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Biomaterials for Gene Delivery Atelocollagen-mediated Controlled Release of Molecular Medicines

机译:基因传递的生物材料Atelocollagen介导的分子药物控制释放。

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摘要

Over the last decade, increasing attention has been paid to the development of systems to deliver drugs for long periods at controlled rates. Some of these systems can deliver drugs continuously for over one year. However, little effort has been given to developing systems for the controlled release of nucleic acids. Recently, a novel gene transfer method which allows prolonged release and expression of plasmid DNA in vivo in normal adult animals was established. In this system, a biocompatible natural polymer such as collagen or its derivatives acts as the carrier for the delivery of DNA vectors. The biomaterial carrying the plasmid DNA was administered into animals and, once introduced, gradually released plasmid DNA in vivo. A single injection of plasmid DNA_biomaterial produced physiologically significant levels of gene-encoding proteins in the local_systemic circulation of animals and resulted in prolonged biological effects. These results suggest that the biomaterials carrying plasmid DNA may enhance the clinical potency of plasmid-based gene transfer, facilitating a more effective and long-term use of naked plasmid vectors for gene therapy. Furthermore, the biomaterials can be removed surgically, minimizing the effect of gene products if some unexpected side effects should be observed after application. The application of these systems to expand the bioavailability of molecular medicine, including antisense oligonucleotides and adenovirus vectors, and to aid in stem cell transplantation in the context of DNA-based tissue engineering will be discussed.
机译:在过去的十年中,人们越来越关注以可控的速率长期输送药物的系统。其中一些系统可以连续一年以上地输送药物。但是,很少有努力开发用于核酸控制释放的系统。最近,建立了一种新的基因转移方法,该方法可以在正常成年动物体内延长质粒DNA的体内释放和表达。在该系统中,生物相容性天然聚合物(例如胶原蛋白或其衍生物)充当DNA载体递送的载体。携带质粒DNA的生物材料被施用于动物,一旦被引入,便在体内逐渐释放质粒DNA。一次注射质粒DNA_生物材料在动物的局部系统循环中产生了生理上显着水平的基因编码蛋白,并导致了延长的生物学效应。这些结果表明,携带质粒DNA的生物材料可以增强基于质粒的基因转移的临床效力,从而促进裸质粒载体更有效和长期地用于基因治疗。此外,如果在使用后应观察到一些意想不到的副作用,则可以通过手术去除生物材料,从而最大程度地降低基因产物的作用。将讨论这些系统在扩展分子药物(包括反义寡核苷酸和腺病毒载体)的生物利用度以及在基于DNA的组织工程背景下辅助干细胞移植中的应用。

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