2013
DOI: 10.1016/j.carbpol.2012.09.014
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A convenient way to synthesize comb-shaped chitosan-graft-poly (N-isopropylacrylamide) copolymer

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Cited by 44 publications
(31 citation statements)
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“…Chen et al have proposed a four-step route where the grafting reaction was directed towards the C-6 position; the method involves [59]:…”
Section: Synthesismentioning
confidence: 99%
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“…Chen et al have proposed a four-step route where the grafting reaction was directed towards the C-6 position; the method involves [59]:…”
Section: Synthesismentioning
confidence: 99%
“…Due to the interesting dual-responsive behaviour of Cs-g-PNIPAm copolymers, the properties of these materials have been thoroughly studied using different techniques such as microdifferential scanning calorimetry (μDSC), dynamic light scattering (DLS), NMR, UV-Vis spectroscopy and rheological measurements, among others [46,51,52,54,[58][59][60][62][63][64][65].…”
Section: Propertiesmentioning
confidence: 99%
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“…living free radical nitroxide-mediated polymerization, atom transfer radical polymerization and reversible addition-fragmentation chain transfer (RAFT) polymerization [30]. Atom transfer radical polymerization (ATRP) refers to a system where equilibrium between dormant species and radicals is established [31]. Reversible addition fragmentation chain transfer (RAFT) is a reversible deactivation of radical polymerization.…”
Section: Chitosan Co-polymersmentioning
confidence: 99%
“…14,15 Taking these differences as a basic concept, various pH and temperature responsive polymers were synthesized and utilized as carriers for stimuli-responsive delivery of anti-cancer drugs. [16][17][18][19][20] Though all these reported polymeric nanoparticles have shown tremendous potential for targeted drug delivery, they have a very low drug loading capacity. Among them, due to the closer LCST (32 o C) of PNIPAAm to normal body temperature, biocompatibility and non-toxicity, chitosan-g-poly(N-isopropylacrylamide) (CS-g-PNIPAAm) co-polymer was most extensively studied as a carrier for anticancer drugs to achieve thermo and pH responsive delivery of drugs to the intended sites with minimal or no adverse effects in cancer therapy.…”
Section: Introductionmentioning
confidence: 99%