Multipathway Antibacterial Mechanism of a Nanoparticle-Supported Artemisinin Promoted by Nitrogen Plasma Treatment

被引:21
作者
Cui, Haiying [1 ]
Chen, Xiaochen [2 ]
Bai, Mei [1 ]
Han, Dong [3 ]
Lin, Lin [1 ]
Dong, Mingdong [2 ]
机构
[1] Jiangsu Univ, Sch Food & Biol Engn, Zhenjiang 212013, Jiangsu, Peoples R China
[2] Aarhus Univ, Interdisciplinary Nanosci Ctr, Sino Danish Ctr Educ & Res, DK-8000 Aarhus, Denmark
[3] Natl Ctr Nanosci & Technol, Beijing 100190, Peoples R China
基金
中国国家自然科学基金; 欧盟地平线“2020”; 新加坡国家研究基金会;
关键词
artemisinin; silica nanoparticles; antibacterial; multipathway mechanism; nitrogen plasma; MESOPOROUS SILICA NANOPARTICLES; ESSENTIAL OIL; IN-VITRO; CHEMICAL-COMPOSITION; SOLUBILITY; DERIVATIVES; EFFICIENT; TARGET; CYCLODEXTRIN; INSIGHTS;
D O I
10.1021/acsami.9b15124
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Artemisinin has excellent antimalarial, antiparasitic, and antibacterial activities; however, the poor water solubility of artemisinin crystal limits their application in antibiosis. Herein, artemisinin crystal was first composited with silica nanoparticles (SNPs) to form an artemisinin@silica nanoparticle (A@SNP). After treating with nitrogen plasma, the aqueous solubility of plasma-treated A@SNP (A@SNP-p) approaches 42.26%, which is possibly attributed to the exposure of hydrophilic groups such as -OH groups on the SNPs during the plasma process. Compared with the pristine A@SNP, the antibacterial activity of A@SNP-p against both Gram-positive and Gram-negative strains is further enhanced, and its bactericidal rate against both strains exceeded 6 log CFU/mL (>99.9999%), which is contributed by the increased water solubility of the A@SNP-p. A possible multipathway antibacterial mechanism of A@SNP was proposed and preliminarily proved by the changes of intracellular materials of bacteria and the inhibition of bacterial metabolism processes, including the HMP pathway in Gram-negative strain and EMP pathway in Gram-positive strain, after treating with A@SNP-p. These findings from the present work will provide a new view for fabricating artemisinin-based materials as antibiotics.
引用
收藏
页码:47299 / 47310
页数:12
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