光热治疗
材料科学
体内
表面等离子共振
纳米颗粒
药物输送
细胞凋亡
纳米技术
生物物理学
癌症研究
化学
生物化学
医学
生物
生物技术
作者
Nick A. Alden,Tyus J. Yeingst,Hanna M. Pfeiffer,Nazmiye Celik,Julien H. Arrizabalaga,Angelica M. Helton,Yiming Liu,Douglas B. Stairs,Adam B. Glick,Neerav Goyal,Daniel J. Hayes
标识
DOI:10.1002/adhm.202303593
摘要
Current nucleic acid delivery methods have not achieved efficient, non-toxic delivery of miRNAs with tumor-specific selectivity. In this study, a new delivery system based on light-inducible gold-silver-gold, core-shell-shell (CSS) nanoparticles is presented. This system delivers small nucleic acid therapeutics with precise spatiotemporal control, demonstrating the potential for achieving tumor-specific selectivity and efficient delivery of miRNA mimics. The light-inducible particles leverage the photothermal heating of metal nanoparticles due to the local surface plasmonic resonance for controlled chemical cleavage and release of the miRNA mimic payload. The CSS morphology and composition result in a plasmonic resonance within the near-infrared (NIR) region of the light spectrum. Through this method, exogenous miR-34a-5p mimics are effectively delivered to human squamous cell carcinoma TE10 cells, leading to apoptosis induction without adverse effects on untransformed keratinocytes in vitro. The CSS nanoparticle delivery system is tested in vivo in Foxn1nu athymic nude mice with bilateral human esophageal TE10 cancer cells xenografts. These experiments reveal that this CSS nanoparticle conjugates, when systemically administered, followed by 850 nm light emitting diode irradiation at the tumor site, 6 h post-injection, produce a significant and sustained reduction in tumor volume, exceeding 87% in less than 72 h.
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