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Updated: May 3, 2026

Confocal Time Lapse Imaging as an Efficient Method for the Cytocompatibility Evaluation of Dental Composites
Published on: November 9, 2014
CYTOTOXICITY ASSESSMENT OF ADHESIVE SYSTEM COMPONENTS CONTAINING METHACRYLOYLOXYDECYL DIHYDROGEN PHOSPHATE
Z Khabadze1, M Dashtieva1, L Chraghyan1
1Peoples' Friendship University of Russia named after Patrice Lumumba (RUDN University), Institute of Medicine, Moscow, Russia.
Introduction:
The safety and biocompatibility of dental adhesive systems remain critical concerns in restorative dentistry due to their close contact with pulp and soft tissues. Methacryloyloxydecyl dihydrogen phosphate (MDP-10) is a widely used monomer in adhesive formulations, yet its cytotoxicity profile remains insufficiently characterized.
Aim:
This study aimed to assess and compare the cytotoxic effects of five MDP-10-containing dental adhesive systems, including a laboratory-synthesized MDP-10 primer, on human gingival mesenchymal stromal cells (hGMSCs) derived from attached and movable gingiva.
Materials And Methods:
Five adhesive materials (UNIVERSAL BOND II, Monobond N, KompoFix Primer, CLEARFIL S3 BOND Universal, and synthesized MDP-10) were tested. Viability of hGMSCs was evaluated using Annexin V-FITC and propidium iodide (PI) staining and analyzed via flow cytometry. Two cell cultures were used, obtained from different gingival sites. Statistical significance was assessed using the Mann-Whitney U test (p≤0.05).
Results:
Substances 1, 3, and 4 exhibited high cytotoxicity, significantly reducing viable cell percentages and increasing apoptotic and necrotic populations. The synthesized MDP-10 primer (Substance 5) showed the lowest cytotoxicity, maintaining over 60% viability in both cell types. No significant differences were observed between attached and movable gingival cultures.
Conclusion:
The results demonstrate that MDP-10-based adhesives differ significantly in cytotoxic potential. Composition and purity play key roles in biocompatibility, and custom-formulated primers may offer safer alternatives for clinical use. These findings support the need for careful material selection and further in vivo validation.
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