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pH-Responsive Cobalt(II)-Coordinated Assembly Containing Quercetin for Antimicrobial Applications
Giuseppina D G Santonoceta1, Carmelo Sgarlata1
1Department of Chemical Sciences, University of Catania, Viale Andrea Doria 6, 95125 Catania, Italy.
Molecules (Basel, Switzerland)
|July 29, 2023
Summary
This study introduces a novel pH-responsive drug delivery system (DDS) using cobalt(II) and quercetin for enhanced antibacterial activity. The system effectively releases drugs in acidic environments, addressing antimicrobial resistance.
Area of Science:
- Materials Science
- Nanotechnology
- Biochemistry
Background:
- Increasing antimicrobial resistance necessitates novel drug delivery systems (DDSs).
- Quercetin and its metal complexes show antibacterial potential but have limitations.
- Existing DDS face challenges in targeted drug release and efficacy.
Purpose of the Study:
- To develop a pH-responsive DDS based on cobalt(II)-coordinated assembly with quercetin and polyacrylic acid.
- To investigate the pH-dependent drug release mechanism exploiting acidic infection sites.
- To enhance the binding and release capabilities of the DDS for improved therapeutic outcomes.
Main Methods:
- Spectrophotometric (UV-Vis) and calorimetric (ITC) techniques to study cobalt(II)-quercetin complex formation.
- Quartz Crystal Microbalance with Dissipation (QCM-D) monitoring for solid-liquid interface interactions.
- Analysis of solution equilibria and species formation for DDS design.
Main Results:
- Formation of cobalt(II) complexes with quercetin and polyacrylic acid was characterized.
- Binding affinities and thermodynamic parameters for drug-carrier interactions were determined.
- Evidence of pH-controlled drug loading and release by the DDS was established.
Conclusions:
- The proposed DDS demonstrates effective pH-responsive drug release for potential antibacterial applications.
- The study provides crucial thermodynamic and binding data for optimizing DDS performance.
- This approach offers a promising strategy to combat antimicrobial resistance through targeted drug delivery.
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