生物利用度
纳米技术
灵活性(工程)
并行传输
艾塞那肽
胰岛素释放
化学
胰岛素
生长素
生化工程
风险分析(工程)
口服途径
计算机科学
弹性(材料科学)
作者
Xihua Liu,Shuangjian Li,Guodong Wu,Jia Wenzhe,Yiguo Zhao,Yapeng Fang,Yiping Cao
标识
DOI:10.1016/j.bioactmat.2025.11.020
摘要
Oral delivery of biologics presents a formidable challenge: achieving high bioavailability without compromising gastrointestinal barrier integrity or clinical scalability—a trilemma that remains unaddressed by existing chemical permeation enhancers, ligand-modified nanoparticles, or exosome platforms. Here, we repurpose β-lactoglobulin (BLG) nanofibrils that resolve this challenge through a unique “enhance-degrade-restore” mechanism. In vivo, these nanofibrils enable oral insulin bioavailability reaching 10.2–12.3 %, and long-term safety studies confirm the absence of intestinal damage. Mechanistic studies reveal that the nanofibrils facilitate Ca2+ influx-induced calpain activation to enhance paracellular permeability, followed by protease-mediated degradation that ensures timely restoration of barrier integrity. Moreover, nanofibrils maintain full adjuvant activity when integrated into commercial milk products, highlighting their formulation flexibility and robustness. This work introduces a sustainable “waste-to-nanomedicine” strategy that unites high-efficiency peptide delivery with environmentally responsible nanomaterial design.
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