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Article

Fluoride Content in Infusions of Selected Teas Available on the Polish Market—An In Vitro Study

1
Department of Biostructure and Animal Physiology, Wroclaw University of Environmental and Life Sciences, Kożuchowska1, 51-631 Wroclaw, Poland
2
Department of Human Nutrition, Faculty of Biotechnology and Food Science, Wroclaw University of Environmental and Life Sciences, Józefa Chełmońskiego 37, 51-630 Wroclaw, Poland
3
Division of Ultrastructural Research, Wroclaw Medical University, Chałubinskiego 6a, 50-368 Wroclaw, Poland
4
Department of Pediatric Dentistry and Preclinical Dentistry, Wroclaw Medical University, Krakowska 26, 50-425 Wroclaw, Poland
5
Institute of Low Temperatures and Structure Research, Polish Academy of Sciences, Okolna 2, 50-422 Wroclaw, Poland
6
Faculty of Dentistry, Wroclaw Medical University, Krakowska 26, 50-425 Wroclaw, Poland
7
Medical Center of Innovation, Wroclaw Medical University, Krakowska 26, 50-425 Wroclaw, Poland
8
Dental Surgery Department, Wroclaw Medical University, Krakowska 26, 50-425 Wroclaw, Poland
*
Authors to whom correspondence should be addressed.
Foods 2025, 14(14), 2452; https://doi.org/10.3390/foods14142452
Submission received: 13 June 2025 / Revised: 2 July 2025 / Accepted: 8 July 2025 / Published: 12 July 2025

Abstract

This study aimed to evaluate the fluoride content and other key physicochemical properties in commercially available black tea infusions, with a focus on tea form and geographic origin, in order to assess their contribution to total dietary fluoride intake. Methods: A total of 121 black tea samples were analyzed, including 66 loose-leaf, 42 bags, and 13 pyramid-bag teas. Infusions were prepared using standardized brewing protocols. Fluoride concentrations were determined with an ion-selective electrode, while the pH, buffer capacity, titratable acidity, calcium, and inorganic phosphorus were also measured. Statistical analysis included ANOVA, Tukey post hoc tests, and Pearson correlation analysis. Results: Fluoride content varied significantly by tea form and origin. Infusion of tea bags exhibited the highest fluoride, calcium, and acidity levels, while loose-leaf teas had the lowest. Teas from Africa contained approximately twice as much fluoride as those from Central or East Asia. Significant correlations between fluoride, calcium, and phosphorus were observed, particularly in tea-bag infusions, suggesting processing influences mineral release. Conclusions: Black tea, particularly in bag form and sourced from African regions, may significantly contribute to daily fluoride intake. Given the potential to exceed recommended fluoride thresholds, especially in individuals consuming multiple cups daily or living in fluoridated areas, these findings underscore the importance of consumer awareness and possible product labeling to guide safe consumption.

