# Robocast Zn- and Co-doped bioactive glass/tricalcium phosphate scaffolds for bone regeneration

**Authors:** Mahdieh Hajian Monfared, Sanam Mohandesnezhad, Mahmoud Azami, Saeed Samani

PMC · DOI: 10.1186/s13036-025-00585-x · Journal of Biological Engineering · 2025-12-06

## TL;DR

This study creates 3D-printed scaffolds with zinc and cobalt that support bone regeneration by enhancing early and late stages of bone cell development.

## Contribution

The novel contribution is the development of Zn- and Co-doped BG/TCP scaffolds that show complementary osteogenic effects in sequential stages.

## Key findings

- Zn-doping enhances early osteogenesis with higher collagen type I and ALP activity.
- Co-doping promotes late-stage maturation with increased osteocalcin and calcium mineralization.
- Scaffolds exhibit mechanical strength comparable to cancellous bone and accelerated hydroxyapatite formation.

## Abstract

Bone tissue engineering requires scaffolds that synergize mechanical strength with bioactivity. This study aimed to develop and characterize 3D-printed zinc (Zn)- and cobalt (Co)-doped 45S5 bioactive glass (BG)/β-tricalcium phosphate (TCP) composite scaffolds for enhanced bone regeneration.

Sol-gel-synthesized BG powders, doped with 3–15% Zn or 1–5% Co, were combined with TCP (50:50 ratio) to fabricate porous scaffolds via robocasting. Scaffolds were screened for cytocompatibility (MTT assay) and ion release (ICP-OES). The optimal compositions (3% Zn and 1% Co) were characterized for mechanical strength, in vitro bioactivity in SBF, and osteogenic potential using hADMSCs through qPCR, ALP activity, immunocytochemistry, and Alizarin Red staining.

The 3% Zn- and 1% Co-doped scaffolds demonstrated excellent cytocompatibility (≥ 90% hADMSC viability) with controlled ion release. They exhibited compressive strengths of 15.67–20.24 MPa, matching cancellous bone, and significantly accelerated hydroxyapatite formation in SBF. Biologically, the scaffolds induced distinct, stage-specific osteogenic responses. Zn-doping preferentially enhanced early osteogenesis, marked by significantly higher collagen type I (COL-1) expression at day 21 and the highest ALP activity at day 14. In contrast, Co-doping specifically promoted late-stage maturation, resulting in superior osteocalcin (OCN) expression and a 2.5-fold increase in calcium mineralization compared to undoped controls, as quantified by Alizarin Red staining. Immunocytochemistry confirmed this trend, with robust expression of both COL-1 and osteopontin in the doped groups.

The results demonstrate that Zn²⁺ and Co²⁺ ions confer complementary biological functions within BG/TCP scaffolds, effectively promoting sequential stages of osteogenesis. The robocast scaffolds successfully combine mechanical competence with enhanced osteoinductivity, presenting a highly promising platform for the repair of load-bearing bone defects.

## Linked entities

- **Genes:** COL1 (CONSTANS-like 1) [NCBI Gene 831442], BGLAP (bone gamma-carboxyglutamate protein) [NCBI Gene 632]
- **Proteins:** bglap2 (bone gamma-carboxyglutamate (gla) protein (osteocalcin) 2), ALPP (alkaline phosphatase, placental)
- **Chemicals:** Zn (PubChem CID 23994), Co (PubChem CID 281), hydroxyapatite (PubChem CID 14781), calcium (PubChem CID 5460341)

## Full-text entities

- **Chemicals:** tricalcium phosphate (MESH:C018392), bioactive glass (-), Co (MESH:D003035), Zn (MESH:D015032)

## Full text

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## Figures

9 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12817833/full.md

## References

3 references — full list in the complete paper: https://tomesphere.com/paper/PMC12817833/full.md

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Source: https://tomesphere.com/paper/PMC12817833