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Dual pH- and thermoresponsive nano-objects with tunable morphologies and dye encapsulation prepared via aqueous emulsion polymerization-induced self-assembly

Title: Dual pH- and thermoresponsive nano-objects with tunable morphologies and dye encapsulation prepared via aqueous emulsion polymerization-induced self-assembly
Authors: Lukáš Petrova, Svetlana; Vragovič, Martina; Pavlova, Ewa; Hrubý, Martin; Pokorný, Václav
Contributors: Ministerstvo Školství, Mládeže a Tělovýchovy; European Union
Source: Royal Society Open Science ; volume 13, issue 3 ; ISSN 2054-5703
Publisher Information: The Royal Society
Publication Year: 2026
Description: Poly(triethylene glycol methyl ether methacrylate)-b-poly[2-(diisopropylamino)ethyl methacrylate] (PTEGMA-b-PDPA) nano-objects, synthesized via polymerization-induced self-assembly (PISA), exhibit dual thermo- and pH-responsive behaviour. The thermoresponsiveness originates from the lower critical solution temperature (LCST) of the PTEGMA block, while the pH-responsiveness arises from protonation of the PDPA block under acidic conditions. The hydrophilic PTEGMA block (degree of polymerization, DP = 120) was first synthesized to serve as a macro-chain transfer agent. This was followed by reversible addition−fragmentation chain-transfer polymerization (RAFT)-mediated PISA emulsion polymerization of the pH-sensitive PDPA block (DP = 35–265) in aqueous solution at a solid content of 10 wt%. During polymerization, the block copolymers self-assembled in situ into diverse and tunable nanostructures, including micelles, branched worms, ‘jellyfish’ and thick-walled vesicles. These nano-objects were thoroughly characterized using cryo-transmission electron microscopy (cryo-TEM), dynamic light scattering (DLS) and small-angle X-ray scattering (SAXS). The in situ drug encapsulation capability of these dual-responsive nano-formulations was demonstrated using Nile Red (NR), a hydrophobic fluorescent model compound. Specifically, thick-walled vesicles (PTEGMA120-b-PDPA265) successfully encapsulated NR during RAFT-PISA synthesis and released it under acidic conditions and/or at mildly elevated temperatures. These results highlight the potential of tailorable PTEGMA-b-PDPA nano-objects as ‘smart’ nanocarriers for targeted and stimuli-responsive drug delivery applications.
Document Type: article in journal/newspaper
Language: English
DOI: 10.1098/rsos.252454
DOI: 10.1098/rsos.252454/6127609/rsos.252454.pdf
Availability: https://doi.org/10.1098/rsos.252454; https://royalsocietypublishing.org/rsos/article-pdf/doi/10.1098/rsos.252454/6127609/rsos.252454.pdf
Rights: http://creativecommons.org/licenses/by/4.0/ ; http://creativecommons.org/licenses/by/4.0/
Accession Number: edsbas.4B1FC1C6
Database: BASE