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Polymer-Coated Echogenic Lipid Nanoparticles with Dual Release Triggers

机译:具有双重释放触发器的聚合物涂层的致癌脂质纳米颗粒

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摘要

Although lipid nanoparticles are promising drug delivery vehicles, passive release of encapsulated contents at the target site is often slow. Herein, we report contents release from targeted, polymer-coated, echogenic lipid nanoparticles in the cell cytoplasm by redox trigger and simultaneously enhanced by diagnostic frequency ultrasound. The lipid nanoparticles were polymerized on the external leaflet using a disulfide cross-linker. In the presence of cytosolic concentrations of glutathione, the lipid nanoparticles released 76% of encapsulated contents. Plasma concentrations of glutathione failed to release the encapsulated contents. Application of 3 MHz ultrasound for 2 min simultaneously with the reducing agent enhanced the release to 96%. Folic acid conjugated, doxorubicin-loaded nanoparticles showed enhanced uptake and higher cytotoxicity in cancer cells overexpressing the folate receptor (compared to the control). With further developments, these lipid nanoparticles have the potential to be used as multimodal nanocarriers for simultaneous targeted drug delivery and ultrasound imaging.
机译:尽管脂质纳米颗粒是有前途的药物递送载体,但是在目标部位被动释放胶囊化内容物通常很慢。在这里,我们报告内容通过氧化还原触发从目标,聚合物涂层,回声脂质纳米粒释放在细胞质中,同时通过诊断频率超声增强。使用二硫键交联剂在外部小叶上聚合脂质纳米颗粒。在谷胱甘肽的胞质浓度存在下,脂质纳米颗粒释放了76%的胶囊化内容物。血浆中的谷胱甘肽浓度未能释放出胶囊化的内容物。在还原剂的同时施加3 MHz超声波2分钟可将释放提高至96%。在过表达叶酸受体的癌细胞中(与对照相比),叶酸偶联的,阿霉素负载的纳米颗粒显示出增加的摄取和更高的细胞毒性。随着进一步的发展,这些脂质纳米颗粒有潜力用作同时靶向药物输送和超声成像的多峰纳米载体。

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