(Ca/Zn)CO <sub>3</sub> Microparticles Loaded with Bacitracin─Antibacterial and Osteogenic Dual Action Carriers

Calcium carbonate (CaCO<sub>3</sub>) microparticles are widely used in biomedical engineering, mainly in the field of bone tissue regeneration. This study aimed at the development of CaCO<sub>3</sub>-based carriers for an antimicrobial peptide, bacitracin (BCT), with antibacterial and osteogenic properties. The first part of the study was devoted to CaCO<sub>3</sub> microparticles obtained by the precipitation method from equimolar Na<sub>2</sub>CO<sub>3</sub> and CaCl<sub>2</sub> solutions. The morphology, size, and surface area of the microparticles were strongly dependent on the parameters used during the reaction (i.e., the mixing speed and geometry of the container). However, BCT adsorption on CaCO<sub>3</sub> microparticles was insufficient (maximum drug loading of approximately 1%); therefore, the microparticles were enriched with Zn<sup>2+</sup> ions (5%, 10%, or 20% vol. of the CaCl<sub>2</sub> solution used for precipitation was exchanged to equimolar ZnCl<sub>2</sub> solution). This innovative approach significantly influenced the properties and BCT adsorption capacity of the microparticles. The microparticles containing Zn<sup>2+</sup> were larger and cubic in shape with a predominant calcite structure. The adsorption efficacy of BCT increased significantly (maximum drug loading of approximately 40%) due to the strong affinity of BCT to Zn<sup>2+</sup>. BCT was released from the microparticles within 24 h, and the degradation of Zn<sup>2+</sup> containing microparticles was three times slower than in the case of nonmodified CaCO<sub>3</sub> microparticles. The microparticles were cytocompatible with L929 fibroblasts and human mesenchymal stem cells (hMSCs), except for the microparticles with the highest Zn<sup>2+</sup> content. The microparticles with adsorbed BCT successfully inhibited the growth of <i>Staphylococcus aureus</i>, <i>Staphylococcus epidermidis</i>, and <i>Streptococcus pyogenes</i>. (Ca/Zn)-CO<sub>3</sub> microparticles enhanced osteogenic differentiation of hMSCs; however, this effect should be attributed to the release of Zn<sup>2+</sup> rather than BCT. The newly developed (Ca/Zn)-CO<sub>3</sub> microparticles with adsorbed BCT could in the future serve as antibacterial and osteogenic materials for the treatment of bacterial infections and regeneration of bone tissue.

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Publication Details

Journal
ACS Omega
Published
2025-12-18
DOI
https://doi.org/10.1021/acsomega.5c06594
Primary Topic
Calcium Carbonate Crystallization and Inhibition
Type
article
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article

(Ca/Zn)CO 3 Microparticles Loaded with Bacitracin─Antibacterial and Osteogenic Dual Action Carriers

Elżbieta Pamuła, Monika Brzychczy‐Włoch, Dorota Ochońska, Kamil Kornaus et al.
ACS Omega
Calcium Carbonate Crystallization and Inhibition
article

(Ca/Zn)CO 3 Microparticles Loaded with Bacitracin─Antibacterial and Osteogenic Dual Action Carriers

Elżbieta Pamuła, Monika Brzychczy‐Włoch, Dorota Ochońska, Kamil Kornaus, Katarzyna Reczyńska-Kolman
article en

Abstract

Calcium carbonate (CaCO<sub>3</sub>) microparticles are widely used in biomedical engineering, mainly in the field of bone tissue regeneration. This study aimed at the development of CaCO<sub>3</sub>-based carriers for an antimicrobial peptide, bacitracin (BCT), with antibacterial and osteogenic properties. The first part of the study was devoted to CaCO<sub>3</sub> microparticles obtained by the precipitation method from equimolar Na<sub>2</sub>CO<sub>3</sub> and CaCl<sub>2</sub> solutions. The morphology, size, and surface area of the microparticles were strongly dependent on the parameters used during the reaction (i.e., the mixing speed and geometry of the container). However, BCT adsorption on CaCO<sub>3</sub> microparticles was insufficient (maximum drug loading of approximately 1%); therefore, the microparticles were enriched with Zn<sup>2+</sup> ions (5%, 10%, or 20% vol. of the CaCl<sub>2</sub> solution used for precipitation was exchanged to equimolar ZnCl<sub>2</sub> solution). This innovative approach significantly influenced the properties and BCT adsorption capacity of the microparticles. The microparticles containing Zn<sup>2+</sup> were larger and cubic in shape with a predominant calcite structure. The adsorption efficacy of BCT increased significantly (maximum drug loading of approximately 40%) due to the strong affinity of BCT to Zn<sup>2+</sup>. BCT was released from the microparticles within 24 h, and the degradation of Zn<sup>2+</sup> containing microparticles was three times slower than in the case of nonmodified CaCO<sub>3</sub> microparticles. The microparticles were cytocompatible with L929 fibroblasts and human mesenchymal stem cells (hMSCs), except for the microparticles with the highest Zn<sup>2+</sup> content. The microparticles with adsorbed BCT successfully inhibited the growth of <i>Staphylococcus aureus</i>, <i>Staphylococcus epidermidis</i>, and <i>Streptococcus pyogenes</i>. (Ca/Zn)-CO<sub>3</sub> microparticles enhanced osteogenic differentiation of hMSCs; however, this effect should be attributed to the release of Zn<sup>2+</sup> rather than BCT. The newly developed (Ca/Zn)-CO<sub>3</sub> microparticles with adsorbed BCT could in the future serve as antibacterial and osteogenic materials for the treatment of bacterial infections and regeneration of bone tissue.

ACS OmegaVol. 11(1)
Jagiellonian University (PL), Institute of Ceramics and Building Materials (PL), AGH University of Krakow (PL)
Openalex Percentile: Top 72%
Calcium Carbonate Crystallization and Inhibition
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