A New In Vitro Blood Flow Model for the Realistic Evaluation of Antimicrobial Surfaces

Abstract

Device‐associated bloodstream infections can cause serious medical problems and cost‐intensive post‐infection management, defining a need for more effective antimicrobial coatings. Newly developed coatings often show reduced bacterial colonization and high hemocompatibility in established in vitro tests, but fail in animal studies or clinical trials. The poor predictive power of these models is attributed to inadequate representation of in vivo conditions. Here, we present a new single‐pass blood flow model, with simultaneous incubation of the test surface with bacteria and freshly‐drawn human blood. The flow model is validated by comparative analysis of a recently developed set of anti‐adhesive and contact‐killing polymer coatings, and the corresponding uncoated polycarbonate surfaces. The results confirm the model's ability to differentiate the antimicrobial activities of the studied surfaces. Blood activation data correlate with bacterial surface coverage: low bacterial adhesion is associated with low inflammation and hemostasis. Shear stress correlates inversely with bacterial colonization, especially on anti‐adhesive surfaces. The introduced model is concluded to enable the evaluation of novel antimicrobial materials under in vivo‐like conditions, capturing interactions between bacteria and biomaterials surfaces in the presence of key components of the ex vivo host response.This article is protected by copyright. All rights reserved

Bioinspired super-hydrophilic zwitterionic polymer armor combats thrombosis and infection of vascular catheters

“…Furthermore, the long-term indwelling of catheters increases the risk of these complications occurring simultaneously. Increasing evidence suggests a pathophysiological relationship between thrombus formation and biofilm growth on the surface of catheters [ [15] , [16] , [17] ]. Proteins in thrombi, such as fibronectin and fibrin, are conducive to bacterial adhesion, facilitating the development of biofilms.…”