†Department of Pharmaceutical Sciences and Moulder Center for Drug Discovery Research, Temple University School of Pharmacy, 3307 North Broad Street, Philadelphia, Pennsylvania 19140, United States.
‡Temple Materials Institute, 1803 North Broad Street, Philadelphia, Pennsylvania 19122, United States.
J Med Chem. 2015 May 28;58(10):4091-130. doi: 10.1021/jm500330k. Epub 2015 Feb 20.
Self-assembled synthetic gene delivery systems represent the bottom-up approach to gene delivery and gene silencing, in which scientists are designing novel cationic and procationic amphiphiles that can pack, transport, and deliver nucleic acids to various targets in the body in a controlled manner. These supramolecular assemblies are safer than viruses, but they are lagging behind them in efficiency. We are presenting recent progress that has narrowed this gap through better understanding the delivery barriers and incorporation of this knowledge in the design of novel synthetic amphiphiles, formulations, and revolutionary screening and optimization processes. Structure-properties and structure-activity relationships were drawn within each amphiphile class, presenting the cellular and animal models used to generate them. We are also revealing pertinent in vitro/in vivo correlations that emphasize promising amphiphiles and successful formulation optimization efforts for efficient in vivo nucleic acid delivery, together with main organ targets and diseases treatable with these revolutionary technologies.
自组装合成基因传递系统代表了基因传递和基因沉默的自下而上的方法,科学家们正在设计新型的阳离子和质子化两亲物,这些两亲物可以以可控的方式将核酸包装、运输并递送到体内的各种靶标。这些超分子组装体比病毒更安全,但它们的效率落后于病毒。我们正在介绍最近的进展,通过更好地了解传递障碍,并将这些知识纳入新型合成两亲物、制剂以及革命性的筛选和优化过程的设计,缩小了这一差距。在每个两亲物类别内都绘制了结构-性质和结构-活性关系,展示了用于生成它们的细胞和动物模型。我们还揭示了相关的体外/体内相关性,强调了有前途的两亲物和成功的制剂优化努力,以实现有效的体内核酸传递,以及这些革命性技术可治疗的主要器官靶标和疾病。