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In this work, amphiphilic block copolymers (BCs) consisting of a hydrophilic poly(ethylene glycol) methyl ether (PEG) and a degradable polycarbonate block derived from 2,2-bis(hydroxymethyl)propionic acid (bis-MPA) with pendant ureido units, along with corresponding homopolycarbonates are described. Polymers are synthesized by combining ring opening polymerization (ROP) and thiol-ene/yne functionalization to incorporate UCST-promoting ureido groups. For homopolycarbonates, increasing the ureido groups density along the polymer chain facilitates the upper critical solution temperature (UCST)-type thermoresponse in water. Because of their amphiphilic character, BCs form stable self-assemblies either by direct dispersion in water, co-solvent method or microfluidics. Upon heating, these self-assemblies swell, and collapse due to extensive hydration of the polycarbonate block, rather than becoming solubilized. Thermoresponsiveness is analyzed in terms of the number of ureido groups in the polycarbonate for a given polycarbonate block length as well as the length of polycarbonate block. As a proof of concept, the potential of these self-assemblies as thermoresponsive drug nanocarriers is evaluated, using curcumin as a hydrophobic model drug.
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http://dx.doi.org/10.1002/marc.202500029 | DOI Listing |
Angew Chem Int Ed Engl
August 2025
State Key Laboratory of Biobased Transportation Fuel Technology, International Research Center for X Polymers, Department of Polymer Science and Engineering, Zhejiang University, Hangzhou, 310027, China.
The development of efficient and selective catalytic methods for synthesizing well-defined polycarbonates and their copolymers represents a significant advancement toward sustainable polymer production. In this study, we report a series of innovative single-molecule hydrogen-bonding catalysts/initiators for the ring-opening polymerization (ROP) of cyclic carbonates, enabling rapid and precise synthesis of polycarbonates and their copolymers with polylactide. These catalysts uniquely facilitate simultaneous activation of both monomer and chain-end within a single molecular architecture, demonstrating superior activity compared to conventional multicomponent hydrogen-bonding initiating systems.
View Article and Find Full Text PDFPolymers (Basel)
June 2025
College of Chemistry, Zhengzhou University, Zhengzhou 450001, China.
A series of PPCDL-PEG-TPU were prepared by melting method using CO based biodegradable polycarbonate diol (PPCDL) and polyethylene glycol (PEG1000) as soft segments, and hexamethylene diisocyanate (HDI) and 1,4-butanediol (BDO) as hard segments. Their structure and properties were characterized to show that the products have nanoscale microphase separation, excellent wear-resistance and high resilience. PPCDL-PEG-TPUs have high tensile strength, high elongation at break, controllable hardness and excellent wear resistance when the content of hard segment is about 20%.
View Article and Find Full Text PDFACS Macro Lett
June 2025
Department of Chemical Science and Engineering, Institute of Science Tokyo, 2-12-1 Ookayama, Meguro-ku, Tokyo 152-8550, Japan.
Cyclic polymers have garnered significant interest due to their unique structure; however, their synthesis remains challenging, often hindered by low yields and limited selectivity. Considering that the cyclization step during the synthesis of cyclic polymers is presumably the most challenging, using a spontaneous and selective cyclization system is ideal. Here, we present a topology transformation from linear to cyclic, which is achieved through the error-checking ability provided by the dynamic covalent bonding between bis(2,2,6,6-tetramethylpiperidin-1-yl)disulfide (BiTEMPS) and its stable radicals with a high bond exchange rate.
View Article and Find Full Text PDFBiomacromolecules
June 2025
Bioprocessing Technology Institute (BTI), Agency for Science, Technology and Research (A*STAR), 20 Biopolis Way, #06-01 Centros, Singapore 138668, Singapore.
Since the remarkable breakthrough of COVID-19 mRNA vaccines, lipid nanoparticles (LNPs) have gained substantial attention as the most cutting-edge clinical formulations for mRNA delivery. PEGylated lipid (PEG-lipid) has been regarded as an essential constituent of LNPs that helps to prolong their systemic circulation by preventing particle aggregation in the blood and sequestration by the mononuclear phagocyte system. Herein, we synthesized a series of mRNA-loaded nanoparticles by replacing ALC-0159 (a PEG-lipid used in the Comirnaty formulation) with amphiphilic PEG-polycarbonate diblock copolymers (PC-HNPs).
View Article and Find Full Text PDFACS Appl Mater Interfaces
April 2025
Department of Chemistry, University of Miami, 1301 Memorial Drive, Coral Gables, Florida 33146, United States.
Self-assembled polymeric micelles formed from amphiphilic block copolymers offer a promising strategy for enhanced drug delivery due to their biocompatibility and controlled release. However, challenges such as their poor colloidal stability under diluted conditions and degradation during storage and circulation limit their further applications. To address these issues, we developed a straightforward method for constructing cross-linked polycarbonate micelles that enhance stability while allowing for controlled stimuli-responsive drug delivery.
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