Strickland Aaron D, Lang Clemens, Manhartseder Stefan, Reichsoellner Raffael, Valliant Esther, Schädl Barbara, Gulle Heinz, Slezak Paul
iFyber LLC, Ithaca, New York, USA.
Ludwig Boltzmann Institute for Traumatology, The Research Center in Cooperation with AUVA, Vienna, Austria.
Surg Infect (Larchmt). 2023 Feb;24(1):82-90. doi: 10.1089/sur.2022.315.
Fibrin sealants are used as antimicrobial-releasing carriers for preventing surgical site infections; however, it is important to determine the release kinetics and antimicrobial effects of drugs added to fibrin sealants and the effects of drugs on clot/clotting properties. The antimicrobial and antibiofilm activity of cefazolin, colistin, gentamicin, oxacillin, tobramycin, and silver nitrate released from fibrin sealant were characterized using in vitro and ex vivo assays against bacteria commonly found on the skin. The effects of antimicrobial agents on the physical structure of the fibrin sealant were assessed with scanning electron microscopy (SEM) and on the clotting rate and strength of fibrin clots using run-off tests and rheology. Generally, antibiotic agents were released gradually from fibrin sealant and were stable after release, with antimicrobial effects evident up to three days. Cefazolin, gentamicin, and oxacillin prevented biofilm formation of in porcine skin explants; gentamicin and colistin prevented biofilm formation of . Gentamicin, cefazolin, colistin, and tobramycin did not affect the structural integrity or viscoelastic properties of fibrin sealant; changes were observed with oxacillin (SEM) and particularly silver nitrate (SEM and rheology). No antimicrobial agents caused deterioration of clotting time (run-off tests). From the antimicrobial agents tested, gentamicin and cefazolin showed prolonged release from fibrin sealant, sustained antimicrobial activity, and biofilm prevention properties against ; similar results were observed for gentamicin and colistin against . For each of these findings, the physical structure of the fibrin sealant, clotting rate, and strength of fibrin clots were unaffected.
纤维蛋白密封剂被用作释放抗菌剂的载体以预防手术部位感染;然而,确定添加到纤维蛋白密封剂中的药物的释放动力学和抗菌效果以及药物对凝块/凝血特性的影响很重要。使用体外和离体试验对从纤维蛋白密封剂中释放的头孢唑林、黏菌素、庆大霉素、苯唑西林、妥布霉素和硝酸银针对皮肤上常见细菌的抗菌和抗生物膜活性进行了表征。使用扫描电子显微镜(SEM)评估抗菌剂对纤维蛋白密封剂物理结构的影响,并使用径流试验和流变学评估对纤维蛋白凝块的凝血速率和强度的影响。一般来说,抗生素从纤维蛋白密封剂中逐渐释放,释放后稳定,抗菌效果在三天内明显。头孢唑林、庆大霉素和苯唑西林可防止猪皮肤外植体中生物膜的形成;庆大霉素和黏菌素可防止生物膜的形成。庆大霉素、头孢唑林、黏菌素和妥布霉素不影响纤维蛋白密封剂的结构完整性或粘弹性;观察到苯唑西林(SEM)尤其是硝酸银(SEM和流变学)有变化。没有抗菌剂导致凝血时间恶化(径流试验)。在所测试的抗菌剂中,庆大霉素和头孢唑林从纤维蛋白密封剂中释放时间延长,具有持续的抗菌活性和针对生物膜的预防特性;庆大霉素和黏菌素针对生物膜也观察到类似结果。对于这些发现中的每一个,纤维蛋白密封剂的物理结构、凝血速率和纤维蛋白凝块的强度均未受影响。