scholarly journals Smear layer removal and chelated calcium ion quantification of three irrigating solutions

2006 ◽  
Vol 17 (4) ◽  
pp. 306-309 ◽  
Author(s):  
Andre Augusto Franco Marques ◽  
Melissa Andréia Marchesan ◽  
Celso Bernardo de Sousa-Filho ◽  
Yara Teresinha Correa Silva-Sousa ◽  
Manoel D. Sousa-Neto ◽  
...  

The purpose of this study was to evaluate, by scanning electron microscopy (SEM), smear layer removal and quantify, by atomic absorption spectrophotometry, the amount of calcium ion present in the chelating solutions after their use. Sixteen extracted canines were instrumented using the step-back technique and were assigned to 3 groups according to the irrigating solution used: G1: 1 mL 17% EDTAC between each file; G2: 1 mL 17% CDTA; G3: 1 mL 17% EGTA. The solutions were collected after use. The teeth were cleaved longitudinally, evaluated under SEM and assessed for smear layer by blinded examiners and scored from 1 to 4. In order to quantify calcium ion release, the collected solutions were examined by atomic absorption spectrophotometry. Freidman's test was used for statistical analysis of SEM values and showed that canals irrigated with 17% EDTAC and 17% CDTA had significantly less smear layer throughout the canals than 17% EGTA (p<0.01). For analysis of the collected solutions, Tukey's test was used and showed that EDTAC and CDTA had a greater amount of calcium ions (22.8±7.54 and 60.6±20.67 µg/mL, respectively) compared to EGTA (70.5±14.2 µg/mL) (p<0.01). The association both methodologies may contribute to the understanding of how these solutions act in the root canal.

2011 ◽  
Vol 19 (6) ◽  
pp. 639-643 ◽  
Author(s):  
George Táccio de Miranda Candeiro ◽  
Isabela Barbosa de Matos ◽  
Clarice Fernandes Eloy da Costa ◽  
Cristiane Sá Roriz Fonteles ◽  
Mônica Sampaio do Vale

1974 ◽  
Vol 20 (11) ◽  
pp. 1444-1445 ◽  
Author(s):  
R Menachè

Abstract The method of Gitelson et al. was modified to a microscale procedure and adapted for atomic absorption spectrophotometry. Oxalic acid in urine is precipitated with excess of calcium ions at pH 5. The excess of calcium present in the supernate and the total calcium added and present in the urine at pH 2 are determined by atomic absorption spectrophotometry. The oxalic acid present in the precipitate is calculated indirectly from the difference between the two determinations of calcium. This method is useful for routine determination of urinary oxalic acid.


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