Line 1: | Line 1: | ||
{{TecCEM}} | {{TecCEM}} | ||
<html> | <html> | ||
− | |||
− | |||
<div id="parallax"> | <div id="parallax"> | ||
</div> | </div> | ||
− | <div class=" | + | <div class="container"> |
− | + | <div class="row"> | |
− | < | + | <h1>Abstract</h1> |
− | <p>Cell lines HaCat and L-929 were used to evaluate a tissue regeneration system incorporating a collagen-based scaffold and encapsulated recombinant growth factors. A collagenous synthetic gene comprising collagen type V heparin binding domain (HepV) was expressed in a bacterial system, constituting the main component of the scaffold. For collagen molecule consists of repetitive G-X-Y triplets, being Y frequently hydroxyproline (Hyp), a method of intracellular accumulation of Hyp is used to co-translationally incorporate this non-canonical amino acid. A chitosan crosslinking procedure is carried out on the expressed collagen to prevent contraction and to finally freeze-dry. Further, a mixture of heparin and tenascin C fibronectin type III domain V (TNCIII5) was added to the scaffold, for the heparin-tenascin C binding has a high affinity with a large number of growth factors. Recombinant human leptin β (LepB) is used as a growth factor and we hypothesize that it may be encapsulated to achieve a controlled drug delivery. Due to its suitability, chitosan nanoencapsulation was employed. To evaluate the efficacy of the system, MTT proliferation assay was performed in 96-well plates. Given the cell lines assessed during this project, this tissue regeneration system proves its ability to be used in the treatment of second degree burns. As a widely new biotechnology procedure for skin regeneration the creation of a new, low cost method, for the silencing of miRNA´s involved in the skin regeneration was created and tested. The project was also tested using a skin chip as a practical and small cell proliferation hardware. </p> | + | <p>Cell lines HaCat and L-929 were used to evaluate a tissue regeneration system incorporating a collagen-based scaffold and encapsulated recombinant growth factors. A collagenous synthetic gene comprising collagen type V heparin binding domain (HepV) was expressed in a bacterial system, constituting the main component of the scaffold. For collagen molecule consists of repetitive G-X-Y triplets, being Y frequently hydroxyproline (Hyp), a method of intracellular accumulation of Hyp is used to co-translationally incorporate this non-canonical amino acid. A chitosan crosslinking procedure is carried out on the expressed collagen to prevent contraction and to finally freeze-dry. Further, a mixture of heparin and tenascin C fibronectin type III domain V (TNCIII5) was added to the scaffold, for the heparin-tenascin C binding has a high affinity with a large number of growth factors. Recombinant human leptin β (LepB) is used as a growth factor and we hypothesize that it may be encapsulated to achieve a controlled drug delivery. Due to its suitability, chitosan nanoencapsulation was employed. To evaluate the efficacy of the system, MTT proliferation assay was performed in 96-well plates. Given the cell lines assessed during this project, this tissue regeneration system proves its ability to be used in the treatment of second degree burns. As a widely new biotechnology procedure for skin regeneration the creation of a new, low cost method, for the silencing of miRNA´s involved in the skin regeneration was created and tested. The project was also tested using a skin chip as a practical and small cell proliferation hardware. </p> |
− | + | </div> | |
− | + | </div> | |
− | + | ||
− | + | ||
− | + | ||
− | + | ||
− | + | ||
− | </div> | + | |
− | + | ||
− | + | ||
− | + | ||
− | + | ||
− | + | ||
− | + | ||
− | + | ||
− | + | ||
− | + | ||
− | + | ||
− | + | ||
− | + | ||
− | + | ||
− | + | ||
− | + | ||
− | + | ||
− | + | ||
− | + | ||
− | + | ||
− | + | ||
− | + | ||
− | + | ||
− | + | ||
− | + | ||
− | + | ||
− | + | ||
− | + | ||
− | + | ||
− | + | ||
− | + | ||
− | + | ||
− | + | ||
− | + | ||
− | + | ||
− | + | ||
− | + | ||
− | + | ||
− | + | ||
− | + | ||
− | + | ||
− | + | ||
− | + | ||
− | + | ||
− | + | ||
− | + | ||
− | + | ||
− | + | ||
− | + | ||
− | + | ||
− | + | ||
− | + | ||
− | + | ||
− | + | ||
− | + | ||
− | + | ||
− | + | ||
− | + | ||
− | + | ||
− | + | ||
− | + | ||
− | + | ||
− | + | ||
− | + | ||
− | + | ||
− | + | ||
− | + | ||
− | + | ||
− | + | ||
− | + | ||
− | + | ||
− | + | ||
− | + | ||
− | + | ||
− | + | ||
− | + | ||
− | + | ||
− | + | ||
− | + | ||
− | + | ||
− | + | ||
− | + | ||
− | + | ||
− | + | ||
− | + | ||
− | + | ||
− | + | ||
− | + | ||
− | + | ||
− | + | ||
− | + | ||
− | + | ||
− | + | ||
− | + | ||
− | + | ||
− | + | ||
− | + | ||
− | + | ||
− | + | ||
− | + | ||
− | + | ||
− | + | ||
− | + | ||
− | + | ||
</html> | </html> | ||
{{TecCEM/Footer}} | {{TecCEM/Footer}} |
Revision as of 03:48, 24 September 2018
Abstract
Cell lines HaCat and L-929 were used to evaluate a tissue regeneration system incorporating a collagen-based scaffold and encapsulated recombinant growth factors. A collagenous synthetic gene comprising collagen type V heparin binding domain (HepV) was expressed in a bacterial system, constituting the main component of the scaffold. For collagen molecule consists of repetitive G-X-Y triplets, being Y frequently hydroxyproline (Hyp), a method of intracellular accumulation of Hyp is used to co-translationally incorporate this non-canonical amino acid. A chitosan crosslinking procedure is carried out on the expressed collagen to prevent contraction and to finally freeze-dry. Further, a mixture of heparin and tenascin C fibronectin type III domain V (TNCIII5) was added to the scaffold, for the heparin-tenascin C binding has a high affinity with a large number of growth factors. Recombinant human leptin β (LepB) is used as a growth factor and we hypothesize that it may be encapsulated to achieve a controlled drug delivery. Due to its suitability, chitosan nanoencapsulation was employed. To evaluate the efficacy of the system, MTT proliferation assay was performed in 96-well plates. Given the cell lines assessed during this project, this tissue regeneration system proves its ability to be used in the treatment of second degree burns. As a widely new biotechnology procedure for skin regeneration the creation of a new, low cost method, for the silencing of miRNA´s involved in the skin regeneration was created and tested. The project was also tested using a skin chip as a practical and small cell proliferation hardware.