2008
DOI: 10.1016/j.colsurfb.2007.07.012
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Self-aggregated nanoparticles from methoxy poly(ethylene glycol)-modified chitosan: Synthesis; characterization; aggregation and methotrexate release in vitro

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Cited by 120 publications
(61 citation statements)
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“…After this initial effect, MTX was released in a continuous way for up to 48 h, reaching percentage of cumulative release close to 60%. Therefore, the self-aggregated nanoparticles delayed the drug release in the release process when these results were compared with the release of the free drug (Yang et al, 2008).…”
Section: Methotrexate (Mtx)mentioning
confidence: 93%
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“…After this initial effect, MTX was released in a continuous way for up to 48 h, reaching percentage of cumulative release close to 60%. Therefore, the self-aggregated nanoparticles delayed the drug release in the release process when these results were compared with the release of the free drug (Yang et al, 2008).…”
Section: Methotrexate (Mtx)mentioning
confidence: 93%
“…PEG and its derivatives can be attached to the polysaccharide structure to form micelles directly in an aqueous medium by adjusting the hydrophobicity/hydrophilicity of the polysaccharide chain. Chitosan has been grafted with different molecules of poly(ethylene glycol), obtaining nanoparticles with an average size ranged between 80-260 nm (Yang et al, 2008;Yoksan et al, 2004).…”
Section: Nanoparticles Obtained From Self-assembling Of Hydrophobicalmentioning
confidence: 99%
“…chitosan -Cyclodextrin (Sakairi et al, 1998;Martel et al, 2001;Aoki et al, 2003) Modification: Sakairi prepared -CD linked chitosan using 2-O-formylmethyl--CD by reductive N-alkylation and confirmed the host-guest complex with p-nitrophenol. Chitosan є-Caprolactone Yang et al, 2008b) Modification: The PCL-graft-chitosan copolymers were synthesized by coupling the hydroxyl end-groups on preformed PCL chains and the amino groups present on 6-Otriphenylmethyl chitosan and by removing the protective 6-O-triphenylmethyl groups in acidic aqueous solution Biomedical grade chitosan Monomethoxy poly(ethyleneglycol) (Zhang et al, 2005;Yang et al, 2008b) Modification: Chitosan was completely dissolved in formic acid by stirring and a suitable amount of mPEG was added. After 15 min, enough formaldehyde solution was added to the above mixture and was stirred for 12 h. Table 2.…”
Section: Chitosanmentioning
confidence: 99%
“…Therefore, poly (ethylene glycol) is widely used as a pharmacological polymer with high hydrophilicity, biocompatibility and biodegradability. In recent years, derivative poly (ethylene glycol)-g-derivative chitosan to obtain nanoparticles has been studied by many researchers (Ouchi et al, 1998;Jung et al, 2006) (Park et al, 2008) (Yang et al, 2008b) (Opanasopit et al, 2007). The grafted poly (ethylene glycol) methyl ether onto N-Phthaloyl chitosan chains, aggregated to obtain sphere-like nanoparticles (an et al, 2004).…”
Section: Linear Hydrophobic Moleculesmentioning
confidence: 99%
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