Title:
Preparation of hybrid triple-stimuli responsive nanogels based on poly(L-histidine)
Languages of Item:
English
Abstract:
A series of novel multi-responsive disulfide cross-linked polypeptide nanogels has been synthesized by a one-step ring-opening polymerization process. The pH-responsive core of the prepared nanogels was based on poly(L-histidine), the difunctional N-carboxy anhydride of l-cystine (l-Cys-NCA) was used as a reduction-cleavable cross-linking agent, while the outer hydrophilic corona was comprised of a poly(ethylene oxide) block. Extensive molecular characterization studies were conducted in order to confirm the formation of the desired polymeric nanostructures and also to prove their responsiveness to external stimuli within the physiological values of healthy and cancer tissues. Furthermore, the disruption of the disulfide-bond linkages between the polymeric chains was achieved by the presence of the reductive tripeptide glutathione (GSH), leading to size variations that were monitored by dynamic light scattering (DLS) and size-exclusion chromatography (SEC). "Stealth" properties of the formed nanostructures were examined by zeta potential measurements. The described nanogels are clearly promising candidates for drug delivery applications. © 2015 Wiley Periodicals, Inc.
Authors:
Panayiotis Bilalis
Spyridon Varlas
Aikaterini Kiafa
Athanassios Velentzas
Dimitrios Stravopodis
Hermis Iatrou
Journal:
Journal of Polymer Science Part A: Polymer Chemistry
Keywords:
Amino acids; Chromatography; Covalent bonds; Crosslinking; Dynamic light scattering; Ethylene; Light scattering; Nanoparticles; Nanostructured materials; Nanostructures; Polyethylene oxides; Polyethylenes; Polymerization; Polypeptides; Size exclusion chromatography, Cross linking agents; Drug delivery applications; Hydrophilic corona; Molecular characterization; Polies (lhistidine); Redox chemistry; Stimuli-responsive; Zeta potential measurements, Ring opening polymerization
Main subject category:
Science
Official URL (Publisher):
