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Optimization of specific cell-peptide interactions at the bio-material interface via regulation of nonspecific biofouling interactions

Optimization of specific cell-peptide interactions at the bio-material interface via regulation of nonspecific biofouling interactions
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摘要 Materials that interact with biological systems in a wellcontrolled,predictable manner are highly sought after for numerous biomedical and biotechnological applications.For example,it is essential that devices such as stents or heart valves in the blood stream of patients do not cause thrombosis or infection,or that biosensors do not lose their function due to adverse interactions with the bio environment.A general approach to the design of biointerfaces that addresses this need has been pursued over a number of years[1].It has two elements:(1)prevention of non-specific interfacial interactions,and(2)promotion of specific biointeractions required for the intended functioning of the material.In practice this means preventing all interactions except for the desired one(s).With respect to the first point it should be appreciated that biological species such as proteins and cells have a natural affinity for the interfacial state.Therefore,the realization of a surface that eliminates the adsorption/adhesion of these species is extremely difficult.Grafting of PEO/PEG,other hydrophilic polymers(PVP,PHEMA),and zwitterionic polymers[2]to the surface is the most common strategy to achieve“bio-resistance”.Regarding the second point,the surface must be designed so that it interacts selectively and exclusively with the component(s)(proteins,cells)that will give the desired bioactivity.For this purpose,“ligands”that bind these specific components are incorporated into the surface[3].
作者 John L.Brash
出处 《Science China Chemistry》 SCIE EI CAS CSCD 2020年第2期143-144,共2页 中国科学(化学英文版)
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