Affiliations 

  • 1 Restorative Dentistry Division, School of Dentistry, IMU, 126, Jalan Jalil Perkasa 19, Bukit Jalil, 57000 Bukit Jalil, Wilayah Persekutuan Kuala Lumpur, Malaysia; Dental Materials Science, Applied Oral Sciences & Community Dental Care, Faculty of Dentistry, The University of Hong Kong, 34 Hospital Road, Sai Ying Pun, Hong Kong Special Administrative Region
  • 2 Medical Education & Research Development Unit (MERDU), Faculty of Medicine, Universiti Malaya 50603 Kuala Lumpur, Malaysia
  • 3 Restorative Dentistry Division, School of Dentistry, IMU, 126, Jalan Jalil Perkasa 19, Bukit Jalil, 57000 Bukit Jalil, Wilayah Persekutuan Kuala Lumpur, Malaysia
  • 4 Faculty of Biomedical Science, School of Health Sciences, International Medical University, Kuala Lumpur; Malaysia
  • 5 Paediatric Dentistry and Orthodontics, Faculty of Dentistry, The University of Hong Kong, Prince Philip Dental Hospital, 34 Hospital Road, Sai Ying Pun, Hong Kong SAR, China
  • 6 Department of Endodontics, Arthur A Dugoni School of Dentistry, University of the Pacific, San Francisco, CA, USA; School of Dentistry, The University of Queensland, Herston, Qld 4006, Australia
  • 7 Dental Materials Science, Applied Oral Sciences & Community Dental Care, Faculty of Dentistry, The University of Hong Kong, 34 Hospital Road, Sai Ying Pun, Hong Kong Special Administrative Region; University of Manchester, School of Medical Sciences, Division of Dentistry, Manchester, M13 9PL, United Kingdom
  • 8 Dental Biomaterials and Minimally Invasive Dentistry, Departmento de Odontologia, Facultad de Ciencias de la Salud Universidad, CEU-Cardenal Herrera, Spain 9; Department of Therapeutic Dentistry, I. M. Sechenov First Moscow State Medical University, Moscow, Russia
  • 9 Faculty of Dentistry, Oral & Craniofacial Sciences, King's College London, London, United Kingdom; Department of Prosthodontics, Semmelweis University, Budapest, Hungary
  • 10 Applied Oral Sciences & Dental Clinical Sciences, Faculty of Dentistry, Dalhousie University, 5981 University Ave, Halifax, Nova Scotia B3H 1W2 Canada
J Dent, 2025 Mar 15.
PMID: 40096879 DOI: 10.1016/j.jdent.2025.105693

Abstract

AIMS AND OBJECTIVES: To analyse development of hydroxyapatite (HAp) crystals doped with glutamic acid and phosphorine residue (Ser-OPO3) having self-remineralization, biocompatible and optimum bonding properties MATERIALS AND METHODS: β-tri calcium phosphate, ammonium phosphate dibasic HAp was dissolved with strontium Flouride Glu or Ser-OPO3 components and utilised in two 0.1% TCPCa3(PO4)2 Str/FL and 0.2% TCPCa3(PO4)2 Str/FL groups. HAp formulation was evaluated for particle-size analysis, crystal size and indices using FTIR. Demineralized enamel specimens were treated and characterized using transmission electron microscopy (TEM), Xray diffraction (XRD), solid state NMR, and mechanical properties. MC3T3 mouse fibroblastic cells were evaluated for alkaline-phosphate activity (ALP). Human gingival fibroblasts (PGF) were evaluated for morphology. After modifying Universal adhesives, tensile force was assessed at 24 hr and 3 months.

RESULT: Increasing concentrations of experimental solution exposure significantly affect mean diameter of HAp. The increasing FTIR intensity, were displayed; 0.2% TCPCa3(PO4)2 Str/FL > 0.1% TCPCa3(PO4)2 Str/FL> control. 0.2% TCPCa3(PO4)2 Str/FL revealed existence of distinct crystals, with planes orientated perpendicular to longer axis of tooth. XRD pattern indicated crystal growth with a rise in peak intensities in 0.2% TCPCa3(PO4)2 Str/FL group. The NMR spectra for Glu and Ser-OPO3 elucidated interactions between carbon atoms in amino acid and hydrogen atoms on HAp surfaces. Surface microhardness of 0.2% TCPCa3(PO4)2 Str/FL specimens showed significantly higher values on day 28 (p< 0.05). ALP density value of cells was significantly higher for 0.2% TCPCa3(PO4)2 Str/FL group on day 7 and 14. 0.1% TCPCa3(PO4)2 Str/FL and 0.2% TCPCa3(PO4)2 Str/FL enhanced migration of PGF cells in comparison to the control group (p<0.05). 0.1% TCPCa3(PO4)2 Str/FL and 0.2% TCPCa3(PO4)2 Str/FL groups showed significant differences in bond strength at different time points CONCLUSION: 0.1% TCPCa3(PO4)2 Str/FL and 0.2% TCPCa3(PO4)2 Str/FL were structurally integrated into the lattice demonstrating changes within the crystallite size and became conducive for adhesive bonding.

CLINICAL SIGNIFICANCE: The new amino acid-based hydroxyapatite formulation is chemically stable due to the substitution of OH- with F- and is crucial in the rehardening of caries and adhesive bonding.

* Title and MeSH Headings from MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.