Andrade Del Olmo Jon, Pérez-Álvarez Leyre, Sáez Martínez Virginia, Benito Cid Sandra, Pérez González Raúl, Vilas-Vilela José Luis, Alonso José María
i+Med S. Coop. Parque Tecnológico de Álava, Albert Einstein 15, Nave 15, 01510 Vitoria-Gasteiz, Spain.
Grupo de Química Macromolecular (LABQUIMAC), Departamento de Química Física, Facultad de Ciencia y Tecnología, Universidad del País Vasco UPV/EHU, 48940 Leioa, Spain.
Gels. 2022 Apr 6;8(4):223. doi: 10.3390/gels8040223.
Hyaluronic acid (HA) injectable biomaterials are currently applied in numerous biomedical areas, beyond their use as dermal fillers. However, bacterial infections and painful inflammations are associated with healthcare complications that can appear after injection, restricting their applicability. Fortunately, HA injectable hydrogels can also serve as drug delivery platforms for the controlled release of bioactive agents with a critical role in the control of certain diseases. Accordingly, herein, HA hydrogels were crosslinked with 1 4-butanediol diglycidyl ether (BDDE) loaded with cefuroxime (CFX), tetracycline (TCN), and amoxicillin (AMX) antibiotics and acetylsalicylic acid (ASA) anti-inflammatory agent in order to promote antibacterial and anti-inflammatory responses. The hydrogels were thoroughly characterized and a clear correlation between the crosslinking grade and the hydrogels' physicochemical properties was found after rheology, scanning electron microscopy (SEM), thermogravimetry (TGA), and differential scanning calorimetry (DSC) analyses. The biological safety of the hydrogels, expected due to the lack of BDDE residues observed in H-NMR spectroscopy, was also corroborated by an exhaustive biocompatibility test. As expected, the in vitro antibacterial and anti-inflammatory activity of the drug-loaded HA-BDDE hydrogels was confirmed against by significantly decreasing the pro-inflammatory cytokine levels.
透明质酸(HA)可注射生物材料目前除了用作真皮填充剂外,还应用于众多生物医学领域。然而,细菌感染和疼痛性炎症与注射后可能出现的医疗并发症相关,限制了它们的适用性。幸运的是,HA可注射水凝胶还可以作为药物递送平台,用于控制释放对某些疾病的控制起关键作用的生物活性剂。因此,在此,HA水凝胶与负载头孢呋辛(CFX)、四环素(TCN)和阿莫西林(AMX)抗生素以及乙酰水杨酸(ASA)抗炎剂的1,4 - 丁二醇二缩水甘油醚(BDDE)交联,以促进抗菌和抗炎反应。对水凝胶进行了全面表征,在流变学、扫描电子显微镜(SEM)、热重分析(TGA)和差示扫描量热法(DSC)分析后,发现交联程度与水凝胶的物理化学性质之间存在明显相关性。由于在核磁共振氢谱(H-NMR)中未观察到BDDE残留,水凝胶的生物安全性也通过详尽的生物相容性测试得到了证实。正如预期的那样,载药HA-BDDE水凝胶的体外抗菌和抗炎活性通过显著降低促炎细胞因子水平得到了证实。