PEG比率
纳米颗粒
药物输送
氧化还原
化学
对偶(语法数字)
纳米技术
毒品携带者
组合化学
化学工程
材料科学
有机化学
艺术
工程类
经济
文学类
财务
作者
Nancy Ferrentino,Taha Behroozi Kohlan,Shokoufeh Mehrtashfar,Anna Finne‐Wistrand,Daniela Pappalardo
出处
期刊:Biomacromolecules
[American Chemical Society]
日期:2024-11-11
卷期号:25 (12): 7660-7673
被引量:16
标识
DOI:10.1021/acs.biomac.4c00889
摘要
Stimuli-responsive polymeric nanoparticles (NPs) can serve as smart drug delivery systems (DDSs) by triggering drug release upon external or internal stimuli. A dual-responsive DDS made of a triblock poly(ε-caprolactone)-poly(ethylene glycol)-poly(ε-caprolactone) (PCL-SS-PEG-SS-PCL) copolymer, bearing disulfide bonds between PCL and PEG, was synthesized. The copolymer was functionalized with coumarin and sensitive to near-infrared (NIR) light irradiation, while the S-S bonds could be cleaved by GSH (10 mM). Characterization was achieved by nuclear magnetic resonance, size exclusion chromatography, and Fourier transform infrared analyses. Nile Red (NR)-loaded NPs were prepared through self-assembly of the copolymer in water and analyzed by dynamic light scattering and field-emission scanning electron microscopy. The NR release upon ultraviolet (UV)/NIR light irradiation as well as by GSH concentrations was monitored by using fluorescence spectroscopy, while simultaneous exposure to UV/NIR light and intracellular GSH concentration led to faster NR release. AlamarBlue assay showed satisfactory cell viability of the NR-loaded NPs, while their cellular uptake in human dermal fibroblast cells was investigated by fluorescence microscopy and fluorescence emission measurements.
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