Sun Xujie, Shan Xiaoting, Zhu Binyu, Cai Ying, He Zongyan, Zhou Lingli, Yin Lixuan, Liu Yiran, Liu Kaiyue, Zhang Tian, Yang Ning, Li Yaping, Lang Tianqun
Lingang Laboratory, Shanghai, 200031, China.
State Key Laboratory of Drug Research & Center of Pharmaceutics, Shanghai Institute of Materia Medica, Chinese Academy of Sciences, Shanghai, 201203, China.
Adv Healthc Mater. 2025 Feb;14(4):e2403587. doi: 10.1002/adhm.202403587. Epub 2024 Dec 15.
The gut microbiota exerts inhibitory effects on the occurrence and progression of colorectal cancer (CRC) through various mechanisms. Compared to traditional microbiota regulation methods, prebiotics and probiotics demonstrate significant advantages in terms of safety and patient adaptability. Their synergy not only improves the intestinal environment but also enhances the host's anti-tumor immune response. 5-Fluorouracil (5-FU) is a first-line chemotherapy drug that has a short half-life and low bioavailability. However, if administered in an untargeted manner, 5-FU also causes adverse reactions. Liposomes can improve the pharmacokinetic profile of drugs and provide targeted delivery to the tumor site, thereby reducing side effects. In this work, a 5-FU-loaded liposome is modified with the prebiotic xylan derivative Sxy and the probiotic Akkermansia muciniphila active phospholipid homolog 1,2-dipalmitoylphosphatidy-lethanolamine (DPPE) to construct FLSK. The latter effectively prolongs the intestinal transport and release of 5-FU, maintaining high drug concentrations at the tumor site. FLSK is found to inhibit tumor growth and significantly extends the survival period of mice. In addition, FLSK promotes anti-tumor immunity and regulation of the gut microbiota. Combining the merits of prebiotics and probiotics, FLSK provides a potential strategy for integrating chemotherapy with gut microbiota regulation therapy for the treatment of CRC.
肠道微生物群通过多种机制对结直肠癌(CRC)的发生和发展发挥抑制作用。与传统的微生物群调节方法相比,益生元和益生菌在安全性和患者适应性方面具有显著优势。它们的协同作用不仅改善肠道环境,还增强宿主的抗肿瘤免疫反应。5-氟尿嘧啶(5-FU)是一种一线化疗药物,半衰期短且生物利用度低。然而,如果以非靶向方式给药,5-FU也会引起不良反应。脂质体可以改善药物的药代动力学特征,并提供肿瘤部位的靶向递送,从而减少副作用。在这项工作中,用益生元木聚糖衍生物Sxy和益生菌嗜黏蛋白阿克曼氏菌活性磷脂同系物1,2-二棕榈酰磷脂酰乙醇胺(DPPE)修饰负载5-FU的脂质体,构建FLSK。后者有效地延长了5-FU在肠道的转运和释放,在肿瘤部位维持高药物浓度。发现FLSK可抑制肿瘤生长并显著延长小鼠的生存期。此外,FLSK促进抗肿瘤免疫和肠道微生物群的调节。结合益生元和益生菌的优点,FLSK为将化疗与肠道微生物群调节疗法相结合治疗CRC提供了一种潜在策略。