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Stimuli-responsive spin crossover nanoparticles for drug delivery and DNA-binding studies
Christina D Polyzou1, Patroula Gkolfi1, Christos T Chasapis2
1Department of Chemistry, Laboratory of Inorganic Chemistry, University of Patras, 26504 Patras, Greece. chpolyzou@upatras.gr.
Dalton Transactions (Cambridge, England : 2003)
|August 3, 2022
Summary
Aminated silica hybrid nanoparticles loaded with (S)-naproxen show potential as drug nanocarriers. Studies investigated their pH-dependent drug release and interactions with DNA and albumin.
Area of Science:
- Materials Science
- Nanotechnology
- Biochemistry
Background:
- Spin-crossover (SCO) nanoparticles offer unique properties for drug delivery applications.
- Aminated silica nanoparticles (AmNPs) provide a versatile platform for drug conjugation.
Purpose of the Study:
- To evaluate aminated silica hybrid nanoparticles coupled with (S)-naproxen (NAP) as potential drug nanocarriers.
- To investigate the pH-dependent drug release profile of these nanocarriers.
- To assess the interaction and binding affinities of the nanoparticles with DNA and serum albumins.
Main Methods:
- Drug release experiments were conducted at various pH values.
- DNA- and albumin-binding studies utilized diverse biophysical techniques.
- Characterization of nanoparticle-drug complex formation and stability.
Main Results:
- The aminated silica hybrid nanoparticles demonstrated controlled release of (S)-naproxen.
- Significant interactions were observed between the nanoparticles and both calf-thymus DNA and serum albumins.
- Binding constants were determined, indicating the affinity of the nanoparticles for biological macromolecules.
Conclusions:
- Aminated silica hybrid nanoparticles coupled with (S)-naproxen show promise as drug nanocarriers.
- The nanoparticles exhibit pH-responsive drug release capabilities.
- Understanding nanoparticle-biomacromolecule interactions is crucial for optimizing drug delivery efficacy and safety.
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