Centro Singular de Investigación en Química Biolóxica e Materiais Moleculares (CIQUS), Departamento de Química Orgánica , Universidade de Santiago de Compostela , 15782 Santiago de Compostela , Spain.
School of Chemistry , University of Birmingham , Birmingham B15 2TT , U.K.
Biomacromolecules. 2018 Jul 9;19(7):2638-2649. doi: 10.1021/acs.biomac.8b00252. Epub 2018 Apr 26.
The recent advances in genetic engineering demand the development of conceptually new methods to prepare and identify efficient vectors for the intracellular delivery of different nucleotide payloads ranging from short single-stranded oligonucleotides to larger plasmid double-stranded circular DNAs. Although many challenges still have to be overcome, polymers hold great potential for intracellular nucleotide delivery and gene therapy. We here develop and apply the postpolymerization modification of polyhydrazide scaffolds, with different degree of polymerization, for the preparation of amphiphilic polymeric vehicles for the intracellular delivery of a circular plasmid DNA. The hydrazone formation reactions with a mixture of cationic and hydrophobic aldehydes proceed in physiologically compatible aqueous conditions, and the resulting amphiphilic polyhydrazones are directly combined with the biological cargo without any purification step. This methodology allowed the preparation of stable polyplexes with a suitable size and zeta potential to achieve an efficient encapsulation and intracellular delivery of the DNA cargo. Simple formulations that performed with efficiencies and cell viabilities comparable to the current gold standard were identified. Furthermore, the internalization mechanism was studied via internalization experiments in the presence of endocytic inhibitors and fluorescence microscopy. The results reported here confirmed that the polyhydrazone functionalization is a suitable strategy for the screening and identification of customized polymeric vehicles for the delivery of different nucleotide cargos.
最近基因工程的进展要求开发新概念的方法,以制备和鉴定有效的载体,用于将不同核苷酸有效负载递送至细胞内,这些有效负载的范围从短的单链寡核苷酸到较大的质粒双链环状 DNA。尽管仍然有许多挑战需要克服,但聚合物在细胞内核苷酸递送和基因治疗方面具有很大的潜力。我们在此开发并应用了聚酰肼支架的聚合后修饰,其聚合度不同,用于制备用于将环状质粒 DNA 递送至细胞内的两亲性聚合物载体。与阳离子和疏水性醛的腙形成反应在生理相容的水性条件下进行,并且所得的两亲性聚酰肼无需任何纯化步骤即可直接与生物货物结合。该方法允许制备具有合适大小和 zeta 电位的稳定的聚合物复合物,以实现 DNA 货物的有效封装和细胞内递送。确定了简单的配方,其效率和细胞活力可与当前的金标准相媲美。此外,通过存在内吞抑制剂的内化实验和荧光显微镜研究了内化机制。这里报道的结果证实,聚酰肼功能化是筛选和鉴定用于递送不同核苷酸有效负载的定制聚合物载体的合适策略。