2005
DOI: 10.1016/j.jconrel.2004.10.021
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Temperature-sensitive chitosan-poly(N-isopropylacrylamide) interpenetrated networks with enhanced loading capacity and controlled release properties

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Cited by 181 publications
(78 citation statements)
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“…However, all hydrogels tested showed a temperature for the phase transition close to that of the pure PNIPAAm hydrogel. It is reasonable to believe that the intrinsic properties of PNIPAAm subchains in CPN, in particular the transition free energy, are very close to those of the reference hydrogel (Alvarez-Lorenzo et al 2005).…”
Section: The Delivery Of Platinum Drugs From Thermosensitive Hydrogelmentioning
confidence: 82%
“…However, all hydrogels tested showed a temperature for the phase transition close to that of the pure PNIPAAm hydrogel. It is reasonable to believe that the intrinsic properties of PNIPAAm subchains in CPN, in particular the transition free energy, are very close to those of the reference hydrogel (Alvarez-Lorenzo et al 2005).…”
Section: The Delivery Of Platinum Drugs From Thermosensitive Hydrogelmentioning
confidence: 82%
“…This property is not found in native xyloglucan [220]. Further, Grinberg et al developed temperature-sensitive chitosan-poly(NIPAM) based interpenetrating networks (IPNs) with enhanced drug loading capacity and exhibiting controlled drug release kinetics [221]. The IPNs were formed by free-radical polymerization using bisacrylamide as crosslinker, followed by subsequent crosslinking of chitosan with glutaraldehyde solutions, to form fully interpenetrated networks.…”
Section: Temperature-sensitive or Thermo-responsive Gelsmentioning
confidence: 99%
“…Also, pH-responsive, freeze-dried chitosan-polyvinyl pyrrolidone (PVP) hydrogels [50] and chitosan-PVA hydrogels [51] were developed for drug delivery applications by cross-linking with glutaraldehyde. The potential of post cross-linking of chitosan, after preparing a semiinterpenetrating polymer network (semi-IPN) with PNIPAAm to create temperature-responsive and pHsensitive IPNs for drug delivery, has also been studied [44]. Further, CMC [52] and N-(2-carboxybenzyl)-chitosan hydrogels [53] have been prepared by reacting glutaraldehyde with the respective chitosan derivative.…”
Section: Glutaraldehydementioning
confidence: 99%
“…Thus, in the current chapter, an overview on the drug delivery applications of cross-linked [23] and chemically modified chitosan is given. Important modified and cross-linked derivatives include carboxymethyl-chitosan (CMC), O-carboxymethyl-chitosan (O-CMC), N,O-carboxymethyl-chitosan (N,O-CMC) and N-carboxymethyl-chitosan (N-CMC) [14][15][16][17][18][19], succinylchitosan [24][25][26][27][28][29][30][31][32], thiolated chitosan [33][34][35][36][37][38][39][40][41][42][43], and chitosan grafted with PNIPAAm and PNVCL (chitosang-PNIPAAm and chitosan-g-PNVCL) [44][45][46][47].…”
Section: Introductionmentioning
confidence: 99%