pH-Responsive Non-Ionic Diblock Copolymers: Ionization of Carboxylic Acid End-Groups Induces an Order–Order Morphological Transition**
نویسندگان
چکیده
A carboxylic acid based reversible additionfragmentation transfer (RAFT) agent is used to prepare gels composed of worm-like diblock copolymers using two non-ionic monomers, glycerol monomethacrylate (GMA) and 2-hydroxypropyl methacrylate (HPMA). Ionization of the carboxylic acid end-group on the PGMA stabilizer block induces a worm-to-sphere transition, which in turn causes immediate degelation. This morphological transition is fully reversible as determined by TEM and rheology studies and occurs because of a subtle change in the packing parameter for the copolymer chains. A control experiment where the methyl ester derivative of the RAFT agent is used to prepare the same diblock copolymer confirms that no pH-responsive behavior occurs in this case. This end-group ionization approach is important for the design of new pH-responsive copolymer nano-objects as, unlike polyacids or polybases, only a minimal amount of added base (or acid) is required to drive the morphological transition.
منابع مشابه
Order–Order Morphological Transitions for Dual Stimulus Responsive Diblock Copolymer Vesicles
A series of non-ionic poly(glycerol monomethacrylate)-poly(2-hydroxypropyl methacrylate) (PGMA-PHPMA) diblock copolymer vesicles has been prepared by reversible addition-fragmentation chain transfer (RAFT) aqueous dispersion polymerization of HPMA at 70 °C at low pH using a carboxylic acid-based chain transfer agent. The degree of polymerization (DP) of the PGMA block was fixed at 43, and the D...
متن کاملThermoresponsive behavior of micellar aggregates from end-functionalized PnBA-b-PNIPAM-COOH block copolymers and their complexes with lysozyme.
The temperature response of micellar aggregates of poly(n-butyl acrylate)-b-poly(N-isopropylacrylamide)-carboxylic acid (PnBA-b-PNIPAM-COOH) end-functionalized diblock copolymers in aqueous solutions is investigated by small angle neutron scattering and light scattering techniques. The particular micellar aggregates present -COOH groups at their surface due to the molecular architecture of the ...
متن کاملNanopatterned Protein Films Directed by Ionic Complexation with Water-Soluble Diblock Copolymers.
The use of ionic interactions to direct both protein templating and block copolymer self-assembly into nanopatterned films with only aqueous processing conditions is demonstrated using block copolymers containing both thermally responsive and pH responsive blocks. Controlled reversible addition-fragmentation chain-transfer (RAFT) polymerization is employed to synthesize poly(N-isopropylacrylami...
متن کاملThermo-Induced Self-Assembly of Responsive Poly(DMAEMA-<italic>b</italic>-DEGMA) Block Copolymers into Multi- and Unilamellar Vesicles
A series of thermoresponsive diblock copolymers of poly[2-(dimethylamino)ethyl methacrylate-block-di(ethyleneglycol) methyl ether methacrylate], poly(DMAEMA-b-DEGMA), were synthesized by reversible addition−fragmentation chain transfer (RAFT) polymerizations. The series consist of diblock and quasi diblock copolymers. Sequential monomer addition was used for the quasi diblock copolymer synthesi...
متن کاملPREPARATION OF pH-SENSITIVE CORE-SHELL TYPE POLYMERIC MICELLE FROM POLY(PEPTIDE-b-LACTIDE) DIBLOCK COPLYMERS AS BIODEGRADABLE MIOMEDICAL MATERIAL
The formation of polymeric micelles by the self-association of diblock copolymers consisting of hydrophilic and hydrophobic segments in aqueous medium is currently a topic of great interest. This interest is motivated by the attractive applications of polymeric micelles to various research areas such as drug delivery carrier technology and nanotechnology. In the biomedical materials field, poly...
متن کامل