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Evaluation of Gross Alpha and Beta Radioactivity Concentrations in Tooth Samples

Year 2022, Volume: 8 Issue: 1, 1 - 8, 25.02.2022
https://doi.org/10.19127/mbsjohs.979585

Abstract

Objective: Teeth are used as an important data source to estimate radioactivity accumulation in individuals. This study aimed to evaluation the gross alpha (GA) and gross beta (GB) radioactivity concentrations in tooth samples.
Methods: Mandibular permanent first molar teeth of individuals living in the Middle Black Sea region were used for the study to ensure standardization. The teeth samples were divided into 4 groups according to the age factor (Group 1: 6-15 years, Group 2: 16-30 years, Group 3: 31-45 years, and Group 4: 46-65 years). Each group was divided into two subgroups according to gender factor. Measurements were completed with a nuclear spectroscopic system containing a gas-flow proportional counter. Data were analyzed statistically.
Results: While a statistically significant difference was detected among groups for GA radioactivity concentration (p<0.05), no significant difference was detected among groups for GB (p>0.05). Mean GA value was higher in Group 1 (6-15 years) compared to the other groups. There was no statistically significant difference between the genders in both GA and GB radioactivity concentrations for all groups (p>0.05).
Conclusion: While the GA radioactivity concentration was affected by the age factor, it was not affected by the gender factor.

