2008
DOI: 10.1016/j.actbio.2008.02.002
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A stimulus-responsive magnetic nanoparticle drug carrier: Magnetite encapsulated by chitosan-grafted-copolymer

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Cited by 223 publications
(101 citation statements)
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“…Several groups have shown the formation of a novel drug delivery device with magnetic targeting capability by coating a magnetic nanoparticle, conjugated to active drug, with a thermoresponsive polymer. Upon heating above the LCST, the coating shrinks and releases the active drug [149,151,152,155,156]. Purushotham also showed the possibility of using a magnetic field to heat the composite and hence release entrapped drugs form the thermoresponsive coating [150].…”
Section: Particlesmentioning
confidence: 99%
“…Several groups have shown the formation of a novel drug delivery device with magnetic targeting capability by coating a magnetic nanoparticle, conjugated to active drug, with a thermoresponsive polymer. Upon heating above the LCST, the coating shrinks and releases the active drug [149,151,152,155,156]. Purushotham also showed the possibility of using a magnetic field to heat the composite and hence release entrapped drugs form the thermoresponsive coating [150].…”
Section: Particlesmentioning
confidence: 99%
“…A variety of smart CAs have been developed that become activated in response to changes in pH, [7][8][9][10][11][12][13] to the presence of metal ions [14][15][16] through enzymatic activation, 17 and to the presence of oxygenated hemoglobin 18 or radicals 19 or upon exposure to ultrasounds 20 or changes in temperature. 21,22 These smart CAs have proven to be excellent MRI tools for very specific targets in vitro and in vivo. 7,8 On the other hand, targeted nanoparticles such as liposomes, 23 dendrimers, 24 and micelles provide several unique features and capabilities such as to house a large number or different types of functional groups that can be used in multiple diagnostic (eg, gadolinium complex) and therapeutic (eg, anticancer) agents.…”
Section: Introductionmentioning
confidence: 99%
“…The developed smart polymer exhibited a LCSTof 38 C. The drug releasewas appreciably low below the LCSTas opposed to temperatures above the LCST. In each case, there was an initial rapid drug release, followed by a controlled release in a second stage, especially in a mild acidic buffer solution [126].…”
Section: Chitosan-grafted Thermosensitive Polymersmentioning
confidence: 99%
“…A novel magnetic nanoparticle drug carrier for controlled drug release has been reported to respond to changes in external temperature or pH, resulting in longer circulation time and reduced side effects of the delivered drug (doxorubicin) as compared to the native drug [126]. The novel nanocarrier is described as a functionalized magnetite (Fe 3 O 4 ) core that is conjugated with doxorubicin via an acid-labile hydrazone bond and encapsulated by the thermosensitive smart polymer, chitosan-g-poly(N-isopropylacrylamide-co-N,N-dimethylacrylamide).…”
Section: Chitosan-grafted Thermosensitive Polymersmentioning
confidence: 99%