Antibacterial Activity of the Vancomycin and Cefotaxime-Incorporated Total Etch Adhesive System – An In Vitro Study

头孢噻肟 万古霉素 体外 胶粘剂 抗菌活性 微生物学 医学 化学 抗生素 生物 金黄色葡萄球菌 细菌 生物化学 遗传学 有机化学 图层(电子)
作者
M. S. Rangareddy,Md. Abdul Wahed,B. Shravan Kumar,Basa Srinivas Karteek,Chavva Lakshmi Charan Reddy,Jagrati Agrawal
出处
期刊:Journal of Pharmacy and Bioallied Sciences [Medknow Publications]
卷期号:16 (Suppl 2): S1705-S1710
标识
DOI:10.4103/jpbs.jpbs_1046_23
摘要

A BSTRACT Background: Marginal failure at the resin dentin interface promotes biofilm formation, which further leads to secondary caries and hypersensitivity. This likelihood also increases if residual bacteria are present following cavity preparation. In order to achieve a proper biological seal without jeopardizing bonding, efforts were made to functionalize the adhesive system with antibacterial activity. Aim and objectives: To appraise the antibacterial activity of a total-etch adhesive system against S . mutans with and without incorporation of antibiotics Vancomycin and Cefotaxime. Materials and Method: A commercially available 5th-generation total-etch bonding agent (Te-Econorm) was used. S. mutans broth had been standardized and streaked over Muller-Hinton agar culture medium and round wells about 6 mm in diameter were made in the centre of the agar plates. Each experimental group comprised 10 samples, which include: Group 1 - 30µg Cefotaxime, Group 2- 30µg Cefotaxime + Bonding agent, Group 3- 30µg Vancomycin, Group 4- 30µg Vancomycin + Bonding agent, Group 5- Bonding agent, and Group 6- No material. Inoculated culture plates were examined for the zone of inhibition after incubation at 37° C for 24 hours. Results: There was a significant difference in the mean diameter of zone of inhibition ( p =0.000), with the maximum exhibited by Group 4, followed by Group 3 and Group 2. The least zone of inhibition was exhibited by Groups 1 and 5. The negative control showed no zone of inhibition. Conclusion: The combination of Vancomycin and bonding agent had superior antibacterial activity against S. mutans in comparison to cefotaxime and bonding agent.
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