Flavia Almeida Amorim, Maria Suzi de Sousa Lopes, Lyzia Vitoria Mendes Rezende, Evanildo Canuto Paz, Marcus Vinícius Oliveira, Glauber Campos Vale
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引用次数: 0
Abstract
Background: Accurate determination of salivary fluoride (F) depends on appropriate analytical conditions, particularly the buffering system used before ion-selective electrode measurements.
Research design and methods: This laboratory-based analytical study addressed the practical challenge of selecting between two total ionic strength adjustment buffers (TISAB II and TISAB III) for salivary F-determination using samples obtained from previously conducted clinical trials. Unstimulated saliva from eight participants was collected at baseline and at 5 min, 30 min, 1 h, 4 h, and 12 h after exposure to three F-treatments: F-varnish, 1,450 ppm F-dentifrice, and 5,000 ppm F-dentifrice. F-concentrations were measured using an F-ion-selective electrode after buffering with either TISAB II or TISAB III. Data were analyzed using paired statistical tests and Pearson correlation analysis (α = 0.05).
Results: No significant differences were observed between the buffers across most conditions, although differences were detected at later time points following dentifrice use. A strong positive correlation was found between the two buffering systems (p < 0.001), and no differences were detected in the area under the concentration-time curve.
Conclusions: These findings indicate that both TISAB II and TISAB III provide comparable analytical performance for salivary fluoride determination under the tested conditions, although differences may occur at lower fluoride concentrations.
BioanalysisBIOCHEMICAL RESEARCH METHODS-CHEMISTRY, ANALYTICAL
CiteScore
3.30
自引率
16.70%
发文量
88
审稿时长
2 months
期刊介绍:
Reliable data obtained from selective, sensitive and reproducible analysis of xenobiotics and biotics in biological samples is a fundamental and crucial part of every successful drug development program. The same principles can also apply to many other areas of research such as forensic science, toxicology and sports doping testing.
The bioanalytical field incorporates sophisticated techniques linking sample preparation and advanced separations with MS and NMR detection systems, automation and robotics. Standards set by regulatory bodies regarding method development and validation increasingly define the boundaries between speed and quality.
Bioanalysis is a progressive discipline for which the future holds many exciting opportunities to further reduce sample volumes, analysis cost and environmental impact, as well as to improve sensitivity, specificity, accuracy, efficiency, assay throughput, data quality, data handling and processing.
The journal Bioanalysis focuses on the techniques and methods used for the detection or quantitative study of analytes in human or animal biological samples. Bioanalysis encourages the submission of articles describing forward-looking applications, including biosensors, microfluidics, miniaturized analytical devices, and new hyphenated and multi-dimensional techniques.
Bioanalysis delivers essential information in concise, at-a-glance article formats. Key advances in the field are reported and analyzed by international experts, providing an authoritative but accessible forum for the modern bioanalyst.