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超声靶向微泡破坏介导的犬肝脏基因转染。

Ultrasound-targeted microbubble destruction-mediated gene delivery into canine livers.

机构信息

Center for Immunity and Immunotherapies, Seattle Children's Research Institute, Seattle, Washington 98101, USA.

出版信息

Mol Ther. 2013 Sep;21(9):1687-94. doi: 10.1038/mt.2013.107. Epub 2013 Jun 4.

Abstract

Ultrasound (US) was applied to a targeted canine liver lobe simultaneously with injection of plasmid DNA (pDNA)/microbubble (MB) complexes into a portal vein (PV) segmental branch and occlusion of the inferior vena cava (IVC) to facilitate DNA uptake. By using a 1.1 MHz, 13 mm diameter transducer, a fivefold increase in luciferase activity was obtained at 3.3 MPa peak negative pressure (PNP) in the treated lobe. For more effective treatment of large tissue volumes in canines, a planar unfocused transducer with a large effective beam diameter (52 mm) was specifically constructed. Its apodized dual element configuration greatly reduced the near-field transaxial pressure variations, resulting in a remarkably uniform field of US exposure for the treated tissues. Together with a 15 kW capacity US amplifier, a 692-fold increase of gene expression was achieved at 2.7 MPa. Transaminase and histology analysis indicated minimal tissue damage. These experiments represent an important developmental step toward US-mediated gene delivery in large animals and clinics.

摘要

超声(US)应用于靶向犬肝叶,同时将质粒 DNA(pDNA)/微泡(MB)复合物注入门静脉(PV)节段分支,并阻断下腔静脉(IVC),以促进 DNA 摄取。使用 1.1 MHz、13 毫米直径的换能器,在处理的肝叶中,在 3.3 MPa 峰值负压(PNP)下,获得了 5 倍的荧光素酶活性增加。为了更有效地治疗犬科动物的大组织体积,专门构建了一种具有较大有效波束直径(52 毫米)的平面无焦点换能器。其变迹双元件结构大大降低了近场横轴向压力变化,从而为处理组织提供了非常均匀的超声照射场。与 15kW 容量的超声放大器一起,在 2.7 MPa 时实现了 692 倍的基因表达增加。转氨酶和组织学分析表明组织损伤最小。这些实验代表了向大动物和临床应用中超声介导基因传递的重要发展步骤。

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