TY - JOUR
T1 - Influence of the polymer structure over self-assembly and thermo-responsive properties
T2 - The case of PEG-b-PCL grafted copolymers via a combination of RAFT and ROP
AU - Sponchioni, Mattia
AU - Ferrari, Raffaele
AU - Morosi, Lavinia
AU - Moscatelli, Davide
PY - 2016
Y1 - 2016
N2 - During the last years, the field of drug delivery has experienced a growing interest toward the so-called thermo-responsive polymers: synthetic materials that, due to the specific hydrophilic-lipophilic balance of their repeating units, exhibit a lower critical solution temperature (LCST) in water associated to a characteristic coil-globule transition. In this work, thermo-responsive amphiphilic block copolymers are synthesized via reversible addition-fragmentation transfer (RAFT) polymerization starting from thermo-responsive monomers and a hydrophobic biodegradable macromonomer, oligo(caprolactone)methacrylate (CL3MA), produced via ring opening polymerization (ROP). The obtained copolymers exhibit an interesting self-assembly behavior leading to nanoparticles (NPs) as long as temperature is kept below the LCST. Otherwise, once this value is overcome, the destabilization of the NPs causes the formation of hydrophobic superstructures that enhance the release of an entrapped lipophilic drug. This characteristic behavior has been systematically studied and related to the copolymer structure. In particular, the self-assembly behavior as well as temperature-triggered NP destabilization have been related to the relative length of the two blocks constituting the copolymers and to their hydrophilic-lipophilic balance (HLB). Finally, the efficacy of the thermo-responsive triggered drug release has been tested in the case of Paclitaxel (PTX).
AB - During the last years, the field of drug delivery has experienced a growing interest toward the so-called thermo-responsive polymers: synthetic materials that, due to the specific hydrophilic-lipophilic balance of their repeating units, exhibit a lower critical solution temperature (LCST) in water associated to a characteristic coil-globule transition. In this work, thermo-responsive amphiphilic block copolymers are synthesized via reversible addition-fragmentation transfer (RAFT) polymerization starting from thermo-responsive monomers and a hydrophobic biodegradable macromonomer, oligo(caprolactone)methacrylate (CL3MA), produced via ring opening polymerization (ROP). The obtained copolymers exhibit an interesting self-assembly behavior leading to nanoparticles (NPs) as long as temperature is kept below the LCST. Otherwise, once this value is overcome, the destabilization of the NPs causes the formation of hydrophobic superstructures that enhance the release of an entrapped lipophilic drug. This characteristic behavior has been systematically studied and related to the copolymer structure. In particular, the self-assembly behavior as well as temperature-triggered NP destabilization have been related to the relative length of the two blocks constituting the copolymers and to their hydrophilic-lipophilic balance (HLB). Finally, the efficacy of the thermo-responsive triggered drug release has been tested in the case of Paclitaxel (PTX).
KW - Block copolymers
KW - LCST
KW - Macromonomers
KW - PCL
KW - PEG
KW - RAFT
KW - Ring opening polymerization
KW - Thermo-responsive
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U2 - 10.1002/pola.28177
DO - 10.1002/pola.28177
M3 - Article
AN - SCOPUS:84977080667
JO - Journal of Polymer Science, Part A: Polymer Chemistry
JF - Journal of Polymer Science, Part A: Polymer Chemistry
SN - 0887-624X
ER -