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Magnetic Nanocomposite Hydrogel for Potential Cartilage Tissue Engineering: Synthesis, Characterization, and Cytocompatibility with Bone Marrow Derived Mesenchymal Stem Cells

Hydrogels possess high water content and closely mimic the microenvironment of extracellular matrix. In this study, we created a hybrid hydrogel containing type II collagen, hyaluronic acid (HA), and polyethylene glycol (PEG) and incorporated magnetic nanoparticles into the hybrid hydrogels of type...

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Published in:ACS applied materials & interfaces 2015-09, Vol.7 (37), p.20987-20998
Main Authors: Zhang, Naiyin, Lock, Jaclyn, Sallee, Amy, Liu, Huinan
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Language:English
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cited_by cdi_FETCH-LOGICAL-a330t-1e312b32885480733ac6b00e1e5510dc7cc82006e1ae9268545d93faf92497283
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creator Zhang, Naiyin
Lock, Jaclyn
Sallee, Amy
Liu, Huinan
description Hydrogels possess high water content and closely mimic the microenvironment of extracellular matrix. In this study, we created a hybrid hydrogel containing type II collagen, hyaluronic acid (HA), and polyethylene glycol (PEG) and incorporated magnetic nanoparticles into the hybrid hydrogels of type II collagen-HA-PEG to produce a magnetic nanocomposite hydrogel (MagGel) for cartilage tissue engineering. The results showed that both the MagGel and hybrid gel (Gel) were successfully cross-linked and the MagGel responded to an external magnet while maintaining structural integrity. That is, the MagGel could travel to the tissue defect sites in physiological fluids under remote magnetic guidance. The adhesion density of bone marrow derived mesenchymal stem cells (BMSCs) on the MagGel group in vitro was similar to the control group and greater than the Gel group. The morphology of BMSCs was normal and consistent in all groups. We also found that BMSCs engulfed magnetic nanoparticles in culture and the presence of magnetic nanoparticles did not affect BMSC adhesion and morphology. We hypothesized that the ingested nanoparticles may be eventually broken down by lysosome and excreted through exocytosis; further studies are necessary to confirm this. This study reports a promising magnetic responsive nanocomposite hydrogel for potential cartilage tissue engineering applications, which should be further studied for its effects on cell functions when combined with electromagnetic stimulation.
doi_str_mv 10.1021/acsami.5b06939
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We hypothesized that the ingested nanoparticles may be eventually broken down by lysosome and excreted through exocytosis; further studies are necessary to confirm this. 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We also found that BMSCs engulfed magnetic nanoparticles in culture and the presence of magnetic nanoparticles did not affect BMSC adhesion and morphology. We hypothesized that the ingested nanoparticles may be eventually broken down by lysosome and excreted through exocytosis; further studies are necessary to confirm this. 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source American Chemical Society:Jisc Collections:American Chemical Society Read & Publish Agreement 2022-2024 (Reading list)
subjects Animals
Biocompatible Materials - pharmacology
Cartilage, Articular - drug effects
Cell Adhesion - drug effects
Cell Count
Cell Shape
Cells, Cultured - drug effects
Collagen - metabolism
Gels
Hydrogel, Polyethylene Glycol Dimethacrylate - chemical synthesis
Hydrogel, Polyethylene Glycol Dimethacrylate - pharmacology
Magnetic Phenomena
Mesenchymal Stromal Cells
Nanocomposites - chemistry
Rats, Sprague-Dawley
Sheep
Solutions
Spectrometry, X-Ray Emission
Spectroscopy, Fourier Transform Infrared
Tissue Engineering - methods
title Magnetic Nanocomposite Hydrogel for Potential Cartilage Tissue Engineering: Synthesis, Characterization, and Cytocompatibility with Bone Marrow Derived Mesenchymal Stem Cells
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