Tihan Graţiela Teodora, Ungureanu Camelia, Rău Ileana, Zgârian Roxana Gabriela, Barbaresso Răzvan Constantin, Albu Kaya Mădălina Georgiana, Dinu-Pîrvu Cristina-Elena, Ghica Mihaela Violeta
Department of General Chemistry, Faculty of Chemical Engineering and Biotechnology, National University of Science and Technology Politehnica of Bucharest, 1-7 Gheorghe Polizu Street, 011061 Bucharest, Romania.
Department of Collagen, Division of Leather and Footwear Research Institute, National Research and Development Institute for Textiles and Leather, 93 Ion Minulescu Str., 031215 Bucharest, Romania.
Materials (Basel). 2025 Aug 28;18(17):4029. doi: 10.3390/ma18174029.
Collagen-based biomaterials are increasingly explored in dentistry for their ability to deliver drugs locally and support healing. In this study, we developed chlortetracycline-loaded collagen sponges aimed at preventing postoperative infections. Five formulations were prepared by lyophilization, each with the same collagen-to-drug ratio but different glutaraldehyde (GA) concentrations: 0%, 0.25%, 0.5%, 0.75%, and 1% (/) relative to dry collagen. The sponges were characterized using FT-IR and UV-VIS-NIR spectroscopy, and their swelling capacity, enzymatic stability, and drug release kinetics were evaluated. Antibacterial activity was tested against , , and . Statistical differences between formulations were assessed using one-way ANOVA followed by Tukey's post hoc test ( < 0.05). All sponges released the antibiotic rapidly within the first 60 min, followed by a sustained release for up to 10 h. The non-crosslinked sponge showed the highest antimicrobial effect, while the 0.25% GA formulation offered a good balance between stability and bioactivity. While higher cross-linking enhanced structural stability, it progressively reduced antimicrobial efficacy, highlighting a crucial design trade-off. These findings underline the need to fine-tune cross-linking conditions to achieve both durability and strong antimicrobial action in collagen-based drug delivery systems for dental applications.
基于胶原蛋白的生物材料因其局部给药和促进愈合的能力而在牙科领域得到越来越多的探索。在本研究中,我们开发了载有金霉素的胶原蛋白海绵,旨在预防术后感染。通过冻干制备了五种配方,每种配方的胶原蛋白与药物比例相同,但戊二醛(GA)浓度不同:相对于干胶原蛋白分别为0%、0.25%、0.5%、0.75%和1%(/)。使用傅里叶变换红外光谱(FT-IR)和紫外-可见-近红外光谱(UV-VIS-NIR)对海绵进行表征,并评估其溶胀能力、酶稳定性和药物释放动力学。测试了对 、 和 的抗菌活性。使用单因素方差分析(one-way ANOVA),然后进行Tukey事后检验( < 0.05)评估配方之间的统计学差异。所有海绵在最初60分钟内迅速释放抗生素,随后持续释放长达10小时。未交联的海绵显示出最高的抗菌效果,而0.25% GA配方在稳定性和生物活性之间提供了良好的平衡。虽然更高程度的交联增强了结构稳定性,但它逐渐降低了抗菌效果,突出了一个关键的设计权衡。这些发现强调了在牙科应用的基于胶原蛋白的药物递送系统中微调交联条件以实现耐久性和强大抗菌作用的必要性。