| 1. |
- Borges, Ana C., et al.
(författare)
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Nanofibrillated cellulose composite hydrogel for the replacement of the Nucleus Pulposus
- 2011
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Ingår i: Acta Biomaterialia. - : Elsevier BV. - 1742-7061 .- 1878-7568. ; 7:9, s. 3412-3421
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Tidskriftsartikel (refereegranskat)abstract
- The swelling and compressive mechanical behavior as well as the morphology and biocompatibility of composite hydrogels based on Tween® 20 trimethacrylate (T3), N-vinyl-2-pyrrolidone (NVP) and nanofibrillated cellulose (NFC) were assessed in the present study. The chemical structure of T3 was verified by FTIR and 1H NMR and the degree of substitution (DS) was found to be around 3. Swelling ratios of neat hydrogels composed of different concentrations of T3 and NVP were found to range from 1.5 to 5.7 with decreasing concentration of T3. Various concentrations of cellulose nanofibrils (0.2 to 1.6 wt%) were then used to produce composite hydrogels that showed lower swelling ratios than neat ones for a given T3 concentration. Neat and composite hydrogels exhibited typical non-linear response under compression. All composite hydrogels showed an increase in elastic modulus compared to neat hydrogel of about 3 to 8-fold, reaching 18 kPa at 0% strain and 62 kPa at 20% strain for the hydrogel with the highest NFC content. All hydrogels presented a porous and homogeneous structure, with interconnected pore cells of around 100 nm in diameter. The hydrogels are biocompatible. The results of this study demonstrate that composite hydrogels reinforced with NFC may be viable as nucleus pulposus implant due to their adequate swelling ratio that may restore annulus fibrosus loading and their increased mechanical properties that could possibly restore the height of intervertebral discs.
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| 2. |
- Karami, Peyman, et al.
(författare)
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An Intrinsically-Adhesive Family of Injectable and Photo-Curable Hydrogels with Functional Physicochemical Performance for Regenerative Medicine
- 2021
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Ingår i: Macromolecular rapid communications. - : Wiley. - 1022-1336 .- 1521-3927. ; 42:10
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Tidskriftsartikel (refereegranskat)abstract
- Attaching hydrogels to soft internal tissues is crucial for the development of various biomedical devices. Tough sticky hydrogel patches present high adhesion, yet with lack of injectability and the need for treatment of contacting surface. On the contrary, injectable and photo-curable hydrogels are highly attractive owing to their ease of use, flexibility of filling any shape, and their minimally invasive character, compared to their conventional preformed counterparts. Despite recent advances in material developments, a hydrogel that exhibits both proper injectability and sufficient intrinsic adhesion is yet to be demonstrated. Herein, a paradigm shift is proposed toward the design of intrinsically adhesive networks for injectable and photo-curable hydrogels. The bioinspired design strategy not only provides strong adhesive contact, but also results in a wide window of physicochemical properties. The adhesive networks are based on a family of polymeric backbones where chains are modified to be intrinsically adhesive to host tissue and simultaneously form a hydrogel network via a hybrid cross-linking mechanism. With this strategy, adhesion is achieved through a controlled synergy between the interfacial chemistry and bulk mechanical properties. The functionalities of the bioadhesives are demonstrated for various applications, such as tissue adhesives, surgical sealants, or injectable scaffolds.
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| 3. |
- Neagu, R. Cristian, et al.
(författare)
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The potential of wood fibers as reinforcement in cellular biopolymers
- 2012
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Ingår i: Journal of cellular plastics (Print). - 0021-955X .- 1530-7999. ; 48:1, s. 71-103
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Tidskriftsartikel (refereegranskat)abstract
- Wood fiber-reinforced polylactic acid composite foams have been successfully produced using supercritical carbon dioxide. The addition of fibers had a strong effect on microstructure of the foams. An increase in wood fiber content implied smaller average cell size and higher average cell wall thickness as estimated from image analysis of scanning electron microscopy micrographs. Addition of 10 wt% wood fibers seemed to be a limit to obtain foams, with the used processing conditions. The stiffness properties of the foams in compression improved upon addition of wood fibers. A significant increase of specific stiffness was achieved by adding 5-10 wt% wood fibers. It was shown that the stiffness was about 50% higher in the transverse direction for reinforced foams. The strength in the transverse direction increased for foams with unmodified wood fibers but decreased for foams with two types of treated wood fibers as compared with the strength of the pure polylactic acid foam of similar density. A butyl tetracarboxylic acid treatment followed by an additional surfactant treatment results in reduced wood fiber network-forming ability and reduced fiber-matrix adhesion. This contributes to the inferior observed strength properties in this study. The experimental stiffness was comparable with a superposed micromechanical model for a three-phase fiber-reinforced foam. The model shows that increasing the relative density, that is, the ratio of the density of the foam to the density of the composite material, by adding wood fibers results in a noteworthy increase in the transverse compression stiffness of the foams but only at relative density values above 0.2 for the used processing conditions in this study. The key factor for reinforcement is the relation between foam relative density and fiber volume fraction in the preform. The foaming conditions have to be adapted for each wood fiber content to obtain foams with the desired relative density.
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