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首页> 外文期刊>Integrative cancer therapies >The tumoricidal effect of sonodynamic therapy (SDT) on S-180 sarcoma in mice.
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The tumoricidal effect of sonodynamic therapy (SDT) on S-180 sarcoma in mice.

机译:声动力学疗法(SDT)对小鼠S-180肉瘤的杀伤作用。

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There are increasing data showing that sonodynamic therapy (SDT), which refers to a synergistic effect of drugs and ultrasound, is a promising new modality for cancer treatment. However, few clinical data on SDT have been published. One reason is the lack of suitable drugs for clinical SDT use. Recently a new sonosensitizing agent has been developed by SonneMed, LLC, referred to as SF1. In this study the effect of SDT with SF1 on S-180 sarcoma in mice was examined. The tumor bearing mice were allocated to the following groups: (1) sham-treatment (control, C); (2) ultrasound treatment (only ultrasound treatment, 1.2 mW/cm2 , without SF1, U); (3) SF1 treatment (SF1 20 mg/kg intraperitoneal [ip] without ultrasound treatment, S); and (4) SF1 + ultrasound treatment (SU). Following treatment, tumor volume was monitored. Tumor growth inhibition was seen only in group SU, and with increasing ultrasound intensity, the inhibitory effect was enhanced. Tumor growth inhibition was also visible even when covered by a barrier of bone. Pathological slices showed coagulated necrosis or metamorphic tissue with inflammatory reaction in the tumor taken from 2 to 36 hours after SDT. These data revealed that SDT with SF1 did inhibit growth of mouse S-180 sarcoma and the inhibitory effect was sound intensity dependent. SDT also induced some inflammation while it destroyed the tumor, indicative of a "vaccine" effect. SF1 shows great promise for clinical use in the future.
机译:越来越多的数据表明,声动力学疗法(SDT)是指药物和超声的协同作用,是一种有望用于癌症治疗的新方法。但是,关于SDT的临床数据很少发表。原因之一是缺乏适合临床SDT使用的药物。最近,SonneMed,LLC开发了一种新的声敏剂,称为SF1。在这项研究中,研究了SDT与SF1对小鼠S-180肉瘤的作用。将荷瘤小鼠分为以下几组:(1)假治疗(对照组,C); (2)超声治疗(仅超声治疗1.2 mW / cm2,无SF1,U); (3)SF1治疗(SF1 20 mg / kg腹膜内[ip],未经超声治疗,S); (4)SF1 +超声治疗(SU)。治疗后,监测肿瘤体积。仅在SU组中观察到肿瘤生长抑制,并且随着超声强度的增加,抑制作用增强。即使被骨屏障覆盖,也可以看到肿瘤生长抑制。病理切片显示在SDT后2至36小时,肿瘤中出现凝固性坏死或变质组织,并伴有炎症反应。这些数据表明,带有SF1的SDT确实抑制了小鼠S-180肉瘤的生长,并且抑制作用与声音强度有关。 SDT在破坏肿瘤的同时也引起了一些炎症,表明有“疫苗”效应。 SF1在未来的临床应用中显示出巨大的希望。

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