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首页> 外文期刊>Dalton transactions: An international journal of inorganic chemistry >Uniform magnesium silicate hollow spheres as high drug-loading nanocarriers for cancer therapy with low systemic toxicity
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Uniform magnesium silicate hollow spheres as high drug-loading nanocarriers for cancer therapy with low systemic toxicity

机译:均匀的硅酸镁空心球作为高载药量的纳米载体,具有低全身毒性的癌症治疗

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摘要

Resulting from their versatile functionality, nanomaterials with low systemic toxicity have offered high-performance diagnostic and therapeutic capabilities. Here, we designed and synthesized uniform magnesium silicate hollow spheres as high drug-loading nanocarriers for cancer therapy. Through a classical St?ber method and a hydrothermal process, well-defined MgSiO _3 hollow spheres were prepared in a facile route with inexpensive inhesion. Compared with routinely used mesoporous silica nanoparticles, our MgSiO_3 hollow spheres with larger void space and mesoporous shell endowed the structures with a much higher storage capacity of guest molecules (2140 mg DOX g~(-1)) and a much more sustained release of anticancer drugs. In detail, the release property and therapeutic efficacy of DOX-loaded nanoparticles were evaluated in vitro and in vivo. In vitro experiments revealed that these nanoparticles were mostly accumulated in lysosome, which facilitated continual drug release and efficient cancer cell destruction. We further demonstrated that these DOX-loaded nanoparticles could effectively suppress tumor growth compared to free DOX in vivo, as DOX-loaded-nanoparticle-treated mice survived over 15 days without obvious detectable tumor growth. Otherwise, long-term toxicity study was also evaluated, indicating their overall safety and great potential in biomedical applications.
机译:由于其多功能性,具有低全身毒性的纳米材料具有高性能的诊断和治疗能力。在这里,我们设计并合成了均匀的硅酸镁空心球,将其作为高载药量的纳米载体用于癌症治疗。通过经典的St?ber方法和水热工艺,以简便的方法制备了定义明确的MgSiO _3中空球体,且粘合力低。与常规使用的介孔二氧化硅纳米粒子相比,我们的MgSiO_3空心球具有更大的空隙空间和介孔壳,使结构具有更高的客体分子存储容量(2140 mg DOX g〜(-1))和更持久的抗癌释放毒品。详细地,在体外和体内评估了负载DOX的纳米颗粒的释放性质和治疗功效。体外实验表明,这些纳米颗粒主要聚集在溶酶体中,这有助于持续释放药物和有效破坏癌细胞。我们进一步证明,与体内的游离DOX相比,这些DOX负载的纳米粒子可以有效地抑制肿瘤的生长,因为DOX负载的纳米粒子治疗的小鼠可以存活15天以上,而没有明显的肿瘤生长。另外,还评估了长期毒性研究,表明它们的总体安全性和在生物医学应用中的巨大潜力。

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