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用于基因转移的DNA控释涂层:在骨骼肌和心肌中的转染

A DNA controlled-release coating for gene transfer: transfection in skeletal and cardiac muscle.

作者信息

Labhasetwar V, Bonadio J, Goldstein S, Chen W, Levy R J

机构信息

Department of Pharmaceutical Sciences, University of Nebraska Medical Center, Omaha, Nebraska 68198, USA. Pediatric Research Center, Room 1170B.

出版信息

J Pharm Sci. 1998 Nov;87(11):1347-50. doi: 10.1021/js980077+.

Abstract

In this paper we report a novel technique of DNA-polymer coating for gene transfer. A proprietary DNA polymer solution was used for thin-layer coating on a chromic gut suture as a model study. The coated sutures were characterized for physical properties such as coating thickness, mass of the DNA deposited on the suture, surface characteristics as determined by scanning electron microscopy, and in vitro DNA release characteristics under simulated physiologic conditions. The in vivo gene transfection using DNA-coated sutures was demonstrated in rat skeletal muscle and in canine atrial myocardium. A heat-stable human placental alkaline phosphatase (AP) plasmid was used as a marker gene. Incisions of 1 to 1.5 cm were made in the rat skeletal muscles or the canine atrial myocardium. The sites were closed with either the DNA-coated sutures or control sutures. Two weeks after the surgery, the tissue samples adjacent to the suture lines were retrieved and analyzed for AP activity. The DNA-coated sutures demonstrated a sustained release of the DNA under in vitro conditions, with an approximately 84% cumulative DNA release occurring in 26 days. An agarose gel electrophoresis of the DNA samples released from the suture demonstrated two bands, with the lower band corresponding to the input DNA (supercoiled). It seems that there was a partial transformation of the DNA from a supercoiled to an open circular form due to the polymer coating. The tissue sites, which received the DNA-coated sutures, demonstrated a significantly higher AP activity compared with the tissue sites that received control sutures. In the rat studies, the mean AP activity (square root of cpm/microgram protein) was 43.6 +/- 3.3 vs 20.6 +/- 2.1 (p = 0.001) at the control sites. Similarly, in the canine studies, the AP activity was 73.6 +/- 7.4 Vs 21.6 +/- 1.4 (p = 0.0009) at the control sites. Thus, our studies demonstrated a successful gene transfer using our DNA-polymer coating technique. This technique could be useful for coating sutures used in vascular and general surgery, and also for coating medical devices, such as stents, catheters, or orthopedic devices, to achieve a site-specific gene delivery.

摘要

在本文中,我们报告了一种用于基因转移的新型DNA聚合物涂层技术。作为模型研究,使用一种专利DNA聚合物溶液在铬肠缝合线上进行薄层涂层。对涂层缝合线的物理性质进行了表征,如涂层厚度、沉积在缝合线上的DNA质量、通过扫描电子显微镜确定的表面特征,以及在模拟生理条件下的体外DNA释放特性。使用DNA涂层缝合线的体内基因转染在大鼠骨骼肌和犬心房心肌中得到了证实。一种热稳定的人胎盘碱性磷酸酶(AP)质粒被用作标记基因。在大鼠骨骼肌或犬心房心肌上制作1至1.5厘米的切口。用DNA涂层缝合线或对照缝合线闭合这些部位。手术后两周,取出缝合线附近的组织样本并分析AP活性。DNA涂层缝合线在体外条件下显示出DNA的持续释放,在26天内约有84%的累积DNA释放。从缝合线释放的DNA样本的琼脂糖凝胶电泳显示出两条带,较低的带对应于输入DNA(超螺旋)。由于聚合物涂层,似乎DNA从超螺旋形式部分转变为开放环状形式。接受DNA涂层缝合线的组织部位与接受对照缝合线的组织部位相比,显示出显著更高的AP活性。在大鼠研究中,对照部位的平均AP活性(每微克蛋白质的cpm平方根)为43.6±3.3,而对照部位为20.6±2.1(p = 0.001)。同样,在犬类研究中,对照部位的AP活性为73.6±7.4,而对照部位为21.6±1.4(p = 0.0009)。因此,我们的研究证明了使用我们的DNA聚合物涂层技术成功进行了基因转移。该技术可用于涂覆血管和普通外科手术中使用的缝合线,也可用于涂覆医疗设备,如支架、导管或骨科设备,以实现位点特异性基因递送。

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