2009
DOI: 10.1016/j.actbio.2009.02.008
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Ocular injectable formulation assessment for oxidized dextran-based hydrogels

Abstract: Initiator-free injectable hydrogels are very interesting for drug and/or cell delivery applications, since they can be administered in a minimally invasive way, and avoid the use of potentially harmful chemical initiators. In the current work, oxidized dextran crosslinked with adipic acid dihydrazide hydrogels were further characterized and tuned to produce formulations, with the aim of producing an injectable formulation for the possible treatment of posterior eye diseases. The gelation rate and the hydrogel … Show more

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Cited by 44 publications
(33 citation statements)
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“…Precipitation formation may complicate NMR readings after reaction between DA and tert ‐butyl carbazate (tBC) due to the bulky butyl group of tBC. For this reason, DO was determined by TNBS assay instead of NMR . Under the described reaction condition, the DO of DA was determined to be 59 ± 1.4% ( n = 3).…”
Section: Resultsmentioning
confidence: 99%
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“…Precipitation formation may complicate NMR readings after reaction between DA and tert ‐butyl carbazate (tBC) due to the bulky butyl group of tBC. For this reason, DO was determined by TNBS assay instead of NMR . Under the described reaction condition, the DO of DA was determined to be 59 ± 1.4% ( n = 3).…”
Section: Resultsmentioning
confidence: 99%
“…DA was prepared using oxidative cleavage, based on previously reported protocols . In brief, 2.5 g dextran was dissolved in 100 mL DI water.…”
Section: Methodsmentioning
confidence: 99%
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“…Despite extensive research on cytotoxicity (effects on cell proliferation/viability) of aldehyde-modified polysaccharides and ADH, genotoxicity studies are still scarce, in particular, on ADHreticulated polyaldehyde-based hydrogels (Bouhadir, Hausman, & Mooney, 1999;Hu et al, 2017;Maia et al, 2009;Schramm et al, 2012;Su, Chen, & Lin, 2010). Genotoxicity is an important endpoint of the safety assessment of regulated products, but no single test is available to detect all types of genotoxicity.…”
Section: Discussionmentioning
confidence: 99%
“…Hereafter, cells were kept in culture at 37 • C in a 5% CO 2 humidified atmosphere, inside an incubator. To evaluate cell behaviour in the presence of the scaffolds, MSCs were seeded with materials in 96-well plates at a density of 2 × 10 4 cells per well, for 72 h. Previously to cell seeding, plates and materials were sterilized by UV irradiation for 30 min [14,21]. Cell growth was monitored using an Olympus CX41 inverted light microscope (Tokyo, Japan) equipped with an Olympus SP-500 UZ digital camera.…”
Section: Proliferation Of Mscs In the Presence Of Ha:cs Scaffoldsmentioning
confidence: 99%