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Targeted cytosolic delivery of hydrogel nanoparticles into HepG2 cells through engineered Sendai viral envelopes
[摘要]

Hydrogel nanoparticles of cross-linked polyvinylpyrrolidone (PVP-NP) (35–50 nm in diameter) containing fluoresceinated dextran (FITC-Dx) were encapsulated in reconstituted Sendai viral envelopes containing only the fusion (F) protein (F-virosomes1). Incubation of these loaded F-virosomes with human hepatoblastoma cells (HepG2) in culture resulted in membrane-fusion-mediated delivery of NPs to the cell cytoplasm, as inferred from the ability of cells to internalize FITC-Dx loaded PVP-NP (PVPf-NP) in the presence of azide (an inhibitor of the endocytotic process). Introduction of PVPf-NP into the HepG2 cells was assured by selective accumulation of FITC fluorescence in the cytosolic compartment. The structural integrity of the internalized PVPf-NP was also confirmed by fluorescence microscopy and ultracentrifugation analysis. The potential usefulness of PVP-NP-mediated cytosolic release of water soluble drugs both in vitro and in vivo has been established for the first time.

[发布日期]  [发布机构] 
[效力级别]  [学科分类] 生物化学/生物物理
[关键词] Hydrogel nanoparticle;Sendai virus;Virosome;Drug delivery;Targeted cytosolic delivery;Controlled release;ASGP-R;asialoglycoprotein receptor;CHO;Chinese hamster ovary;DMEM;Dulbecco's modified Eagle's medium;DPBS;Dulbecco's phosphate-buffered saline;EDTA;ethylenediaminetetraacetate (disodium salt);F;fusion protein;FCS;fetal calf serum;FITC-Dx;fluorescein isothiocyanate dextran (mol wt. 19.3 kDa);PL;polylysine;PVPf-NP;FITC-Dx-loaded polyvinylpyrrolidone nanoparticle;TBS;Tris-buffered saline [时效性] 
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