
Lie Ma*,**,#, Ailin Shen**,#, Jiayu Gu*, Honghua Hu**, Guoshou Jin**, Jiangfeng Cai**,
Bing Feng**, Xiaodong He**,†
, and Jun Ling*,† 
*MOE Key Laboratory of Macromolecular Synthesis and Functionalization, Department of Polymer Science and Engineering, Zhejiang University, Hangzhou 310058, China
**Zhejiang Wedu Medical Co., Ltd., Hengdian Industrial Zone, Dongyang 322118, China
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Poly(L-lactide) (PLLA) microspheres have excellent biocompatibility and biodegradability and already been applied as biomedical materials in tissue engineering. However, hydrophobic PLLA exhibits low degradation rate, bringing an obstacle to the generation of new tissues. Incorporating hydrophilic blocks endows diblock copolymer poly(L-lactide)-b-poly(ethylene glycol) (PELA) with improved biodegradability. In the present contribution, degradation behaviors of PLLA and PELA microspheres including mass loss, molecular weight changes, viscosity variation and microscopic morphology difference are monitored and analyzed. The accelerating of PEG blocks is validated. The addition of enzymes including proteinase K and lipase shows negligible effect on the degradation, thus hydrolysis in bulk polymer is proved to be the dominant degradation mechanism. Degradation characteristics including accelerates degradation rate, low surface degradation efficiency and hydrolysis nature make PELA microspheres promising candidate for dermal filler materials.
Keywords: degradation, biomaterials, sustainable materials, block copolymers.
This Article2026; 50(2): 220-225
Published online Mar 25, 2026
Correspondence to*MOE Key Laboratory of Macromolecular Synthesis and Functionalization, Department of Polymer Science and Engineering, Zhejiang University, Hangzhou 310058, China
**Zhejiang Wedu Medical Co., Ltd., Hengdian Industrial Zone, Dongyang 322118, China