2018
DOI: 10.1007/978-981-13-0950-2_13
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Growth Factor Delivery Systems for Tissue Engineering and Regenerative Medicine

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Cited by 27 publications
(19 citation statements)
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“…Nevertheless, this approach raises concerns regarding the GF duration, dosage or immune response when they enter into the mammalian body. To solve this issue, current knowledge combines various controlled delivery systems with GFs, such as direct incorporation, layer-by-layer technology or multiphase loading methods, which allow GF release in a sequential and spatiotemporal fashion, leading to GFs being retained by the region of interest with a desirable concentration [ 17 , 22 ]. In addition, the biocompatibility of GF-based delivery systems also needs to be considered because this determines whether they can be applied in clinical practice.…”
Section: Introductionmentioning
confidence: 99%
“…Nevertheless, this approach raises concerns regarding the GF duration, dosage or immune response when they enter into the mammalian body. To solve this issue, current knowledge combines various controlled delivery systems with GFs, such as direct incorporation, layer-by-layer technology or multiphase loading methods, which allow GF release in a sequential and spatiotemporal fashion, leading to GFs being retained by the region of interest with a desirable concentration [ 17 , 22 ]. In addition, the biocompatibility of GF-based delivery systems also needs to be considered because this determines whether they can be applied in clinical practice.…”
Section: Introductionmentioning
confidence: 99%
“…To date, the majority of the literature has focused on the production of immobilized GF (iGF) for tissue engineering applications (Lee et al, 2011;Cabanas-Danés et al, 2014;Reed and Wu, 2014;Hajimiri et al, 2015;Wang et al, 2017;Atienza-Roca et al, 2018). Therefore, this review aims to discuss general approaches to immobilize GFs in the context of cell therapy manufacturing.…”
Section: Introductionmentioning
confidence: 99%
“…52 Regeneration of wounded tissues and wounded skin depends on the action of a number of factors including RTK ligands, such as EGF (stimulates proliferation and migration of keratinocytes and increases tensile strength of new skin), PDGF (acts as a chemoattractant for mesenchymal cells), FGF (stimulates proliferation, migration and angiogenesis in injured skin), and VEGF (initiates angiogenesis and stimulates proliferation and migration of endothelial cells). 9 Insufficient production of these GFs may diminish regenerative capacity of wounded tissues (Table 2). a Abbreviations: TrkAtropomyosin receptor kinase A; NGFneurotrophic growth factor; EGFepidermal growth factor; PDGFplatelet derived growth factor; EGFR -EGF receptor; PDGFR -PDGF receptor; c-Mettyrosine-protein kinase Met; HGFhepatocyte growth factor.…”
Section: Opto-rtks For Non-neural Tissue Regeneration and Tissue Engimentioning
confidence: 99%
“…It can be achieved by engineering of sophisticated delivery vehicles that are reviewed elsewhere. 9 Recently, two novel technologies to control RTK activity and its downstream signaling with light have been developed. In the rst one, optogenetic control of RTK signaling relies on genetically encoded chimeric proteins, called opto-RTKs, which are engineered to comprise photoreceptors fused to intracellular RTK domains.…”
Section: Introductionmentioning
confidence: 99%