Antifouling Microparticles To Scavenge Lipopolysaccharide from Human Blood Plasma
Language English Country United States Media print-electronic
Document type Journal Article, Research Support, Non-U.S. Gov't
- MeSH
- Adsorption MeSH
- Acrylamides metabolism MeSH
- Coated Materials, Biocompatible pharmacology MeSH
- Biofouling prevention & control MeSH
- Epoxy Compounds metabolism MeSH
- Plasma metabolism MeSH
- Humans MeSH
- Lipopolysaccharides metabolism MeSH
- Methacrylates metabolism MeSH
- Polymerization drug effects MeSH
- Polymers chemistry MeSH
- Polymyxin B pharmacology MeSH
- Surface Properties drug effects MeSH
- Proteins metabolism MeSH
- Check Tag
- Humans MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Names of Substances
- Acrylamides MeSH
- Coated Materials, Biocompatible MeSH
- Epoxy Compounds MeSH
- glycidyl methacrylate MeSH Browser
- Lipopolysaccharides MeSH
- methacrylamide MeSH Browser
- Methacrylates MeSH
- Polymers MeSH
- Polymyxin B MeSH
- Proteins MeSH
Currently, one of the most promising treatments of lipopolysaccharides (LPS)-induced sepsis is based on hemofiltration. Nevertheless, proteins rapidly adsorbed on the artificial surface of membranes which leads to activation of coagulation impairing effective scavenging of the endotoxins. To overcome this challenge, we designed polymer-brush-coated microparticles displaying antifouling properties and functionalized them with polymyxin B (PMB) to specifically scavenge LPS the most common endotoxin. Poly[( N-(2-hydroxypropyl) methacrylamide)- co-(carboxybetaine methacrylamide)] brushes were grafted from poly(glycidyl methacrylate) microparticles using photoinduced single-electron transfer living radical polymerization (SET-LRP). Notably, only parts-per-million of copper catalyst were necessary to achieve brushes able to repel adsorption of proteins from blood plasma. The open porosity of the particles, accessible to polymerization, enabled us to immobilize sufficient PMB to selectively scavenge LPS from blood plasma.
References provided by Crossref.org