Tung Ching-Hsuan, Han Myung Shin, Kim Young, Qi Jianjun, O'Neill Brian E
Molecular Imaging Innovations Institute, Department of Radiology, Weill Cornell Medicine, New York, NY, United States; Department of Translational Imaging, Houston Methodist Research Institute, Houston, TX, United States.
Molecular Imaging Innovations Institute, Department of Radiology, Weill Cornell Medicine, New York, NY, United States.
J Control Release. 2017 Jul 28;258:67-72. doi: 10.1016/j.jconrel.2017.05.009. Epub 2017 May 10.
The cell membrane is a semi-fluid container that defines the boundary of cells, and provides an enclosed environment for vital biological processes. A sound excitable drug (SED) that is non-cytotoxic to cells is developed to disrupt the plasma membrane under gentle ultrasound insonation, 1MHz, 1W/cm. The frequency and power density of insonation are within the physical therapy and medical imaging windows; thus the applied ultrasound is safe and not harmful to tissues. The insertion of SEDs into the plasma membrane is not toxic to cells; however, the intruding SEDs weaken the membrane's integrity. Under insonation, the ultrasound energy destabilized the SED disrupted membranes, resulting in membrane rupture and eventual cell death. In a xenograft breast tumor model, the SED alone or the ultrasound alone caused little adverse effects to tumor tissue, while the combined treatment triggered necrosis with a brief local insonation of 3min. The described sono-membrane rupture therapy could be a safe alternative to the currently used high-energy tissue ablation technology, which uses X-rays, gamma rays, electron beams, protons, or high-intensity focused ultrasound.
细胞膜是一个半流体容器,它界定了细胞的边界,并为重要的生物过程提供了一个封闭的环境。一种对细胞无细胞毒性的声敏药物(SED)被研发出来,在1MHz、1W/cm的温和超声照射下破坏质膜。照射的频率和功率密度处于物理治疗和医学成像窗口范围内;因此,所施加的超声是安全的,对组织无害。将SED插入质膜对细胞无毒;然而,侵入的SED会削弱膜的完整性。在超声照射下,超声能量使SED破坏的膜不稳定,导致膜破裂并最终导致细胞死亡。在异种移植乳腺肿瘤模型中,单独使用SED或单独使用超声对肿瘤组织几乎没有不良影响,而联合治疗在3分钟的短暂局部照射下引发了坏死。所描述的声膜破裂疗法可能是目前使用的高能组织消融技术的一种安全替代方法,后者使用X射线、γ射线、电子束、质子或高强度聚焦超声。