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Unveiling the differences: A comprehensive multi-technique analysis of hard and soft nanoparticles
Eleonora D'Intino1, Domenico Chirico1, Maria Gioia Fabiano1
1Department of Drug Chemistry and Technology, Sapienza University of Rome, Rome, Italy.
International Journal of Pharmaceutics
|April 21, 2025
Summary
This study compares soft niosomes (NVs) and hard Iron Oxide Nanoparticles (IONPs) for drug delivery. Surface modification of NVs with chitosan enhanced cellular uptake, showing potential for targeted therapies.
Area of Science:
- Nanotechnology and Materials Science
- Biomedical Engineering
- Pharmacology and Drug Delivery
Background:
- Nanoparticles (NPs) are crucial for advanced applications like biomedicine and drug delivery due to their unique interactions with biological systems.
- Soft nanocarriers (niosomes, NVs) and hard nanocarriers (Iron Oxide Nanoparticles, IONPs) present distinct advantages for targeted therapy and diagnostics.
- Understanding the behavior of different NP types, particularly concerning surface modifications, is vital for optimizing drug delivery systems.
Purpose of the Study:
- To conduct a comprehensive, multi-disciplinary evaluation of soft niosomes (NVs) and hard Iron Oxide Nanoparticles (IONPs).
- To compare the physicochemical properties, cellular uptake, and cytotoxicity profiles of NVs and IONPs.
- To investigate the impact of surface modifications, specifically chitosan coating on NVs, on their performance in drug delivery applications.
Main Methods:
- Characterization of nanoparticle physicochemical properties using Dynamic Light Scattering (DLS) and Atomic Force Microscopy (AFM).
- Assessment of cellular uptake via magnetic cell separation for IONPs and confocal microscopy for calcein-loaded NVs.
- Evaluation of nanoparticle biocompatibility through cytotoxicity studies on Calu-3 lung adenocarcinoma cells.
Main Results:
- Chitosan modification of NVs (NVsB-Chit) increased particle dimensions and shifted zeta potential to positive values, enhancing cellular interactions and uptake.
- NVsB-Chit exhibited zeta potential comparable to commercial coated ferrofluids.
- Both NVs and IONPs (FluidMAG) demonstrated minimal cytotoxicity on Calu-3 cells, especially at lower concentrations.
Conclusions:
- Surface modifications significantly influence nanoparticle behavior, with chitosan-coated niosomes showing improved cellular uptake.
- Both niosomes and IONPs exhibit good biocompatibility, making them suitable candidates for drug delivery systems.
- An interdisciplinary approach combining physicochemical and biological evaluations is crucial for designing efficient, safe, and targeted nanomedicines.

