Advanced Biomaterials 2009
DOI: 10.1002/9780470891315.ch6
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Injectable Hydrogels as Biomaterials

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Cited by 11 publications
(10 citation statements)
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“…Targeted delivery of therapeutic molecules to the desired area with injectable hydrogels can be carried out by incorporating these agents into the precursor solution. However, it is possible that the bioactive agents incorporated in an injectable hydrogel being damaged by exposing them to toxic agents or inducing non-physiological conditions [11,12]. For instance, 2-hydroxy-1-[4-(2-hydroxyethoxy) phenyl]-2-methyl-1-propanone-1-one (Irgacure 2959), a typical photoinitiator used for UV crosslinking of photocrosslinkable hydrogels, showed high cytotoxicity even at low dosages to human aortic smooth muscle cells [13].…”
Section: Introductionmentioning
confidence: 99%
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“…Targeted delivery of therapeutic molecules to the desired area with injectable hydrogels can be carried out by incorporating these agents into the precursor solution. However, it is possible that the bioactive agents incorporated in an injectable hydrogel being damaged by exposing them to toxic agents or inducing non-physiological conditions [11,12]. For instance, 2-hydroxy-1-[4-(2-hydroxyethoxy) phenyl]-2-methyl-1-propanone-1-one (Irgacure 2959), a typical photoinitiator used for UV crosslinking of photocrosslinkable hydrogels, showed high cytotoxicity even at low dosages to human aortic smooth muscle cells [13].…”
Section: Introductionmentioning
confidence: 99%
“…For instance, 2-hydroxy-1-[4-(2-hydroxyethoxy) phenyl]-2-methyl-1-propanone-1-one (Irgacure 2959), a typical photoinitiator used for UV crosslinking of photocrosslinkable hydrogels, showed high cytotoxicity even at low dosages to human aortic smooth muscle cells [13]. Moreover, in situ crosslinking of the hydrogels can either result in the leakage of initial precursor solution to the adjacent tissue or blood stream, or blockage of the catheters due to premature polymerization [11,14].…”
Section: Introductionmentioning
confidence: 99%
“…However, the need to chemically modify chitosan to exhibit the sol-gel transition could significantly affect its biodegradability and bioactivity [4]. We have previously developed a thermal and pH responsive in situ gelling chitosan solution without chemically modifying chitosan [5,6]. The injectable system was shown to undergo thermo gelation under mild physiological conditions and support the viability of encapsulated cells [5,6].…”
Section: Introductionmentioning
confidence: 99%
“…26,27 Moreover, injectable hydrogels are highly advantageous for growth factor and cellular delivery due to their hydrophilic nature, viscoelasticity and stimuli-responsiveness. [28][29][30][31][32] Chitosan is a cationic polysaccharide of b(1-4)-linked D-glucosamine and N-acetyl-Dglucosamine and has been extensively investigated as a biomaterial for various biomedical applications, due to its excellent biocompatibility, biodegradability and bioactivities. [33][34][35] Chitosan based thermogels raise significant interest as an injectable vehicle for drug as well as cell delivery applications.…”
Section: Introductionmentioning
confidence: 99%
“…Injectable scaffolds have recently gained attention due to the growing popularity of minimally invasive arthroscopic and orthopaedic procedures . Moreover, injectable hydrogels are highly advantageous for growth factor and cellular delivery due to their hydrophilic nature, viscoelasticity and stimuli‐responsiveness . Chitosan is a cationic polysaccharide of β(1–4)‐linked D‐glucosamine and N‐acetyl‐D‐glucosamine and has been extensively investigated as a biomaterial for various biomedical applications, due to its excellent biocompatibility, biodegradability and bioactivities .…”
Section: Introductionmentioning
confidence: 99%