subject predicate object context
43397 Creator c3baa1aae2495d9fcf383c433b46bfe0
43397 Creator ext-6e29ad3acdfb81991cdda8ab78d6daa4
43397 Creator ext-166730dd7686ed65658572a63dc56440
43397 Creator ext-5dd898e63c5aebd98edd26dbe39e98d7
43397 Creator ext-cac0fd4001e38af13ddc4387c35f1a8d
43397 Creator ext-ddb3f3a24bfda014f1c5bf48f15d7907
43397 Date 2013-06-16
43397 Is Part Of repository
43397 abstract Hydrogels have been widely used in biomedical applications such as scaffolds for tissue engineering, biosensing, drug delivery and cell immobilization. Due to their 3D structure, tunable mechanical properties, and their ability to mimic the cellular environment, these materials have been extensively studied and analysed in order to investigate their potential characteristics in the biomaterials field. Alginate is one of the most commonly used hydrogels, which is derived from brown algae, a polysaccharide that is composed of (1-4)-linked β-D-mannuronic acid and α-L-guluronic acid monomers. The crosslinks within the alginate hydrogel typically utilize divalent cations to co-ordinate carboxyl and hydroxyl moieties on the polymer chain. Employing a novel system geometry for rapid manufacture, we report an in-depth study of the variables that can be used to modulate the mechanical and rheological properties of the resultant tissue analogue. Specifically we investigate the influence of (i) the divalent cation, (ii) the cation concentration, (iii) the alginate concentration, (iv) the composition of the aqueous medium, and (v) fibroblast encapsulation and concentration in the hydrogel. Spherical indentation is employed to measure the short-time Young’s modulus as a means of characterising the mechanical properties. More detailed rheological properties are obtained by transient and oscillatory measurements with a parallel plate configuration. Staining protocols were used to verify cellular viability in the hydrogel post-manufacture. It is shown that the hydrogel modulus can be tailored up to approximately 500 kPa through careful selection of the alginate and cation concentration. Furthermore, fibroblast viability is not attenuated upon incorporation into the hydrogel; a range of cell growth media can be used without influencing mechanical properties.
43397 authorList authors
43397 presentedAt ext-11fe46c10245fe14239f419fcdac4d33
43397 status nonPeerReviewed
43397 type AcademicArticle
43397 type Article
43397 label Kaklamani, Georgia; Cheneler, David; Bowen, James ; Anthony, Carl J.; Grover, Liam M. and Adams, Michael J. (2013). Towards rapid manufacture of externally gelated tissue analogues. In: 4th International Conference from Nanoparticles and Nanomaterials to Nanodevices and Nanosystems, 16-20 Jun 2013, Corfu, Greece.
43397 label Kaklamani, Georgia; Cheneler, David; Bowen, James ; Anthony, Carl J.; Grover, Liam M. and Adams, Michael J. (2013). Towards rapid manufacture of externally gelated tissue analogues. In: 4th International Conference from Nanoparticles and Nanomaterials to Nanodevices and Nanosystems, 16-20 Jun 2013, Corfu, Greece.
43397 Title Towards rapid manufacture of externally gelated tissue analogues
43397 in dataset oro