Supporting Institution

Ordu University, Scientific Research Projects Coordination Unit

Project Number

AP-1704

References

  • 1. Aghamiri SMR, Ghorbani Z, Darafsheh A, Torabzadeh H, Fathivand AA, Minuchehr A, et al. 226Ra concentration in the teeth of habitants of areas with high level of natural radioactivity in Ramsar. J Environ Radioact. 2006;89(3):212-218.
  • 2. White SC, Pharoah MJ. Oral Radiology principals and ınterpretation. 7 th ed. Mosby, Canada, 2014. p. 1-28.
  • 3. Cinelli G, Tollefsen T, Bossew P, Gruber V, Bogucarskis K, De Felice L, et al. Digital version of the European Atlas of natural radiation. J Environ Radioact. 2019;196:240-252.
  • 4. Sogut O, Aydin MF, Kucukonder E, Zorer OS, Dogru M. Measurement of gross alpha and gross beta activity concentrations in human tooth. J Environ Radioact. 2010;101(3):226-229.
  • 5. Taskin H, Kobya Y, Tokgoz M, Bassari A, Yesilkanat CM. Biomonitoring of trace elements and gross alpha/ beta radioactivity levels in human teeth: A case study from Istanbul, Turkey. Microchemical Journal. 2018;141:458-465.
  • 6. Clemente GF, Renzetti A, Santori G, Steinhäusler F, Pohl-Ruling J. Relationship between the 210Pb content of teeth and exposure to Rn and Rn daughters. Health Phys. 1984;47(2):253-262.
  • 7. Delibacak S, Ongun AR. Influence of treated sewage sludge applications on corn and second crop wheat yield and some soil properties of sandy loam soil. Fresen Environ Bull. 2016;25(1):43-54.
  • 8. Kir I, Erdogan M, Engin MS, Cay S. Trace metals in sediment, water and their bioaccumalation in Carp (Cyprinus Carpio L., 1758) samples, captured from the Karacaoren (I) Dam Lake, Turkey. Fresen Environ Bull. 2016;25(9):3557-3562.
  • 9. Beir VI. Report of the Committee on the Biological effects of Ionizing Radiation, National. Research, Council. 1999.
  • 10. Brown CJ, Chenery SR, Smith B, Mason C, Tomkins A, Roberts GJ, et al. Environmental influences on the trace element content of teeth—implications for disease and nutritional status. Arch Oral Biol. 2004;49(9):705-717.
  • 11. Corbacho JA, Zapata-García D, Montaña M, Fons J, Camacho A, Guillén J, et al. Selection of the appropriate radionuclide source for the efficiency calibration in methods of determining gross alpha activity in water. J Environ Radioact 2016;151:22-7.
  • 12. Butler FE. Strontium-90 in human teeth. Natur. 1961;11(189):848-849.
  • 13. Yamamoto M, Hinoide M, Ohkubo Y, Ueno K. Concentration of 226Ra in human teeth. Health Phys. 1994;67(5):535-540.
  • 14. Kulev YD, Polikarpov GG, Prigodey EV, Assimakopoulos PA. Strontium-90 concentrations in human teeth in South Ukraine, 5 years after the Chernobyl accident. Sci Total Environ. 1994;155(3):215-219.
  • 15. Baltas H, Sirin M, Senel F, Devran F. Determination of natural radionuclides and some metal concentrations in human tooth samples in the Rize province, Turkey Int J Environ Health Res. 2019; 31(1):20-33.
  • 16. Kavun Y, Boztosun I, Ðapo H, Maras I, Segebade C. Determination of the Sr/Ca ratio of tooth samples by photoactivation analysis in Southern Turkey. Radiochimica Acta. 2018;106(9):759-768.
  • 17. Ugur A, Sahan H, Sahan M, Yegingil Z, Gorur S. Investigation of the relation between environmental radioactivity and radioactivity in human teeth who lives in this environment. Fizika (Baku). 2010;16:537-540.
  • 18. Mangano JJ, Gould JM, Sternglass EJ, Shermand JD, McDonnelle W. An unexpected rise in strontium-90 in US deciduous teeth in the 1990s. Sci Total Environ. 2003;317 (1-3):37-51.
  • 19. Dogru M, Kulahci F. Iso-radioactivity curves of the water of the Hazar Lake, Elazig, Turkey. J Radioanal Nucl Chem. 2004;260(3):557-562. 20. Zorer OS, Ceylan H, Dogru M. Assessment of some trace heavy metals and radioactivity concentration in water of Bendimahi River Basin (Van, Turkey). Environ Monit Assess. 2008;147(1-3),183-90.
  • 21. Zorer OS, Ceylan H, Dogru M. Determination of heavy metals and comparison to gross radioactivity concentration in soil and sediment samples of the Bendimahi River Basin (Van, Turkey). Water, air, and Soil Pollution. 2009;196:75-87.
  • 22. Zorer OS, Ceylan H, Dogru M. Gross alpha and beta radioactivity concentration in water, soil and sediment of the Bendimahi River and Van Lake (Turkey). Environ Monit Assess. 2009;148(1-4):39-46.
  • 23. Rothe WE. Gross alpha radioactivity of human bones and teeth. Radiol Health Data Rep. 1966;7(3):204-205.
  • 24. Dewit T, Clulow V, Jackson JS, Mitchel REJ. Uranium and uranium decay series radionuclide dynamics in bone of rats following chronic uranium ore dust inhalation. Health Phys. 2001;81(5):502-513.
  • 25. Wrenn ME, Durbin PW, Howard B, Lipsztein J, Rundo J, Still ET, et al. Metabolism of ingested U and Ra. Health Phys. 1985;48(5):601-633.
  • 26. Penna-Franca E. Review of Brazilian investigations in areas of high natural radioactivity part II: internal exposure and cytogenetic survey. In: Proceedings of the International Symposium on Areas of High Natural Radioactivity, Pocosde caldas, Brazil, 1977; 29–48

Evaluation of Gross Alpha and Beta Radioactivity Concentrations in Tooth Samples

Year 2022, Volume: 8 Issue: 1, 1 - 8, 25.02.2022
https://doi.org/10.19127/mbsjohs.979585