1. Introduction

Tea, derived from the leaves of Camellia sinensis, is one of the most widely consumed beverages globally and is available in several primary types—green, black, white, and oolong—each distinguished by unique processing methods and chemical profiles [1,2,3]. Black tea, the most popular type on the global market, has the highest degree of oxidation, leading to the formation of theaflavins and thearubigins—polyphenolic compounds produced from the transformation of catechin during fermentation —which are largely responsible for its antioxidant, anti-inflammatory, and cardiometabolic effects [4,5].
In addition to these bioactive compounds, black tea contains flavonols, gallic acid, caffeine, L-theanine, and a range of minerals [6,7,8]. Among these constituents, fluoride (F) is of particular interest, as it naturally accumulates in tea leaves and is commonly present in both the dry leaves and brewed infusions. While fluoride provides protective benefits for dental health, excessive intake may lead to adverse effects [9,10]. Its concentration in tea varies widely depending on factors such as geographic origin, agricultural practices, processing techniques, and the form in which the tea is marketed [11]. Black tea products—including loose leaf, tea bags, instant powders, and concentrated extracts—differ in their fluoride content and release characteristics [8]. Therefore, evaluating fluoride concentrations across various black tea products is essential for better understanding their contribution to total dietary fluoride intake and potential health implications.
Fluoride is an essential micronutrient that plays a key role in dental prevention. The relationship between fluoride and human health exemplifies a dose–response effect, where insufficient intake is associated with an increased risk of tooth decay. At optimal concentrations, fluoride enhances enamel mineralization through the formation of fluorapatite, increasing the resistance of teeth to acid-induced demineralization and thereby reducing the incidence of dental caries [12,13]. The cariostatic properties of fluoride include both the remineralization of enamel and the inhibition of caries-causing microorganisms such as Streptococcus mutans, by reducing their adhesion to the tooth surface [14,15,16,17]. Conversely, excessive fluoride intake, particularly over extended periods, poses well-documented health risks. In children, chronic overexposure can lead to dental fluorosis, a condition characterized by enamel hypomineralization, often irreversible. In adults, long-term intake exceeding safe thresholds may contribute to skeletal fluorosis, which can cause joint pain, reduced mobility, increased bone fragility, and potentially systemic effects, including neurological and endocrine disorders [18,19,20,21].
Dietary sources contribute significantly to total fluoride intake, with drinking water traditionally considered the primary source in many communities, though considerable variation exists depending on geographical location, food processing methods, and individual dietary patterns [12,13]. The World Health Organisation (WHO) recommends a fluoride concentration in drinking water of between 0.5 and 1.5 mg/L, with an optimum concentration of around 1 mg/L [14]. In contrast, the U.S. National Institutes of Health (NIH) recommends an adequate intake (AI) of fluoride of 3 mg/day for adult women and 4 mg/day for adult men, while the upper intake limit (UL) is 10 mg/day for adults and 0.1 mg/kg per day for children [19,20,22,23]. The European Food Safety Authority (EFSA) makes similar recommendations, noting the risk of chronic fluorosis [15,16]. The WHO advises that total fluoride intake should not exceed 0.05 mg/kg per day from all sources, including water, food, beverages, and dental products [15]. Polish national recommendations align closely with international standards. The Polish Society of Pediatric Dentistry and other expert bodies emphasize individualized fluoride prophylaxis, particularly in children and adolescents. They recommend a daily intake of 0.05 mg/kg and strongly advise against additional systemic fluoride use without assessing total environmental and dietary exposure [17,18]. Tea, particularly black tea, has been identified as a significant dietary source of fluoride due to the plant’s ability to bioaccumulate the element. The fluoride content of black tea depends, among other factors, on the form of the tea (such as tea bags, sticks, or granules), brewing time, brewing temperature, water quality, and the age of the leaves—with older leaves typically containing more fluoride [24,25,26,27,28,29,30,31]. According to scientific studies, consuming 1 to 1.5 liters of black tea per day (approximately 4–6 cups) may provide 50–100% of the recommended AI of fluoride for adults, and, in some cases, certain varieties may even exceed the tolerable upper intake level (UL) [32,33,34]. In populations with habitual tea consumption, especially where water is also fluoridated, the risk of overexposure increases significantly [35,36]. The bioavailability of tea-derived fluoride appears comparable to that of fluoridated water, suggesting equivalent biological activity [19,37]. Understanding these exposure parameters becomes essential for risk assessment and developing appropriate dietary recommendations, particularly for vulnerable populations including children, pregnant women, and individuals residing in areas with naturally high fluoride concentrations in water supplies [22,35,36]. This becomes particularly significant in the context of public health recommendations, where the maximum daily fluoride intake is established at 3–4 mg/day for adults and 0.05 mg/kg body weight for children [20,23,38].
In view of the growing interest in tea as a potentially important source of fluoride and the lack of detailed data on its content in various commercial forms, we decided to undertake a study focused on black teas commonly available on the market. Despite existing research pointing to notable fluoride levels in tea, comprehensive comparisons across product types and regions of origin remain scarce. Our goal was to explore how tea form (e.g., bags, loose-leaf, and pyramid bags), geographical origin, fluoride concentrations, and other physicochemical properties of tea infusions, such as calcium (Ca) and phosphorus (P) content, pH, buffering capacity, and titratable acidity, thereby contributing to a comprehensive understanding of the potential reciprocal effects on fluoride bioavailability and its impact on human health. The presence of calcium and phosphorus ions, as well as the pH of the infusion, can influence the degree of fluoride dissolution and complexation, thereby modifying its bioavailability. Conversely, the acidity and buffering capacity of the infusion may affect the stability of fluoride compounds and their interactions with other components of the beverage [21,24,39,40]. This research is particularly relevant in light of the public health concerns regarding cumulative fluoride exposure from multiple sources. By providing a clearer understanding of how different tea products contribute to total fluoride intake, our findings may help guide more informed consumer choices and support the development of targeted dietary recommendations—especially for groups at higher risk of overexposure.

2. Materials and Methods

2.1. Study Groups

The study investigated 124 black tea products from various producers, purchased from retail stores in Wrocław, Poland. It focused on the following three types of tea: loose-leaf (n = 66), standard tea bags (n = 42), and pyramid bags (n = 13). The teas were categorized geographically into the following three regions: Africa (n = 16), Central Asia (n = 81), and East Asia (n = 14). The detailed characteristics of the black teas are included in Table 1.

2.2. Preparation of Tea Infusions

Tea bags, each weighing between 1.4 and 2.0 g, were infused with 200 mL of commercial deionized water (EUROMEX Sp. z o. o., Szczucin, Poland) at the temperature recommended by the manufacturer (95–100 °C). The quality of water was measured with TDS (total dissolved solids) meter (TDS-3, ABC-RC, Wieprz, Poland). The TDS value was 7 mg/L. An electric kettle (Amica model KM6011, Wronki, Poland) was used to control the temperature of the water used to prepare tea infusions. The bags were brewed for three minutes under a cover to prevent evaporation. For loose-leaf teas, 2.0 g of tea was similarly infused with 200 mL of deionized water at the indicated temperature and brewed for three minutes under cover. To obtain a clear infusion, the tea was filtered through filter paper. For tea bags weighing less than 2.0 g (e.g., 1.4 g, 1.5 g, or 1.75 g), the results were normalized to a 2.0 g equivalent to match the mass of the loose-leaf samples. After cooling to room temperature, the infusions were subjected to laboratory analysis. Each of the examined parameters was measured in triplicate to ensure the reliability of the results.

