Halimeda gracilis as a bioactive resource: exploring its antioxidant, antibiofilm, anti-inflammatory, and antibacterial potential for dental applications.

Biomaterial investigations in dentistry Pub Date : 2025-05-14 eCollection Date: 2025-01-01 DOI:10.2340/biid.v12.43612
Dileepkumar Hemamalini, S Shantha Sundari, K M Shahul Hameed Faizee, Sivakamavalli Jeyachandran
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Abstract

Aim: This study aimed to evaluate the antibacterial, antibiofilm, antioxidant and anti-inflammatory properties and of Halimeda gracilis extracts.

Materials and methods: The H. gracilis sample was washed and extracted using methanol. The mixture was homogenized using a blender and centrifuged at high speed (10,000 × g) for 2 min, then stirred at room temperature for 30 min using magnetic stirrer, to ensure thorough extraction. Afterward, it was centrifuged at 5,000 × g for 10 min to separate the dissolved components from undissolved debris. Following this antioxidant activity was assessed using DPHH assay, the antimicrobial effects were tested against Streptococcus mutans, Escherichia coli, Enterococcus faecalis and Shigella sonnei using Kirby-Bauer disk diffusion, biofilm inhibition assay was done to assess biofilm inhibition against S. mutans, E. coli, E. faecalis and S. sonnei. Finally, the anti-inflammatory activities of the H. gracilis were determined using a modified version of the BSA assay.

Results: When tested against S. mutans, E. coli, E. faecalis, and S. sonnei strains, the antimicrobial evaluation revealed that the extract successfully inhibited biofilm formation when tested against the same organism, and it also demonstrated increased activity with increasing concentration. The zone of inhibition progressively expanded with increasing concentration, reaching a maximum of 17 mm ± 0.1 for 100 µg/mL. In terms of antioxidant activity, the H. gracilis metholic extract gradually increased from 10 µg/mL to a higher activity at 40 µg/mL in comparison to the control and blank, and then decreased at a dose of 50 µg/mL. At different doses, the anti-inflammatory action of H. gracilis extracts successfully inhibited BSA denaturation, which causes inflammation; the maximum activity has been observed.

Conclusion: This comprehensive analysis highlights H. gracilis as a valuable natural resource with multifaceted biological activities, supporting its further investigation for therapeutic applications in dentistry.

作为一种生物活性资源:探索其抗氧化、抗生物膜、抗炎和抗菌在牙科方面的应用潜力。
目的:评价薄叶垂叶提取物的抗菌、抗生物膜、抗氧化和抗炎作用。材料和方法:用甲醇洗涤和提取样品。混合均匀后,高速(10000 × g)离心2 min,室温下磁力搅拌器搅拌30 min,确保提取彻底。随后,5000 × g离心10min,将溶解组分与未溶解碎屑分离。采用DPHH法测定其抗氧化活性,采用Kirby-Bauer圆盘扩散法测定其对变形链球菌、大肠杆菌、粪肠球菌和索内志贺菌的抑菌作用,采用生物膜抑制法测定生物膜对变形链球菌、大肠杆菌、粪肠球菌和索内志贺菌的抑菌作用。最后,用改良版的BSA测定法测定了薄叶菊的抗炎活性。结果:对变形链球菌、大肠杆菌、粪肠杆菌和sonnei链球菌进行抑菌试验,结果表明,该提取物在对同一种细菌进行抑菌试验时,成功地抑制了生物膜的形成,并且随着浓度的增加,活性也有所增加。随着浓度的增加,抑制区逐渐扩大,当浓度为100µg/mL时,抑制区最大可达17 mm±0.1。在抗氧化活性方面,与对照和空白相比,细叶菊甲氧基提取物的抗氧化活性从10µg/mL逐渐升高到40µg/mL时活性更高,然后在50µg/mL剂量下活性下降。在不同剂量下,股薄草提取物的抗炎作用成功地抑制了引起炎症的牛血清白蛋白变性;已观察到最大活动。结论:本综合分析结果表明,股薄草是一种具有多方面生物活性的珍贵天然资源,支持其在牙科治疗中的进一步研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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