Biopolymer-Based Formulations 2020
DOI: 10.1016/b978-0-12-816897-4.00035-7
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Collagen-based 3D structures—versatile, efficient materials for biomedical applications

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Cited by 10 publications
(14 citation statements)
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“…Thus, drug-coated ceramics [ 19 ] are described in the literature, as well as composites of hydrogels introduced into the ceramics [ 20 ] to achieve a delayed drug release. Other approaches are also being pursued by adding the ceramics as powder or granules to scaffolds made of hydrogels [ 21 ] or xerogels, e.g., collagen [ 22 , 23 ]. This offers the advantage of being able to print these gels by means of 3D extrusion.…”
Section: Introductionmentioning
confidence: 99%
“…Thus, drug-coated ceramics [ 19 ] are described in the literature, as well as composites of hydrogels introduced into the ceramics [ 20 ] to achieve a delayed drug release. Other approaches are also being pursued by adding the ceramics as powder or granules to scaffolds made of hydrogels [ 21 ] or xerogels, e.g., collagen [ 22 , 23 ]. This offers the advantage of being able to print these gels by means of 3D extrusion.…”
Section: Introductionmentioning
confidence: 99%
“…Protein-based micro-and nanoparticles present high biodegradability and low thermal and mechanical stability, which lead to collagen chemical modification (maintaining its native structure) or the combination with other biopolymers or synthetic polymers or even inorganic materials, also allowing to increase the system functionality [107,108] and to modulate their properties according to the desired application. Thus, several collagen-based micro-and nanoparticles were developed with different biomedical applications (tissue engineering, imagistic/diagnosis, and drug/gene delivery) [109].…”
Section: Nanomicrofibers and Nanomicroparticlesmentioning
confidence: 99%
“…Modifications were introduced into the emulsification method to improve the delivery kinetics, maintaining the collagen meshwork biocompatibility as the replacement of chemicals for photochemical crosslinking or the use of self-assembling collagen fiber reconstitution [ 114 ]. However, the emulsion method remains to present poor control of the particle shape and size, as well as a reduced loading level [ 109 ], which leads to the exploitation of other strategies to produce micro- or nanoparticles.…”
Section: Development Of Marine-polymeric Architectures Via Ionic Lmentioning
confidence: 99%
“…Collagen-based 3D materials are extensively used in biomedical applications (scaffolds in tissue engineering, lab models for drug screening, modern wound dressings, and drug delivery devices) due to their protein properties. The most envisaged are: biocompatibility and inherent bio-functionality enabling cells' proliferation and differentiation, coupled with haemostatic properties, low immunogenicity, a rich chemistry and high water-holding capacity [1,2]. A porous architecture facilitates cell adhesion and improves flexibility and substance permeability, finally promoting 3D structure biomimicry [3,4].…”
Section: Introductionmentioning
confidence: 99%
“…A porous architecture facilitates cell adhesion and improves flexibility and substance permeability, finally promoting 3D structure biomimicry [3,4]. However, the application of this protein for biomedical devices, as a unique raw source, is limited by some disadvantages, such as the poor mechanical and antibacterial properties, fast degradation, modification and processing difficulties, some batch-to-batch variations and risk of human transgenic disease transmission [1]. Cross-linking (by physical, chemical or combined techniques) and combination with other polymers (natural or synthetic) or materials (i.e., ceramics) may be used as topical, convenient routes to avoid the biopolymer drawbacks and to improve/control the physico-chemical and biological properties of collagen-based materials, to meet specific needs [1,[5][6][7].…”
Section: Introductionmentioning
confidence: 99%