2018
DOI: 10.1016/j.carbpol.2017.11.027
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Chitosan-based polymer hybrids for thermo-responsive nanogel delivery of curcumin

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Cited by 129 publications
(70 citation statements)
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“…On the other hand, at pH 5.4, the release rates are a little higher than that of pH 7.4 and all loaded Imatinib molecules release within 120 min. It means that the drug release rate of Fe 3 O 4 @CS/Imatinib is pH dependent and lower pH levels lead to faster release of Imatinib from this nanocomposite. It should be noted that, compared with the release behavior of the other Fe 3 O 4 @CS/drug nanocomposites, the Fe 3 O 4 @CS/Imatinib NPs do not involve any burst phenomenon at the beginning of the release trials.…”
Section: Resultsmentioning
confidence: 99%
“…On the other hand, at pH 5.4, the release rates are a little higher than that of pH 7.4 and all loaded Imatinib molecules release within 120 min. It means that the drug release rate of Fe 3 O 4 @CS/Imatinib is pH dependent and lower pH levels lead to faster release of Imatinib from this nanocomposite. It should be noted that, compared with the release behavior of the other Fe 3 O 4 @CS/drug nanocomposites, the Fe 3 O 4 @CS/Imatinib NPs do not involve any burst phenomenon at the beginning of the release trials.…”
Section: Resultsmentioning
confidence: 99%
“…All these advantageous characteristics make stimulus-responsive hydrogels an optimal option for the robust loading of therapeutic drugs and the subsequent controllable release of those drugs when and where they are needed through precise modulation of the surrounding environment (e.g., pH, temperature, and light) or the application of external physical fields (e.g., magnetic and electric fields) 97,[129][130][131][132] . The corresponding applications of drug-delivery systems based on stimulus-responsive hydrogels include neural disease treatment, cancer chemotherapy, and wound healing [133][134][135][136] .…”
Section: Drug Deliverymentioning
confidence: 99%
“…Having a volume-/phase-transition temperature (LCST of 32°C) close to the human physiological temperature (37°C), the drug release from the PNIPAAm-based system can be spontaneously activated as soon as the drug enters the human body. This drug-unloading mechanism brings about unparalleled easy accessibility without any further applied stimuli; thus, PNIPAAm has been highlighted as an appealing candidate in bioactuator design and fabrication for thermally induced drug release 56,133,[136][137][138] . The PNIPAAm hydrogel has been shown to efficiently release drugs (e.g., doxorubicin and lysozyme 56 ) under heating, which can be explained by the collapse of chains and the shrinkage of the hydrogel network.…”
Section: Drug Deliverymentioning
confidence: 99%
“…This provided a ‘bridge’ for the combination of hydrophobic drugs with hydrophilic materials. Chitosan, derived from chitin deacetylation, is a linear polysaccharide consisting of β ‐(1–4)‐linked d ‐glucosamine residues and N ‐acetylglucosamine groups and has been widely used in biomedical applications due to its biocompatibility, nontoxicity, bio‐activity, biodegradability, etc . In addition, chitosan is a polyelectrolyte with positive charge due to the presence of amino groups on the polyglycidic chain.…”
Section: Introductionmentioning
confidence: 99%