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Updated: May 14, 2025

Surgical Retrieval, Isolation and In vitro Expansion of Human Anterior Cruciate Ligament-derived Cells for Tissue Engineering Applications
Published on: April 30, 2014
Optimizing Vancomycin Soaking Protocols for Anterior Cruciate Ligament Reconstruction
Wachiraphan Parinyakhup1, Piya Chavalparit1, Dennapa Saeloh Sotthibandhu2
1Department of Orthopedics, Faculty of Medicine, Prince of Songkla University, Hat Yai 90110, Songkhla, Thailand.
Abstract:
Background/Objectives: Although current guidelines recommend soaking anterior cruciate ligament autografts in 5 mg/mL vancomycin for 20 min to reduce postoperative infections, practical constraints often limit soaking to 5 min. This study aimed to evaluate the bacterial eradication efficacy and cytotoxicity of various vancomycin concentrations and application methods within a 5 min soaking period. Methods: Human semitendinosus tendons were inoculated with one of four bacterial pathogens, including Staphylococcus aureus, Staphylococcus epidermidis with biofilm-producing and non-biofilm-producing strains, and Enterococcus faecalis. Samples were treated by direct soaking in 5 mg/mL vancomycin or gauze wrapping with 2.5, 5, or 10 mg/mL vancomycin for 5 min. Bacterial elimination was assessed using agar plating. Cytotoxicity toward human tenocytes and mesenchymal stem cells was evaluated at 6, 12, 24, and 72 h. Vancomycin release was measured using an immunofluorescence assay with the Cobas C311 Roche analyzer. Results: Complete bacterial eradication was achieved by direct soaking at 5 mg/mL and gauze wrapping at 10 mg/mL. All concentrations maintained cell viability above 70%, with no significant cytotoxicity. Vancomycin release was the highest in the direct soaking group, while it remained below the toxicity threshold for chondrocytes. Conclusions: Direct soaking at 5 mg/mL and gauze wrapping at 10 mg/mL for 5 min effectively eradicated bacterial contamination without compromising cell viability.

