A New Antibiotic-Loaded Sol-Gel can Prevent Bacterial Intravenous Catheter-Related Infections.
John Jairo Aguilera-CorreaRosa Vidal-LasoRafael Alfredo Carias-CálixBeatriz ToiracAmaya García-CasasDiego Velasco-RodríguezPilar Llamas-SilleroAntonia Jiménez-MoralesJaime Esteban MorenoPublished in: Materials (Basel, Switzerland) (2020)
The aim of this study was to evaluate the effectiveness of a moxifloxacin-loaded organic-inorganic sol-gel (A50) by locally preventing the catheter-related bloodstream infection (CRBSI) provoked by Staphylococcus epidermidis (S. epidermidis) and the effect resulting from its hydrolytic degradation on coagulation by using a rabbit in-vivo model. A50 coating can completely inhibit growth and would locally prevent CRBSI provoked by S. epidermidis. None of the coagulation blood parameters showed a significant difference constant over time between the control catheter group and the A50-coated catheter group, despite the visible silica release resulting from physiological A50 sol-gel degradation detected in serum at least during the first week. At pathological level, foreign body reaction was present in both of types of catheter, and it was characterized by the presence of macrophages and foreign body giant cell. However, this reaction was different in each group: the A50-coated catheter group showed a higher inflammation with histiocytes, which were forming granuloma-like aggregates with an amorphous crystalline material inside, accompanied by other inflammatory cells such as plasma cells, lymphocytes and mast cells. In conclusion, A50 coating a venous catheter showed excellent bactericidal anti-biofilm response since it completely inhibited S. epidermidis biofilm development and, far from showing procoagulant effects, showed slightly anticoagulant effects.
Keyphrases
- biofilm formation
- ultrasound guided
- induced apoptosis
- staphylococcus aureus
- pseudomonas aeruginosa
- oxidative stress
- drug delivery
- randomized controlled trial
- wound healing
- systematic review
- cell cycle arrest
- escherichia coli
- cystic fibrosis
- cancer therapy
- room temperature
- low dose
- signaling pathway
- hyaluronic acid
- multidrug resistant
- pi k akt
- klebsiella pneumoniae