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- W4236876235 abstract "Abstract Nanoparticles show great potential for drug delivery. However, suitable nanostructures capable of loading a range of drugs together with the co‐delivery of siRNAs, which avoid the problem of cation‐associated cytotoxicity, are lacking. Herein, we report an small interfering RNA (siRNA)‐based vesicle (siRNAsome), which consists of a hydrophilic siRNA shell, a thermal‐ and intracellular‐reduction‐sensitive hydrophobic median layer, and an empty aqueous interior that meets this need. The siRNAsome can serve as a versatile nanostructure to load drug agents with divergent chemical properties, therapeutic proteins as well as co‐delivering immobilized siRNAs without transfection agents. Importantly, the inherent thermal/reduction‐responsiveness enables controlled drug loading and release. When siRNAsomes are loaded with the hydrophilic drug doxorubicin hydrochloride and anti‐P‐glycoprotein siRNA, synergistic therapeutic activity is achieved in multidrug resistant cancer cells and a tumor model." @default.
- W4236876235 created "2022-05-12" @default.
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- W4236876235 date "2019-03-03" @default.
- W4236876235 modified "2023-10-15" @default.
- W4236876235 title "The siRNAsome: A Cation‐Free and Versatile Nanostructure for siRNA and Drug Co‐delivery" @default.
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- W4236876235 doi "https://doi.org/10.1002/ange.201814289" @default.
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