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Determination of Anions in Toothpaste by Ion Chromatography

Applications | 2016 | Thermo Fisher ScientificInstrumentation
Ion chromatography
Industries
Manufacturer
Thermo Fisher Scientific

Summary

Significance of the Topic


The precise quantification of fluoride and related anions in toothpaste is essential for ensuring product efficacy and consumer safety. Fluoride compounds such as stannous fluoride, sodium fluoride, and sodium monofluorophosphate (MFP) prevent dental caries, but may interact with other ingredients to form insoluble species, reducing their therapeutic value. Reliable analytical methods are therefore critical for quality control and stability assessment.

Objectives and Study Overview


This work presents a single-run ion chromatography (IC) method for the direct determination of free fluoride, MFP, and other anionic additives in toothpaste. The goals were to achieve high reproducibility, minimize sample preparation time, and apply the method to multiple commercial toothpaste products for comparative analysis.

Methodology and Instrumentation


Toothpaste samples were dispersed (1 g in 100 mL deionized water), vortexed, and filtered through a 0.45 µm membrane. Two gradient elution programs were evaluated using hydroxide eluents generated electrolytically:
  • Method A (IonPac AS18 column): 22–60 mM KOH gradient over 20 min at 1.0 mL/min, 30 °C, 25 µL injection, suppressed conductivity detection.
  • Method B (IonPac AS17 column): 3–40 mM KOH gradient over 18 min at 1.5 mL/min, 30 °C, 25 µL injection, suppressed conductivity detection.

Used Instrumentation


The analysis employed a Dionex ICS-2000 RFIC system with:
  • Integrated eluent generator (EluGen EGC-KOH cartridge)
  • Column heater
  • Pump degas and CR-ATC suppressor
  • ASRS ULTRA suppressor (recycle mode)
  • AS50 autosampler
  • Chromeleon chromatography workstation

Main Results and Discussion


Calibration curves for fluoride, chloride, MFP, sulfate, benzoate, and phosphate exhibited excellent linearity (r² ≥ 0.9991) over relevant concentration ranges. Method A achieved <0.2% RSD in retention times and <0.9% RSD in peak areas across ten replicates. Analysis of three commercial toothpastes revealed:
  • Two products contained MFP as primary fluoride source (0.65–0.81 %), with minimal free fluoride.
  • One product used sodium fluoride (0.083 %) and displayed higher levels of pyrophosphate, indicating tartar control formulation.
Column capacity influenced selectivity: AS18 tolerated high-ionic matrices, while AS17 provided better separation of strongly retained anions like pyrophosphate and saccharin.

Benefits and Practical Applications


Electrolytically generated eluents eliminate manual preparation errors, improve reproducibility, and allow rapid gradient adjustments. The direct IC approach streamlines analysis by avoiding derivatization or hydrolysis steps required in GC or colorimetric assays. This method is applicable to routine quality control, stability studies, and regulatory compliance in dental product manufacturing.

Future Trends and Opportunities


Advancements may include miniaturized IC systems for point-of-use testing, coupling with mass spectrometry for structural confirmation, and further automation of sample handling. Green chemistry approaches could focus on reduced reagent consumption and recyclable suppressors.

Conclusion


The presented ion chromatography method with reagent-free eluent generation offers a robust, precise, and time-efficient solution for simultaneous determination of fluoride, MFP, and other anions in toothpaste. Its high reproducibility and minimal sample preparation make it well suited for industrial and regulatory laboratories.

Reference


1. McCoy MC. US Food and Drug Administration Viewpoints. EN 2001 Apr;42.
2. Wang P, Li SFY, Lee HK. J Chromatogr A. 1997;765:353–359.
3. Biemer TA, Asral N, Sippy AJ. J Chromatogr A. 1997;771:355–359.
4. Official Journal of the European Communities. L291. 1983:37–40.
5. Borissova R, Debouki A, Nikolov T. Fresenius J Anal Chem. 1993;347:63–66.
6. Hattab J. Dent. 1989;17:77–83.
7. Farcas F, Chaussadent T, Fiaud C, Mabille I. Anal Chim Acta. 2002;472:37–43.
8. Murawski DJ. J Chromatogr A. 1991;546:351–367.

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