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Licensed Unlicensed Requires Authentication Published online by De Gruyter January 23, 2024

Effect of calcium phosphate/bovine serum albumin coated Al2O3–Ti biocomposites on osteoblast response

  • Hamid Reza Sameni , Samaneh Arab EMAIL logo , Nesa Doostmohammadi and Marjan Bahraminasab ORCID logo EMAIL logo

Abstract

Objectives

The biological performance of aluminum oxide-titanium (Al2O3-Ti) composites requires special attention to achieve improved osteoblastic differentiation, and subsequent osseointegration/strong anchorage with the surrounding bone. Therefore, the aim of this study was to improve them by providing calcium phosphate (Ca-P)/bovine serum albumin (BSA) coating on their surfaces.

Methods

Ca-P)/BSA coatings were prepared on the surfaces of 75vol.%Ti composites (75Ti-BSA) and pure Ti (100Ti-BSA as a control). The surface characteristics, phase analysis, micro-hardness, BSA release profile and biological responses including cytotoxicity, cell viability, differentiation, mineralization, and cell adhesion were evaluated.

Results

The results showed that lower cytotoxicity% and higher mitochondrial activity or viability % were associated with the samples with Ca-P/BSA coatings (particularly 75Ti-BSA having 21.3% cytotoxicity, 111.4% and 288.6% viability at day 1 and 7, respectively). Furthermore, the Ca-P/BSA coating could highly enhance the differentiation of pre-osteoblast cells into osteoblasts in 75Ti-BSA group (ALP concentration of 4.8 ng/ml). However, its influence on cell differentiation in 100Ti-BSA group was negligible. Similar results were also obtained from mineralization assay. The results on cell adhesion revealed that the Ca-P/BSA coated samples differently interacted with MC3T3-E1 cells; enlarged flat cells on 75Ti-BSA vs more spindle-shaped cells on 100Ti-BSA.

Conclusions

Ca-P/BSA coated Al2O3-Ti provided promising biological performance, superior to that of uncoated composites. Therefore, they have the potential to improve implant osseointegration.


Corresponding authors: Samaneh Arab and Marjan Bahraminasab, Nervous System Stem Cells Research Center, Semnan University of Medical Sciences, Semnan, Iran; and Department of Tissue Engineering and Applied Cell Sciences, School of Medicine, Semnan University of Medical Sciences, Semnan, Iran, E-mail: samaneh.arab@gmail.com (S. Arab); (M. Bahraminasab)

  1. Research ethics: This article does not contain any studies with human participants or animals performed by any of the authors.

  2. Informed consent: Not applicable.

  3. Author contributions: Hamid Reza Sameni: experiment design, and writing and reviewing. Samaneh Arab: conceptualization, experiment design, experimentation, writing and reviewing. Nesa Doostmohammadi: experimentation, writing and reviewing. Marjan Bahraminasab: conceptualization, experimentation, data analysis, provision of study materials, writing and reviewing.

  4. Competing interests: The authors declared no potential conflicts of interest with respect to the research, authorship, and/or publication of this article.

  5. Research funding: Semnan University of Medical Sciences (No. 1310).

  6. Data availability: The data that support the findings of this study will be available from the corresponding authors upon reasonable request.

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Received: 2023-04-02
Accepted: 2024-01-10
Published Online: 2024-01-23

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