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Distinctive Features of the Buffer Capacity of Polyelectrolyte Microcapsules Formed on MnCO3 Core
Aleksandr L Kim1, Alexey V Dubrovskii2, Sergey A Tikhonenko2
1Moscow Polytechnic University (Moscow Polytech), Bolshaya Semyonovskaya Str., 38, 107023 Moscow, Russia.
Polymers
|August 14, 2025
Summary
Manganese carbonate microcapsules (PMCs) show stable buffer capacity under heating, unlike calcium carbonate or polystyrene cores. This core material choice is key for adaptable biosensing and drug delivery systems.
Area of Science:
- Materials Science
- Nanotechnology
- Biomedical Engineering
Background:
- Layer-by-layer polyelectrolyte microcapsules (PMCs) require defined buffer capacity (BC) for stable biomedical and materials science applications.
- Manganese carbonate (MnCO3) is a promising core material for hollow structures, but its interaction with polyelectrolytes and effect on BC are not well understood.
Purpose of the Study:
- To determine the buffer capacity (BC) of PMCs templated on MnCO3 cores.
- To investigate the influence of ionic strength and temperature on MnCO3-templated PMCs (PMC_Mn).
- To compare the BC of PMC_Mn with PMCs templated on CaCO3 (PMC_Ca) and polystyrene (PMC_PS) cores.
Main Methods:
- Fabrication of PMCs using layer-by-layer assembly on MnCO3, CaCO3, and PS cores.
- Measurement of BC under varying ionic strength (0.22-3 M NaCl) and temperatures (60-90 °C).
- Comparative analysis of BC performance across different core materials and conditions.
Main Results:
- PMC_Mn exhibited identical BC dynamics in water as PMC_Ca.
- At pH < 5, BC of PMC_Mn and PMC_PS remained constant across ionic strengths; at pH > 8.5, PMC_Mn BC increased only at 3 M NaCl.
- PMC_Mn demonstrated stable BC under heating, while PMC_Ca and PMC_PS showed decreased BC.
Conclusions:
- The core material significantly dictates the functionality and stability of PMCs.
- MnCO3-templated PMCs offer enhanced thermal stability compared to PMC_Ca and PMC_PS.
- These findings support the development of adaptive systems for biosensing and controlled drug delivery.
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