| 1. |
- Kisiel, Marta, et al.
(författare)
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Improving the osteogenic potential of BMP-2 with hyaluronic acid hydrogel modified with integrin-specific fibronectin fragment
- 2013
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Ingår i: Biomaterials. - : Elsevier BV. - 0142-9612 .- 1878-5905. ; 34:3, s. 704-712
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Tidskriftsartikel (refereegranskat)abstract
- While human bone morphogenetic protein-2 (rhBMP-2) is a promising growth factor for bone regeneration, its clinical efficacy has recently shown to be below expectation. In order to improve the clinical translation of rhBMP-2, there exists strong motivation to engineer better delivery systems. Hyaluronic acid (HA) hydrogel is a suitable carrier for the delivery of rhBMP-2, but a major limitation of this scaffold is its low cell adhesive properties. In this study, we have determined whether covalent grafting of an integrin-specific ligands into HA hydrogel could improve cell attachment and further enhance the osteogenic potential of rhBMP-2. A structurally stabilized fibronectin (FN) fragment containing the major integrin-binding domain of full-length FN (FN III9 *-10) was engineered, in order to be incorporated into HA hydrogel. Compared to non-functionalized HA hydrogel, HA-FN hydrogel remarkably improved the capacity of the material to support mesenchymal stem cell attachment and spreading. In an ectopic bone formation model in the rat, delivery of rhBMP-2 with HA-FN hydrogel resulted in the formation of twice as much bone with better organization of collagen fibers compared to delivering the growth factor in non-functionalized HA hydrogel. This engineered hydrogel carrier for rhBMP-2 can be relevant in clinical bone repair.
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| 2. |
- Nijhuis, Arnold W. G., et al.
(författare)
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Rapid Screening of Mineralization Capacity of Biomaterials by Means of Quantification of Enzymatically Deposited Calcium Phosphate
- 2014
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Ingår i: Tissue Engineering. Part C, Methods. - : Mary Ann Liebert Inc. - 1937-3384 .- 1937-3392. ; 20:10, s. 838-850
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Tidskriftsartikel (refereegranskat)abstract
- The current study focused on the development of a rapid, straightforward quantification method based on the use of enzymatic decomposition of urea using urease to assess the mineralization capacity of a wide range of biomaterials for bone regeneration. Urea-containing mineralizing solutions (MSs) (containing: Na2HPO4, CaCl2, and NaCl at 37 degrees C and pH 6.0) were used in the mineralization experiments. Urease was added to these solutions to induce enzymatic decomposition of urea resulting in increased pH and deposition of calcium phosphate. By optimizing the ionic and urease concentrations in these MSs, it was shown that the proposed system could mineralize titanium substrates with six different pretreatments, as opposed to normal simulated body fluid that mineralized only two of them. It was possible to rank the mineralization capacity of these substrates by measuring the amount of calcium deposited. Furthermore, the ranking of (i) various polymeric substrates and (ii) hydrogels with and without functionalization with calcium-binding bisphosphonate groups was also possible. These results confirm that the proposed testing system has a broad applicability in the field of biomaterials due to its inherent versatility and discriminative power.
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| 3. |
- Bermejo-Velasco, Daniel, 1985-, et al.
(författare)
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Injectable hyaluronic acid hydrogels with the capacity for magnetic resonance imaging
- 2018
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Ingår i: Carbohydrate Polymers. - : Elsevier. - 0144-8617 .- 1879-1344. ; 197, s. 641-648
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Tidskriftsartikel (refereegranskat)abstract
- Monitoring hydrogel degradation in real time using noninvasive imaging techniques is of great interest for designing a scaffold in tissue engineering. We report the preparation of gadolinium (Gd)-labeled and injectable hyaluronic acid (HA) hydrogels that can be visualized using T-1- and T-2-weighted magnetic resonance imaging (MRI). An HA derivative functionalized with thiol and hydrazide was labeled using a diethylenetriaminepentaacetate complex modified with "clickable" dithiopyridyl functionalities (degree of modification was 3.77% with respect to HA repeat units). The HA derivative modified with cross-linkable groups and Gd complex exhibited relaxivities r(1) = 3.78 mM(-1)s(-1) and r(2) = 56.3 mM(-1)s(-1). A hydrazone hydrogel network was obtained by mixing Gd-labeled HA-hydrazide and HA-aldehyde derivatives. Enzymatic hydrogel degradation could be followed using MRI because the MR images showed great correlation with the hydrogel mass loss. Ex vivo MRI of injected Gd-labeled hydrogels demonstrated that they show a significant contrast difference (SNRcoronal = 456; SNRaxial = 459) from the surrounding tissues. These results indicate that our Gd-labeled HA hydrogel has great potential as an injectable biocompatible hydrogel that can be used for longitudinal tracking in vivo using MRI.
