
FOLLOWUS
Key Laboratory for Waste Plastics Biocatalytic Degradation and Recycling, College of Biotechnology and Pharmaceutical Engineering, Nanjing Tech University, Nanjing 211816, China
State Key Laboratory of Materials—Oriented Chemical Engineering, Nanjing Tech University, Nanjing 211816, China
Jiangsu National Synergetic Innovation Center for Advanced Materials (SICAM), Nanjing Tech University, Nanjing 211816, China
*Corresponding authors. E-mail addresses:xlzhou@njtech.edu.cn(X. Zhou)
*Corresponding authors. E-mail addresses:yujia_peng@njtech.edu.cn(Y. Peng).
收稿:2025-09-16,
修回:2026-01-15,
录用:2026-02-01,
网络首发:2026-04-03,
纸质出版:2026-07
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Lu Jianqi, Fan Lingling, Wang Yihu, 等. Controllable self-biodegradation of polycaprolactone/polyurethane composite sutures enabled by random heteropolymers-immobilized lipase[J]. 中国化学工程学报(英文), 2026,95(7):139-150.
Lu Jianqi, Fan Lingling, Wang Yihu, et al. Controllable self-biodegradation of polycaprolactone/polyurethane composite sutures enabled by random heteropolymers-immobilized lipase[J]. Chinese Journal of Chemical Engineering, 2026, 95(7): 139-150.
Lu Jianqi, Fan Lingling, Wang Yihu, 等. Controllable self-biodegradation of polycaprolactone/polyurethane composite sutures enabled by random heteropolymers-immobilized lipase[J]. 中国化学工程学报(英文), 2026,95(7):139-150. DOI:
Lu Jianqi, Fan Lingling, Wang Yihu, et al. Controllable self-biodegradation of polycaprolactone/polyurethane composite sutures enabled by random heteropolymers-immobilized lipase[J]. Chinese Journal of Chemical Engineering, 2026, 95(7): 139-150. DOI:
Current absorbable sutures face challenges in matching heterogeneous tissue healing timelines
leading to postoperative complications from delayed degradation. Thus
self-biodegradable polycaprolactone/polyurethane (PCL/PU) composite sutures
via
electrospinning
incorporating
Burkholderia cepacia
lipase (BCL) stabilized by random heteropolymers (RHP) was developed in this research. RHP can maintain BCL activity retention at 40%—90% in organic solvents. The PCL70/PU30 suture exhibited optimal mechanics (tensile strength was (28.44 ± 1.25) MPa and Young's modulus was (42.43 ± 5.3) MPa)
following the incorporation of the BCL-RHP complex
the suture's key mechanical properties were largely maintained and remained within the range compatible with typical suture applications. Enzyme-loading gradients (0.05%—0.5% (mass)) enabled precise degradation control. 0.5% (mass) enzyme-loaded sutures fully disintegrated spontaneously in simulated wound fluid within 15 days
this timeframe aligns with the typical epidermal healing cycle (approximately 2 weeks)
suggesting the potential for achieving dynamic degradation-healing synchronization
in vivo
. In addition
functionalization of self-biodegradable composite sutures was achieved by embeddin
g thymol for synergistic bioactivity. Thymol achieved a cumulative release of 86.76% ± 1.34% over 120 h
endowing the self-biodegradable composite sutures with sustained antioxidant (79.85% ABTS
+
scavenging rate) and antibacterial activity (significantly suppressing the growth of
Staphylococcus aureus
). Concurrently
the self-biodegradable composite sutures demonstrated favorable cytocompatibility in L929 fibroblast cell. The RHP-enabled enzyme stabilization strategy overcomes clinical-ecological limitations of conventional sutures
offering programmable degradation and multifunctionality for precision medicine.
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