Determination of antibiotics and detergent residues in decellularized tissue-engineered heart valves using LC-MS/MS.
Leticia KraftVictoria Stadler Tasca RibeiroLuciana Cristina Ferretti de Nazareno WollmannPaula Hansen SussFelipe Francisco TuonPublished in: Cell and tissue banking (2020)
Residual chemicals that are presented during tissue processing in human tissue banks can be a risk for the allograft recipient. Determine the residual concentrations of the antibiotics and detergent used in the process of human decellularized tissue-engineered heart valves stored in isotonic saline solution up to 18 months. A total of 24 human decellularized allografts were stored in sterile sodium chloride and analyzed immediately after the decellularization process (0 months) and after storage for 6, 12, and 18 months, which includes the use of sodium dodecyl sulfate (SDS) and antibiotics (cefoxitin, vancomycin hydrochloride, lincomycin hydrochloride, polymyxin B sulfate). These valves were used for suitability tests, the zone of inhibition evaluation, and direct contact cytotoxicity assay. The stock solution from 32 valves was used for LC-MS/MS analysis of antibiotics and SDS. Tissue samples from decellularized valves showed a zone of inhibition formation for S. aureus and B. subtilis, suggesting the presence of an inhibitory molecule in the tissue. Cytotoxicity tests were negative. Polymyxin B, vancomycin, and SDS were detected and quantified in human decellularized aortic and pulmonary allografts during all periods of the study. There were no traces of residual cefoxitin and lincomycin in the tissue stock solution. We found residual concentrations of the antibiotics and detergent used in the process of human decellularized tissue-engineered heart valves stored in isotonic saline solution up to 18 months.
Keyphrases
- endothelial cells
- aortic valve
- extracellular matrix
- induced pluripotent stem cells
- heart failure
- aortic valve replacement
- pluripotent stem cells
- tissue engineering
- transcatheter aortic valve replacement
- coronary artery
- pulmonary artery
- mass spectrometry
- pulmonary arterial hypertension
- multidrug resistant
- kidney transplantation
- ejection fraction
- tandem mass spectrometry