Lo Justin H, Kwon Ester J, Zhang Angela Q, Singhal Preeti, Bhatia Sangeeta N
Koch Institute for Integrative Cancer Research, MIT , 500 Main Street, Cambridge, Massachusetts 02139, United States.
Department of Medicine, Brigham and Women's Hospital , 75 Francis Street, Boston, Massachusetts 02115, United States.
Bioconjug Chem. 2016 Oct 19;27(10):2323-2331. doi: 10.1021/acs.bioconjchem.6b00304. Epub 2016 Sep 16.
Nanoparticulate systems have shown great promise in overcoming the considerable trafficking barriers associated with systemic nucleic acid delivery, which must be addressed to unlock the full potential of technologies such as RNAi and gene editing in vivo. In addition to mediating the cytoplasmic delivery of nucleic cargo and shielding it from nuclease degradation and immunostimulation, nucleic-acid-containing nanomaterials delivered intravenously must also be stable in the bloodstream after administration to avoid toxicity and off-target delivery. To this end, the hydrophilic molecule polyethylene glycol (PEG) has been deployed in many different nanoparticle systems to prevent aggregation and recognition by the reticuloendothelial system. However, the optimal strategy for incorporating PEG into self-assembled nucleic acid delivery systems to obtain nanoparticle stability while retaining important functions such as receptor targeting and cargo activity remains unclear. In this work, we develop substantially improved formulations of tumor-penetrating nanocomplexes (TPNs), targeted self-assembled nanoparticles formulated with peptide carriers and siRNA that have been shown to mitigate tumor burden in an orthotopic model of ovarian cancer. We specifically sought to tailor TPNs for intravenous delivery by systematically comparing formulations with three different classes of modular PEG incorporation (namely PEG graft polymers, PEG lipids, and PEGylated peptide), each synthesized using straightforward bioconjugation techniques. We found that the addition of PEG lipids or PEGylated peptide carriers led to the formation of small and stable nanoparticles, but only nanoparticles formulated with PEGylated peptide carriers retained substantial activity in a gene silencing assay. In vivo, this formulation significantly decreased accumulation in off-target organs and improved initial availability in circulation compared to results from the original non-PEGylated particles. Thus, from among a set of candidate strategies, we identified TPNs with admixed PEGylated peptide carriers as the optimal formulation for systemic administration of siRNA on the basis of their performance in a battery of physicochemical and biological assays. Moreover, this optimized formulation confers pharmacologic advantages that may enable further translational development of tumor-penetrating nanocomplexes, highlighting the preclinical value of comparing formulation strategies and the relevance of this systematic approach for the development of other self-assembled nanomaterials.
纳米颗粒系统在克服与全身核酸递送相关的巨大转运障碍方面显示出巨大潜力,要释放RNA干扰(RNAi)和体内基因编辑等技术的全部潜力,就必须解决这些障碍。除了介导核酸货物的细胞质递送并使其免受核酸酶降解和免疫刺激外,静脉内递送的含核酸纳米材料在给药后还必须在血流中保持稳定,以避免毒性和脱靶递送。为此,亲水分子聚乙二醇(PEG)已被应用于许多不同的纳米颗粒系统中,以防止聚集和被网状内皮系统识别。然而,将PEG纳入自组装核酸递送系统以获得纳米颗粒稳定性,同时保留受体靶向和货物活性等重要功能的最佳策略仍不明确。在这项工作中,我们开发了显著改进的肿瘤穿透纳米复合物(TPN)制剂,这是一种用肽载体和小干扰RNA(siRNA)配制的靶向自组装纳米颗粒,已证明其在卵巢癌原位模型中可减轻肿瘤负担。我们特别试图通过系统比较具有三种不同类型模块化PEG掺入(即PEG接枝聚合物、PEG脂质和聚乙二醇化肽)的制剂来定制用于静脉内递送的TPN,每种制剂都使用简单的生物共轭技术合成。我们发现,添加PEG脂质或聚乙二醇化肽载体导致形成小而稳定的纳米颗粒,但只有用聚乙二醇化肽载体配制的纳米颗粒在基因沉默试验中保留了显著活性。在体内,与原始非聚乙二醇化颗粒的结果相比,这种制剂显著降低了在脱靶器官中的积累,并提高了循环中的初始可用性。因此,在一系列候选策略中,我们根据其在一系列物理化学和生物学试验中的表现,确定了含有混合聚乙二醇化肽载体的TPN是用于全身递送siRNA的最佳制剂。此外,这种优化的制剂具有药理学优势,可能使肿瘤穿透纳米复合物能够进一步转化发展,突出了比较制剂策略的临床前价值以及这种系统方法对其他自组装纳米材料开发的相关性。