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Collagen grafting

Furthermore, soluble collagen grafted with polyacrylamide formed fibrils on heating to 37 °C at neutral pH, but unlike the native collagen, these fibrils did not redissolve on cooling to 2°C (8). These results indicate that the redispersion property of soluble collagen is impaired, probably by attachment of the polyacrylamide side chains to the collagen molecule. [Pg.192]

Figure 7.76 Development of human osteoblasts on the surfaces of as-HVOF-sprayed (a), alkali treated (b) and collagen grafted (c) HAp/Ti02 coatings. Fluorescence staining shows that in live cells the non-fluorescent calcein-AM is converted to a... Figure 7.76 Development of human osteoblasts on the surfaces of as-HVOF-sprayed (a), alkali treated (b) and collagen grafted (c) HAp/Ti02 coatings. Fluorescence staining shows that in live cells the non-fluorescent calcein-AM is converted to a...
Tong, X.J., Hirai, K., Shimada, H., Mizutani, Y., Izumi, T., Toda, N., Yu, R, 1994. Sciatic nerve regeneration navigated by laminin-fibronectin double coated biodegradable collagen grafts in rats. Brain Res. 663, 155-162. [Pg.117]

Huynh, T. et al., Remodehng of an acellular collagen graft into a physiologically responsive neovessel. Nat Biotechnol, 1999.17(11) 1083-86. [Pg.702]

Figure 1. Kinetics of skin wound contraction in the presence of polymeric grafts which undergo enzymatic degradation at two different rates, R = 17 enzyme units (e.u.) and R = 231 e.u. The variation in R was achieved by controlling the duration of cross-linking of the collagen-graft-glycosaminoglycan in aqueous glutaraldehyde. Figure 1. Kinetics of skin wound contraction in the presence of polymeric grafts which undergo enzymatic degradation at two different rates, R = 17 enzyme units (e.u.) and R = 231 e.u. The variation in R was achieved by controlling the duration of cross-linking of the collagen-graft-glycosaminoglycan in aqueous glutaraldehyde.
Hydroxyapatite constitutes -65% of human bone by weight. There is another 18% collagen fiber which makes the bone flexible and more durable. Then, there is -10% genetic tissue (mostly living bone cells). This tissue carries the genetic code of the person or animal and unless it is in a denatured form, which also kills the bone, it is likely to be rejected in the body as a bone graft. Therefore, it is impossible to successfully implant living bone even from closely related donors. The remainder of bone is composed of capillaries, nerves, and so on. [Pg.317]

Figure 26. Reconstruction of the tunica intima on the inner surface of a clinically used polyethylene terephtalate vascular prosthesis. A non-modified inner surface of the prosthesis, B immobilization of defined assemblies of protein molecules (e.g., collagenfiarninin or collagen+fibrin) on the inner surface of the graft, C immunofluorescence of von Willebrand factor, a marker of the identity a differentiation of vascular endothelial cells, in human saphenous vein endothelial cells in cultures on the inner surface of a prosthesis coated with collagen and larninin, D detail of a layer of endothelial cells growing on a layer of collagen and fibrin. Note well developed talin-containing focal adhesion plaques. A, B conventional optical microscope, C, D confocal microscope Leica DM 2500 [30,31]. Figure 26. Reconstruction of the tunica intima on the inner surface of a clinically used polyethylene terephtalate vascular prosthesis. A non-modified inner surface of the prosthesis, B immobilization of defined assemblies of protein molecules (e.g., collagenfiarninin or collagen+fibrin) on the inner surface of the graft, C immunofluorescence of von Willebrand factor, a marker of the identity a differentiation of vascular endothelial cells, in human saphenous vein endothelial cells in cultures on the inner surface of a prosthesis coated with collagen and larninin, D detail of a layer of endothelial cells growing on a layer of collagen and fibrin. Note well developed talin-containing focal adhesion plaques. A, B conventional optical microscope, C, D confocal microscope Leica DM 2500 [30,31].
When collagen-GAG matrices which can significantly delay the onset of wound contraction are seeded with a minimum density of easily separable skin cells (basal cells) from the same animal, and the cell-seeded matrices are then grafted, wound healing is affected in an even more profound way In this case,... [Pg.236]

Fig. 9. Variation of half-life of skin wound with the average pore diameter of collagen-GAG matrices used as grafts for full-thickness skin wounds in the guinea pig. The vertical broken lines at about 20 and 120 pm mark the limits of matrix activity. Outside these approximate limits the wound half-life rapidly drops to the level of the ungrafted wound. The horizontal scale is logarithmic [79]... Fig. 9. Variation of half-life of skin wound with the average pore diameter of collagen-GAG matrices used as grafts for full-thickness skin wounds in the guinea pig. The vertical broken lines at about 20 and 120 pm mark the limits of matrix activity. Outside these approximate limits the wound half-life rapidly drops to the level of the ungrafted wound. The horizontal scale is logarithmic [79]...

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