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Aim: This study evaluates the cytotoxicity, anti-inflammatory effects, and drug release profiles of an allicin-incorporated graphene oxide-silver nanoparticle (GO-AgNP) hydrogel as an intracanal medicament.
Materials And Methods: The allicin-incorporated GO-AgNP hydrogel was synthesized and characterized using transmission electron microscopy. Human periodontal ligament (PDL) fibroblasts were used for 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide cytotoxicity assays, assessing cell viability at 10, 25, 50, and 100 µg/mL concentrations over 24, 48, and 72 hours. Anti-inflammatory effects were evaluated by analyzing interleukin (IL)-6, IL-8, and tumor necrosis factor (TNF)-α expression in lipopolysaccharide (LPS)-induced RAW 264.7 macrophage cells via quantitative polymerase chain reaction at 24 hours and 7 days. Drug release was assessed using ultraviolet-visible spectrophotometry over 168 hours in root canal-treated teeth.
Results: The allicin-incorporated GO-AgNP hydrogel exhibited concentration-dependent cytotoxicity, with cell viability exceeding 90% at 10-20 µg/mL but decreasing significantly at 50-100 µg/mL ( < 0.05). The half-maximal inhibitory concentration was approximately 45 µg/mL. Anti-inflammatory assays showed a reduction in IL-6 (45%), IL-8 (38%), and TNF-α (42%) compared with the LPS-treated control ( < 0.05). Drug release analysis revealed a sustained release pattern, with the 20 µg/mL hydrogel demonstrating a higher cumulative release than the 10 µg/mL hydrogel.
Conclusion: The allicin-incorporated GO-AgNP hydrogel demonstrates potential as a biocompatible intracanal medicament with anti-inflammatory properties and controlled drug release. Further optimization is required for clinical application.
Clinical Significance: This allicin-incorporated GO-AgNP hydrogel shows promise as an intracanal medicament due to its biocompatibility, anti-inflammatory properties, and controlled drug release. By modulating the inflammatory response, it may contribute to reduced postoperative discomfort and improved periapical healing. Additionally, its bioactive properties may support tissue repair and regeneration, making it a potential candidate for regenerative endodontic procedures. How to cite this article: Piriyanga R, Ranjan M, Bathla S, Comparative Evaluation of Cytotoxicity, Anti-inflammatory, and Drug Release Profiles of Allicin-incorporated GO-AgNP Hydrogel: An Study. J Contemp Dent Pract 2025;26(1):71-76.
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http://dx.doi.org/10.5005/jp-journals-10024-3812 | DOI Listing |
BMC Biotechnol
September 2025
Zoology Department, Faculty of Science, Cairo University, Giza, 12613, Egypt.
Fundam Clin Pharmacol
October 2025
Postgraduate Program in Pharmaceutical Science, Federal University of Juiz de Fora, Juiz de Fora, Minas Gerais, Brazil.
This review highlights the integration of drug repurposing and nanotechnology-driven delivery strategies as innovative approaches to enhance the antifungal activity of statins against mucosal candidiasis, providing a framework for future translational research and clinical application. The rising prevalence of antifungal resistance and virulence factors of Candida albicans underscore the limitations of current therapies. Statins, commonly used as lipid-lowering agents, have emerged as attractive repurposed drug candidates due to their ability to interfere with fungal ergosterol biosynthesis and Ras-mediated signaling pathways.
View Article and Find Full Text PDFNat Nanotechnol
September 2025
Department of Bioengineering, Rice University, Houston, TX, USA.
Maintaining safe and potent drug levels in vivo is challenging. Multidomain peptides assemble into supramolecular hydrogels with a well-defined, highly porous nanostructure that makes them attractive for drug delivery. However, their ability to extend release is typically limited by rapid drug diffusion.
View Article and Find Full Text PDFInt J Biol Macromol
September 2025
Tianjin Key Laboratory of Composite and Functional Materials, School of Materials Science and Engineering, Tianjin University, Tianjin, 300350, PR China. Electronic address:
Balancing antibacterial efficacy, mechanical integrity, and biocompatibility remains a critical challenge in drug release systems for wound dressings. Many antimicrobial agents exhibit inherent cytotoxicity, compromising cell viability and tissue compatibility. To address this, an Absorbable Gelatine Sponge was synthetised based on high-viscosity hydroxypropyl methylcellulose (HPMC K100M) and loaded with silver citrate nanorods (AgCit), which confine silver nanoparticles to enable controlled ion release.
View Article and Find Full Text PDFInt J Biol Macromol
September 2025
Department of Pharmaceutical Technology, Faculty of Pharmacy, University of Malaya, Kuala Lumpur, 50603, Malaysia. Electronic address:
This study aimed to characterize, in vitro dissolution, and evaluate the release kinetics of salicylamide in capsule shells made from κ-carrageenan-HPMC. The capsule shell was prepared using the dipping method with CRG: HPMC (1:1, 1:2, 1:3) ratio, supplemented with sorbitol and antifoam silicone emulsion. Characterization was conducted using FTIR, SEM-EDX mapping, AFM, hardness, and swelling degree experiments.
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