Clay nanotube–biopolymer composite scaffolds for tissue engineering
Композитные каркасы из глинистых нанотрубок и биополимеров для тканевой инженерии
2016-01-01
SCID: 54.1/q8bym2ub
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biopolymer hydrogel scaffoldsfreeze-dryinghalloysite nanotubesin vivo biocompatibilitytissue engineering
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Abstract (AI)
Porous biopolymer hydrogels doped at 3-6 wt% with 50 nm diameter/0.8 μm long natural clay nanotubes were produced without any cross-linkers using the freeze-drying method. The enhancement of mechanical strength (doubled pick load), higher water uptake and thermal properties in chitosan-gelatine-agarose hydrogels doped with halloysite was demonstrated. SEM and AFM imaging has shown the even distribution of nanotubes within the scaffolds. We used enhanced dark-field microscopy to visualise the distribution of halloysite nanotubes in the implantation area. In vitro cell adhesion and proliferation on the nanocomposites occur without changes in viability and cytoskeleton formation. In vivo biocompatibility and biodegradability evaluation in rats has confirmed that the scaffolds promote the formation of novel blood vessels around the implantation sites. The scaffolds show excellent resorption within six weeks after implantation in rats. Neo-vascularization observed in newly formed connective tissue placed near the scaffold allows for the complete restoration of blood flow. These phenomena indicate that the halloysite-doped scaffolds are biocompatible as demonstrated both in vitro and in vivo. The chitosan-gelatine-agarose doped clay nanotube nanocomposite scaffolds fabricated in this work are promising candidates for tissue engineering applications.
Key Findings
1
Halloysite nanotube incorporation doubled pick load and improved water uptake and thermal properties of the biopolymer hydrogels.
2
Porous chitosan–gelatine–agarose scaffolds containing 3–6 wt% halloysite clay nanotubes were fabricated by freeze-drying without cross-linkers.
3
Rat studies demonstrated biocompatibility, biodegradability, neovascularization, restoration of local blood flow, and near-complete scaffold resorption within six weeks.
4
SEM and AFM showed uniform nanotube distribution, while enhanced dark-field microscopy visualized nanotubes in implantation areas.
5
The nanocomposite scaffolds supported in vitro cell adhesion and proliferation without compromising viability or cytoskeleton formation.
Research Object
Halloysite-doped chitosan–gelatine–agarose biopolymer composite scaffolds for tissue engineering
Research Subject
The scaffolds’ mechanical, water-uptake, thermal, structural, cellular, biocompatibility, biodegradability, resorption, and neo-vascularization properties
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2016-01-01
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