Department of Chemical Engineering and Institute of Biomedical Engineering, National Tsing Hua University, Hsinchu 30013, Taiwan, ROC.
Biomaterials. 2013 Sep;34(28):6930-7. doi: 10.1016/j.biomaterials.2013.05.049. Epub 2013 Jun 13.
Many human diseases carry at least two independent gene mutations, further exacerbating clinical disorders. In this work, disulfide bond-conjugated dual PEGylated siRNAs were synthesized, capable of specifically targeting and silencing two genes simultaneously. To achieve efficient delivery, the conjugated siRNAs were formulated with the cationic chitosan together with an anionic polymer, poly(γ-glutamic acid) (γPGA), to form a ternary complex. Experimental results indicate that the incorporated γPGA could significantly enhance their intracellular delivery efficiency, allowing for reduction of the disulfide bond-conjugated PEGylated siRNAs delivered to the PEGylated siRNAs in the reductive cytoplasmic environment. The PEGylated siRNAs could more significantly increase their enzymatic tolerability, effectively silence multiple genes, and prolong the duration of their gene silencing capability than the unmodified siRNAs could. Silencing of different genes simultaneously significantly contributes to the efforts to treat multiple gene disorders, and prolonged duration of gene silencing can reduce the need for frequent administrations.
许多人类疾病至少携带两个独立的基因突变,进一步加重了临床疾病的复杂性。在这项工作中,合成了二硫键连接的双聚乙二醇化 siRNA,能够特异性地同时靶向和沉默两个基因。为了实现高效传递,将共轭的 siRNA 与阳离子壳聚糖和阴离子聚合物聚(γ-谷氨酸)(γPGA)一起配制,形成三元复合物。实验结果表明,所包含的 γPGA 可以显著提高其细胞内传递效率,减少在还原性细胞质环境中传递的二硫键连接的聚乙二醇化 siRNA。与未修饰的 siRNA 相比,聚乙二醇化的 siRNA 能够显著增加其酶耐受性,有效地沉默多个基因,并延长其基因沉默能力的持续时间。同时沉默不同的基因有助于治疗多种基因疾病,延长基因沉默的持续时间可以减少频繁给药的需求。