Rosecler S. Klein
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Research Subjects
Research Interests
Rosecler S. Klein has a total of 6 co-authors. Here are the top co-authors by number of shared publications:
- Alessandro Franscisco Martins
State University of Maringá
1 shared publication - Ariel C. de Oliveira
Laboratory of Materials, Macromolecules, and Composites, Federal University of Technology-Paraná (UTFPR), Apucarana 86812-460, PR, Brazil
1 shared publication - Débora A. de Almeida
Laboratory of Materials, Macromolecules, and Composites, Federal University of Technology-Paraná (UTFPR), Apucarana 86812-460, PR, Brazil
1 shared publication - Elton Guntendorfer Bonafe
Laboratory of Food Chemistry, Postgraduate Program in Food Science, State University of Maringá, Maringá, PR, 87020-900, Brazil; Laboratory of Materials, Macromolecules, and Composites (LaMMAC), Federal University of Technology - Paraná (UTFPR), Apucarana, PR, 86812-460, Brazil
1 shared publication - Johny Paulo Monteiro
Laboratory of Materials, Macromolecules, and Composites (LaMMAC)
1 shared publication - Roberta Maia Sabino
Department of Chemical and Biomedical Engineering, University of Wyoming (UW), Laramie, WY 82071, USA
1 shared publication
Latest Publications
- Open Access
- 22 January 2025
- Published by MDPI AG in Nanomaterials
- Vol. 15 (3) , 161
Iota-Carrageenan/Chitosan Nanoparticles via Coacervation: Achieving Stability for Tiny Particles
This study investigated the influence of parameters such as pH condition, polyelectrolyte concentration, polymer ratio, and order of addition of the commercial polyelectrolytes chitosan and iota-carrageenan (ι-carrageenan) on the formation of polymeric nanoparticles in suspension (coacervates). A preliminary purification step of the polymers was essential for obtaining stable nanoparticles with small sizes as impurities, particularly metal ions that interfere with complexation, are removed by dialysis. Microparticles (13.5 μm in dry diameter) are obtained when aliquots of chitosan solution are poured into the ι-carrageenan solution. In general, an excess of chitosan results in the formation of agglomerated particles. The addition of an aliquot of ι-carrageenan solution (30 mL at 0.6 mg/mL and pH 4.0) to the chitosan solution (6.0 mL at 0.3 mg/mL and pH 4.0) leads to dispersed nanoparticles with a hydrodynamic radius of 278 ± 5 nm, a zeta potential of −31 ± 3 mV, and an average dry diameter of 45 ± 11 nm. The hydrodynamic radius increases as the pH rises. The partial deprotonation of ι-carrageenan chains enhances the interaction with water molecules, causing the particles to swell. These findings contribute to the fundamental understanding of polyelectrolyte complexation processes in aqueous suspension and provide insights for developing stable nanomaterials for potential practical applications.
- 22 January 2025
- Published by MDPI AG in Nanomaterials
- Vol. 15 (3) , 161
Open AccessIota-Carrageenan/Chitosan Nanoparticles via Coacervation: Achieving Stability for Tiny Particles
This study investigated the influence of parameters such as pH condition, polyelectrolyte concentration, polymer ratio, and order of addition of the commercial polyelectrolytes chitosan and iota-carrageenan (ι-carrageenan) on the formation of polymeric nanoparticles in suspension (coacervates). A preliminary purification step of the polymers was essential for obtaining stable nanoparticles with small sizes as impurities, particularly metal ions that interfere with complexation, are removed by dialysis. Microparticles (13.5 μm in dry diameter) are obtained when aliquots of chitosan solution are poured into the ι-carrageenan solution. In general, an excess of chitosan results in the formation of agglomerated particles. The addition of an aliquot of ι-carrageenan solution (30 mL at 0.6 mg/mL and pH 4.0) to the chitosan solution (6.0 mL at 0.3 mg/mL and pH 4.0) leads to dispersed nanoparticles with a hydrodynamic radius of 278 ± 5 nm, a zeta potential of −31 ± 3 mV, and an average dry diameter of 45 ± 11 nm. The hydrodynamic radius increases as the pH rises. The partial deprotonation of ι-carrageenan chains enhances the interaction with water molecules, causing the particles to swell. These findings contribute to the fundamental understanding of polyelectrolyte complexation processes in aqueous suspension and provide insights for developing stable nanomaterials for potential practical applications.