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镁离子掺杂的二氧化硅纳米片作为具有增强抗菌活性和细胞摄取能力的可降解药物载体。

Magnesium-ion-doped silica nanosheets as degradable drug carriers with enhanced antibacterial activity and cellular uptake.

作者信息

Liao Ruohan, Zhang Chengdong, Wang Zechuang, Li Xingping, Pu Chao, Luo Xuwei, Feng Gang, Su Qiang, Xiao Dongqin

机构信息

Research Institute of Tissue Engineering and Stem Cells, Department of Pharmacy, The Second Clinical College of North Sichuan Medical College Nanchong Sichuan 637000 China

Department of Orthopaedics, Chengfei Hospital Chengdu Sichuan 610091 China.

出版信息

RSC Adv. 2025 Jan 31;15(5):3183-3191. doi: 10.1039/d4ra07626e. eCollection 2025 Jan 29.

Abstract

Mesoporous silica nanoparticles (MSNs) have attracted significant interest in drug delivery applications due to their good biocompatibility and high specific surface area. However, conventional MSNs typically have small pore sizes and low degradation rates, resulting in limited drug loading capacity and potential nanoparticle accumulation. This study focuses on the synthesis of novel magnesium (Mg) ion-doped silica nanoparticles (MgMSNs) using a chemical precipitation method followed by calcination. In contrast to the nanorod-shaped MSNs, the Mg ion-doped silica nanoparticles exhibited a nanosheet-shaped morphology. When the added Mg concentration was 5 mM, the prepared nanosheets (5MgMSNs) showed superior antibacterial activity and increased curcumin-loading capacity compared to pure silica nanoparticles. Additionally, the natural green fluorescence of curcumin allowed for the visualization of cellular uptake, confirming the efficient internalization of 5MgMSNs by L929 cells. Notably, under acidic conditions, the release of Mg ions and the degradability of the nanoparticles were enhanced, indicating pH-responsive release behavior. Overall, these results highlight the favorable degradability and improved cellular uptake capacity of nanosheet Mg-incorporated silica nanoparticles, suggesting their potential for loading polyphenol drugs such as curcumin and achieving efficient drug release within cells.

摘要

介孔二氧化硅纳米颗粒(MSNs)因其良好的生物相容性和高比表面积而在药物递送应用中引起了广泛关注。然而,传统的MSNs通常孔径较小且降解率较低,导致药物负载能力有限以及潜在的纳米颗粒积累。本研究重点采用化学沉淀法随后煅烧来合成新型镁(Mg)离子掺杂的二氧化硅纳米颗粒(MgMSNs)。与纳米棒状的MSNs不同,镁离子掺杂的二氧化硅纳米颗粒呈现出纳米片状形态。当添加的镁浓度为5 mM时,所制备的纳米片(5MgMSNs)与纯二氧化硅纳米颗粒相比表现出优异的抗菌活性和提高的姜黄素负载能力。此外,姜黄素的天然绿色荧光使得细胞摄取可视化,证实了5MgMSNs能被L929细胞有效内化。值得注意的是,在酸性条件下,镁离子的释放和纳米颗粒的降解性增强,表明具有pH响应释放行为。总体而言,这些结果突出了纳米片状含镁二氧化硅纳米颗粒良好的降解性和改善的细胞摄取能力,表明它们在负载姜黄素等多酚类药物以及在细胞内实现高效药物释放方面的潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bb2e/11783045/e8d313f09621/d4ra07626e-f1.jpg

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