# Novel Metformin-Encapsulating Poly(lactic-co-glycolic acid) Microspheres in Calcium Phosphate Pulp-Capping Cement with Dental Pulp Stem Cells for Regenerative Applications

**Authors:** Mohammad Alenizy, Abdullah Alhussein, Nader Almutairi, Ibrahim Ba-Armah, Heba Alqarni, Yazeed Altamimi, Ayman Altamimi, Tao Ma, Man-Kyo Chung, Michael D. Weir, Abraham Schneider, Hockin H. K. Xu

PMC · DOI: 10.3390/ma19030487 · Materials · 2026-01-26

## TL;DR

This study develops a new dental cement with metformin-releasing microspheres that supports stem cell compatibility and fast setting for pulp regeneration.

## Contribution

A novel metformin-encapsulating PLGA microsphere system is integrated into calcium phosphate cement for dental pulp regeneration.

## Key findings

- Met-PLGA-CPCC showed comparable or better mechanical properties than CPCC and MTA.
- Metformin release increased with higher microsphere content.
- hDPSCs exhibited high viability and attachment on the material.

## Abstract

Metformin is a promising small molecule for dentin regeneration, but an effective local delivery system for pulp applications has been underexplored. This study encapsulated metformin in poly(lactic-co-glycolic acid) (PLGA) microspheres and incorporated them into calcium phosphate–chitosan cement (CPCC) as a direct pulp-capping material (DPC). Metformin-PLGA microspheres were prepared by double emulsion and mixed with CPCC at a concentration of 0% to 20% by weight. Microsphere morphology, encapsulation efficiency, chemical composition, and physico-mechanical properties were characterized, and compatibility with human dental pulp stem cells (hDPSCs) was evaluated by live/dead assay and SEM. The microspheres were spherical (5.43 ± 0.17 µm) with (51 ± 3.69%) encapsulation efficiency, and FTIR confirmed metformin incorporation. The 15% Met-PLGA-CPCC group showed flexural strength (15.22 ± 1.98 MPa), elastic modulus (4.60 ± 0.73 GPa), and work of fracture (104.96 ± 12.48 J/m2) comparable to or higher than CPCC and MTA, while all Met-PLGA-CPCC groups had shorter setting times ranging from 18 min to 27 min than CPCC (39.15 ± 2.10 min) and MTA (123 ± 4.2 min). Metformin release increased proportionally with Met-PLGA content. hDPSCs exhibited good attachment and high viability on all materials over the evaluated period. In conclusion, Met-PLGA-CPCC provides fast-setting and favorable physico-mechanical properties, sustained metformin delivery, and excellent hDPSC compatibility. These properties support its potential as a bioactive direct pulp-capping material and as a versatile platform for regenerative applications.

## Linked entities

- **Chemicals:** Metformin (PubChem CID 4091), chitosan (PubChem CID 129662530), calcium phosphate (PubChem CID 24456)
- **Species:** Homo sapiens (taxon 9606)

## Full-text entities

- **Chemicals:** Calcium Phosphate (MESH:C020243), chitosan (MESH:D048271), PLGA (MESH:D000077182), Met (MESH:D008715), Metformin (MESH:D008687), MTA (MESH:D000068437)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

9 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12897909/full.md

## References

60 references — full list in the complete paper: https://tomesphere.com/paper/PMC12897909/full.md

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Source: https://tomesphere.com/paper/PMC12897909