2.3. Measuring the pH of Herbal Infusions

The pH was measured using a Eurosensor pH electrode (Eurosensor, Gliwice, Poland) connected to a CPI-505 pH/ion meter (Elmetron, Zabrze, Poland). All measurements were performed at room temperature using freshly prepared infusions. The reagents used were of analytical grade, and solutions were prepared with deionized water (TDS = 7 mg/L, EUROMEX Sp. z o. o., Szczucin, Poland).

2.4. Measuring the Buffering Capacity of Tea Infusions

Buffering capacity refers to a substance’s ability to resist changes in pH upon the addition of an acid or base. In this study, the buffering capacity was determined by adding 0.1 M HCL (reagent grade, Chempur, Poland) to the infusion and calculated using the following formula:
B u f f e r   c a p a c i t y   ( m o l / L ) = ( 0.01 / V ) × ( p H 2 p H 1 )
where
pH1 is the pH of the brewed tea;
pH2 is the pH after the addition of 0.1 M HCl.

2.5. Determination of Titratable Acidity of Tea Infusions

Titratable acidity, expressed in millimoles per liter (mmol/L), represents the volume of 0.1 M NaOH (reagent grade, Chempur, Poland) needed to neutralize all acidic components in the solution to a pH of 7.

2.6. Determination of Inorganic Phosphorus and Calcium in Tea Infusions

The concentration of inorganic phosphorus was determined using the phosphomolybdate method at a wavelength of 340 nm, with deionized water as a reference (TDS = 7 mg/L, EUROMEX Sp. z o. o., Szczucin, Poland). The method is based on the formation of a phosphomolybdate complex in an acidic medium, followed by reduction to a molybdenum blue complex measurable spectrophotometrically. The reagents used were ammonium molybdate, sulphuric acid, and detergents (reagent grade, Spinreact Kit, Spinreact, S.A./S.A.U., Sant Esteve de Bas, Spain).
Calcium was determined using the Arsenazo III method at a wavelength of 630 nm, also with deionized water (TDS = 7 mg/L, EUROMEX Sp. z o. o., Szczucin, Poland) as a reference. The method is based on the formation of a stable purple complex between calcium ions and arsenazo III in imidazole buffer pH 6.5 (reagent grade, Spinreact Kit, Spinreact, S.A./S.A.U., Sant Esteve de Bas, Spain).

2.7. Determination of Fluoride Content in Tea Infusions

Fluoride was determined using an ORION 9609 ion-selective electrode (Thermo Fisher Scientific, Waltham, MA, USA), in accordance with the manufacturer’s instructions, in conjunction with a CPI-551 ELMETRON pH/ionometer microcomputer (Elmetron, Zabrze, Poland). This electrode is classified as a combined electrode, meaning that a separate reference electrode was not required.

2.8. Statistical Analysis

The statistical analysis performed in this study focused on identifying differences between tea types (bags, loose-leaf, and pyramid bags) and regions (Africa, Central Asia, and East Asia), as well as on finding correlations between the evaluated variables. Therefore, an ANOVA test with a Tukey post hoc test and a Pearson correlation test were used. Correlation analysis was performed for all evaluated teas, as well as for tea-type subgroups. The analysis was conducted using the Jamovi software v. 2.6 (Jamovi, Sydney, Australia) and R Statistical Environment (R Core Team, Vienna, Austria).

3. Results

3.1. Physicochemical Properties of Teas

Statistically significant differences in the analyzed physicochemical properties are presented in Figure 1. The effect of tea form on the results is shown in Figure 1A–D. Tea bags exhibit the highest levels of fluoride, calcium, titratable acidity, and buffer capacity. Teas in pyramid bags and loose-leaf form tend to show similar values, except for titratable acidity, where loose-leaf tea displays the lowest value. The raw descriptive values for the different groups are included in Supplementary Table S1.
Teas produced in different regions exhibit similar characteristics. The only statistically significant difference was observed in fluoride concentration, with teas from Africa containing approximately twice as much fluoride as those from Central or East Asia (Figure 1E).

3.2. Correlation Analysis Among Physicochemical Properties

Statistically significant correlations are presented in Figure 2. Correlation analysis was conducted for all evaluated teas, as well as within specific tea-type subgroups. Overall, the concentrations of all analyzed elements showed significant mutual correlations, as follows: fluoride with calcium (r = 0.46), fluoride with inorganic phosphorus (r = 0.43), and inorganic phosphorus with calcium (r = 0.45). Additionally, all three elements correlated significantly with titratable acidity (fluoride: r = 0.68, calcium: r = 0.40, and phosphorus: r = 0.41).
Notably, when the correlations were analyzed within individual subgroups, they remained significant only for tea-bag infusions. In loose-leaf teas, the correlations between calcium and fluoride, as well as phosphorus and fluoride, were not statistically significant. Tea in pyramid bags showed a significant correlation only between fluoride and titratable acidity.

