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April 24, 2026Biomacromolecules1 citationsOpen Access

Biofilm- and Spore-Disruptive Star-Shaped Poly( l -lysine)/Hyaluronic Acid Microgels for Targeted Oral Therapy of Clostridioides difficile Infection

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ILI Shiuan LinE-Da HospitalCCC Y ChouNational Cheng Kung UniversityYCYu‐Fang ChenChina Medical University

Key Points

  • The study aims to develop microgels for targeted oral therapy against Clostridioides difficile infection while preserving gut microbiota.
  • Formulated star-shaped poly(l-lysine) into hyaluronic acid microgels for oral delivery.
  • Evaluated antimicrobial effects in a murine model of Clostridioides difficile infection.
  • Analyzed spore inhibition and biofilm disruption compared to vancomycin.
  • G3-PLL9 microgels showed superior spore and biofilm disruption than vancomycin.
  • Treatment reduced clinical symptoms and tissue damage in murine models.
  • Microgels preserved gut microbiota better than conventional antibiotics.

Abstract

Clostridioides difficile infection (CDI) remains a major healthcare challenge due to recurrent disease, spore persistence, and biofilm-associated tolerance, while conventional antibiotics often disrupt gut microbiota. Here, we report a star-shaped poly(l-lysine) dendrimer (G3-PLL9) formulated into hyaluronic acid-based microgels for targeted oral delivery to the inflamed colon. G3-PLL9 exhibited potent antimicrobial activity, including rapid bactericidal effects, superior spore inhibition compared with vancomycin, and robust biofilm disruption at subinhibitory concentrations. In a murine CDI model, rectal administration of G3-PLL9 alleviated clinical symptoms, reduced tissue damage, and lowered recurrence risk. To enable oral therapy, G3-PLL9 was incorporated into hyaluronic acid microgels, achieving site-specific release through hyaluronidase-mediated degradation in the inflamed colon. Importantly, treatment preserved commensal gut microbiota more effectively than vancomycin. Collectively, these findings highlight G3-PLL9 microgels as a microbiota-sparing therapeutic that targets multiple stages of CDI pathogenesis─including spores and biofilms─and demonstrate their potential for clinical translation.

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Cite This Study

Lin et al. (2026) studied this question.

synapsesocial.com/papers/69eb0ac4553a5433e34b4b0dhttps://doi.org/10.1021/acs.biomac.5c02037
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