Improved Cell Transfection of siRNA by pH-Responsive Nanomicelles Self-Assembled with mPEG‑<i>b</i>‑PHis‑<i>b</i>‑PEI Copolymers

Published on 2018-06-08T00:00:00Z (GMT) by
Here, the novel pH-responsive nanomicelles self-assembled with amphipathic meo-poly­(ethylene glycol)-<i>b</i>-poly­(l-histidine)-<i>b</i>-polyethylenimine (mPEG-<i>b</i>-PHis-<i>b</i>-PEI, EHE) copolymers based on hydrophobic interaction of PHis with deprotonation of imidazoles were developed for siRNA transfection. The cationic nanomicelles could electrostatically compact siRNA into stable EHE/siRNA nanoplexes with a hydrodynamic diameter of ∼190 nm and present a low toxicity in normal physiological condition (pH ∼ 7.4). Different from pH-irresponsive ECE/siRNA nanoplexes based on mPEG-<i>b</i>-poly­(ε-caprolactone)-<i>b</i>-PEI (ECE), the EHE/siRNA nanoplexes exhibited a higher cellular uptake along with an increased ζ-potential (from +18 to +32 mV) when the pH changed from 7.4 to 6.8 (extracellular acidic microenvironments). After cell internalization, the EHE/siRNA nanoplexes also exhibited an enhanced nanostructural disassembling and release of siRNA from lysosomal acidic microenvironments (pH ∼ 5.5). Furthermore, it was demonstrated that the EHE/siEGFR nanoplexes downregulated the expression levels of the corresponding mRNA and protein more efficiently than ECE/siEGFR in HeLa cells. The improved siRNA silencing effects of EHE/siEGFR nanoplexes resulted from the higher cellular uptake and enhanced endosomal/lysosomal escape, which is associated with the pH-responsive disassembly of nanostructure as well as the synergistic “proton sponge” effects of PHis and PEI in EHE copolymers. Therefore, the pH-responsive EHE nanomicelles would be promising and potential carriers for cell transfection of siRNA.

Cite this collection

Xu, Bin; Zhu, Yuan-Jun; Wang, Cheng-Han; Qiu, Chong; Sun, Jing; Yan, Yi; et al. (2018): Improved Cell Transfection of siRNA by pH-Responsive

Nanomicelles Self-Assembled with mPEG‑b‑PHis‑b‑PEI Copolymers. ACS Publications. Collection. https://doi.org/10.1021/acsami.8b04301