4. Discussion

The present study demonstrates that the physical form and processing method of black tea significantly affects fluoride content in brewed infusions. The results indicate that tea bags showed the highest fluoride concentrations compared with loose-leaf and pyramid bags, consistent with previous observations [1,4] that a smaller particle size and increased surface area increase fluoride extraction during brewing [8,25]. Additionally, the quality grading system often assigns lower-grade leaves with potentially higher fluoride accumulation to tea bags, while premium whole leaves are reserved for loose-leaf products [11,26]. This increased extraction efficiency in tea bags is concerning from a public health perspective, as tea bags are the most widely consumed form of black tea in the world. The strong correlations between fluoride and other minerals (calcium r = 0.46 and inorganic phosphorus r = 0.43) observed exclusively in tea bags suggest that the processing and packaging methods significantly alter the chemical matrix and release characteristics of bioactive compounds. These findings extend beyond previous studies that focused primarily on brewing parameters, demonstrating that the commercial form of tea itself is a critical determinant of fluoride exposure, with bag varieties potentially contributing disproportionately to total dietary fluoride intake.
The significant regional variation in fluoride content observed in this study, particularly the elevated levels in African-sourced teas compared with Central and East Asian varieties, reflects the complex interaction between environmental factors and tea plant fluoride bioaccumulation, confirming previous observations by Pavlovič et al. regarding geographic variability in tea fluoride content [25]. For populations in areas with fluoridated water supplies, the cumulative effect of tea consumption could easily exceed safe fluoride thresholds, especially in children, whose lower body weight makes them more susceptible to fluoride toxicity [27,36]. These findings support the need for evidence-based consumption guidelines that consider tea form, origin, and individual risk factors [36]. Our results indicating approximately twice the fluoride concentrations in African teas support previous studies showing that Camellia sinensis acts as a bioaccumulator and that fluoride uptake depends on soil composition, water quality, and agricultural practices specific to growing regions [28,29,30]. This geographic variability has major implications for dietary risk assessment, as consumers of teas from Africa may experience significantly higher fluoride exposure than those consuming teas from other regions. The observed bioaccumulation patterns are consistent with established knowledge that mature tea leaves concentrate fluoride over time, but our findings uniquely quantify the regional discrepancies that exist in commercial tea products. Public health recommendations should include fluoride labeling on tea products, especially for high-risk varieties, and educational initiatives to promote awareness of cumulative fluoride exposure from all dietary sources, as suggested by Satou et al. in their risk assessment framework [31].
The clinical significance of our findings lies in the potential impact of chronic tea consumption on fluoride-related health outcomes, both beneficial and adverse. While moderate fluoride intake provides well-documented prevention of dental caries through enamel remineralization and antimicrobial activity against caries-forming bacteria [32,33,34,41], our results indicate that consumption at the level of 3–4 cups per day, especially of high-fluoride varieties, may result in fluoride intake approaching or exceeding recommended thresholds, especially when combined with other fluoride sources. The link between fluoride and health outcomes suggests that elevated concentrations observed in certain forms and origins of tea may contribute to dental fluorosis in children and, with prolonged exposure, potentially to skeletal fluorosis [19,42,43]. However, the antioxidant, anti-inflammatory, and cardiovascular benefits of black tea compounds such as theaflavins and thearubigins should be weighed against fluoride risks in clinical decision making. Our results support the implementation of individualized dietary counseling that takes into account total fluoride exposure from all sources, including tea consumption patterns, particularly for patients at high risk for fluoride-related adverse effects. This personalized approach is consistent with contemporary principles of preventive medicine and the growing recognition that dietary interventions must address cumulative patterns of exposure rather than isolated dietary components.
The findings of this study underscore the potential of black tea—especially in bag form—as a significant and often underestimated source of dietary fluoride, with clear implications for public health. Infusion of tea bags exhibited consistently higher fluoride concentrations than infusion of loose-leaf and pyramid bags, likely due to differences in physical form and infusion efficiency. Notably, only tea-bag infusions demonstrated strong correlations between fluoride and other elements, indicating their distinct role in cumulative fluoride exposure. These distinctions are especially salient considering that regular consumption of black tea, estimated at 1–1.5 L per day, may contribute 50–100% of the AI, and in some instances may approach or exceed UL, particularly in populations with additional exposure from fluoridated water or dental products [44]. The substantial regional variability observed—especially the elevated fluoride levels in African-sourced teas—further emphasizes the need for individualized risk assessment. These findings align with current recommendations from global and national health authorities, including the WHO, EFSA, and Polish expert bodies, and contribute novel and form- and origin-specific data essential for refining dietary guidelines and optimizing preventive strategies against fluoride-related health risks [45,46].
The infusion water used is a critical factor in determining the overall fluoride content of the beverage. The final fluoride content of the tea extract is influenced by water-related factors, including water hardness, calcium and fluoride content, and pH. Our experience from previous studies [47] shows that tap water varies greatly in terms of the aforementioned parameters, even within a single city. For instance, in the city of Wrocław (Poland), the calcium content of the water measured at three water production stations (‘Na Grobli’, ‘Mokry Dwór’, and ‘Leśnica—pumping station II degree’) was found to be within the range of 0.0860–0.1490 mg/mL. Furthermore, the presence of a range of physico-chemical parameters in commercially available bottled water samples on the Polish market is likely to result in fluctuations in fluoride levels in the beverage. The utilization of deionized water in our experimental protocol was intended to provide an objective assessment of the fluoride content in extracts obtained from individual teas. It is important to note that these conditions are essential for ensuring the reliability of the measurement process. Consequently, the fluoride content of the tea sample is the only source of variation in the results.
The aluminum (Al3+) present in the extracts demonstrates a pronounced propensity to form complexes with fluoride (Al-F), particularly in acidic environments, where it is present as soluble ions. This results in a reduction in the concentration of free fluoride ions (F-) in solution. In the Al3+/F- system, forms such as AlF2+, AlF2+, AlF30, AlF4, AlF52−, and AlF63− occur, and their distribution depends on pH, among other factors [48,49,50]. In the context of scientific studies, it has been demonstrated that within an environment characterized by a pH value of approximately 4–6, a substantial proportion of fluoride, estimated to be over 78%, is found to be complexed with aluminum. This observation indicates that a mere 21% of the fluoride remains in its free state [51,52]. The addition of milk or sugar to infusions by consumers has been demonstrated to influence the fluoride delivery with the beverage. The high calcium content of milk has been shown to reduce the bioavailability of fluoride by approximately 20–80% through the formation of insoluble CaF2 in the gastrointestinal tract, thereby reducing the absorption of this element [53,54]. Conversely, the addition of sugar has been observed to enhance the extraction of fluoride during the initial minutes of tea steeping [55]. It is, therefore, postulated that knowledge of the aforementioned interactions may serve to lower the threshold for potentially harmful fluoride intake.
While this study offers valuable insights into the fluoride content of black tea infusions across different forms and regions, several limitations should be acknowledged. The analysis was limited to teas available in a single market (Poland), which may affect the generalizability of the findings to other regions with different consumption patterns and product types. Although fluoride levels were measured under standardized conditions, real-life variables—such as water fluoride content, brewing duration, and temperature—may significantly alter actual exposure. The study also did not account for individual variability in fluoride absorption and metabolism, which can influence systemic fluoride burden. As a cross-sectional analysis, it cannot inform long-term health outcomes. Future research should include a wider geographic scope, more diverse brewing scenarios, and a comprehensive assessment of all fluoride sources. Longitudinal studies are particularly needed to assess the cumulative health effects of fluoride from tea, with particular attention paid to children who are most susceptible to dental fluorosis due to their greater sensitivity to fluoride during tooth development.

