ArticleiScience2025
Stability and biocompatibility of hBD3 with different chiral configurations and their therapeutic efficacy in periodontitis.
Article in iScience, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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9 authors.
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Abstract
Periodontitis is characterized by progressive destruction of the periodontal attachment apparatus caused by dental plaque accumulation, which can lead to tooth loosening and permanent loss. Human β-defensin 3 (hBD3) exhibits broad-spectrum antibacterial activity and exerts critical immunomodulatory functions. Modifying amino acid chirality represents a novel strategy for the development of next-generation antibacterial agents. In this study, D-hBD3 and L-hBD3 were synthesized via solid-phase peptide synthesis, with recombinant hBD3 (r-hBD3) as control, and their therapeutic efficacy was evaluated in experimental periodontitis mice. Our findings demonstrated that D-hBD3 exhibited remarkable stability, potent antibacterial activity
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