Cytotoxicity of intracanal dressings on apical papilla cells differ upon activation with E. faecalis LTA

التفاصيل البيبلوغرافية
العنوان: Cytotoxicity of intracanal dressings on apical papilla cells differ upon activation with E. faecalis LTA
المؤلفون: Celso Luiz Caldeira, Carla Renata Sipert, Aline Pereira de Oliveira
المصدر: Journal of Applied Oral Science, Volume: 27, Article number: e20180291, Published: 21 FEB 2019
Journal of Applied Oral Science v.27 2019
Journal of applied oral science
Universidade de São Paulo (USP)
instacron:USP
Journal of Applied Oral Science
Journal of Applied Oral Science, Vol 27, Iss 0 (2019)
بيانات النشر: Faculdade De Odontologia De Bauru - USP, 2019.
سنة النشر: 2019
مصطلحات موضوعية: Lipopolysaccharides, Male, Time Factors, Adolescent, Cell Survival, Context (language use), Enterococcus faecalis, Calcium Hydroxide, 030207 dermatology & venereal diseases, 03 medical and health sciences, 0302 clinical medicine, Tooth Apex, Ciprofloxacin, Metronidazole, Cytotoxic T cell, Humans, MTT assay, Viability assay, Cefaclor, Cytotoxicity, General Dentistry, Dental Papilla, Cells, Cultured, Analysis of Variance, Immunity, Cellular, biology, Root Canal Irrigants, Chemistry, Reproducibility of Results, 030206 dentistry, biology.organism_classification, Dental pulp cavity, Molecular biology, Anti-Bacterial Agents, lcsh:RK1-715, Teichoic Acids, Cell culture, lcsh:Dentistry, Female, Original Article, Lipoteichoic acid, Cell culture techniques
الوصف: Objective The aim of this study was to investigate the cytotoxic effects of modified triple antibiotic paste and an experimental composition using calcium hydroxide on lipoteichoic acid (LTA)-primed apical papilla cells (APC). Material and Methods Human APC were tested for in vitro cytotoxicity of modified Triple Antibiotic Paste (mTAP – Ciprofloxacin, Metronidazole and Cefaclor at 1:1:1) and of a paste of Ciprofloxacin, Metronidazole and Calcium hydroxide (CMC – 1:1:2) and modified CMC (mCMC – 2:2:1) by using MTT assay. The substances were reconstituted in DMEM at 1,000 µg/mL and ¼ serially diluted before being kept in contact with cells for 1, 3, 5 and 7 days. Further, cells were primed with 1 µg/mL of Enterococcus faecalis LTA for 7 days prior to the viability test with 1,000 µg/mL of each substance. Statistical analysis was performed using one-way analysis of variance (ANOVA) and two-way ANOVA respectively followed by Tukey’s post-test. Significance levels were set at p
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