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1.
Appl Opt ; 58(8): 1895-1899, 2019 Mar 10.
Article in English | MEDLINE | ID: mdl-30874053

ABSTRACT

Laser-induced breakdown spectroscopy (LIBS) assisted with laser-induced fluorescence (LIF) was introduced to detect trace aluminum in steatite ceramics in this work. The mechanism and transition process of laser-induced aluminum atomic fluorescence in laser-induced plasma was described and discussed. Selective enhancement of LIF and temporal synchronicity between radiation laser and fluorescence were studied. The influences of ablation laser energy, power density of the radiation laser, and interpulse delay were experimentally investigated. The results showed that 60 mJ in ablation laser energy and 4 µs in interpulse delay were the optimal choice for fluorescent intensity. The fluorescence was increased to the saturation level over 4 MW/cm2. Spectral stability improvement of LIBS-LIF was also discovered in this work. The results proved that LIBS-LIF is a feasible and effective modification of LIBS for ceramics analysis.

2.
J Endod ; 41(4): 479-86, 2015 Apr.
Article in English | MEDLINE | ID: mdl-25492490

ABSTRACT

INTRODUCTION: Sphingosine-1-phosphate receptor 1 (S1P1) is crucial for regulation of immunity and bone metabolism. This study aimed to investigate the expression of S1P1 in rat periapical lesions and its relationship with receptor activator of nuclear factor kappa B ligand (RANKL) and regulatory T (Treg) cells. METHODS: Periapical lesions were induced by pulp exposure in the first lower molars of 55 Wistar rats. Thirty rats were killed on days 0, 7, 14, 21, 28, and 35, and their mandibles were harvested for x-ray imaging, micro-computed tomography scanning, histologic observation, immunohistochemistry, enzyme histochemistry, and double immunofluorescence analysis. The remaining 25 rats were killed on days 0, 14, 21, 28, and 35, and mandibles were harvested for flow cytometry. RESULTS: The volume and area of the periapical lesions increased from day 0 to day 21 and then remained comparably stable after day 28. S1P1-positive cells were observed in the inflammatory periapical regions; the number of S1P1-positive cells peaked at day 14 and then decreased from day 21 to day 35. The distribution of S1P1-positive cells was positively correlated with the dynamics of RANKL-positive cells but was negatively correlated with that of Treg cells. CONCLUSIONS: S1P1 expression was differentially correlated with RANKL and Treg cell infiltration in the periapical lesions and is therefore a contributing factor to the pathogenesis of such lesions.


Subject(s)
Periapical Diseases/metabolism , RANK Ligand/metabolism , Receptors, Lysosphingolipid/metabolism , T-Lymphocytes, Regulatory/metabolism , Animals , Female , Flow Cytometry , Osteoclasts/metabolism , Periapical Diseases/pathology , Rats , Rats, Wistar
3.
Acta Biomater ; 10(12): 5156-5168, 2014 Dec.
Article in English | MEDLINE | ID: mdl-25182220

ABSTRACT

Bioactive materials play an important role in facilitating dental pulp repair when living dental pulp is exposed after injuries. Mineral trioxide aggregate is the currently recommended material of choice for pulp repair procedures though has several disadvantages, especially the inconvenience of handling. Little information is yet available about the early events and molecular mechanisms involved in bioceramic-mediated dental pulp repair. We aimed to characterize and determine the apatite-forming ability of the novel ready-to-use nanoparticulate bioceramic iRoot BP Plus, and investigate its effects on the in vitro recruitment of human dental pulp stem cells (DPSCs), as well as its capacity to induce dentin bridge formation in an in vivo model of pulp repair. It was found that iRoot BP Plus was nanosized and had excellent apatite-forming ability in vitro. Treatment with iRoot BP Plus extracts promoted the adhesion, migration and attachment of DPSCs, and optimized focal adhesion formation (Vinculin, p-Paxillin and p-Focal adhesion kinase) and stress fibre assembly. Consistent with the in vitro results, we observed the formation of a homogeneous dentin bridge and the expression of odontogenic (dentin sialoprotein, dentin matrix protein 1) and focal adhesion molecules (Vinculin, p-Paxillin) at the injury site of pulp repair model by iRoot BP Plus. Our findings provide valuable insights into the mechanism of bioceramic-mediated dental pulp repair, and the novel revolutionary ready-to-use nanoparticulate bioceramic paste shows promising therapeutic potential in dental pulp repair application.


Subject(s)
Bone Cements/chemistry , Dental Porcelain/chemistry , Dental Pulp/chemistry , Dental Pulp/cytology , Nanoparticles/chemistry , Stem Cells/chemistry , Stem Cells/cytology , Cell Movement/physiology , Cell Proliferation/physiology , Cells, Cultured , Ceramics , Dental Pulp/physiology , Drug Evaluation, Preclinical , Humans , Materials Testing , Ointments , Stem Cells/physiology
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