4-Sulfonatocalixarene-induced nanoparticle formation of methylimidazolium-conjugated dextrans: Utilization for drug encapsulation. (1st November 2019)
- Record Type:
- Journal Article
- Title:
- 4-Sulfonatocalixarene-induced nanoparticle formation of methylimidazolium-conjugated dextrans: Utilization for drug encapsulation. (1st November 2019)
- Main Title:
- 4-Sulfonatocalixarene-induced nanoparticle formation of methylimidazolium-conjugated dextrans: Utilization for drug encapsulation
- Authors:
- Wintgens, Véronique
Guigner, Jean-Michel
Miskolczy, Zsombor
Amiel, Catherine
Biczók, László - Abstract:
- Highlights: Imidazolium-grafted dextrans self-assemble with sulfonatocalixarenes into nanoparticles. Spherical particle morphology and stoichiometry close to charge compensation are found. Nanoparticle diameter barely depends on macrocycle size and molecular mass of polymer. Decrease of substitution degree substantially diminishes the stability of the associates. Association efficiency of 99% can be reached with coralyne alkaloid. Abstract: Methylimidazolium side groups were grafted via ether linkage to dextran and the self-assembly of these polymers with 4-sulfonato-calix[n]arenes (SCXn) was studied in aqueous solutions. Dynamic light scattering and zeta potential measurements revealed the mixing ratio ranges of the constituents where stable nanoparticles could be created. The macrocycle size of SCXn and the molecular mass of the polymer barely affected the nanoparticle diameter, but the lowering of the imidazolium degree of substitution substantially diminished the stability of the associates. The pH change from neutral to acidic also unfavourably influenced the self-organization owing mainly to the decrease of the SCXn charge. Cryogenic transmission electron microscopy images proved the spherical morphology of the nanoproducts in which the stoichiometry of the constituents was always close to the one corresponding to charge compensation. The flexible and positively charged dextran-chains are compacted by the polyanionic SCXn. Coralyne, a pharmacologically importantHighlights: Imidazolium-grafted dextrans self-assemble with sulfonatocalixarenes into nanoparticles. Spherical particle morphology and stoichiometry close to charge compensation are found. Nanoparticle diameter barely depends on macrocycle size and molecular mass of polymer. Decrease of substitution degree substantially diminishes the stability of the associates. Association efficiency of 99% can be reached with coralyne alkaloid. Abstract: Methylimidazolium side groups were grafted via ether linkage to dextran and the self-assembly of these polymers with 4-sulfonato-calix[n]arenes (SCXn) was studied in aqueous solutions. Dynamic light scattering and zeta potential measurements revealed the mixing ratio ranges of the constituents where stable nanoparticles could be created. The macrocycle size of SCXn and the molecular mass of the polymer barely affected the nanoparticle diameter, but the lowering of the imidazolium degree of substitution substantially diminished the stability of the associates. The pH change from neutral to acidic also unfavourably influenced the self-organization owing mainly to the decrease of the SCXn charge. Cryogenic transmission electron microscopy images proved the spherical morphology of the nanoproducts in which the stoichiometry of the constituents was always close to the one corresponding to charge compensation. The flexible and positively charged dextran-chains are compacted by the polyanionic SCXn. Coralyne, a pharmacologically important alkaloid was efficiently embedded by self-assembly in the produced nanoparticles reaching 99% association efficiency. … (more)
- Is Part Of:
- Carbohydrate polymers. Volume 223(2019)
- Journal:
- Carbohydrate polymers
- Issue:
- Volume 223(2019)
- Issue Display:
- Volume 223, Issue 2019 (2019)
- Year:
- 2019
- Volume:
- 223
- Issue:
- 2019
- Issue Sort Value:
- 2019-0223-2019-0000
- Page Start:
- Page End:
- Publication Date:
- 2019-11-01
- Subjects:
- Cationic polymer -- Macrocycle -- Self-assembly -- Alkaloid -- Drug delivery
Polysaccharides -- Periodicals
Polysaccharides -- Periodicals
Polysaccharides -- Périodiques
Electronic journals
547.78 - Journal URLs:
- http://www.sciencedirect.com/science/journal/01448617 ↗
http://www.elsevier.com/journals ↗ - DOI:
- 10.1016/j.carbpol.2019.115071 ↗
- Languages:
- English
- ISSNs:
- 0144-8617
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3050.990480
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 11403.xml