Affiliation:
1. Key Laboratory of Applied Surface and Colloid Chemistry Ministry of Education School of Chemistry and Chemical Engineering Shaanxi Normal University Xi'an 710119 China
2. Xi'an Key Laboratory of Polymeric Soft Matter School of Chemistry and Chemical Engineering Shaanxi Normal University Xi'an 710119 China
3. International Joint Research Center on Functional Fiber and Soft Smart Textile School of Chemistry and Chemical Engineering Shaanxi Normal University Xi'an 710119 China
4. School of Materials and Chemical Engineering Xi'an Technological University Xi'an 710021 China
5. Frontiers Science Center for Flexible Electronics (FSCFE) Xi'an Institute of Flexible Electronics (IFE) and Xi'an Institute of Biomedical Materials & Engineering (IBME) Northwestern Polytechnical University 127 West Youyi Road Xi'an 710072 China
Abstract
AbstractBiocompatible adsorbents play an essential role in hemoperfusion. Nevertheless, there are no hemoperfusion adsorbents that can simultaneously remove small and medium toxins, including bilirubin, urea, phosphor, heavy metals, and antibiotics. This bottleneck significantly impedes the miniaturization and portability of hemoperfusion materials and devices. Herein, a biocompatible protein‐polysaccharide complex is reported that exhibits “multi‐in‐one” removal efficacy for liver and kidney metabolism wastes, toxic metal ions, and antibiotics. Through electrostatic interactions and polysaccharide‐mediated coacervation, adsorbents can be prepared by simply mixing lysozyme (LZ) and sodium alginate (SA) together in seconds. The LZ/SA absorbent presented high adsorption capacities for bilirubin, urea, and Hg2+ of up to 468, 331, and 497 mg g−1, respectively, and the excellent anti‐protein adsorption endowed LZ/SA with a record‐high adsorption capacity for bilirubin in the interference of serum albumin to simulate the physiological environment. The LZ/SA adsorbent also has effective adsorption capacity for heavy metals (Pb2+, Cu2+, Cr3+, and Cd2+) and multiple antibiotics (terramycin, tetracycline, enrofloxacin, norfloxacin, roxithromycin, erythromycin, sulfapyrimidine, and sulfamethoxazole). Various adsorption functional groups exposed on the adsorbent surface significantly contribute to the excellent adsorption capacity. This fully bio‐derived protein/alginate‐based hemoperfusion adsorbent has great application prospects in the treatment of blood‐related diseases.
Funder
National Science Fund for Distinguished Young Scholars
Higher Education Discipline Innovation Project
National Natural Science Foundation of China
Subject
Pharmaceutical Science,Biomedical Engineering,Biomaterials
Cited by
9 articles.
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