Abstract

Objective: Teeth are used as an important data source to estimate radioactivity accumulation in individuals. This study aimed to evaluation the gross alpha (GA) and gross beta (GB) radioactivity concentrations in tooth samples.
Methods: Mandibular permanent first molar teeth of individuals living in the Middle Black Sea region were used for the study to ensure standardization. The teeth samples were divided into 4 groups according to the age factor (Group 1: 6-15 years, Group 2: 16-30 years, Group 3: 31-45 years, and Group 4: 46-65 years). Each group was divided into two subgroups according to gender factor. Measurements were completed with a nuclear spectroscopic system containing a gas-flow proportional counter. Data were analyzed statistically.
Results: While a statistically significant difference was detected among groups for GA radioactivity concentration (p<0.05), no significant difference was detected among groups for GB (p>0.05). Mean GA value was higher in Group 1 (6-15 years) compared to the other groups. There was no statistically significant difference between the genders in both GA and GB radioactivity concentrations for all groups (p>0.05).
Conclusion: While the GA radioactivity concentration was affected by the age factor, it was not affected by the gender factor.

Project Number

AP-1704

References

  • 1. Aghamiri SMR, Ghorbani Z, Darafsheh A, Torabzadeh H, Fathivand AA, Minuchehr A, et al. 226Ra concentration in the teeth of habitants of areas with high level of natural radioactivity in Ramsar. J Environ Radioact. 2006;89(3):212-218.
  • 2. White SC, Pharoah MJ. Oral Radiology principals and ınterpretation. 7 th ed. Mosby, Canada, 2014. p. 1-28.
  • 3. Cinelli G, Tollefsen T, Bossew P, Gruber V, Bogucarskis K, De Felice L, et al. Digital version of the European Atlas of natural radiation. J Environ Radioact. 2019;196:240-252.
  • 4. Sogut O, Aydin MF, Kucukonder E, Zorer OS, Dogru M. Measurement of gross alpha and gross beta activity concentrations in human tooth. J Environ Radioact. 2010;101(3):226-229.
  • 5. Taskin H, Kobya Y, Tokgoz M, Bassari A, Yesilkanat CM. Biomonitoring of trace elements and gross alpha/ beta radioactivity levels in human teeth: A case study from Istanbul, Turkey. Microchemical Journal. 2018;141:458-465.
  • 6. Clemente GF, Renzetti A, Santori G, Steinhäusler F, Pohl-Ruling J. Relationship between the 210Pb content of teeth and exposure to Rn and Rn daughters. Health Phys. 1984;47(2):253-262.
  • 7. Delibacak S, Ongun AR. Influence of treated sewage sludge applications on corn and second crop wheat yield and some soil properties of sandy loam soil. Fresen Environ Bull. 2016;25(1):43-54.
  • 8. Kir I, Erdogan M, Engin MS, Cay S. Trace metals in sediment, water and their bioaccumalation in Carp (Cyprinus Carpio L., 1758) samples, captured from the Karacaoren (I) Dam Lake, Turkey. Fresen Environ Bull. 2016;25(9):3557-3562.
  • 9. Beir VI. Report of the Committee on the Biological effects of Ionizing Radiation, National. Research, Council. 1999.
  • 10. Brown CJ, Chenery SR, Smith B, Mason C, Tomkins A, Roberts GJ, et al. Environmental influences on the trace element content of teeth—implications for disease and nutritional status. Arch Oral Biol. 2004;49(9):705-717.
  • 11. Corbacho JA, Zapata-García D, Montaña M, Fons J, Camacho A, Guillén J, et al. Selection of the appropriate radionuclide source for the efficiency calibration in methods of determining gross alpha activity in water. J Environ Radioact 2016;151:22-7.