5. Conclusions

Black tea, particularly in bag form and sourced from Africa, is a notable contributor to daily fluoride intake. With regular consumption, especially alongside other fluoride sources, like drinking water or dental products, there is potential to exceed recommended intake levels—posing a risk, particularly for children. The study highlights that both tea form and origin significantly influence fluoride content, with tea bags showing the highest concentrations and strongest mineral correlations. These findings support the need for clearer labeling of fluoride content on tea products and greater consumer awareness. Public health recommendations should account for individual consumption habits and regional product differences to better manage fluoride exposure and its associated health risks.

Supplementary Materials

The following supporting information can be downloaded at: https://www.mdpi.com/article/10.3390/foods14142452/s1, Table S1: Raw descriptive statistics.

Author Contributions

Conceptualization, A.M. and M.D.; methodology, A.M., A.W., and M.K.; software, A.M., M.S., and J.M.; validation, A.M., J.M., and M.D.; formal analysis, J.M., M.J., and M.D.; investigation, A.M., A.W., and M.K.; resources, A.M., A.W., and M.D.; data curation, A.M. and A.W.; writing—original draft preparation, A.M., J.K., A.K., and I.Z.; writing—review and editing, A.M., A.W., J.K., A.K., I.Z., J.M., and M.D.; visualization, M.K.; supervision, J.M., M.J., and M.D.; project administration, A.M. and M.D.; funding acquisition, M.J. and M.S. All authors have read and agreed to the published version of the manuscript.

Funding

This work was financed by a subsidy from Wroclaw Medical University, number SUBZ.B180.23.054. The APC was co-financed by Wrocław University of Environmental and Life Sciences.

Institutional Review Board Statement

Not applicable.

Informed Consent Statement

Not applicable.

Data Availability Statement

The original contributions presented in this study are included in the article/Supplementary Materials. Further inquiries can be directed to the corresponding authors.

Conflicts of Interest

The authors declare no conflicts of interest.

