Nishimura Koyo, Fumoto Shintaro, Fuchigami Yuki, Hagimori Masayori, Maruyama Kazuo, Kawakami Shigeru
a Graduate School of Biomedical Sciences , Nagasaki University , Nagasaki , Japan and.
b Faculty of Pharma-Sciences , Teikyo University , Tokyo , Japan.
Drug Deliv. 2017 Nov;24(1):737-744. doi: 10.1080/10717544.2017.1319433.
In this study, we demonstrate the low toxicity and highly efficient and spatially improved transfection of plasmid DNA (pDNA) with liposomal nanobubbles (bubble liposomes [BLs]) using ultrasound (US) irradiation in mice. Naked pDNA with BLs was intraperitoneally injected, followed by US irradiation. The injection volume, the duration of US irradiation, and the dose of BLs were optimized. Both BLs and US irradiation were essential to achieve high transgene expression from naked pDNA. We observed transgene expression in the entire peritoneal tissues, including the peritoneal wall, liver, spleen, stomach and small and large intestines. The area of transfection could be controlled with focused US irradiation. There were few changes in the morphology of the peritoneum, the peritoneal function or serum alanine aminotransferase levels, suggesting the safety of BLs with US irradiation. Using a tissue-clearing method, the spatial distribution of transgene expression was evaluated. BLs with US irradiation delivered pDNA to the submesothelial layer in the peritoneal wall, whereas transgene expression was restricted to the surface layer in the liver and stomach. Therefore, BLs with US irradiation could be an effective and safe method of gene transfection to the peritoneum.
在本研究中,我们证明了在小鼠中使用超声(US)照射,脂质体纳米气泡(气泡脂质体[BLs])对质粒DNA(pDNA)具有低毒性、高效且空间上改善的转染效果。将携带BLs的裸pDNA进行腹腔注射,随后进行US照射。对注射体积、US照射持续时间和BLs剂量进行了优化。BLs和US照射对于实现裸pDNA的高转基因表达均至关重要。我们在整个腹膜组织中观察到了转基因表达,包括腹膜壁、肝脏、脾脏、胃以及小肠和大肠。可以通过聚焦US照射来控制转染区域。腹膜形态、腹膜功能或血清丙氨酸转氨酶水平几乎没有变化,这表明BLs联合US照射具有安全性。使用组织透明化方法评估了转基因表达的空间分布。US照射下的BLs将pDNA递送至腹膜壁的间皮下层,而转基因表达则局限于肝脏和胃的表层。因此,US照射下的BLs可能是一种有效且安全的腹膜基因转染方法。