Kuo Tai-Tzung, Wang Chung-Hsin, Wang Jir-You, Chiou Hong-Jen, Fan Ching-Hsiang, Yeh Chih-Kuang
Department of Biomedical Engineering and Environmental Sciences, National Tsing Hua University, Hsinchu 30013, Taiwan.
Department of Neurosurgery, Hsin-chu Mackay Memorial Hospital, Hsinchu 30071, Taiwan.
Pharmaceutics. 2019 May 8;11(5):223. doi: 10.3390/pharmaceutics11050223.
Osteosarcoma (OS) is the most common bone tumor in children and teenagers. The multidrug resistant property of OS produces a major obstacle to chemotherapy, since the effective drug dose cannot be achieved via conventional drug delivery routes without serious systemic cytotoxicity. Microbubbles in conjunction with ultrasound (US) has recently been shown to spatially and temporally permeabilize the cellular membrane, promoting drug penetration into tumors. Here, we investigated whether drug (doxorubicin, DOX)-loaded bubbles (DOX-bubbles) can serve as drug-loaded carriers in combination with US in order to facilitate tumor drug delivery. The proposed bubbles have a high payload capacity (efficiency of 69.4 ± 9.1%, payload of 1.4 mg/mL) for DOX. In vitro data revealed that when used in combination with US (1-MHz), these DOX-bubbles facilitate DOX entering into tumor cells. In tumor-bearing animals, DOX-bubbles + US could provide 3.7-fold suppression of tumor growth compared with the group without insonation (1.8 ± 0.9 cm vs. 8.5 ± 2.2 cm) because of the acceleration of DOX-induced tumor necrosis. In the meantime, the tumor perfusion and volume can be monitored by DOX-bubbles with contrast-enhanced ultrasound imaging. Our data provide useful information in support of translating the use of theranostic US-responsive bubbles for regulated tumor drug delivery into clinical use.
骨肉瘤(OS)是儿童和青少年中最常见的骨肿瘤。OS的多药耐药特性给化疗带来了重大障碍,因为在不产生严重全身细胞毒性的情况下,通过传统给药途径无法达到有效的药物剂量。最近研究表明,微泡与超声(US)联合使用可在空间和时间上使细胞膜通透,促进药物渗透到肿瘤中。在此,我们研究了载药(阿霉素,DOX)微泡(DOX-微泡)是否可作为载药载体与超声联合使用,以促进肿瘤药物递送。所提出的微泡对DOX具有高载药量(效率为69.4±9.1%,载药量为1.4mg/mL)。体外数据显示,当与超声(1MHz)联合使用时,这些DOX-微泡可促进DOX进入肿瘤细胞。在荷瘤动物中,由于DOX诱导的肿瘤坏死加速,DOX-微泡+超声组与未进行超声照射的组相比,肿瘤生长抑制率提高了3.7倍(1.8±0.9cm对8.5±2.2cm)。同时,可通过DOX-微泡和超声造影成像监测肿瘤灌注和体积。我们的数据为支持将用于调控肿瘤药物递送的治疗诊断性超声响应微泡的应用转化为临床应用提供了有用信息。