References

  1. Khan, N.; Mukhtar, H. Tea and Health: Studies in Humans. Curr. Pharm. Des. 2013, 19, 6141–6147. [Google Scholar] [CrossRef] [PubMed]
  2. Małyszek, A.; Kiryk, S.; Kensy, J.; Kotela, A.; Michalak, M.; Kiryk, J.; Janeczek, M.; Matys, J.; Dobrzyński, M. Identification of Factors Influencing Fluoride Content in Tea Infusions: A Systematic Review. Appl. Sci. 2025, 15, 5974. [Google Scholar] [CrossRef]
  3. Lakshmanan, L.; Gurunathan, D.; Shanmugam, R. Effectiveness of White Tea-Mediated Silver Nanoparticles as an Intracanal Irrigant against Enterococcus Faecalis: An in Vitro Study. Dent. Med. Probl. 2024, 61, 593–598. [Google Scholar] [CrossRef] [PubMed]
  4. Yao, L.H.; Jiang, Y.M.; Caffin, N.; D’Arcy, B.; Datta, N.; Liu, X.; Singanusong, R.; Xu, Y. Phenolic Compounds in Tea from Australian Supermarkets. Food Chem. 2006, 96, 614–620. [Google Scholar] [CrossRef]
  5. Vastrad, J.V.; Badanayak, P.; Goudar, G. Phenolic Compounds in Tea: Phytochemical, Biological, and Therapeutic Applications. In Phenolic Compounds—Chemistry, Synthesis, Diversity, Non-Conventional Industrial, Pharmaceutical and Therapeutic Applications; IntechOpen: London, UK, 2022. [Google Scholar]
  6. Lin, J.-K.; Lin, C.-L.; Liang, Y.-C.; Lin-Shiau, S.-Y.; Juan, I.-M. Survey of Catechins, Gallic Acid, and Methylxanthines in Green, Oolong, Pu-Erh, and Black Teas. J. Agric. Food Chem. 1998, 46, 3635–3642. [Google Scholar] [CrossRef]
  7. Kaczmarek, U. PH Values and Fluoride Levels in Some Tea Brands. Ann. Acad. Med. Stetin. 2004, 50 (Suppl. 1), 58–61. [Google Scholar]
  8. Koblar, A.; Tavčar, G.; Ponikvar-Svet, M. Fluoride in Teas of Different Types and Forms and the Exposure of Humans to Fluoride with Tea and Diet. Food Chem. 2012, 130, 286–290. [Google Scholar] [CrossRef]
  9. Abanto Alvarez, J.; Rezende, K.M.P.C.; Marocho, S.M.S.; Alves, F.B.T.; Celiberti, P.; Ciamponi, A.L. Dental Fluorosis: Exposure, Prevention and Management. Med. Oral Patol. Oral Cir. Bucal 2009, 14, E103–E107. [Google Scholar]
  10. Manjunathappa, T.H.; Devegowda, D.; Mysore, N.K.; Vishwanath, P.; Narayana, P.S. Association between Drinking Water Fluoride and the Serum Alkaline Phosphatase and Phosphate Levels in Pregnant Women and Newborn Infants. Dent. Med. Probl. 2023, 60, 569–575. [Google Scholar] [CrossRef]
  11. Lu, Y.; Guo, W.-F.; Yang, X.-Q. Fluoride Content in Tea and Its Relationship with Tea Quality. J. Agric. Food Chem. 2004, 52, 4472–4476. [Google Scholar] [CrossRef]
  12. Levy, S.M.; Guha-Chowdhury, N. Total Fluoride Intake and Implications for Dietary Fluoride Supplementation. J. Public Health Dent. 1999, 59, 211–223. [Google Scholar] [CrossRef] [PubMed]
  13. Rodrigues, M.H.C.; Leite, A.L.; Arana, A.; Villena, R.S.; Forte, F.D.S.; Sampaio, F.C.; Buzalaf, M.A.R. Dietary Fluoride Intake by Children Receiving Different Sources of Systemic Fluoride. J. Dent. Res. 2009, 88, 142–145. [Google Scholar] [CrossRef] [PubMed]
  14. World Health Organization. Guidelines for Drinking-Water Quality, 4th ed.; World Health Organization: Geneva, Switzerland, 2011. [Google Scholar]
  15. Dobrzyński, W.; Nikodem, A.; Diakowska, D.; Wiglusz, R.J.; Watras, A.; Dobrzyński, M.; Mikulewicz, M. Comparison of the fluoride ion release from nanofluorapatite-modified orthodontic cement under different pH conditions—An in vitro study. Acta Bioeng. Biomech. 2023, 25, 159–176. [Google Scholar] [CrossRef]
  16. European Food Safety Authority. Overview on Tolerable Upper Intake Levels as Derived by the Scientific Committee on Food (SCF) and the EFSA Panel on Dietetic Products, Nutrition and Allergies (NDA); European Food Safety Authority: Parma, Italy, 2024. [Google Scholar]
