Restructuring the Interface of Silk-Polycaprolactone Biocomposites Using Rigid-Flexible Agents

Natural fiber-reinforced biocomposites with excellent mechanical and biological properties have attractive prospects for internal medical devices. However, poor interfacial adhesion between natural silk fiber and the polymer matrix has been a disturbing issue for such applications. Herein, rigid-flexible agents, such as polydopamine (PDA) and epoxy soybean oil (ESO), were introduced to enhance the interfacial adhesion between Antheraea pernyi (Ap) silk and a common medical polymer, polycaprolactone (PCL). We compared two strategies of depositing PDA first (Ap- PDA-ESO) and grafting ESO first (Ap-ESO-PDA). The rigidflexible interfacial agents introduced multiple molecular interactions at the silk-PCL interface. The Ap-PDA-ESO strategy exhibited a greater enhancement in interfacial adhesion, and interfacial toughening mechanisms were proposed. This work sheds light on engineering strong and tough silk fiber-based biocomposites for biomedical applications.

Automated summary

Natural fiber-reinforced biocomposites with excellent mechanical and biological properties have attractive prospects for internal medical devices. However, poor interfacial adhesion between natural silk fiber and the polymer matrix has been a disturbing issue for such applications. In this study, rigid-flexible agents, such as polydopamine (PDA) and epoxy soybean oil (ESO), were introduced to enhance the interfacial adhesion between Antheraea pernyi (Ap) silk and polycaprolactone (PCL). The Ap-PDA-ESO strategy exhibited a greater enhancement in interfacial adhesion, and proposed interfacial toughening mechanisms.