| RRC ID |
71793
|
| 著者 |
Suma T, Miyata K, Anraku Y, Watanabe S, Christie RJ, Takemoto H, Shioyama M, Gouda N, Ishii T, Nishiyama N, Kataoka K.
|
| タイトル |
Smart multilayered assembly for biocompatible siRNA delivery featuring dissolvable silica, endosome-disrupting polycation, and detachable PEG.
|
| ジャーナル |
ACS Nano
|
| Abstract |
Multifunctional delivery systems of small interfering RNA (siRNA) are needed to overcome the intrinsic biological barriers toward efficient gene silencing in the cell cytoplasm. In this report, a smart multilayered assembly (SMA) was fabricated by a layer-by-layer method with polyionic materials. The SMA was designed to feature a siRNA-loaded core, a transiently core-stabilizing silica interlayer, an endosome-disrupting polycation interlayer, and a biocompatible poly(ethylene glycol) (PEG) shell with reductive environment-responsive detachability. The SMA was confirmed to be approximately 160 nm in size with narrow distribution and spherical morphology by DLS and TEM analyses. The PEG detachability of the SMA based on disulfide cleavage was also confirmed by the increase in both ζ-potential and size due to the exposure of the polycation interlayer and the compromised colloidal stability. The silica interlayer rendered the SMA highly tolerant to dissociation induced by anionic lipids, while after 24 h dialysis siRNA release from the SMA was clearly observed, presumably due to gradual dissolution of the silica interlayer based on the equilibrium shift to silicate ions. The entrapment ratio of siRNA delivered by the SMA within the endosome was significantly lower than that by nondisulfide control (NDC) without PEG detachability, suggesting the improved endosomal escape of SMA with the exposed, endosome-disrupting interlayer after PEG detachment. SMAs induced significantly higher gene silencing efficiency in various cultured cells, compared to NDC, without associated cytotoxicity. The systemic administration of SMAs for subcutaneous tumor-bearing mice achieved significant endogenous gene silencing in tumor tissue without hematological toxicity.
|
| 巻・号 |
6(8)
|
| ページ |
6693-705
|
| 公開日 |
2012-8-28
|
| DOI |
10.1021/nn301164a
|
| PMID |
22835034
|
| MeSH |
Animals
Crystallization / methods
Delayed-Action Preparations / administration & dosage
Delayed-Action Preparations / chemistry*
Endosomes / chemistry*
Endosomes / physiology*
Macromolecular Substances / chemistry
Materials Testing
Mice
Molecular Conformation
Nanocapsules / chemistry*
Nanocapsules / ultrastructure
Neoplasms, Experimental / genetics*
Particle Size
Polyethylene Glycols / chemistry
RNA, Small Interfering / administration & dosage
RNA, Small Interfering / chemistry
RNA, Small Interfering / genetics*
Surface Properties
Transfection / methods*
|
| IF |
14.588
|
| リソース情報 |
| ヒト・動物細胞 |
OS-RC-2(RCB0735) |
