Toward clinical translation: montmorillonite-enhanced Lactobacillus biofilm alleviates colitis by modulating the gut microbiota-bile acid axis

  • Mater Today Bio. 2026 May 8:38:103211. doi: 10.1016/j.mtbio.2026.103211.
Zhongyuan Wang  1 Feng Zhu  1 Jie Zhang  1 Kangkang Feng  2 Waresi Abudourexiti  1 Song Li  1 Yanzhe Guo  1 Mingfei Chen  1 Zeqian Yu  1 Lei Zhao  3  4 Zhen Guo  5 Chao Ding  6 Jianfeng Gong  1
Affiliations
  • 1. Department of General Surgery, Jinling Hospital, Affiliated Hospital of Medical School, Nanjing University, Nanjing, China.
  • 2. State Key Laboratory of Pharmaceutical Biotechnology, Chemistry and Biomedicine Innovation Center [ChemBIC], Jiangsu Key Laboratory of Molecular Medicine, Medical School of Nanjing University, Nanjing, China.
  • 3. Department of Anorectal Surgery, The Quzhou Affiliated Hospital of Wenzhou Medical University, Quzhou People' s Hospital, Quzhou, Zhejiang, China.
  • 4. Department of General Surgery, Jinling Clinical Medical College, Nanjing University of Chinese Medicine, Nanjing, Jiangsu, China.
  • 5. Department of General Surgery, Nanjing Women and Children's Healthcare Hospital, Women's Hospital of Nanjing Medical University, Nanjing, China.
  • 6. Department of General Surgery, Nanjing Drum Tower Hospital, Affiliated Hospital of Medical School, Nanjing University, Nanjing, China.
Abstract

Oral probiotics hold therapeutic potential for ulcerative colitis (UC), but their low bioavailability greatly limits clinical efficacy. Here, we designed a montmorillonite-Lactobacillus acidophilus biofilm (MLB) delivery strategy to enhance probiotic stability, intestinal adhesion, and therapeutic efficiency. MLB was prepared by inducing the clinically common strain Lactobacillus acidophilus to form biofilms on montmorillonite, an antidiarrheal agent widely used in clinics. The in vitro assays demonstrated that montmorillonite significantly promoted biofilm formation, thereby improving Bacterial survival in gastrointestinal conditions and enhancing mucosal adhesion. In vivo, MLB showed superior efficacy in alleviating DSS-induced colitis compared with free bacteria or non-biofilm mixtures. Mechanistically, MLB remodeled gut microbiota composition and restored microbial bile acid metabolism through elevated bile salt hydrolase activity. This led to increased production of secondary bile acids, which in turn promoted anti-inflammatory macrophage polarization and facilitated inflammation resolution. Together, these findings demonstrate that MLB enhances the efficacy of oral probiotics by targeting the microbiota-bile acid-immune axis, representing a safe and practical approach for UC treatment.

Keywords
Bile acid metabolism; Biofilm; Oral probiotic delivery; Ulcerative colitis.
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