Show/Hide Menu
Hide/Show Apps
Logout
Türkçe
Türkçe
Search
Search
Login
Login
OpenMETU
OpenMETU
About
About
Open Science Policy
Open Science Policy
Open Access Guideline
Open Access Guideline
Postgraduate Thesis Guideline
Postgraduate Thesis Guideline
Communities & Collections
Communities & Collections
Help
Help
Frequently Asked Questions
Frequently Asked Questions
Guides
Guides
Thesis submission
Thesis submission
MS without thesis term project submission
MS without thesis term project submission
Publication submission with DOI
Publication submission with DOI
Publication submission
Publication submission
Supporting Information
Supporting Information
General Information
General Information
Copyright, Embargo and License
Copyright, Embargo and License
Contact us
Contact us
Development and characterization of manganese-doped hydroxyapatite-incorporated wet-electrospun polycaprolactone scaffolds
Download
Samiei_2026_Biomed._Mater._21_015007.pdf
Date
2025-12-12
Author
Samiei, Alaleh
Jodati, Hossein
Evis, Zafer
Keskin, Dilek
Metadata
Show full item record
This work is licensed under a
Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License
.
Item Usage Stats
100
views
104
downloads
Cite This
Bioceramic-incorporated polymer-based scaffolds have gained more interest as a promising and effective approach in bone tissue engineering (BTE) applications. This study is the first to investigate the role of incorporated manganese-doped hydroxyapatite (Mn-HA) and gelatin coating in increased bioactivity and biological properties, specifically the cell attachment potencies of three-dimensional (3D) porous electrospun polycaprolactone (PCL). In this context, novel 3D porous composite scaffolds were synthesized by wet electrospinning of PCL incorporated with Mn-HA. The scaffolds were then coated with a thin gelatin layer to enhance the cell adhesion capacity. The effects of Mn-HA and the gelatin coating were evaluated in terms of structural, physicochemical, and biological properties. The results demonstrated that Mn-HA was successfully synthesized with doping of 2 mol% Mn, with MnSO4(manganese sulfate) and MnCl2(manganese chloride) precursors. Mn-HA powder with a MnSO4precursor indicated better cell viability results. Therefore, Mn-HA/PCL scaffolds with 2.5% and 5% (w/w) bioceramic content were prepared with the MnSO4precursor. The scaffolds' porosity increased from 24% (PCL/gelatin group) to approximately 34% in both the 2.5% and 5% (w/w) bioceramic-containing groups. The addition of Mn-HA powder improved thein vitrobioactivity and degradation rate of the scaffolds. Specifically, the 5% and 2.5% (w/w) Mn-HA incorporated scaffolds indicated 40% and 30% weight loss after 21 d of incubation, respectively. In contrast to the PCL/gelatin and HA-containing groups, the Mn-doped HA containing scaffolds exhibited a weight loss of around 17%-20%, indicating a decrease in degradation. The presence of the Mn-HA powder and gelatin coating elevated the cell viability results significantly, as opposed to the PCL scaffolds. Incorporation of 5% (w/w) Mn-HA improved the alkaline phosphatase activity and intracellular calcium levels, contrary to other groups. Thus, the incorporation of Mn-doped HA and gelatin into the PCL scaffold supports the potency towards properties required for BTE applications and suggests it as a prospective biomaterial for further evaluations.
Subject Keywords
bone tissue engineering
,
manganese-doped hydroxyapatite
,
PCL/gelatin scaffold
,
wet electrospinning
URI
https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=105024804665&origin=inward
https://hdl.handle.net/11511/117945
Journal
Biomedical materials (Bristol, England)
DOI
https://doi.org/10.1088/1748-605x/ae1c07
Collections
Department of Engineering Sciences, Article
Citation Formats
IEEE
ACM
APA
CHICAGO
MLA
BibTeX
A. Samiei, H. Jodati, Z. Evis, and D. Keskin, “Development and characterization of manganese-doped hydroxyapatite-incorporated wet-electrospun polycaprolactone scaffolds,”
Biomedical materials (Bristol, England)
, vol. 21, no. 1, pp. 0–0, 2025, Accessed: 00, 2025. [Online]. Available: https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=105024804665&origin=inward.