Gangolli Riddhi, Pushalkar Smruti, Beutel Bryan G, Danna Natalie, Duarte Simone, Ricci John L, Fleisher Kenneth, Saxena Deepak, Coelho Paulo G, Witek Lukasz, Tovar Nick
Biomaterials Division, NYU Dentistry, New York, NY 10010, USA.
Center for Genomics and Systems Biology, Department of Biology, New York University, New York, NY 10003, USA.
Materials (Basel). 2024 Aug 17;17(16):4086. doi: 10.3390/ma17164086.
The purpose of this in vitro study was to develop calcium sulfate (CS)-based disks infused with an antimicrobial drug, which can be used as a post-surgical treatment modality for osteomyelitis. CS powder was embedded with 10% antibiotic, amoxicillin (AMX) or moxifloxacin (MFX), to form composite disks 11 mm in diameter that were tested for their degradation and antibiotic release profiles. For the disk degradation study portion, the single drug-loaded disks were placed in individual meshes, subsequently submerged in phosphate-buffered saline (PBS), and incubated at 37 °C. The disks were weighed once every seven days and analyzed via Fourier-transform infrared spectroscopy, X-ray diffraction, energy dispersive X-ray spectroscopy, and scanning electron microscopy. During the antibiotic release analysis, composite disks were placed in PBS solution, which was changed every 3 days, and analyzed for antibiotic activity and efficacy. The antibacterial effects of these sustained-release composites were tested by agar diffusion assay using () UA 159 as an indicator strain. The degradation data showed significant increases in the degradation of all disks with the addition of antibiotics. Following PBS incubation, there were significant increases in the amount of phosphate and decreases in the amount of sulfate. The agar diffusion assay demonstrated that the released concentrations of the respective antibiotics from the disks were significantly higher than the minimum inhibitory concentration exhibited against over a 2-3-week period. In conclusion, CS-antibiotic composite disks can potentially serve as a resorbable, osteoconductive, and antibacterial therapy in the treatment of bone defects and osteomyelitis.
本体外研究的目的是开发一种注入抗菌药物的硫酸钙(CS)基盘,其可作为骨髓炎的术后治疗方式。将CS粉末与10%的抗生素阿莫西林(AMX)或莫西沙星(MFX)混合,制成直径为11毫米的复合盘,并对其降解和抗生素释放情况进行测试。在盘片降解研究部分,将单药负载的盘片置于单独的网孔中,随后浸入磷酸盐缓冲盐水(PBS)中,并在37°C下孵育。每七天对盘片称重一次,并通过傅里叶变换红外光谱、X射线衍射、能量色散X射线光谱和扫描电子显微镜进行分析。在抗生素释放分析过程中,将复合盘片置于PBS溶液中,每3天更换一次溶液,并分析抗生素的活性和功效。以()UA 159作为指示菌株,通过琼脂扩散试验测试这些缓释复合材料的抗菌效果。降解数据显示,添加抗生素后所有盘片的降解均显著增加。在PBS孵育后,磷酸盐含量显著增加,硫酸盐含量显著降低。琼脂扩散试验表明,在2至3周的时间内,从盘片中释放的各抗生素浓度显著高于对()所显示的最低抑菌浓度。总之,CS-抗生素复合盘片在治疗骨缺损和骨髓炎方面可能具有可吸收、骨传导和抗菌治疗的作用。