hrvatski jezikClear Cookie - decide language by browser settings

Bone Tissue Engineering in a Perfusion Bioreactor Using Dexamethasone-Loaded Peptide Hydrogel

Panek, Marina; Antunović, Maja; Pribolšan, Lidija; Ivković, Alan; Gotić, Marijan; Vukasović, Andreja; Caput Mihalić, Katarina; Pušić, Maja; Jurkin, Tanja; Marijanović, Inga (2019) Bone Tissue Engineering in a Perfusion Bioreactor Using Dexamethasone-Loaded Peptide Hydrogel. Materials, 12 (6). ISSN 1996-1944

[img]
Preview
PDF - Published Version - article
Available under License Creative Commons Attribution.

Download (1MB) | Preview

Abstract

The main goal of this study was the formation of bone tissue using dexamethasone (DEX)-loaded [COCH3]-RADARADARADARADA-[CONH2] (RADA 16-I) scaffold that has the ability to release optimal DEX concentration under perfusion force. Bone-marrow samples were collected from three patients during a hip arthroplasty. Human mesenchymal stem cells (hMSCs) were isolated and propagated in vitro in order to be seeded on scaffolds made of DEX-loaded RADA 16-I hydrogel in a perfusion bioreactor. DEX concentrations were as follows: 4 × 10−3, 4 × 10−4 and 4 × 10−5 M. After 21 days in a perfusion bioreactor, tissue was analyzed by scanning electron microscopy (SEM) and histology. Markers of osteogenic differentiation were quantified by real-time polymerase chain reaction (RT-PCR) and immunocytochemistry. Minerals were quantified and detected by the von Kossa method. In addition, DEX release from the scaffold in a perfusion bioreactor was assessed. The osteoblast differentiation was confirmed by the expression analysis of osteoblast-related genes (alkaline phosphatase (ALP), collagen I (COL1A1) and osteocalcin (OC). The hematoxylin/eosin staining confirmed the presence of cells and connective tissue, while SEM revealed morphological characteristics of cells, extracellular matrix and minerals—three main components of mature bone tissue. Immunocytochemical detection of collagen I is in concordance with given results, supporting the conclusion that scaffold with DEX concentration of 4 × 10−4 M has the optimal engineered tissue morphology. The best-engineered bone tissue is produced on scaffold loaded with 4 × 10−4 M DEX with a perfusion rate of 0.1 mL/min for 21 days. Differentiation of hMSCs on DEX-loaded RADA 16-I scaffold under perfusion force has a high potential for application in regenerative orthopedics.

Item Type: Article
Uncontrolled Keywords: hydrogel ; RADA 16-I ; dexamethasone ; perfusion bioreactor ; osteodifferentiation ; human mesenchymal stem cells
Subjects: NATURAL SCIENCES > Biology
TECHNICAL SCIENCES > Chemical Engineering
BIOMEDICINE AND HEALTHCARE > Basic Medical Sciences
BIOTECHNICAL SCIENCES > Biotechnology
Divisions: Division of Materials Chemistry
Depositing User: Marijan Gotić
Date Deposited: 10 Jun 2019 12:07
URI: http://fulir.irb.hr/id/eprint/4533
DOI: 10.3390/ma12060919

Actions (login required)

View Item View Item

Downloads

Downloads per month over past year

Contrast
Increase Font
Decrease Font
Dyslexic Font
Accessibility