2009
DOI: 10.1016/j.reactfunctpolym.2008.11.003
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Direct introduction of phosphonate by the surface modification of polymers enhances biocompatibility

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Cited by 29 publications
(17 citation statements)
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“…Further, the immobilization of natural molecules by chemical modification and plasma surface treatments have also been studied [11]. However, the low stability of the modified polymers and the difficulty associated with their quantitative analysis remain unresolved [12].…”
Section: Introductionmentioning
confidence: 99%
“…Further, the immobilization of natural molecules by chemical modification and plasma surface treatments have also been studied [11]. However, the low stability of the modified polymers and the difficulty associated with their quantitative analysis remain unresolved [12].…”
Section: Introductionmentioning
confidence: 99%
“…7 The method relies upon the generation of carbenes by thermolytic or photolytic methods and their irreversible attachment by insertion into available surface chemical groups; a similar approach has recently been reported by Hayes. [8][9][10] Significantly, this approach permits the possibility of a post-polymerisation step for control of surface properties, but without changing the bulk characteristics of the underlying substrate, and since the applicable substrates may be both organic and inorganic polymers and materials, it is potentially very wide in scope.…”
Section: Introductionmentioning
confidence: 99%
“…In this work, a gelatin membrane, prepared by electrospinning in order to generate a porous structure, was surface modified with two bis(diaryldiazomethane)s. This modified gelatin membrane was a further example of the carbene modification of natural polymers, which had already been applied for the modification of color, hydrophobicity, biocompatibility, protein binding and adsorption, and payload delivery effects on various surfaces. The subsequent cross‐linking reaction between the end‐group amines and diisocyanates gave a structurally robust surface, which was expected to bind hydrogen peroxide and largely endowed with the antibacterial activity.…”
Section: Introductionmentioning
confidence: 99%