Photofrin or ALA that also received 50 to 100 J./cm.(2) Median survival in rats treated with ALA intravesically plus 75 J./cm.(2) (77 days), Photofrin intravesically plus 50 (67) or 100 J./cm.(2) (76) and Photofrin intravenously plus 50 J./cm.(2) (60) were significantly different from that in controls (44). CONCLUSIONS: Intravesical instillation of Photofrin or ALA can achieve the same photodynamic therapy efficacy as intravenous Photofrin in this orthotopic rat bladder tumor model with less phototoxicity to normal tissues.
机译:目的:静脉注射光敏蛋白(QLT Phototherapeutics,温哥华,不列颠哥伦比亚省,加拿大)后进行光动力疗法会导致收缩的膀胱和皮肤光敏性,从而限制了其临床应用。为了克服这些限制,探索了在原位大鼠膀胱肿瘤模型中膀胱内滴注Photofrin或5-氨基乙酰丙酸(ALA)后的光动力疗法,并与静脉内Photofrin进行了光动力疗法功效和光毒性比较。材料与方法:在膀胱植入1.5 x 10(6)AY-27肿瘤细胞后2周,将动物随机分组。施用光敏蛋白(静脉内5mg / kg,膀胱内2mg / ml)。膀胱内滴注的ALA浓度为300 mM。药物给药后4小时,用分级剂量的光(λ= 630 nm。)进行全膀胱光动力疗法。评价肿瘤控制和并发症。结果:静脉注射Photofrin加上100 J./cm.(2)的光动力疗法导致严重的膀胱损伤。在10只大鼠中有6只死亡,而接受50 J./cm。的10只大鼠中有2只死亡。接受Photofrin或ALA膀胱内滴注的组也没有与光动力疗法相关的死亡,该组也接受50至100 J./cm.(2)膀胱内ALA加75 J./cm.(2)治疗的大鼠的中位生存期(77)天),Photofrin膀胱内加50(67)或100 J./cm.(2)(76)和Photofrin静脉内加50 J./cm.(2)(60)与对照组相比有显着差异(44)。结论:在此原位大鼠膀胱肿瘤模型中,膀胱内注射Photofrin或ALA可以达到与静脉内Photofrin相同的光动力治疗功效,对正常组织的光毒性较小。

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