Keywordspolyphosphate; microparticles; delayed wound healing; collagen; PAI-1; re-epithelialization; diabetic mice; directional alignment into fibers; polyfluorene copolymers; liquid-solid interfaces; polarization spectroscopy; photoconductivity; polylactide; urea; inclusion complex; crystallization; stereocomplex; polymers; cyclodextrins; inclusion compounds; coalescence; biopolymers; polysaccharides; polysaccharide-based metallic nanoparticles; host–guest strategy; preparation and characterization; application; toxicity evaluation; host-guest chemistry; layer-by-layer self-assembly; pillar[6]arene; pH-responsiveness; amylose host; enzymatic polymerization; hierarchical structured material; inclusion complex; vine-twining polymerization; ionic polyglutamic acid complexes; biocide polyglutamic acid; comb-like polyglutamic acid complexes; ethyl lauroyl arginate; antibacterial polymer complexes; polyelectrolyte complexes; dendrimers; frontal analysis continuous capillary electrophoresis; counter-ion release; binding constants; ionic strength dependence; antibacterial meshes; guest molecule; cyclodextrin grafting; polypropylene; oxygen plasma; polyrotaxane; silver sulfadiazine; mechanism; antibacterial; α-cyclodextrin; α-cyclodextrin nanosponges; α-cyclodextrin polymers; oxygen delivery; myocardial infarction; ischemia; reperfusion; quantum dots; host–guest interactions; xerogel; poly(lactic acid); poly(ε-caprolactone); cyclodextrins; cyclodextrin-inclusion complexes; controlled drug delivery; rapid dissolution; pseudorotaxanes; mechanical properties; host–guest polymer complex; microgel; hydrogel; β-cyclodextrin polymer; rheology; temperature-induced sol–gel transition; n/a
