聚乙烯亚胺
吸附
纤维素
水解
化学
离子强度
化学工程
石英晶体微天平
高分子化学
聚电解质
图层(电子)
醋酸纤维素
再生纤维素
材料科学
有机化学
聚合物
生物化学
工程类
水溶液
基因
转染
作者
Ghania Tiliket,Guy Ladam,Quang Trong Nguyen,Laurent Lebrun
标识
DOI:10.1016/j.apsusc.2016.02.165
摘要
Thin regenerated cellulose films are prepared by hydrolysis of cellulose acetate (CA). A polycation, namely polyethylenimine (PEI), is then adsorbed onto the films. From QCM-D analysis, PEI readily adsorbs from a 0.1% w/v solution in NaCl 0.2 M (ca. 100 ng cm−2). Further PEI adsorption steps at higher PEI concentrations induce a linear growth of the PEI films, suggesting that free adsorption sites still exist after the initial adsorption. The adsorbed PEI chains are resistant to variations of the ionic strength up to NaCl 1 M. Promisingly, the adsorption of T4D bacteriophages are 15-fold more efficient onto the PEI-treated, compared to the native regenerated cellulose films, as measured by QCM-D. This confirms the strong affinity between the negatively charged viruses and PEI, even at low PEI concentration, probably governed by strong electrostatic attractive interactions. This result explains the remarkable improvement of the affinity of medical masks for virus droplets when one of their cellulose layers was changed by two-PEI-functionalized cellulose-based filters.
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