Efficient Synthesis of Hydrophilic Hairy Semihollow Molecularly Imprinted Polymer Microcapsules with Ultrahigh Drug
Yan Zhou1, Yanyan Mu1, Huiqi Zhang1
1State Key Laboratory of Medicinal Chemical Biology, Key Laboratory of Functional Polymer Materials (Ministry of Education), and College of Chemistry, Nankai University, Tianjin 300071, China.
Abstract:
A highly efficient approach to obtaining well-defined hydrophilic hairy semihollow molecularly imprinted polymer (MIP) microcapsules with ultrahigh drug loading and pH-responsive sustained release properties is described, which involves grafting of a thin propranolol-MIP layer and poly(2-hydroxyethyl methacrylate) (PHEMA) brushes onto the "living" poly(methacrylic acid) (PMAA) microspheres (prepared by one-pot reversible addition-fragmentation chain transfer (RAFT) precipitation polymerization) via two-step surface-initiated RAFT polymerization and rapid etching of part of the PMAA core from the resulting core-shell-corona-structured MIP particles by methanol washing. Both the MIP layer thickness and etching degrees of the obtained core-shell-structured MIP particles could be easily tuned by adjusting the polymerization time, and the surface-grafting of PHEMA brushes was well-controlled. The unique structure of the semihollow MIP microcapsules with PMAA chains inside cavities endowed them with ultrahigh template loading capacities (1637 and 1065 μmol/g for MIP microcapsules without and with PHEMA brushes, respectively, which are much higher than those of the previously reported propranolol-MIPs (from dozens to 600 μmol/g)). Additionally, they showed high flexibility, obvious molecular imprinting effects, and extremely fast template binding kinetics (the semihollow MIP microcapsules without PHEMA brushes reaching equilibrium binding within 1 min). Furthermore, the pH-responsive sustained drug release of the propranolol-loaded hydrophilic hairy semihollow MIP microcapsules in PBS buffer solutions was also demonstrated. The high versatility of RAFT polymerization techniques and robust nature of the facile sacrificial PMAA core-etching method make our strategy a general and efficient way for developing advanced hydrophilic hairy semihollow MIP micro/nanocapsules highly promising in drug delivery and various bioanalytical applications.
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