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| 4. |
- Han, Yuanyuan, et al.
(författare)
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Graphene Based Mechanical Biosensor by Employing Non-covalent Stacking Functionalization
- 2019
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Annan publikation (övrigt vetenskapligt/konstnärligt)abstract
- Herein we demonstrate a novel methodology to achieve mechanical biosensor by employing the distinguished interaction forces between the atomic force microscope (AFM) probe and sensor surfaces as the response signal. This mechanical biosensor is fabricated by utilizing the non-covalent π-π stacking of pyrene-maltose onto graphene surfaces with Concanavalin A (Con A) as a target protein. The atomic resolution scanning tunneling microscopy (STM) images indicate the successful formation of the self-assembled and densely packed pyrene-maltose layer on the sensor surface, which gives distinct atomic lattice structure as compared to pristine graphene. This mechanical biosensor exhibits detection of Con A with the sensitivity down to nanomolar level. Therefore, this proposed mechanical biosensor has the potential to be employed in a variety of bio-sensing applications.
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| 5. |
- Han, Yuanyuan, et al.
(författare)
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Optimization and analysis of pyrene-maltose functionalized graphene surfaces for Con A detection
- 2020
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Ingår i: Applied Surface Science. - : ELSEVIER. - 0169-4332 .- 1873-5584. ; 510
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Tidskriftsartikel (refereegranskat)abstract
- Utilizing the non-covalent pi-pi stacking of pyrene functionalized molecules onto graphene surfaces has achieved great success in the detection of various bio-objects, while the fundamental investigations on surface modifications stills remain rarely exploited. Here, we report the nano and atomic scale analysis of the pi-pi stacking functionalized graphene surface regarding to its surface topography, molecular self-assembly as well as process optimizations. The 'amphipathic' molecule, pyrene-maltose, is used for the non-covalent functionalization of graphene and systematical analysis is performed to understand the influence of different solvents on the molecular surface arrangement. Atomic force microscopy (AFM) and spectroscopy analysis indicate the successful formation of pyrene-maltose layer on graphene surface and it is further confirmed by scanning tunneling microscopy, depicting the self-assembled and densely packed pyrene-maltose layer that give distinguished and ordered diamond-shape lattice as compared to triangular lattice in pristine graphene. We also demonstrated that the interfacial adhesion forces between the AFM probe and the functionalized surfaces allow the detection of the lectin protein Concavalin A through selective absorption. This work provides essential evidence of the pi-pi interactions between pyrene molecules and graphene, and the AFM based adhesion measurement also has the potential to be employed in a variety of bio-detection applications.
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| 6. |
- Kheirabadi, Malihe, et al.
(författare)
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Improvement in Mechanical Performance of Anionic Hydrogels Using Full-Interpenetrating Polymer Network Reinforced with Graphene Oxide Nanosheets
- 2016
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Ingår i: Advances in Polymer Technology. - : Wiley. - 0730-6679 .- 1098-2329. ; 35:4, s. 386-395
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Tidskriftsartikel (refereegranskat)abstract
- Weak mechanical possession is one of the limiting factors in application of hydrogels. To modify this inherent disadvantage, different approaches have been studied including synthesizing interpenetrating polymer network (IPN) and nanocomposite hydrogels. So, this study has focused on preparation of a novel full-IPN structure based on anionic monomers of 2-acrylamido-2-methylpropane sulfonic acid/acrylic acid-sodium acrylate via facile solution polymerization technique in an aqueous media with incorporation of graphene oxide (GO) nanosheets. Mechanical performance of materials in the as-prepared condition and swollen state was characterized via tensile, compression, and rheology tests, respectively. Significant improvement of both elastic and storage modulus (ca. four times higher than pure hydrogel) is observed in this approach. Also dynamic mechanical thermal analysis results revealed that incorporation of high GO content (0.5 wt%) can suppress formation of full-IPN structure, whereas low GO content has not such an effect, interestingly. Moreover, these novel hydrogels could easily be stretched or compressed followed by full recovery after unloading.
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| 7. |
- Kheirabadi, Malihe, et al.
