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Delivery of Chondrocytes

Lee, H. and Park, T. G. 2009. Photo-crossUnkable, biomimetic, and thermo-sensitive pluronic grafted hyaluronic acid copolymers for injectable delivery of chondrocytes. / Biomed Mater Res Part A 88A 797-806. [Pg.404]

Samuel R E, et al. (2002). Delivery of plasmid DNA to articular chondrocytes via novel collagen-glycosaminoglycan matrices. Hum. Gene Ther. 13 791-802. [Pg.1056]

Park, H., Temenoff, J. S., Holland, T. A., Tahata, Y. Mikos, A. G. (2005b) Delivery of TGF-/31 and chondrocytes via injectable, biodegradable hydrogels for cartilage tissue engineering apphcations. Biomaterials, 26, 7095-103. [Pg.177]

X. Xu, R.M. Capito, M. Spector, Delivery of plasmid IGF-1 to chondrocytes via cation-ized gelatin nanoparticles. Journal of Biomedical Materials Research 84A (2008) 73-83. [Pg.312]

Na K, et al. Delivery of dexamethasone, ascorbate, and growth factor (TGF beta-3) in thermo-reversible hydrogel constructs embedded with rabbit chondrocytes. Biomaterials 2006 27 5951-7. [Pg.201]

BMPs stimulate matrix production in chondrocytes [51-53] however, their effects on zonal cell populations are less documented. A recent study showed adenovirus-mediated delivery of both BMP 2 and 7 resulted in increased matrix accumulation in only superficial cell culture pellets [54]. These results indicate that BMPs maybe more appropriate for delivery to superficial zone cell populations. [Pg.600]

Coculture and conditioned media models have also demonstrated success for differentiating MSCs. Cartilage chips [84], mixed micromass pellets of chondrocytes and MSCs [93], and chondrocyte-conditioned media [94] have all resulted in MSC chondrogenesis independent of TGF-P delivery. Table 30.2 lists details of these, and other popular methods, for MSC chondrogenesis. [Pg.606]

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Chondrocyte

Chondrocytes

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