scholarly journals Modular bioink for 3D printing of biocompatible hydrogels: sol–gel polymerization of hybrid peptides and polymers

RSC Advances ◽  
2017 ◽  
Vol 7 (20) ◽  
pp. 12231-12235 ◽  
Author(s):  
C. Echalier ◽  
R. Levato ◽  
M. A. Mateos-Timoneda ◽  
O. Castaño ◽  
S. Déjean ◽  
...  
Keyword(s):  
3D Printing ◽  
Sol Gel ◽  
Cross Linking ◽  
Hybrid Peptides ◽  
Peptide Hydrogels

Inorganic polymerization as a cross-linking method for 3D printing of PEG–peptide hydrogels.

scholarly journals Synthesis of Nanogels: Current Trends and Future Outlook

Gels ◽  
2021 ◽  
Vol 7 (2) ◽  
pp. 36
Author(s):  
Emanuele Mauri ◽  
Sara Maria Giannitelli ◽  
Marcella Trombetta ◽  
Alberto Rainer
Keyword(s):  
3D Printing ◽  
Ad Hoc ◽  
Sol Gel ◽  
Controlled Polymerization ◽  
Current Trends ◽  
Chip Technology ◽  
Physico Chemical ◽  
Physical Interactions ◽  
Sol Gel Transition ◽  
Gel Transition

Nanogels represent an innovative platform for tunable drug release and targeted therapy in several biomedical applications, ranging from cancer to neurological disorders. The design of these nanocarriers is a pivotal topic investigated by the researchers over the years, with the aim to optimize the procedures and provide advanced nanomaterials. Chemical reactions, physical interactions and the developments of engineered devices are the three main areas explored to overcome the shortcomings of the traditional nanofabrication approaches. This review proposes a focus on the current techniques used in nanogel design, highlighting the upgrades in physico-chemical methodologies, microfluidics and 3D printing. Polymers and biomolecules can be combined to produce ad hoc nanonetworks according to the final curative aims, preserving the criteria of biocompatibility and biodegradability. Controlled polymerization, interfacial reactions, sol-gel transition, manipulation of the fluids at the nanoscale, lab-on-a-chip technology and 3D printing are the leading strategies to lean on in the next future and offer new solutions to the critical healthcare scenarios.

Lateral sol–gel cross-linking of polyurethane using the a grafted triethoxysilyl group

2014 ◽  
Vol 72 (3) ◽  
pp. 543-552 ◽  
Author(s):  
Yong-Chan Chung ◽  
Kyung Suk Kang ◽  
Byoung Chul Chun
Keyword(s):  
Sol Gel ◽  
Cross Linking

EXPERIMENTAL VALIDATION OF THE CHARLESBY AND HORIKX MODELS APPLIED TO DE-VULCANIZATION OF SULFUR AND PEROXIDE VULCANIZATES OF NR AND EPDM

2016 ◽  
Vol 89 (4) ◽  
pp. 671-688 ◽  
Author(s):  
M. A. L. Verbruggen ◽  
L. van der Does ◽  
W. K. Dierkes ◽  
J. W. M. Noordermeer
Keyword(s):  
Experimental Validation ◽  
Main Chain ◽  
Sol Gel ◽  
Chain Scission ◽  
Cross Linking ◽  
Cross Link ◽  
Practical Reality ◽  
Cross Links ◽  
The Cross ◽  
Theoretical Considerations

ABSTRACT The theoretical model developed by Charlesby to quantify the balance between cross-links creation of polymers and chain scission during radiation cross-linking and further modifications by Horikx to describe network breakdown from aging were merged to characterize the balance of both types of scission on the development of the sol content during de-vulcanization of rubber networks. There are, however, disturbing factors in these theoretical considerations vis-à-vis practical reality. Sulfur- and peroxide-cured NR and EPDM vulcanizates were de-vulcanized under conditions of selective cross-link and random main-chain scissions. Cross-link scission was obtained using thiol-amine reagents for selective cleavage of sulfur cross-links. Random main-chain scission was achieved by heating peroxide vulcanizates of NR with diphenyldisulfide, a method commonly employed for NR reclaiming. An important factor in the analyses of these experiments is the cross-linking index. Its value must be calculated using the sol fraction of the cross-linked network before de-vulcanization to obtain reliable results. The values for the cross-linking index calculated with sol-gel data before de-vulcanization appear to fit the experimentally determined modes of network scission during de-vulcanization very well. This study confirms that the treatment of de-vulcanization data with the merged Charlesby and Horikx models can be used satisfactorily to characterize the de-vulcanization of NR and EPDM vulcanizates.

