Molecular Imaging Laboratory, MGH/MIT/HMS Athinoula A. Martinos Center for Biomedical Imaging, Massachusetts General Hospital and Harvard Medical School, Charlestown, MA, USA.
Wiley Interdiscip Rev Nanomed Nanobiotechnol. 2012 Jul-Aug;4(4):428-37. doi: 10.1002/wnan.1158. Epub 2012 Jan 6.
Short interfering RNAs (siRNAs) have emerged as a potent new class of therapeutics, which regulate gene expression through sequence-specific inhibition of mRNA translation. Human trials of siRNAs have highlighted the need for robust delivery and detection techniques that will enable the application of these therapeutics to increasingly complex disease and organ systems. Efforts to monitor the in vivo trafficking and efficacy of siRNAs have routinely involved bioluminescence imaging of naked siRNA molecules. More recently, siRNAs have been incorporated into a variety of molecular imaging probes to promote their detection with clinically relevant imaging modalities. Lipid-, polymer-, and nanoparticle-based siRNA delivery vehicles have proven effective in improving the stability, bioavailability, and target specificity of siRNAs following systemic administration in vivo. Additionally, these methods provide a platform to modify siRNAs with a variety of contrast agents and have enabled nuclear and magnetic resonance imaging of siRNA delivery in preclinical studies. These image-guided delivery approaches represent a crucial step in the transition of siRNA therapeutics to the clinic.
短干扰 RNA(siRNA)已成为一种强大的新型治疗药物,通过序列特异性抑制 mRNA 翻译来调节基因表达。siRNA 的人体试验强调了需要强大的输送和检测技术,以使这些治疗药物能够应用于越来越复杂的疾病和器官系统。监测 siRNA 的体内迁移和疗效的努力通常涉及裸 siRNA 分子的生物发光成像。最近,siRNA 已被纳入各种分子成像探针中,以促进其与临床相关成像方式的检测。基于脂质、聚合物和纳米颗粒的 siRNA 递药载体已被证明可有效提高 siRNA 在体内系统给药后的稳定性、生物利用度和靶向特异性。此外,这些方法为 siRNA 提供了一个用各种对比剂进行修饰的平台,并使核和磁共振成像能够在临床前研究中对 siRNA 递药进行成像。这些图像引导的递药方法代表着 siRNA 治疗药物向临床应用的重要一步。