BL2                         My Program 


Biomaterials, Bio-fluid Dynamics and Biorheology


Using exogenous polymers to engineer biofilm viscoelasticity


October 20, 2025 (Monday) 10:10


Track 6 / Sweeney Ballroom C

(Click on name to view author profile)

  1. Bhattarai, Bikash (Texas Tech University)
  2. Christopher, Gordon F. (Texas Tech University)

(in printed abstract book)
Bikash Bhattarai and Gordon F. Christopher
Texas Tech University, Lubbock, TX 79410


Bhattarai, Bikash


biomaterials; biorheology


Using Exogenous Polymers to Engineer Biofilm Viscoelasticity Abstract A large percentage of bacteria exist in sessile communities surrounded by self-secreted extracellular polymeric substances (EPS), better known as biofilms. Biofilms are increasingly found in applications in which their viscoelasticity influences outcomes including bioremediation, wastewater cleanup, and/or biofuel production. Ideally, to improve outcomes, biofilm viscoelasticity could be manipulated to achieve a desired response. Exogenous polymers are well known to impact planktonic bacterial behavior and previous work from our lab has demonstrated they can also substantially alter biofilm mechanics. However, the potential influence of polymers on biofilm viscoelasticity is largely unexplored. Building on previous results, we investigate how exogenous polysaccharides with varying charge and molecular weights can be used to impact biofilm viscoelasticity in a controlled manner.

Biofilms of Pseudomonas aeruginosa, which has a well characterized EPS, are grown in the presence of negative, neutral, and positive polysaccharides of varying molecular weight at concentrations where there is no planktonic antibacterial effect. Passive microrheology was employed to evaluate biofilms viscoelasticity. Results showed that neutral polymers had minimal impact on biofilms viscoelasticity whereas all charged polymers, both anionic and cationic, exhibited a stiffening effect on biofilms. In addition, the increase in stiffening is linked to the stiffness of the individual polymer incorporated into the biofilm.