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      Non-thermally initiated RAFT polymerization-induced self-assembly

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          Abstract

          This review summarizes the recent non-thermal initiation methods in RAFT mediated polymerization-induced self-assembly (PISA), including photo-, redox/oscillatory reaction-, enzyme- and ultrasound wave-initiation.

          Abstract

          The reversible addition–fragmentation chain transfer (RAFT) mediated polymerization-induced self-assembly (PISA) enables efficient and convenient syntheses of polymeric nanoparticles, generally based on thermal initiation. However, thermal initiation confines the incorporation of temperature-sensitive biomolecules into nanoparticles. Recently, developments in non-thermally initiated RAFT PISA have addressed this problem, allowing precise regulation of polymerization and the incorporation of biomolecules under mild conditions, which is promising for bio-related applications. In this review, we try to summarize recent progress in PISA mediated by non-thermal initiation techniques, including photo-, redox/oscillatory reaction-, enzyme- and ultrasound wave-initiation.

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          Controlled/living radical polymerization: Features, developments, and perspectives

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            Design of polymeric nanoparticles for biomedical delivery applications.

            Polymeric nanoparticles-based therapeutics show great promise in the treatment of a wide range of diseases, due to the flexibility in which their structures can be modified, with intricate definition over their compositions, structures and properties. Advances in polymerization chemistries and the application of reactive, efficient and orthogonal chemical modification reactions have enabled the engineering of multifunctional polymeric nanoparticles with precise control over the architectures of the individual polymer components, to direct their assembly and subsequent transformations into nanoparticles of selective overall shapes, sizes, internal morphologies, external surface charges and functionalizations. In addition, incorporation of certain functionalities can modulate the responsiveness of these nanostructures to specific stimuli through the use of remote activation. Furthermore, they can be equipped with smart components to allow their delivery beyond certain biological barriers, such as skin, mucus, blood, extracellular matrix, cellular and subcellular organelles. This tutorial review highlights the importance of well-defined chemistries, with detailed ties to specific biological hurdles and opportunities, in the design of nanostructures for various biomedical delivery applications.
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              Self-assembly of block copolymers.

              Block copolymer (BCP) self-assembly has attracted considerable attention for many decades because it can yield ordered structures in a wide range of morphologies, including spheres, cylinders, bicontinuous structures, lamellae, vesicles, and many other complex or hierarchical assemblies. These aggregates provide potential or practical applications in many fields. The present tutorial review introduces the primary principles of BCP self-assembly in bulk and in solution, by describing experiments, theories, accessible morphologies and morphological transitions, factors affecting the morphology, thermodynamics and kinetics, among others. As one specific example at a more advanced level, BCP vesicles (polymersomes) and their potential applications are discussed in some detail.
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                Author and article information

                Contributors
                Journal
                PCOHC2
                Polymer Chemistry
                Polym. Chem.
                Royal Society of Chemistry (RSC)
                1759-9954
                1759-9962
                June 8 2021
                2021
                : 12
                : 22
                : 3220-3232
                Affiliations
                [1 ]Key Lab of Organic Optoelectronics and Molecular Engineering of Ministry of Education
                [2 ]Department of Chemistry
                [3 ]Tsinghua University
                [4 ]100084 Beijing
                [5 ]China
                Article
                10.1039/D1PY00216C
                adb45ee4-df31-43cd-aaae-d037c86d65d0
                © 2021

                http://rsc.li/journals-terms-of-use

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