(författare)
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In situ forming interpenetrating hydrogels of hyaluronic acid hybridized with iron oxide nanoparticles
- 2015
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Ingår i: Biomaterials Science. - : Royal Society of Chemistry (RSC). - 2047-4830 .- 2047-4849. ; 3:11, s. 1466-1474
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Tidskriftsartikel (refereegranskat)abstract
- Four derivatives of hyaluronic acid (HA) bearing thiol (HA-SH), hydrazide (HA-hy), 2-dithiopyridyl (HA-SSPy), and aldehyde groups (HA-al) respectively were synthesized. Thiol and 2-dithiopyridyl as well as hydrazide and aldehyde make up two chemically orthogonal pairs of chemo-selective functionalities that allow in situ formation of interpenetrating (IPN) disulfide and hydrazone networks simultaneously upon the mixing of the above derivatives at once. The formation of IPN was demonstrated by comparing it with the formulations of the same total HA concentration but lacking one of the reactive components. The hydrogel composed of all four components was characterized by a larger elastic modulus than those of the control single networks (either disulfide or hydrazone) and the three component formulations gave the softest hydrogels. Moreover, a hydrazone cross-linkage was designed to contain a 1,2-diol fragment. This allowed us to partially disassemble one type of network in the IPN leaving another one unaffected. In particular, treatment of the IPN with either sodium periodate or dithiothreitol resulted in disassembly of the hydrazone and disulfide networks respectively and thus softening of the hydrogel. Contrarily, the single network hydrogels completely dissolved under the corresponding conditions. In corroboration with this, enzymatic degradation of the IPN by hyaluronidase was also substantially slower than the degradation of the single networks. In order to further improve the mechanical properties of the elaborated injectable IPN, it has been in situ hybridized with iron oxide nanoparticles (IONPs). The mesh size of the IPN was smaller than the size of the IONPs resulting in the retention of nanoparticles in the matrix under equilibrium swelling conditions. However, these nanoparticles were released upon enzymatic degradation suggesting their use as MRI tags for non-invasive tracking of the hydrogel material in vivo. Additionally, this injectable hybridized hydrogel with encapsulated IONPs can be used in hyperthermia cancer therapy.
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| 8. |
- Kim, Yang-Hee, et al.
(författare)
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Bisphosphonate nanoclay edge-site interactions facilitate hydrogel self-assembly and sustained growth factor localization
- 2020
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Ingår i: Nature Communications. - : Springer Nature. - 2041-1723. ; 11:1
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Tidskriftsartikel (refereegranskat)abstract
- Nanoclays have generated interest in biomaterial design for their ability to enhance the mechanics of polymeric materials and impart biological function. As well as their utility as physical cross-linkers, clays have been explored for sustained localization of biomolecules to promote in vivo tissue regeneration. To date, both biomolecule-clay and polymer-clay nanocomposite strategies have utilised the negatively charged clay particle surface. As such, biomolecule-clay and polymer-clay interactions are set in competition, potentially limiting the functional enhancements achieved. Here, we apply specific bisphosphonate interactions with the positively charged clay particle edge to develop self-assembling hydrogels and functionalized clay nanoparticles with preserved surface exchange capacity. Low concentrations of nanoclay are applied to cross-link hyaluronic acid polymers derivatised with a pendant bisphosphonate to generate hydrogels with enhanced mechanical properties and preserved protein binding able to sustain, for over six weeks in vivo, the localized activity of the clinically licensed growth factor BMP-2.
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| 9. |
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| 10. |
- Lunzer, Markus, et al.
(författare)
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A Modular Approach to Sensitized Two-Photon Patterning of Photodegradable Hydrogels
- 2018
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Ingår i: Angewandte Chemie International Edition. - : WILEY-V C H VERLAG GMBH. - 1433-7851 .- 1521-3773. ; 57:46, s. 15122-15127
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Tidskriftsartikel (refereegranskat)abstract
- Photodegradable hydrogels have emerged as useful platforms for research on cell function, tissue engineering, and cell delivery as their physical and chemical properties can be dynamically controlled by the use of light. The photo-induced degradation of such hydrogel systems is commonly based on the integration of photolabile o-nitrobenzyl derivatives to the hydrogel backbone, because such linkers can be cleaved by means of one-and two-photon absorption. Herein we describe a cytocompatible click-based hydrogel containing o-nitrobenzyl ester linkages between a hyaluronic acid backbone, which is photodegradable in the presence of cells. It is demonstrated for the first time that by using a cyclic benzylidene ketone-based small molecule as photosensitizer the efficiency of the two-photon degradation process can be improved significantly. Biocompatibility of both the improved two-photon micropatterning process as well as the hydrogel itself is confirmed by cell culture studies.
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