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Mesoporous Silica Nanoparticles for Dual-Mode Chemo-Sonodynamic Therapy by Low-Energy Ultrasound

机译:低能超声介孔二氧化硅纳米粒子用于双模式化学声动力学治疗

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摘要

Low-energy ultrasound (LEUS), exhibiting obvious advantages as a safe therapeutic strategy, would be promising for cancer therapy. We had synthesized a LEUS-responsive targeted drug delivery system based on functional mesoporous silica nanoparticle for cancer therapy. Paclitaxel (PTX) was loaded in mesoporous silica nanoparticles with a hydrophobic internal channel, and folic acid (FA) functionalized β-Cyclodextrin (β-CD) was capped on the surface of the nanoparticles (DESN), which acted as a cancer-targeting moiety and solubilizer. The existence of a hydrophobic internal channel in the DESN was beneficial to the storage of hydrophobic PTX, along with the enhancement of the cavitation effect produced by mild low-energy ultrasound (LEUS, ≤1.0 W/cm2, 1 MHz). The DESN showed significantly enhanced cavitation effect, selective targeting, and achieved a rapid drug release under mild LEUS. To investigate the in vivo antitumor efficacy of the DESN upon LEUS irradiation, we established a 4T1 mammary tumor model. The DESN were confirmed to be of great biodegradability/biocompatibility. The tumor growth was significantly inhibited when the mice were treated with DESN (10 mg/kg) + LEUS with the relative tumor volume reduced to 4.72 ± 0.70 compared with the control group (V/V0 = 17.12 ± 2.75). The DESN with LEUS represented excellent inhibiting effect on tumor cell in vivo. This work demonstrated that DESN mediating dual mode chemo-sonodynamic therapy could be triggered by extracorporeal remote control, may suggest a promising clinical application in cancer therapy.
机译:低能量超声(LEUS)作为一种安全的治疗策略具有明显的优势,将有望用于癌症治疗。我们已经基于功能性介孔二氧化硅纳米粒子合成了LEUS反应性靶向药物递送系统,用于癌症治疗。将紫杉醇(PTX)加载到具有疏水性内部通道的中孔二氧化硅纳米颗粒中,并将叶酸(FA)功能化的β-环糊精(β-CD)封盖在纳米颗粒(DESN)的表面上,这是一种靶向癌症的药物部分和增溶剂。 DESN中疏水性内部通道的存在有利于疏水性PTX的存储,并增强了轻度低能超声(LEUS,≤1.0W / cm 2 )产生的空化作用,1 MHz)。 DESN在轻度LEUS下显示出明显增强的空化作用,选择性靶向并实现了快速药物释放。为了研究LEUS照射后DESN的体内抗肿瘤功效,我们建立了4T1乳腺肿瘤模型。证实DESN具有很大的生物降解性/生物相容性。当用DESN(10 mg / kg)+ LEUS治疗小鼠时,肿瘤生长被显着抑制,与对照组相比,相对肿瘤体积降低到4.72±0.70(V / V0 = 17.12±2.75)。具有LEUS的DESN在体内对肿瘤细胞具有优异的抑制作用。这项工作表明DESN介导双模式化学-超声动力疗法可以由体外遥控触发,可能表明在癌症治疗中有希望的临床应用。

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