Preparation of the polymerizable titania oriented to 3D printing and the laser-induced crystallization

2018 ◽  
Vol 24 (9) ◽  
pp. 1421-1427 ◽  
Author(s):  
Feng Liu ◽  
Shaoai Xie ◽  
Yan Wang ◽  
Jianjun Yu ◽  
Qinghua Meng
Keyword(s):  
3D Printing ◽  
Sol Gel ◽  
Crystal Form ◽  
Tetrabutyl Titanate ◽  
Content Type ◽  
Functional Additives ◽  
Sol Gel Process ◽  
Photosensitive Resin ◽  
Induced Crystallization

PurposeThe titania (titanium dioxide) is one of the important functional additives in the photosensitive resin and encounters the problem of stabilization in the photosensitive resin for 3D printing. This study aims to achieve enhancement in stabilization by preparation of the polymerizable titania andin situlaser-induced crystallization during 3D printing.Design/methodology/approachA type of polymerizable titania (AAEM@TiO2) was designed and prepared from tetrabutyl titanate (TBT) and 2-(acetoacetoxy)ethyl methacrylate (AAEM) via the sol–gel process, which was characterized by Fourier-transform infrared (FTIR) spectra, ultraviolet–visible (UV-Vis) spectra, surface bonding efficiency (SBE) and settling height (H). AAEM acted on both bonding to the titania and polymerization with the monomer in resin for stabilization. The polymerizable titania could be converted to the pigmented titania by means of laser-induced crystallization. The photosensitive resin was then formulated on the basis of optimization and used in a stereolithography apparatus (SLA) for 3D printing.FindingsThe stabilization effect of AAEM on TiO2was achieved and the mechanism of competition in the light-consuming reactions during photocuring was proposed. The ratio of nAAEM/nTBTin AAEM@TiO2, the concentration of AAEM@TiO2and photoinitiator (PI) used in the photosensitive resin were optimized. The anatase crystal form was indicated by X-ray diffraction (XRD) and clustering of nanocrystals was revealed by scanning electron microscopy (SEM) after SLA 3D printing.Originality/valueThis investigation provides a novel method of pigmentation by preparation of the polymerizable titania andin situlaser-induced crystallization for SLA 3D printing.

Synthesis and Characterizations of Strontium Substituted Hydroxyapatite Thin Films

2010 ◽  
Vol 93-94 ◽  
pp. 231-234
Author(s):  
B. Hongthong ◽  
Satreerat K. Hodak ◽  
Sukkaneste Tungasmita
Keyword(s):  
Thin Film ◽  
Thin Films ◽  
Chemical Composition ◽  
Spin Coating ◽  
Phase Structure ◽  
Sol Gel ◽  
Cross Linking ◽  
X Ray Diffraction ◽  
X Ray ◽  
Sol Gel Process

Strontium substituted hydroxyapatite(SrHAp) were fabricated both in the form of powder as reference and thin film by using inorganic precursor reaction. The sol-gel process has been used for the deposition of SrHAp layer on stainless steal 316L substrate by spin coating technique, after that the films were annealed in air at various temperatures. The chemical composition of SrHAp is represented (SrxCa1-x)5(PO4)3OH, where x is equal to 0, 0.5 and 1.0. Investigations of the phase structure of SrHAp were carried out by using X-ray diffraction technique (XRD). The results showed that strontium is incorporated into hydroxyapatite where its substitution for calcium increases in the lattice parameters, and Sr3(PO4)2 can be detected at 900°C. The SEM micrographs showed that SrHAp films exhibited porous structure before develop to a cross-linking structure.

scholarly journals On-Chip Fabrication and In-Flow 3D-Printing of Cell-Laden Microgel Constructs: From Chip to Scaffold Materials in One Integral Process

2021 ◽  
Author(s):  
Stephan Förster ◽  
Jürgen Groll ◽  
Benjamin Reineke ◽  
Stephan Hauschild ◽  
Ilona Paulus ◽  
...  
Keyword(s):  
3D Printing ◽  
Three Dimensional ◽  
Cross Linking ◽  
Cell Protection ◽  
Free Standing ◽  
Produce Cell ◽  
Chip Fabrication ◽  
Integral Process ◽  
Scaffold Materials ◽  
On Chip

Bioprinting has evolved into a thriving technology for the fabrication of cell-laden scaffolds. Bioinks are the most critical component for bioprinting. Recently, microgels have been introduced as a very promising bioink enabling cell protection and the control of the cellular microenvironment. However, their microfluidic fabrication inherently seemed to be a limitation. Here we introduce a direct coupling of microfluidics and 3D-printing for the microfluidic production of cell-laden microgels with direct in-flow bioprinting into stable scaffolds. The methodology enables the continuous on-chip encapsulation of cells into monodisperse microdroplets with subsequent in-flow cross-linking to produce cell-laden microgels, which after exiting a microtubing are automatically jammed into thin continuous microgel filaments. The integration into a 3D printhead allows direct in-flow printing of the filaments into free-standing three-dimensional scaffolds. The method is demonstrated for different cross-linking methods and cell lines. With this advancement, microfluidics is no longer a bottleneck for biofabrication. <br>

scholarly journals Printable Alginate Hydrogels with Embedded Network of Halloysite Nanotubes: Effect of Polymer Cross-Linking on Rheological Properties and Microstructure

