Evidence map›Paper›PMID 41137437›Full record

ArticleAdvanced healthcare materials2026

Strontium-Containing Bioactive Glass Nanoparticles Stimulate Osteogenesis and Suppress Osteoclast Formation in Co-Culture.

Parichart Naruphontjirakul, Alexandra E Porter, Julian R Jones

Abstract read
In one paragraph

Article in Advanced healthcare materials, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

3 authors.

Parichart NaruphontjirakulBiological Engineering Program, Faculty of Engineering, King Mongkut's University of Technology Thonburi, Bangkok, 10140, Thailand.ORCID https://orcid.org/0000-0001-9998-6700
Alexandra E PorterDepartment of Materials, Imperial College London, South Kensington Campus, London, SW7 2AZ, UK.
Julian R JonesDepartment of Materials, Imperial College London, South Kensington Campus, London, SW7 2AZ, UK.ORCID https://orcid.org/0000-0002-2647-8024

Funding

Engineering and Physical Sciences Research Council EP/M004414/1King Mongkut's University of Technology Thonburi (KMUTT)National Science, Research and Innovation Fund (NSRF) EPSRC (EP/M004414/1)National Science, Research and Innovation Fund (NSRF) FRB670016/0164Thailand Science Research and Innovation (TSRI)
6 · The paper itself

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% SrO

Indexed as

GlassNanoparticlesOsteoclastsOsteogenesisStrontiumAnimalsCell DifferentiationCell LineCoculture TechniquesMiceOsteoblastsRANK LigandRAW 264.7 CellsRANK LigandStrontiumanti‐osteoclastic activitybioactive glassindirect co‐culture systemnanoparticlesosteoblast activitystrontium

Identifiers

PMID41137437
PMCPMC12864587

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.