Nothing Special   »   [go: up one dir, main page]

Gréant et al., 2023 - Google Patents

Digital light processing of poly (ε-caprolactone)-based resins into porous shape memory scaffolds

Gréant et al., 2023

View PDF
Document ID
12380050318764479287
Author
Gréant C
Van Durme B
Van Damme L
Brancart J
Van Hoorick J
Van Vlierberghe S
Publication year
Publication venue
European Polymer Journal

External Links

Snippet

Digital light processing (DLP) is a promising 3D printing technique with excellent resolution, enabling the fabrication of complex structures to serve the tissue engineering (TE) field. However, its full potential in this regard remains insufficiently explored by the scarcity of …
Continue reading at cris.vub.be (PDF) (other versions)

Classifications

    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G18/00Polymeric products of isocyanates or isothiocyanates
    • C08G18/06Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/28Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
    • C08G18/40High-molecular-weight compounds
    • C08G18/42Polycondensates having carboxylic or carbonic ester groups in the main chain
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G63/00Macromolecular compounds obtained by reactions forming a carboxylic ester link in the main chain of the macromolecule
    • C08G63/91Polymers modified by chemical after-treatment
    • C08G63/912Polymers modified by chemical after-treatment derived from hydroxycarboxylic acids
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G18/00Polymeric products of isocyanates or isothiocyanates
    • C08G18/06Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/70Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the isocyanates or isothiocyanates used
    • C08G18/72Polyisocyanates or polyisothiocyanates
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61LMETHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION, OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS, OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS, OR SURGICAL ARTICLES
    • A61L27/00Materials for grafts or prostheses or for coating grafts or prostheses
    • A61L27/14Macromolecular materials
    • A61L27/18Macromolecular materials obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G65/00Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61LMETHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION, OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS, OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS, OR SURGICAL ARTICLES
    • A61L27/00Materials for grafts or prostheses or for coating grafts or prostheses
    • A61L27/50Materials characterised by their function or physical properties, e.g. injectable or lubricating compositions, shape-memory materials, surface modified materials

Similar Documents

Publication Publication Date Title
Aduba Jr et al. Vat photopolymerization 3D printing of acid-cleavable PEG-methacrylate networks for biomaterial applications
AU2019237219B2 (en) 3D printing composition for biomaterials
Martin et al. A porous tissue engineering scaffold selectively degraded by cell-generated reactive oxygen species
Gréant et al. Digital light processing of poly (ε-caprolactone)-based resins into porous shape memory scaffolds
Elomaa et al. Preparation of poly (ε-caprolactone)-based tissue engineering scaffolds by stereolithography
Arslan et al. Polymer architecture as key to unprecedented high-resolution 3D-printing performance: The case of biodegradable hexa-functional telechelic urethane-based poly-ε-caprolactone
Grijpma et al. Preparation of biodegradable networks by photo-crosslinking lactide, ε-caprolactone and trimethylene carbonate-based oligomers functionalized with fumaric acid monoethyl ester
Berg et al. Synthesis of photopolymerizable hydrophilic macromers and evaluation of their applicability as reactive resin components for the fabrication of three‐dimensionally structured hydrogel matrices by 2‐photon‐polymerization
Firoozi et al. A highly elastic and autofluorescent poly (xylitol-dodecanedioic acid) for tissue engineering
Thijssen et al. Volumetric printing of thiol‐ene photo‐cross‐linkable poly (ε‐caprolactone): a tunable material platform serving biomedical applications
Wright et al. Synthesis of functionalized poly (lactic acid) using 2-Bromo-3-hydroxypropionic acid
Wang et al. Synthesis of a photocurable acrylated poly (ethylene glycol)-co-poly (xylitol sebacate) copolymers hydrogel 3D printing ink for tissue engineering
Hong et al. Synthesis and characterization of biodegradable poly (ɛ-caprolactone-co-β-butyrolactone)-based polyurethane
Karamzadeh et al. High‐Resolution Additive Manufacturing of a Biodegradable Elastomer with A Low‐Cost LCD 3D Printer
Hou et al. Creep-resistant elastomeric networks prepared by photocrosslinking fumaric acid monoethyl ester-functionalized poly (trimethylene carbonate) oligomers
Samson et al. Tough, Resorbable Polycaprolactone‐Based Bimodal Networks for Vat Polymerization 3D Printing
Sharifi et al. Photopolymerization and shrinkage kinetics of in situ crosslinkable N‐vinyl‐pyrrolidone/poly (ε‐caprolactone fumarate) networks
JP7544361B2 (en) Acrylate end-capped urethane or urea polymers
EP1641471B1 (en) Biocompatible polymer networks
US20210380826A1 (en) Polyesters, polymer compositions, and methods of using thereof
Pien et al. Tailorable acrylate-endcapped urethane-based polymers for precision in digital light processing: Versatile solutions for biomedical applications
Melchels Preparation of advanced porous structures by stereolithography for application in tissue engineering
Theiler et al. Synthesis, characterization and in vitro degradation of 3D-microstructured poly (ε-caprolactone) resins
Wang Synthesis and application of bis (acyl) phosphane oxide photoinitiators
De Man Development of acrylate-endcapped urethane-based POSS/PLA scaffolds towards breast reconstruction