Department of Physics, Norwegian University of Science and Technology, Trondheim, Norway.
Ultrasound Med Biol. 2013 Jul;39(7):1255-66. doi: 10.1016/j.ultrasmedbio.2013.02.010. Epub 2013 Apr 30.
Combining liposomally encapsulated cytotoxic drugs with ultrasound exposure has improved the therapeutic response to cancer in animal models; however, little is known about the underlying mechanisms. This study focused on investigating the effect of ultrasound exposures (1 MHz and 300 kHz) on the delivery and distribution of liposomal doxorubicin in mice with prostate cancer xenografts. The mice were exposed to ultrasound 24 h after liposome administration to study the effect on release of doxorubicin and its penetration through the extracellular matrix. Optical imaging methods were used to examine the effects at both microscopic subcellular and macroscopic tissue levels. Confocal laser scanning microscopy revealed that ultrasound-exposed tumors had increased levels of released doxorubicin compared with unexposed control tumors and that the distribution of liposomes and doxorubicin through the tumor tissue was improved. Whole-animal optical imaging revealed that liposomes were taken up by both abdominal organs and tumors.
将脂质体包裹的细胞毒性药物与超声辐射相结合已提高了动物模型中癌症的治疗反应;然而,其潜在机制知之甚少。本研究专注于调查超声辐射(1 MHz 和 300 kHz)对荷前列腺癌异种移植瘤小鼠中脂质体阿霉素递送和分布的影响。在给予脂质体 24 小时后对小鼠进行超声辐射,以研究其对阿霉素释放及其穿过细胞外基质的穿透性的影响。光学成像方法用于检查微观亚细胞和宏观组织水平的影响。共聚焦激光扫描显微镜显示,与未暴露的对照肿瘤相比,超声暴露的肿瘤中释放的阿霉素水平增加,并且通过肿瘤组织的脂质体和阿霉素分布得到改善。全动物光学成像显示,脂质体被腹部器官和肿瘤吸收。
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