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Microbial biofilms in catheter lumens are complex, multicellular communities of microorganisms encased in a self-produced extracellular polymeric substance (EPS) matrix consisting of polysaccharides, proteins, and extracellular DNA (Donlan, R. M., 2001, PMID: 11281858). These biofilms develop on the internal surfaces of indwelling medical devices, such as central venous catheters (CVCs) and urinary catheters, where they serve as a reservoir for persistent infections (StatPearls, 2023, NBK535361). The biofilm structure provides a physical and chemical barrier that protects embedded pathogens from host immune responses and increases their tolerance to systemic antibiotics by up to 1,000-fold compared to planktonic cells (CDC, 2011). Therapeutic interventions specifically target the biofilm by using antimicrobial lock solutions (e.g., taurolidine, ethanol), impregnated coatings (e.g., minocycline-rifampin), or enzymatic agents designed to degrade the EPS matrix (NIH, 2022). Eradicating these biofilms is essential for preventing catheter-related bloodstream infections (CRBSIs) and catheter-associated urinary tract infections (CAUTIs), which are major causes of morbidity in healthcare settings.
Disruption of the extracellular polymeric substance (EPS) matrix, inhibition of microbial adhesion, and bactericidal activity against sessile organisms.
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