Sustainable and Surfactant-Free Synthesis of Negatively Charged Acrylamide Nanogels for Biomedical Applications

Nanogels offer unique advantages, like high surface-to-volume ratio, scalable synthetic methods, and easily tailored formulations, that allow us to control size and introduce stimuli-responsive properties. Their potential for drug delivery is significant due to their biocompatibility, high drug loading capacity, and controlled and sustained drug release. The development of greener and sustainable processes is essential for large-scale applications. We report the synthesis in water of covalently cross-linked acrylamide-based nanogels, both neutral and negatively charged, with varying amounts of acryloyl-l-proline, using high-dilution radical polymerization, without the need for surfactants. The use of a water-based synthesis resulted in nanogels with high monomer conversions and chemical yields, as well as lower polydispersity and smaller particle sizes for the negatively charged nanogels, leading to a more efficient synthetic methodology, with reduced loss of starting materials, higher potential for scalability, and reduction in costs. The suitability of these nanogels for biomedical applications was supported by cytotoxicity studies showing no significant reduction in viability on a human neuroblastoma cell line.

Authors

Institutions

Publication Details

Journal
Macromolecules
Published
2025-01-23
DOI
https://doi.org/10.1021/acs.macromol.4c02128
Citations
2
Primary Topic
Nanoparticle-Based Drug Delivery
Type
article
Field-Weighted Citation Impact
1.19

Funders

Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Sustainable and Surfactant-Free Synthesis of Negatively Charged Acrylamide Nanogels for Biomedical Applications

Vaidehi Roy Chowdhury, Alexander Röntgen, Michele Vendruscolo, Marina Resmini et al.
2 citations
Macromolecules
Nanoparticle-Based Drug Delivery
1.19
article

Sustainable and Surfactant-Free Synthesis of Negatively Charged Acrylamide Nanogels for Biomedical Applications

Vaidehi Roy Chowdhury, Alexander Röntgen, Michele Vendruscolo, Marina Resmini, Gabriela Rath, Davide Mazzali
article en
2 citations

Abstract

Nanogels offer unique advantages, like high surface-to-volume ratio, scalable synthetic methods, and easily tailored formulations, that allow us to control size and introduce stimuli-responsive properties. Their potential for drug delivery is significant due to their biocompatibility, high drug loading capacity, and controlled and sustained drug release. The development of greener and sustainable processes is essential for large-scale applications. We report the synthesis in water of covalently cross-linked acrylamide-based nanogels, both neutral and negatively charged, with varying amounts of acryloyl-l-proline, using high-dilution radical polymerization, without the need for surfactants. The use of a water-based synthesis resulted in nanogels with high monomer conversions and chemical yields, as well as lower polydispersity and smaller particle sizes for the negatively charged nanogels, leading to a more efficient synthetic methodology, with reduced loss of starting materials, higher potential for scalability, and reduction in costs. The suitability of these nanogels for biomedical applications was supported by cytotoxicity studies showing no significant reduction in viability on a human neuroblastoma cell line.

MacromoleculesVol. 58(3)
Queen Mary University of London (GB), University of Cambridge (GB), Samodzielny Publiczny Centralny Szpital Kliniczny (PL)
European Commission, H2020 Marie Skłodowska-Curie Actions
Responsible consumption and production
Openalex Percentile: Top 25%
Nanoparticle-Based Drug Delivery
1.19
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.