# Strontium-doped hydroxyapatite microspheres loaded with iloprost promote dentin–pulp complex regeneration

**Authors:** Jilong Chen, Jingyi Di, Qiming Yu, Hui Xiao, Ting Wang, Li He

PMC · DOI: 10.3389/fbioe.2025.1726285 · Frontiers in Bioengineering and Biotechnology · 2026-01-14

## TL;DR

A new material combining strontium-doped hydroxyapatite and iloprost improves dentin-pulp regeneration in teeth.

## Contribution

A novel Sr-doped hydroxyapatite microsphere loaded with iloprost is developed for enhanced pulp repair.

## Key findings

- 5% Sr-HA showed optimal ion release and cytocompatibility for pulp cell growth.
- Ilo@Sr-HA enhanced dentin bridge formation and reduced inflammation in rat models.
- Ilo@Sr-HA increased mineralized nodule formation and odontogenic gene expression in vitro.

## Abstract

Vital pulp therapy (VPT) aims to preserve pulp vitality and tooth function. However, materials like calcium hydroxide and mineral trioxide aggregate have limitations in bioactivity, underscoring the need for improved biomaterials. Strontium-doped hydroxyapatite (Sr-HA) and pro-angiogenic agents have emerged as promising strategies to enhance dentin–pulp complex regeneration.

Hollow hydroxyapatite microspheres with 5%, 10%, and 15% Sr substitution were synthesized, and the optimal concentration was identified through Sr2+ release profiling and CCK-8-based cytocompatibility screening. Iloprost was subsequently loaded onto the selected 5% Sr-HA to obtain Ilo@Sr-HA. Human dental pulp stem cells (hDPSCs) were isolated from healthy extracted premolars using the tissue-explant method and identified by flow cytometry and multilineage differentiation assays. The identified cells were used to assess viability, ALP activity, mineralized nodule formation, and odontogenic gene expression. A bilateral rat pulp-exposure model (N = 40; n = 10/group: Blank, Dycal, Sr-HA, Ilo@Sr-HA) was established. Reparative outcomes were quantified using micro-CT and histological scoring at days 7 and 28.

Preliminary screening identified 5% Sr-HA as optimal, with the best ion release and cytocompatibility. Ilo@Sr-HA showed a biphasic release and no cytotoxicity toward hDPSCs. In vitro, Ilo@Sr-HA enhanced hDPSCs proliferation and ALP activity compared with HA and Sr-HA. Mineralized nodule formation increased, with significant DMP1 and DSPP upregulation (P < 0.05). In vivo, Ilo@Sr-HA enhanced reparative dentin formation, with DV/TV reaching 38.91% at 4 weeks vs. 26.53% for Dycal (P < 0.01). Histology confirmed continuous dentin bridges in the Ilo@Sr-HA group, contrasting with incomplete structures in Dycal and Sr-HA. Lower inflammation and better pulp preservation were also observed.

Ilo@Sr-HA combines Sr2+ ionic cues with iloprost’s pharmacological effects to form a bioactive microenvironment that supports pulp repair and reparative dentinogenesis. Ilo@Sr-HA is a promising material for VPT and dentin–pulp regeneration.

## Linked entities

- **Genes:** DMP1 (dentin matrix acidic phosphoprotein 1) [NCBI Gene 1758], DSPP (dentin sialophosphoprotein) [NCBI Gene 1834]
- **Chemicals:** iloprost (PubChem CID 5311181), strontium (PubChem CID 5359327), calcium hydroxide (PubChem CID 6093208)
- **Species:** Homo sapiens (taxon 9606), Mus musculus (taxon 10090)

## Full-text entities

- **Genes:** DMP1 (dentin matrix acidic phosphoprotein 1) [NCBI Gene 1758] {aka ARHP, ARHR, DMP-1}, ATHS (atherosclerosis susceptibility (lipoprotein associated)) [NCBI Gene 470] {aka ALP}, DSPP (dentin sialophosphoprotein) [NCBI Gene 1834] {aka DFNA39, DGI1, DMP3, DPP, DSP}
- **Diseases:** cytotoxicity (MESH:D064420), inflammation (MESH:D007249)
- **Chemicals:** hydroxyapatite (MESH:D017886), Ilo@Sr-HA (-), calcium hydroxide (MESH:D002126), Sr (MESH:D013324), mineral trioxide aggregate (MESH:C086631), Iloprost (MESH:D016285), CCK-8 (MESH:D012844)
- **Species:** Rattus norvegicus (brown rat, species) [taxon 10116], Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

7 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12847251/full.md

## References

61 references — full list in the complete paper: https://tomesphere.com/paper/PMC12847251/full.md

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Source: https://tomesphere.com/paper/PMC12847251