Drug pipeline
Full profile accessExplore the programs pursuing this target and their development progress.
- Drug candidates
- Developers
- Development stage
Target intelligence / Profile preview
The bacterial cell surface and extracellular biofilm matrix constitute a complex, protective microenvironment that shields microbial communities from host immune defenses and antimicrobial agents. The matrix is primarily composed of extracellular polymeric substances (EPS), including exopolysaccharides, proteins, lipids, and extracellular DNA (eDNA), which provide structural stability and facilitate surface attachment (Flemming & Wingender, 2010, Nature Reviews Microbiology). This assembly acts as a physical and chemical barrier, contributing to the high levels of antibiotic tolerance observed in chronic infections such as those associated with cystic fibrosis, indwelling medical devices, and non-healing wounds (Hall-Stoodley et al., 2004, Nature Reviews Microbiology). Therapeutic targeting of the matrix involves the use of enzymes like DNase I (Dornase alfa) to degrade eDNA or glycosyl hydrolases to break down polysaccharides, thereby destabilizing the biofilm architecture (Tetz & Tetz, 2010, Antimicrobial Agents and Chemotherapy). By disrupting these surfaces, drugs aim to increase the susceptibility of the encased bacteria to conventional antibiotics and facilitate their clearance by the host immune system (Karygianni et al., 2020, Frontiers in Cellular and Infection Microbiology).
Enzymatic degradation of extracellular DNA and polysaccharides, chelation of stabilizing divalent cations, inhibition of matrix synthesis, and disruption of cell wall/membrane integrity to enhance antibiotic penetration and immune clearance.
7 more in the full profile.
Beyond the preview
Explore the evidence, development activity, and competitive landscape with Gosset’s full data platform.
Explore the programs pursuing this target and their development progress.
Follow the clinical studies evaluating therapies directed at this target.
Compare approaches across drug candidates, modalities, and indications.
Investigate the research and source evidence behind target biology and development.
Explore patent activity around therapies and technologies addressing this target.
Connect target biology, drug development, and emerging evidence in your research.
See how Gosset can support your research on Bacterial cell surface and extracellular biofilm matrix (EPS matrix).