  17. Olczak-Kowalczyk, D.; Mielczarek, A.; Jackowska, T.; Mielnik-Błaszczak, M.; Turska-Szybka, A.; Opydo-Szymaczek, J.; Jurczak, A.; Kaczmarek, U. Środki Fluorkowe w Zapobieganiu i Leczeniu Próchnicy i Erozji Zębów u Dzieci, Młodzieży i Dorosłych–Rekomendacje Polskich Ekspertów. Aktualizacja Zaleceń: Indywidualna Profilaktyka Fluorkowa u Dzieci, Młodzieży–Rekomendacje Polskich Ekspertów. Nowa Stomatol. 2022, 27, 35–59. [Google Scholar] [CrossRef]
  18. Herman, K.; Wujczyk, M.; Dobrzynski, M.; Diakowska, D.; Wiglusz, K.; Wiglusz, R.J. In Vitro Assessment of Long-Term Fluoride Ion Release from Nanofluorapatite. Materials 2021, 14, 3747. [Google Scholar] [CrossRef]
  19. Veneri, F.; Iamandii, I.; Vinceti, M.; Birnbaum, L.S.; Generali, L.; Consolo, U.; Filippini, T. Fluoride Exposure and Skeletal Fluorosis: A Systematic Review and Dose-Response Meta-Analysis. Curr. Environ. Health Rep. 2023, 10, 417–441. [Google Scholar] [CrossRef]
  20. Institute of Medicine (US) Standing Committee on the Scientific Evaluation of Dietary Reference Intakes. Dietary Reference Intakes for Calcium, Phosphorus, Magnesium, Vitamin D, and Fluoride; National Academies Press: Washington, DC, USA, 1997; ISBN 978-0-309-06403-3.
  21. Linhares, D.P.S.; Garcia, P.V.; Amaral, L.; Ferreira, T.; dos Santos Rodrigues, A. Safety Evaluation of Fluoride Content in Tea Infusions Consumed in the Azores—A Volcanic Region with Water Springs Naturally Enriched in Fluoride. Biol. Trace Elem. Res. 2017, 179, 158–164. [Google Scholar] [CrossRef] [PubMed]
  22. Malinowska, E.; Inkielewicz, I.; Czarnowski, W.; Szefer, P. Assessment of Fluoride Concentration and Daily Intake by Human from Tea and Herbal Infusions. Food Chem. Toxicol. 2008, 46, 1055–1061. [Google Scholar] [CrossRef]
  23. European Food Safety Authority (EFSA). Opinion of the Scientific Panel on Dietetic Products, Nutrition and Allergies (NDA) on a Request from the Commission Related to the Tolerable Upper Intake Level of Fluoride. EFSA J. 2005, 3, 192. [Google Scholar] [CrossRef]
  24. Erdemoglu, S.B.; Türkdemir, H.; Gücer, S. Determination of Total and Fluoride Bound Aluminium in Tea Infusions by Ion Selective Electrode and Flame Atomic Absorption Spectrometry. Anal. Lett. 2000, 33, 1513–1529. [Google Scholar] [CrossRef]
  25. Pavlovič, A.; Tavčar, G.; Ponikvar-Svet, M. Fluoride and Aluminium in Tea (Camellia sinensis L.)—Tea Quality Indicators and Risk Factors for Consumers. Molecules 2023, 28, 6396. [Google Scholar] [CrossRef]
  26. Herman, K.; Czajczyńska-Waszkiewicz, A.; Kowalczyk-Zając, M.; Dobrzyński, M. Assessment of the influence of vegetarian diet on the occurrence of erosive and abrasive cavities in hard tooth tissues. Postepy Hig. Med. Dosw. 2011, 65, 764–769. [Google Scholar]
  27. Lubojanski, A.; Piesiak-Panczyszyn, D.; Zakrzewski, W.; Dobrzynski, W.; Szymonowicz, M.; Rybak, Z.; Mielan, B.; Wiglusz, R.J.; Watras, A.; Dobrzynski, M. The Safety of Fluoride Compounds and Their Effect on the Human Body—A Narrative Review. Materials 2023, 16, 1242. [Google Scholar] [CrossRef]
  28. Ruan, J.; Ma, L.; Shi, Y.; Han, W. The Impact of PH and Calcium on the Uptake of Fluoride by Tea Plants (Camellia sinensis L.). Ann. Bot. 2004, 93, 97–105. [Google Scholar] [CrossRef]
  29. Zhang, L.; Li, Q.; Ma, L.; Ruan, J. Characterization of Fluoride Uptake by Roots of Tea Plants (Camellia sinensis (L.) O. Kuntze). Plant Soil 2013, 366, 659–669. [Google Scholar] [CrossRef]
  30. Li, Q.-S.; Lin, X.-M.; Qiao, R.-Y.; Zheng, X.-Q.; Lu, J.-L.; Ye, J.-H.; Liang, Y.-R. Effect of Fluoride Treatment on Gene Expression in Tea Plant (Camellia sinensis). Sci. Rep. 2017, 7, 9847. [Google Scholar] [CrossRef]
  31. Satou, R.; Oka, S.; Sugihara, N. Risk Assessment of Fluoride Daily Intake from Preference Beverage. J. Dent. Sci. 2021, 16, 220–228. [Google Scholar] [CrossRef] [PubMed]
