# Strontium‐Containing Bioactive Glass Nanoparticles Stimulate Osteogenesis and Suppress Osteoclast Formation in Co‐Culture

**Authors:** Parichart Naruphontjirakul, Alexandra E. Porter, Julian R. Jones

PMC · DOI: 10.1002/adhm.202503671 · Advanced Healthcare Materials · 2025-10-24

## TL;DR

Strontium-containing bioactive glass nanoparticles promote bone formation and reduce bone breakdown in a lab model, suggesting potential for treating osteoporosis.

## Contribution

Strontium-containing bioactive glass nanoparticles are shown to stimulate osteoblasts and suppress osteoclasts in co-culture systems.

## Key findings

- Sr-BGNPs reduced osteoclast differentiation and activity in monoculture and co-culture.
- Sr-BGNPs increased osteoblast differentiation and mineralized matrix formation in co-culture.
- The nanoparticles show potential for osteoporosis treatment by balancing bone formation and resorption.

## Abstract

The effect of monodispersed bioactive glass nanoparticles containing strontium (9.4 mol % SrO and 4.4 mol% SrO) and their dissolution products on osteoclast differentiation are investigated in monoculture and in an osteoblast‐osteoclast in vitro co‐culture system. Under standard conditions, RAW264.7 cells efficiently differentiate into osteoclast‐like cells upon RANKL stimulation, making them a well‐established monoculture model for osteoclastogenesis. The viability of RAW264.7 cells exposed to nanoparticles is dose‐ and time‐dependent. Indirect co‐culture of pre‐osteoblast MC3T3‐E1 and mouse monocyte RAW264.7 cells is carried out using Millipore cell culture plate inserts, with and without RANKL. Osteoclast differentiation, indicated by tartrate‐resistant acid phosphatase (TRAP) activity and the formation of multinucleated osteoclasts, is significantly reduced in RAW264.7 cells exposed to Sr‐BGNPs and their dissolution products, compared to RANKL‐stimulated control cells. Therefore, the observed reduction in osteoclast differentiation following exposure to Sr‐BGNPs and their ionic dissolution products indicates a potential inhibitory effect on this process. In co‐culture, bioactive glass nanoparticles containing 9.4 mol% SrO2 promoted differentiation of osteoblasts, relative to basal media and osteogenic media controls, measured as an increase in Alkaline phosphotase (ALP) activity and formation of mineralized matrix, while differentiation of osteoclasts decreased, measured as a reduction in TRAP activity and multinucleated osteoclast formation.

Spherical bioactive glass nanoparticles containing strontium inhibit osteoclast differentiation and activity, but promote osteoblast activity in osteoblast‐osteoclast in vitro co‐culture. The nanoparticles could be used for the treatment of osteoporosis.

## Linked entities

- **Chemicals:** TRAP (PubChem CID 88776687), ALP (PubChem CID 1392)
- **Diseases:** osteoporosis (MONDO:0005298)
- **Species:** Mus musculus (taxon 10090)

## Full-text entities

- **Genes:** Tnfsf11 (tumor necrosis factor (ligand) superfamily, member 11) [NCBI Gene 21943] {aka Ly109l, ODF, OPGL, RANKL, Trance}, Acp5 (acid phosphatase 5, tartrate resistant) [NCBI Gene 11433] {aka TRACP, TRAP}
- **Chemicals:** Sr-BGNPs (-), Strontium (MESH:D013324)
- **Species:** Mus musculus (house mouse, species) [taxon 10090]
- **Cell lines:** RAW264.7 — Mus musculus (Mouse), Mouse leukemia, Cancer cell line (CVCL_0493), MC3T3-E1 — Mus musculus (Mouse), Spontaneously immortalized cell line (CVCL_0409)

## Full text

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## Figures

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## References

55 references — full list in the complete paper: https://tomesphere.com/paper/PMC12864587/full.md

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Source: https://tomesphere.com/paper/PMC12864587