Janus particles with obvious chemical compartition can perform their functions independently, so they have attracted much attention in biomedical materials. Herein, a mesoporous silica/silver Janus nanoparticle modified with cardanol (C-MSN@Ag) was designed and synthesized redox and click chemical reactions and was further evaluated as a highly efficient hemostatic dressing. This Janus structure endowed C-MSN@Ag with both prominent hemostatic and antibacterial performance. The hemostatic time of C-MSN@Ag on rat liver laceration was up to 40% shorter than that of MSN and MSN@Ag because of adhesion of phenolic compounds on the tissue and the blocking effect of the hydrophobic alkyl chains from cardanol. Besides, C-MSN@Ag could promote coagulation by forming a three-dimensional network with fibrin more quickly than MSN and MSN@Ag. Additionally, due to the released silver ions and phenolic hydroxyl groups of cardanol, C-MSN@Ag exhibited a broad-spectrum antibacterial rate (∼99%) against both and . C-MSN@Ag also possessed non-cytotoxicity. This work not only provides a way for the fabrication of silica-based Janus hemostatic agents by the atom-economical click reaction but also gives a direction for the application of the sustainable naturally occurring cardanol.
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http://dx.doi.org/10.1021/acsabm.0c01267 | DOI Listing |
ACS Appl Bio Mater
December 2020
College of Chemistry and Materials Science, Fujian Normal University, Fuzhou 350007, People's Republic of China.
Janus particles with obvious chemical compartition can perform their functions independently, so they have attracted much attention in biomedical materials. Herein, a mesoporous silica/silver Janus nanoparticle modified with cardanol (C-MSN@Ag) was designed and synthesized redox and click chemical reactions and was further evaluated as a highly efficient hemostatic dressing. This Janus structure endowed C-MSN@Ag with both prominent hemostatic and antibacterial performance.
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