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Related Concept Videos

Anionic Chain-Growth Polymerization: Overview01:20

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The polymerization process that involves carbanion as an intermediate is called anionic polymerization. It is also a type of addition or chain-growth polymerization. Anionic polymerization gets initiated by a strong nucleophile such as an organolithium or a Grignard reagent. The most commonly used initiator for anionic polymerization is butyl lithium. Monomers involved in anionic polymerization must possess a vinyl group bonded to one or two electron-withdrawing groups. For instance,...
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The cationic polymerization mechanism consists of three steps: initiation, propagation, and termination. In the initiation step of the polymerization process, the π bond of a monomer gets protonated by the Lewis acid catalyst, which is formed from boron trifluoride and water. The protonation of the π bond generates a carbocation stabilized by the electron‐donating group. In the propagation step, the π bond of the second monomer acts as a nucleophile and attacks the...
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Related Experiment Video

Updated: May 20, 2025

Synthesis of Thermogelling PolyN-isopropylacrylamide-graft-chondroitin Sulfate Composites with Alginate Microparticles for Tissue Engineering
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Improving Complex Coacervate Tissue Adhesive Performance Using Bridging Polymer Chains.

Ayla N Kwant1,2,3,4, Julien S Es Sayed1,5, Nawal Aledlbi6,7

  • 1Polymer Science, Zernike Institute for Advanced Materials (ZIAM), University of Groningen, Groningen 9747AG, The Netherlands.

Biomacromolecules
|March 25, 2025
PubMed
Summary
This summary is machine-generated.

Bridging polymers enhance complex coacervate adhesives (CCAs) for tissue repair. Pretreatment with poly(allylamine hydrochloride) (pAH) improved adhesion on dynamic tissues by forming a bridging layer, increasing robustness.

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Area of Science:

  • Biomaterials Science
  • Polymer Chemistry
  • Tissue Engineering

Background:

  • Complex coacervates (CCAs) show promise as tissue adhesives due to tunable properties and wet adhesion.
  • Maintaining stable adhesion on soft, dynamic biological tissues is a significant challenge for current CCAs.

Purpose of the Study:

  • To investigate the use of a bridging polymer to enhance the adhesive properties of a poly(allylamine hydrochloride) (pAH) and polysulfopropyl methacrylate (pSPMA) based CCA.
  • To understand the mechanism by which bridging polymers improve CCA adhesion on biological substrates.

Main Methods:

  • Fabrication of a CCA from pAH and pSPMA, which solidifies via salt concentration changes.
  • Pretreatment of model hydrogels and biological tissues with pAH or pSPMA.
  • Measurement of adhesion energy and analysis of interfacial polymer distribution.

Main Results:

  • Pretreatment with pAH, but not pSPMA, significantly enhanced adhesion energy on both hydrogels and tissues.
  • A polymer-rich bridging layer formed at the interface due to pAH accumulation in superficial layers.
  • The pAH bridging layer increased the CCA's ability to withstand deformation before failure.

Conclusions:

  • Bridging polymers, specifically pAH, can significantly improve the adhesion of CCAs on dynamic tissues.
  • The mechanism involves the formation of an interfacial bridging layer that enhances mechanical robustness.
  • This strategy holds potential for advancing CCAs and other biomedical adhesives.