Strong and Tough Polylactide via Branched Rigid-Flexible Hybrid Segments

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Authors: Ning Du, Yinglei Ma, Zhen Wu, Yongqiang Wen, Heng An, Guojie Wang
Cited by: 1
References: 62

Abstract

Polylactide (PLA), as a biodegradable polymer, holds great promise in biomedicine, packaging, and sustainable materials. However, inherent brittleness and low fracture toughness limit its practical applications. To address the strength–toughness trade-off, we designed and prepared a high-molecular weight ( M η > 260 kDa) branched block copolymer, branched polyethylene glycol-polylactide (B-PELA). This architecture was constructed by using a branched polyester as a macroinitiator for the ring-opening polymerization of l -lactide, successfully integrating rigid PLA and flexible polyethylene glycol (PEG) segments. Specifically, the long-chain branched physical network significantly enhances chain entanglements to retain structural integrity for high strength. Concurrently, the branched PEG nodes act as topological anchors to efficiently dissipate strain energy and guide extensive plastic deformation. The synergy enables B-PELA to achieve high tensile strength (64.4 MPa), high elongation at break (52%), and superior toughness (30.6 MJ·m –3 ). Furthermore, B-PELA exhibits excellent biocompatibility and hemocompatibility. Therefore, this work provides a novel strategy for constructing high-performance PLA, enabling its potential application in bioimplants.

Fields of Study & Subjects

biodegradable polymer synthesis and properties Polymer Foaming and Composites Polymer composites and self-healing

Publication details

Journal / source
ACS Applied Polymer Materials
Publisher
American Chemical Society (ACS)
Volume
8
Issue
11
Pages
8913–8923
Publication date
20 May 2026
Language
EN