  • 12. Butler FE. Strontium-90 in human teeth. Natur. 1961;11(189):848-849.
  • 13. Yamamoto M, Hinoide M, Ohkubo Y, Ueno K. Concentration of 226Ra in human teeth. Health Phys. 1994;67(5):535-540.
  • 14. Kulev YD, Polikarpov GG, Prigodey EV, Assimakopoulos PA. Strontium-90 concentrations in human teeth in South Ukraine, 5 years after the Chernobyl accident. Sci Total Environ. 1994;155(3):215-219.
  • 15. Baltas H, Sirin M, Senel F, Devran F. Determination of natural radionuclides and some metal concentrations in human tooth samples in the Rize province, Turkey Int J Environ Health Res. 2019; 31(1):20-33.
  • 16. Kavun Y, Boztosun I, Ðapo H, Maras I, Segebade C. Determination of the Sr/Ca ratio of tooth samples by photoactivation analysis in Southern Turkey. Radiochimica Acta. 2018;106(9):759-768.
  • 17. Ugur A, Sahan H, Sahan M, Yegingil Z, Gorur S. Investigation of the relation between environmental radioactivity and radioactivity in human teeth who lives in this environment. Fizika (Baku). 2010;16:537-540.
  • 18. Mangano JJ, Gould JM, Sternglass EJ, Shermand JD, McDonnelle W. An unexpected rise in strontium-90 in US deciduous teeth in the 1990s. Sci Total Environ. 2003;317 (1-3):37-51.
  • 19. Dogru M, Kulahci F. Iso-radioactivity curves of the water of the Hazar Lake, Elazig, Turkey. J Radioanal Nucl Chem. 2004;260(3):557-562. 20. Zorer OS, Ceylan H, Dogru M. Assessment of some trace heavy metals and radioactivity concentration in water of Bendimahi River Basin (Van, Turkey). Environ Monit Assess. 2008;147(1-3),183-90.
  • 21. Zorer OS, Ceylan H, Dogru M. Determination of heavy metals and comparison to gross radioactivity concentration in soil and sediment samples of the Bendimahi River Basin (Van, Turkey). Water, air, and Soil Pollution. 2009;196:75-87.
  • 22. Zorer OS, Ceylan H, Dogru M. Gross alpha and beta radioactivity concentration in water, soil and sediment of the Bendimahi River and Van Lake (Turkey). Environ Monit Assess. 2009;148(1-4):39-46.
  • 23. Rothe WE. Gross alpha radioactivity of human bones and teeth. Radiol Health Data Rep. 1966;7(3):204-205.
  • 24. Dewit T, Clulow V, Jackson JS, Mitchel REJ. Uranium and uranium decay series radionuclide dynamics in bone of rats following chronic uranium ore dust inhalation. Health Phys. 2001;81(5):502-513.
  • 25. Wrenn ME, Durbin PW, Howard B, Lipsztein J, Rundo J, Still ET, et al. Metabolism of ingested U and Ra. Health Phys. 1985;48(5):601-633.
  • 26. Penna-Franca E. Review of Brazilian investigations in areas of high natural radioactivity part II: internal exposure and cytogenetic survey. In: Proceedings of the International Symposium on Areas of High Natural Radioactivity, Pocosde caldas, Brazil, 1977; 29–48
There are 25 citations in total.

Details

Primary Language English
Subjects Health Care Administration
Journal Section Research articles
Authors

Zerrin Ünal Erzurumlu 0000-0002-8693-1206

Arzu Şahin 0000-0002-8789-4582

Çiğdem Güler 0000-0002-2581-9050

Mehmet Melih Ömezli 0000-0002-6606-6593

Mehmet Emin Korkmaz 0000-0001-8815-5629

Osman Ağar 0000-0003-3807-1587

Soner Çankaya 0000-0001-8056-1892

Project Number AP-1704
Publication Date February 25, 2022
Published in Issue Year 2022 Volume: 8 Issue: 1

Cite

Vancouver Ünal Erzurumlu Z, Şahin A, Güler Ç, Ömezli MM, Korkmaz ME, Ağar O, Çankaya S. Evaluation of Gross Alpha and Beta Radioactivity Concentrations in Tooth Samples. Mid Blac Sea J Health Sci. 2022;8(1):1-8.

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