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Ultrasound with microbubbles enhances gene expression of plasmid DNA in the liver via intraportal delivery.携带微泡的超声通过门静脉给药增强肝脏中质粒DNA的基因表达。
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Ultrasound-Mediated Gene Therapy in Swine Livers Using Single-Element, Multi-lensed, High-Intensity Ultrasound Transducers.使用单元素、多透镜、高强度超声换能器在猪肝脏中进行超声介导的基因治疗。
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Ultrasound-Mediated Gene Therapy in Swine Livers Using Single-Element, Multi-lensed, High-Intensity Ultrasound Transducers.使用单元素、多透镜、高强度超声换能器在猪肝脏中进行超声介导的基因治疗。
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Prolonging pulse duration in ultrasound-mediated gene delivery lowers acoustic pressure threshold for efficient gene transfer to cells and small animals.延长超声介导基因传递中的脉冲持续时间可降低声压阈值,从而实现高效的细胞和小动物基因转移。
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Enhanced effect of nuclear localization signal peptide during ultrasound‑targeted microbubble destruction‑mediated gene transfection.核定位信号肽在超声靶向微泡破坏介导的基因转染过程中的增强作用。
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本文引用的文献

1
Efficient microbubble- and ultrasound-mediated plasmid DNA delivery into a specific rat liver lobe via a targeted injection and acoustic exposure using a novel ultrasound system.通过使用新型超声系统进行靶向注射和声暴露,高效地将微泡和超声介导的质粒DNA递送至特定大鼠肝叶。
Mol Pharm. 2012 Aug 6;9(8):2187-96. doi: 10.1021/mp300037t. Epub 2012 Jul 25.
2
Overview of therapeutic ultrasound applications and safety considerations.治疗超声应用概述及安全注意事项。
J Ultrasound Med. 2012 Apr;31(4):623-34. doi: 10.7863/jum.2012.31.4.623.
3
Explorations of high-intensity therapeutic ultrasound and microbubble-mediated gene delivery in mouse liver.高强度治疗超声和微泡介导的基因传递在小鼠肝脏中的探索。
Gene Ther. 2011 Oct;18(10):1006-14. doi: 10.1038/gt.2011.34. Epub 2011 Mar 31.
4
Evaluation of transfection efficiency in skeletal muscle using nano/microbubbles and ultrasound.利用纳米/微泡和超声评价骨骼肌转染效率。
Ultrasound Med Biol. 2010 Jul;36(7):1196-205. doi: 10.1016/j.ultrasmedbio.2010.04.016.
5
Progress in the development of ultrasound-mediated gene delivery systems utilizing nano- and microbubbles.超声介导的利用纳米和微泡的基因传递系统的发展进展。
J Control Release. 2011 Jan 5;149(1):36-41. doi: 10.1016/j.jconrel.2010.05.009. Epub 2010 May 12.
6
Ultrasound bioeffects and safety.超声生物效应与安全性。
Proc Inst Mech Eng H. 2010;224(2):363-73. doi: 10.1243/09544119JEIM613.
7
Sonoporation, drug delivery, and gene therapy.超声穿孔、药物递送与基因治疗。
Proc Inst Mech Eng H. 2010;224(2):343-61. doi: 10.1243/09544119JEIM565.
8
Cavitation and contrast: the use of bubbles in ultrasound imaging and therapy.空化与造影剂:气泡在超声成像与治疗中的应用。
Proc Inst Mech Eng H. 2010;224(2):171-91. doi: 10.1243/09544119JEIM622.
9
Image-guided, intravascular hydrodynamic gene delivery to skeletal muscle in pigs.血管内血流动力学导向的基因递送至猪骨骼肌。
Mol Ther. 2010 Jan;18(1):93-100. doi: 10.1038/mt.2009.206. Epub 2009 Sep 8.
10
Acoustic dose and acoustic dose-rate.声剂量和声剂量率。
Ultrasound Med Biol. 2009 Oct;35(10):1679-85. doi: 10.1016/j.ultrasmedbio.2009.05.001. Epub 2009 Aug 3.

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.

DOI:10.1038/mt.2013.107
PMID:23732985
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3776626/
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。