# Mesoporous Bioactive Glass: Preparation, Characterisation, and Emerging Applications in Regenerative Medicine and Dentistry

**Authors:** Bakhtawar Mobeen, Nawshad Muhammad, Minati Choudhury, Ayesha Feroz, Sandleen Feroz

PMC · DOI: 10.1016/j.identj.2026.109454 · International Dental Journal · 2026-02-25

## TL;DR

Mesoporous bioactive glasses are promising biomaterials for regenerative medicine and dentistry due to their unique structure and properties, though clinical use is limited by challenges like mechanical strength and scalability.

## Contribution

This review summarizes the synthesis, properties, and biomedical applications of mesoporous bioactive glasses, emphasizing their translational potential.

## Key findings

- Mesoporous bioactive glasses enable rapid hydroxyapatite formation and improved cell adhesion due to their high surface area and tunable pore sizes.
- Applications include bone regeneration, drug delivery, wound healing, and dental treatments like enamel remineralization and implant modification.
- Despite promising pre-clinical results, clinical translation is hindered by mechanical limitations and lack of large-scale manufacturing solutions.

## Abstract

Mesoporous bioactive glasses have emerged as advanced biomaterials due to their highly ordered mesoporous structure, large surface area, and enhanced biological reactivity. These properties distinguish them from conventional bioactive glasses and underpin their growing interest in regenerative medicine and dentistry. This review aims to summarise the development, synthesis, structural characteristics, and applications of mesoporous bioactive glasses, with a focus on their translational potential.

A narrative review of the literature was conducted using major scientific databases to identify peer-reviewed studies related to the preparation, characterisation, and biomedical and dental applications of mesoporous bioactive glasses. Relevant in vitro and in vivo studies were critically analysed to synthesise current evidence and emerging trends.

Mesoporous bioactive glasses exhibit tunable pore sizes, high surface area, and enhanced ion and drug release capabilities, resulting in rapid hydroxyapatite formation and improved cell adhesion and proliferation. Various synthesis approaches, including sol–gel and templating techniques, allow precise control over composition and mesostructure. Reported applications include bone and soft tissue regeneration, drug delivery, wound healing, and antimicrobial therapies. In dentistry, mesoporous bioactive glasses have been explored for enamel remineralisation, periodontal regeneration, dentin hypersensitivity management, orthodontic applications, endodontic therapy, and implant surface modification. Most evidence remains pre-clinical.

Mesoporous bioactive glasses have emerged as a promising class of biomaterials for regenerative and dental applications. However, limitations related to mechanical strength, manufacturing scalability, and the lack of clinical studies currently restrict widespread clinical applications.

Mesoporous bioactive glasses offer enhanced bioactivity and therapeutic delivery compared with conventional bioactive glasses, highlighting their potential to improve regenerative and restorative dental outcomes once translational challenges are addressed

## Full-text entities

- **Genes:** TGFB1 (transforming growth factor beta 1) [NCBI Gene 7040] {aka CAEND1, CED, DPD1, IBDIMDE, LAP, TGF-beta1}, BMP1 (bone morphogenetic protein 1) [NCBI Gene 649] {aka OI13, PCOLC, PCP, TLD}, PTHLH (parathyroid hormone like hormone) [NCBI Gene 5744] {aka BDE2, HHM, PLP, PTHR, PTHRP}, VEGFA (vascular endothelial growth factor A) [NCBI Gene 7422] {aka L-VEGF, MVCD1, VEGF, VPF}, BDNF (brain derived neurotrophic factor) [NCBI Gene 627] {aka ANON2, BULN2}
- **Diseases:** cytotoxicity (MESH:D064420), bone abnormalities (MESH:D001847), infection (MESH:D007239), craniomaxillofacial deformities (MESH:D000077275), dentin hypersensitivity (MESH:D003807), peri-implantitis (MESH:D057873), cancer (MESH:D009369), fracture (MESH:D050723), inflammatory (MESH:D007249)
- **Chemicals:** Pluronic P123 (MESH:C464484), glas (MESH:D017965), silanol (MESH:C082343), hydroxyapatite (MESH:D017886), amine (MESH:D000588), titanium (MESH:D014025), cetyltrimethylammonium bromide (MESH:D000077286), carbon nanotubes (MESH:D037742), Pluronic (MESH:D020442), tetra-methyl orthosilicate (MESH:C500739), SiO 2 (MESH:D012822), Calcium nitrate (MESH:C059948), graphene (MESH:D006108), BAGs (-), oxides (MESH:D010087), calcium (MESH:D002118), PGA (MESH:D011454), strontium (MESH:D013324), CaO (MESH:C016538), Mg (MESH:D008274), Mo (MESH:D008982), alcohol (MESH:D000438), PLGA (MESH:D000077182), borate (MESH:D001881), Na2O (MESH:C096707), phosphonic acid (MESH:C570063), polymers (MESH:D011108), calcium silicate (MESH:C031293), P2O5 (MESH:C012500), ammonia (MESH:D000641), oxygen (MESH:D010100), zinc (MESH:D015032), salts (MESH:D012492), phosphate (MESH:D010710), P (MESH:D010758), tetraethyl orthosilicate (MESH:C040733), silicate (MESH:D017640), metal (MESH:D008670), B (MESH:D001895), Cerium (MESH:D002563), hydrochloric acid (MESH:D006851), Cu (MESH:D003300), Gentamicin (MESH:D005839), Ag+ (MESH:D012834), calcium phosphate (MESH:C020243), PVP (MESH:D011205), water (MESH:D014867)
- **Species:** Bacteria Latreille et al. 1825 (Bacteria stick insect, genus) [taxon 629395], Mus musculus (house mouse, species) [taxon 10090], Candida albicans (species) [taxon 5476], Enterococcus faecalis (species) [taxon 1351]
- **Cell lines:** Saos-2 — Homo sapiens (Human), Osteosarcoma, Cancer cell line (CVCL_0548), NCTC — Mus musculus (Mouse), Spontaneously immortalized cell line (CVCL_K271), L929 — Mus musculus (Mouse), Spontaneously immortalized cell line (CVCL_AR58)

## Full text

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## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12955637/full.md

## References

65 references — full list in the complete paper: https://tomesphere.com/paper/PMC12955637/full.md

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Source: https://tomesphere.com/paper/PMC12955637