Polymers ◽  
2021 ◽  
Vol 13 (23) ◽  
pp. 4130
Author(s):  
Svetlana A. Glukhova ◽  
Vyacheslav S. Molchanov ◽  
Boris V. Lokshin ◽  
Andrei V. Rogachev ◽  
Alexey A. Tsarenko ◽  
...  
Keyword(s):  
3D Printing ◽  
Rheological Properties ◽  
Shear Thinning ◽  
Halloysite Nanotubes ◽  
Polymer Chains ◽  
Cross Linking ◽  
Saxs Data ◽  
Nanocomposite Hydrogels ◽  
Embedded Network ◽  
The Cross

Rapidly growing 3D printing of hydrogels requires network materials which combine enhanced mechanical properties and printability. One of the most promising approaches to strengthen the hydrogels consists of the incorporation of inorganic fillers. In this paper, the rheological properties important for 3D printability were studied for nanocomposite hydrogels based on a rigid network of percolating halloysite nanotubes embedded in a soft alginate network cross-linked by calcium ions. Particular attention was paid to the effect of polymer cross-linking on these properties. It was revealed that the system possessed a pronounced shear-thinning behavior accompanied by a viscosity drop of 4–5 orders of magnitude. The polymer cross-links enhanced the shear-thinning properties and accelerated the viscosity recovery at rest so that the system could regain 96% of viscosity in only 18 s. Increasing the cross-linking of the soft network also enhanced the storage modulus of the nanocomposite system by up to 2 kPa. Through SAXS data, it was shown that at cross-linking, the junction zones consisting of fragments of two laterally aligned polymer chains were formed, which should have provided additional strength to the hydrogel. At the same time, the cross-linking of the soft network only slightly affected the yield stress, which seemed to be mainly determined by the rigid percolation network of nanotubes and reached 327 Pa. These properties make the alginate/halloysite hydrogels very promising for 3D printing, in particular, for biomedical purposes taking into account the natural origin, low toxicity, and good biocompatibility of both components.

Bioinspired Synthesis of Cross-Linking of Dopamine-Containing Block Copolymers to Form Thermosensitive Covalent Hydrogels

2012 ◽  
Vol 531-532 ◽  
pp. 238-241 ◽  
Author(s):  
Kui Huang ◽  
Jin San Chen ◽  
Yang Liu
Keyword(s):  
Sol Gel ◽  
Coupling Efficiency ◽  
Pluronic F127 ◽  
Cross Linking ◽  
Inversion Method ◽  
Sustained Drug Delivery ◽  
Vis Spectroscopy ◽  
Marine Mussels ◽  
Mussel Adhesive ◽  
Adhesive Proteins

Marine mussels secrete remarkable mussel adhesive proteins (MAPs) for adherence to the substrates upon which they reside. Inspired by the intermolecular cross-linking characteristics of MAPs, we report the synthesis of thermosensitive dopamine modified Pluronic copolymer (PluF127-Dopa) with high coupling efficiency. Under certain temperature and concentration, PluF127-Dopa copolymers in aqueous solution self-assemble into micelles and are able to rapidly form a more stable hydrogels upon addition of oxidizing reagents such as NaIO4, resulting from oxidative cross-linking of dopamine. UV-vis spectroscopy was utilized to identify the reaction intermediates. The sol-gel transition curves of cross-linked PluF127-Dopa hydrogels (CL-PluF127-Dopa) were determined by a vial inversion method. The critical gelation concentration of CL-PluF127-Dopa hydrogels was significantly lower than those for PluF127-Dopa and unmodified Pluronic F127. The apparent mechanical strength of CL-PluF127-Dopa hydrogels was dramatically enhanced compared to those unmodified Pluronic copolymer hydrogels, suitable for sustained drug delivery. These new biomimetic materials are expected to have potential uses in biomedical applications.

Research Progress of Preparation Technology of Nano Copper Powder for 3D Printing

2018 ◽  
Vol 777 ◽  
pp. 150-157
Author(s):  
Jing Min Shi ◽  
Jian Wei Wang ◽  
Wei Xiao
Keyword(s):  
3D Printing ◽  
Copper Powder ◽  
Physical Vapor Deposition ◽  
Sol Gel ◽  
Radiation Chemistry ◽  
Research Progress ◽  
Chemical Methods ◽  
Advantages And Disadvantages ◽  
Explosion Method ◽  
Physical And Chemical

Nanocopper has become one of the research hotspots of metal powder for 3D printing, due to its excellent properties. In this paper, technical methods, process flow and research progress were systematically introduced of nanocopper powder for 3D printing. Preparation of nano-copper powder for 3D printing are mainly physical and chemical methods. Physical methods include atomization method, physical vapor deposition method, grinding method, electric explosion method. Chemical methods include sol-gel method, radiation chemistry, plasma, microemulsion, hydrothermal, liquid reduction and so on. The advantages and disadvantages of these methods were compared in detail, and the future development direction of nano-copper powder for 3D printing was look forward to.

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