Antimicrobial Activity and Physicochemical Properties of Calcium Hydroxide Pastes Used as Intracanal Medication

Abstract Introduction The aim of the present study was to evaluate the pH, calcium release, solubility, and antimicrobial action against biofilms of calcium hydroxide + saline solution, Calen (SS White Artigos Dentários Ltd, Rio de Janeiro, Brazil) (CH/P), Calen camphorated paramonochlorophenol (CMC...

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Veröffentlicht in:Journal of endodontics 2016-12, Vol.42 (12), p.1822-1828
Hauptverfasser: Zancan, Rafaela Fernandes, MSc, Vivan, Rodrigo Ricci, PhD, Milanda Lopes, Marcelo Ribeiro, MSc, Weckwerth, Paulo Henrique, PhD, de Andrade, Flaviana Bombarda, PhD, Ponce, José Burgos, PhD, Duarte, Marco Antonio Hungaro, PhD
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Sprache:eng
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Zusammenfassung:Abstract Introduction The aim of the present study was to evaluate the pH, calcium release, solubility, and antimicrobial action against biofilms of calcium hydroxide + saline solution, Calen (SS White Artigos Dentários Ltd, Rio de Janeiro, Brazil) (CH/P), Calen camphorated paramonochlorophenol (CMCP) (CH/CMPC), and calcium hydroxide + chlorhexidine (CH/CHX) pastes. Methods The pH of the pastes was determined with a calibrated pH meter placed in direct contact with each paste. The root canals of acrylic teeth ( N  = 10) were filled with the previously mentioned intracanal dressings and immersed in ultrapure water to measure hydroxyl (pH meter) and calcium ion release (atomic absorption spectrophotometer) at time intervals of 3, 7, 15, and 30 days. To assess solubility, the root canals of acrylic teeth ( N  = 10) were filled with the previously mentioned pastes and scanned by micro–computed tomographic imaging before (initial) and after 7, 15, and 30 days of immersion in ultrapure water. The solubility of each specimen was the difference between the initial and final volume scanning. For antimicrobial analysis, monospecies and dual-species biofilms were in vitro induced on dentin blocks ( N  = 20). Afterward, they were treated with the pastes for 7 days. Live/dead dye and a confocal microscope were used to measure the percentage of living cells. Data were statistically compared ( P  
ISSN:0099-2399
1878-3554
DOI:10.1016/j.joen.2016.08.017