School of Chemical Engineering, The University of Adelaide, Engineering North Building, 5005, Adelaide, Australia.
Faculty of Pharmacy, Assiut University, 71526, Assiut, Egypt.
Adv Healthc Mater. 2016 Oct;5(20):2667-2678. doi: 10.1002/adhm.201600688. Epub 2016 Sep 5.
Drug delivery using synthetic nanoparticles including porous silicon has been extensively used to overcome the limitations of chemotherapy. However, their synthesis has many challenges such as lack of scalability, high cost, and the use of toxic materials with concerning environmental impact. Nanoscale materials obtained from natural resources are an attractive option to address some of these disadvantages. In this paper, a new mesoporous biodegradable silicon nanoparticle (SiNP) drug carrier obtained from natural diatom silica mineral available from the mining industry is presented. Diatom silica structures are mechanically fragmented and converted into SiNPs by simple and scalable magnesiothermic reduction process. Results show that SiNPs have many desirable properties including high surface area, high drug loading capacity, strong luminescence, biodegradability, and no cytotoxicity. The in-vitro release results from SiNPs loaded with anticancer drugs (doxorubicin) demonstrate a pH-dependent and sustained drug release with enhanced cytotoxicity against cancer cells. The cells study using doxorubicin loaded SiNPs shows a significantly enhanced cytotoxicity against cancer cells compared with free drug, suggesting their considerable potential as theranostic nanocarriers for chemotherapy. Their low-cost manufacturing using abundant natural materials and outstanding chemotherapeutic performance has made them as a promising alternative to synthetic nanoparticles for drug delivery applications.
利用包括多孔硅在内的合成纳米粒子进行药物输送已被广泛用于克服化疗的局限性。然而,它们的合成存在许多挑战,例如缺乏可扩展性、成本高以及使用对环境有影响的有毒材料。从天然资源中获得的纳米级材料是解决其中一些缺点的一个有吸引力的选择。本文提出了一种新的介孔可生物降解硅纳米颗粒(SiNP)药物载体,它是从采矿业可用的天然硅藻硅矿物质中获得的。通过简单且可扩展的镁热还原工艺,将硅藻硅结构机械破碎并转化为 SiNPs。结果表明,SiNPs 具有许多理想的特性,包括高比表面积、高载药能力、强发光性、生物降解性和无细胞毒性。负载抗癌药物(阿霉素)的 SiNPs 的体外释放结果表明,药物释放具有 pH 依赖性和持续释放特性,对癌细胞的细胞毒性增强。用载有阿霉素的 SiNPs 进行的细胞研究表明,与游离药物相比,对癌细胞的细胞毒性显著增强,表明它们作为化疗治疗性纳米载体具有相当大的潜力。它们使用丰富的天然材料进行低成本制造和出色的化疗性能,使它们成为药物输送应用中合成纳米粒子的有前途的替代品。