Evidence map›Paper›PMID 39154380›Full record

ArticleMicroscopy research and technique2025

Amino acid surface modified bioglass: A candidate biomaterial for bone tissue engineering

Yasin Özkabadayı, Mustafa Türk, Ali Kumandaş, Siyami Karahan

Abstract read
In one paragraph

Article in Microscopy research and technique, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

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4 · The record

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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

4 authors.

Yasin ÖzkabadayıFaculty of Veterinary Medicine, Department of Histology and Embryology, Kirikkale University, Kirikkale, Turkey.ORCID https://orcid.org/0000-0003-0326-3407
Mustafa TürkFaculty of Engineering and Natural Sciences, Department of Bioengineering, Kirikkale University, Kirikkale, Turkey.
Ali KumandaşFaculty of Veterinary Medicine, Department of Surgery, Kirikkale University, Kirikkale, Turkey.
Siyami KarahanFaculty of Veterinary Medicine, Department of Histology and Embryology, Kirikkale University, Kirikkale, Turkey.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Bioglasses are solid materials consisted of sodium oxide, calcium oxide, silicon dioxide and phosphorus in various proportions and have used in bone tissue engineering. There have been ongoing efforts to improve the surface properties of bioglasses to increase biocompatibility and performance. The aim of the present study is to modify the bioglass surface with an amino acid mixture consisting of arginine, aspartic acid, phenylalanine, cysteine, histidine and lysine, to characterize the surface, and to evaluate the performance and biocompatibility in vitro and in vivo. The untreated bioglass, bioglass kept in simulated body fluid (SBF), and modified bioglass were used in further evaluation. After confirmation of the surface modification with FT-IR analyses and SEM analyses, MC3T3-E1 preosteoblasts adhesion on the surface was also revealed by SEM. The modified bioglass had significantly higher ALP activity in colorimetric measurement, rate of calcium accumulations in Alizarin red s staining, lower rate of cell death in Annexin-V/PI staining to determine apoptosis and necrosis. Having higher cell viability rate in MTT test and absence of genotoxicity in micronucleus test (OECD 487), the modified bioglass was further confirmed for biocompatibility in vitro. The results of the rat tibial defect model revealed that the all bioglass treatments had a significantly better bone healing score compared to the untreated negative control. However, the modified bioglass exhibited significantly better bone healing efforts especially during the first and the second months compared to the other bioglass treatment treatments. As a result, the amino acid surface modification of bioglasses improves the surface biocompatibility and osteogenic performance that makes the amino acid modified bioglass a better candidate for bone tissue engineering. RESEARCH HIGHLIGHTS: Bioglass surface modification with amino acids contributes to bioglass-tissue interaction with an improved cell attachment. Modified bioglass increases in vitro Alp activity and calcium accumulation, and also positively affects cell behavior by supporting cell adaptation. Bioglass exerts osteogenic potential in vivo especially during early bone healing.

Indexed as

Amino AcidsBiocompatible MaterialsCeramicsOsteoblastsSurface PropertiesTissue EngineeringAnimalsBone and BonesCell AdhesionCell LineCell SurvivalMaleMaterials TestingMiceOsteogenesisRatsAmino AcidsBiocompatible MaterialsBioglassamino acid modificationbiocompatibilitybioglassbone tissue engineering

Identifiers

PMID39154380
PMCPMC11652810

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LicenceCC BY-NC-ND
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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.