2011
DOI: 10.1016/j.jconrel.2011.08.096
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Synthesis and controlled release of mitomycin C from a chitosan-based polymeric prodrug

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Cited by 6 publications
(6 citation statements)
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“…This has been examined in the animal models of bone injury repair, skin wound repair, and prevention of cardiac fibrosis after myocardial infarction (MI) and cancer treatment. 116,117 Hydrogels, similar to the ECM, are three-dimensional (3D) networks comprising hydrophilic polymer chains that are physically or chemically cross-linked to absorb water. 118 Hydrogel systems have been widely applied in drug delivery and regenerative medicine because of their biodegradability, injectability, and biocompatibility.…”
Section: Extracellular Vesicle Delivery Strategies In Liver Diseases ...mentioning
confidence: 99%
“…This has been examined in the animal models of bone injury repair, skin wound repair, and prevention of cardiac fibrosis after myocardial infarction (MI) and cancer treatment. 116,117 Hydrogels, similar to the ECM, are three-dimensional (3D) networks comprising hydrophilic polymer chains that are physically or chemically cross-linked to absorb water. 118 Hydrogel systems have been widely applied in drug delivery and regenerative medicine because of their biodegradability, injectability, and biocompatibility.…”
Section: Extracellular Vesicle Delivery Strategies In Liver Diseases ...mentioning
confidence: 99%
“…That is possible to deal with the application of chitosan as a carrier for water-insoluble and water-soluble drug conjugates in anti-scarring therapy. Izume summarized the toxicity of chitosan including a skin sensitization study, temporal skin irritation study, ophthalmic sensitization test, mutagenicity test and patch test for humans; every study and test showed low toxicity of chitosan, which can function well as a drug carrier due to long systemic retention, low toxicity and accumulation in the target tissue[ 24 - 26 ].…”
Section: Presentation Of Hypothesismentioning
confidence: 99%
“…When the m CS-CHO / m MMC was 5/1, 10/1 and 25/1, the initial release amount of MMC was 65%, 50% and 45%. There was an obvious initial release within the initial 8 h, and the concentration of MMC in dialysis medium remained unchanged during the following 60 h. Furthermore, the cytotoxicity study on chitosan-based polymeric predrug encapsulated fibroblast indicated that the maximum non-toxic concentration of CS-CHO was 8.3, 42.3 and 54.7 mg/ml in the 24, 48 and 72 h[ 26 ]. Therefore, the concentration of CS-CHO in the practical application should be lower than the corresponding concentration.…”
Section: Testing the Hypothesismentioning
confidence: 99%
“…Moreover, the polymeric prodrug with abundant active groups can be further functionalized . Lastly, the decelerated hydrolysis and enzymolysis due to stereo‐specific blockade allows the active cargo to gradually fall off from the polymer backbone, thus realizing sustained drug release .…”
Section: Introductionmentioning
confidence: 99%