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Using a Commercial Ultrasound Contrast Agent for Viral-Mediated Gene Transfer In Vitro and In Vivo

机译:使用商业超声造影剂进行病毒介导的基因在体外和体内转移

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This study evaluated the feasibility of site-specific gene delivery mediated by diagnostic ultrasound using genes encapsulated in commercially available ultrasound contrast agents in vitro and in vivo. Five different commercially available contrast agents were tested in vitro for their ability to enclose an adenoviral vector carrying GFP. Prostate cancer cells (DU 145) or non small cell lung cancer cells (H23) were plated in 80 culture wells and insonified at 207 or 535 kPa peak negative pressure for 1 min after administration of 0.1 ml of bubbles reconstituted with the viral vector. Experiments were repeated with the delivery vehicle incubated with complement to inactivate unenclosed Adeno-GFP and with controls. After 24 hours transduction efficiency was demonstrated by fluorescent microscopy. In vivo 15 nude mice with 21 melanoma tumors (DB-1) implanted received 0.1 ml injections of contrast. Mice were split into 3 control and 4 active groups and ultrasound was performed for 4 min at 4 MHz using an Aplio scanner (Toshiba America Medical Systems, Tustin, CA). Tumors, heart, lungs and liver were harvested 48 hours later. Specimens underwent regular and fluorescent microscopy and were stained using an antibody against GFP. In vitro all contrast agents produced more fluorescence at 207 kPa than at 535 kPa. However, only Imagent (IMCOR Pharmaceuticals, San Diego, CA) was able to induce marked gene transduction with the inactivating agent. In vivo systemic delivery of Adeno-GFP carrying microbubbles following pre-treatment with the inactivating agent resulted in specific transduction of the tumor cells only with no uptake in heart, lungs or liver (unlike the controls). In conclusion, specific viral gene transduction has been obtained in vitro and in vivo through the use of ultrasound and Imagent microbubbles as delivery vehicles.
机译:该研究评估了使用在体外和体内在市售的超声造影剂中包封的基因诊断超声诊断超声介导的特异性基因递送的可行性。在体外测试五种不同的商业上可用的造影剂,以其包围携带GFP的腺病毒载体的能力。将前列腺癌细胞(DU 145)或非小细胞肺癌细胞(H23)在80个培养孔中铺板,并在施用0.1ml与病毒载体重构的气泡后,在207或535kPa峰值负压下呈1分钟。用递送的载体重复实验,与补体孵育以灭活未经活化的腺泡-GFP和对照。 24小时后,通过荧光显微镜证明转导效率。在体内15个裸鼠中,具有21个黑色素瘤肿瘤(DB-1)植入的对比度的0.1ml注射。将小鼠分成3个对照,使用APLIO扫描仪(Toshiba America Medical Systems,Tustin,CA),在4 MHz下进行4分钟,4分钟进行4个活性组和超声。在48小时后收获肿瘤,心脏,肺和肝脏。试样常规和荧光显微镜检查,并使用针对GFP的抗体染色。体外所有造影剂在207kPa下产生的荧光高于535kPa。但是,只有想象者(IMCor Pharmaceuticals,San Diego,CA)能够用灭活剂诱导标记的基因转导。在用灭活剂预处理后的腺泡-GFP携带微泡的体内递送,导致肿瘤细胞的特异性转导,没有心脏,肺或肝脏(与对照不同)。总之,通过使用超声和想象者微泡作为递送载体,在体外和体内获得特异性病毒基因转导。

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