  32. Wei, J.; Wang, J.; Shan, W.; Liu, X.; Ma, J.; Liu, C.; Fang, J.; Wei, S. Development of Fluorapatite Cement for Dental Enamel Defects Repair. J. Mater. Sci. Mater. Med. 2011, 22, 1607–1614. [Google Scholar] [CrossRef]
  33. Vieira, A.; Hancock, R.; Limeback, H.; Schwartz, M.; Grynpas, M. How Does Fluoride Concentration in the Tooth Affect Apatite Crystal Size? J. Dent. Res. 2003, 82, 909–913. [Google Scholar] [CrossRef] [PubMed]
  34. Rošin-Grget, K. The Cariostatic Mechanisms of Fluoride. Acta Med. Acad. 2013, 42, 179–188. [Google Scholar] [CrossRef]
  35. Waugh, D.; Potter, W.; Limeback, H.; Godfrey, M. Risk Assessment of Fluoride Intake from Tea in the Republic of Ireland and Its Implications for Public Health and Water Fluoridation. Int. J. Environ. Res. Public Health 2016, 13, 259. [Google Scholar] [CrossRef]
  36. Peng, C.; Cai, H.; Zhu, X.; Li, D.; Yang, Y.; Hou, R.; Wan, X. Analysis of Naturally Occurring Fluoride in Commercial Teas and Estimation of Its Daily Intake through Tea Consumption. J. Food Sci. 2016, 81, H235–H239. [Google Scholar] [CrossRef]
  37. van der Hoeven, J.S.; Franken, H.C. Effect of Fluoride on Growth and Acid Production by Streptococcus Mutans in Dental Plaque. Infect. Immun. 1984, 45, 356–359. [Google Scholar] [CrossRef]
  38. National Research Council. Fluoride in Drinking Water; National Academies Press: Washington, DC, USA, 2006; ISBN 978-0-309-10128-8.
  39. Maleki, A.; Abulmohammadi, P.; Teymouri, P.; Zandi, S.; Daraei, H.; Mahvi, A.H.; Shahsawari, S. Effect of Brewing Time and Water Hardness on Fluoride Release from Different Iranian Teas. Fluoride 2016, 49, 263–273. [Google Scholar]
  40. Morés, S.; Monteiro, G.C.; Santos, F.da.S.; Carasek, E.; Welz, B. Determination of Fluorine in Tea Using High-Resolution Molecular Absorption Spectrometry with Electrothermal Vaporization of the Calcium Mono-Fluoride CaF. Talanta 2011, 85, 2681–2685. [Google Scholar] [CrossRef]
  41. Oleniacz-Trawińska, M.; Kotela, A.; Kensy, J.; Kiryk, S.; Dobrzyński, W.; Kiryk, J.; Gerber, H.; Fast, M.; Matys, J.; Dobrzyński, M. Evaluation of Factors Affecting Fluoride Release from Compomer Restorative Materials: A Systematic Review. Materials 2025, 18, 1627. [Google Scholar] [CrossRef]
  42. DenBesten, P.; Li, W. Chronic Fluoride Toxicity: Dental Fluorosis. Monogr. Oral Sci. 2011, 22, 81–96. [Google Scholar]
  43. Choi, A.L.; Sun, G.; Zhang, Y.; Grandjean, P. Developmental Fluoride Neurotoxicity: A Systematic Review and Meta-Analysis. Environ. Health Perspect. 2012, 120, 1362–1368. [Google Scholar] [CrossRef]
  44. Inoue-Choi, M.; Ramirez, Y.; Cornelis, M.C.; Berrington de González, A.; Freedman, N.D.; Loftfield, E. Tea Consumption and All-Cause and Cause-Specific Mortality in the UK Biobank. Ann. Intern. Med. 2022, 175, 1201–1211. [Google Scholar] [CrossRef]
  45. Kaczmarek, U.; Jackowska, T.; Mielnik-Błaszczak, M.; Jurczak, A.; Olczak-Kowalczyk, D. Individualised Caries Prevention with Fluoride in Children and Adolescents–Recommendations of Polish Experts. Nowa Stomatol. 2019, 24, 70–85. [Google Scholar] [CrossRef]
  46. EFSA Panel on Dietetic Products, Nutrition, and Allergies (NDA). Scientific Opinion on Dietary Reference Values for Fluoride. EFSA J. 2013, 11, 3332. [Google Scholar] [CrossRef]
  47. Piszko, P.J.; Kulus, M.; Piszko, A.; Kiryk, J.; Kiryk, S.; Kensy, J.; Małyszek, A.; Michalak, M.; Dobrzyński, W.; Matys, J.; et al. The Influence of Calcium Ions and PH on Fluoride Release from Commercial Fluoride Gels in an In Vitro Study. Gels 2025, 11, 486. [Google Scholar] [CrossRef]
  48. Wang, W.; Yang, H.; Wang, X.; Jiang, J.; Zhu, W. Factors Effecting Aluminum Speciation in Drinking Water by Laboratory Research. J. Environ. Sci. 2010, 22, 47–55. [Google Scholar] [CrossRef]
  49. Townsend, G.S.; Bache, B.W. Kinetics of Aluminium Fluoride Complexation in Single- and Mixed-Ligand Systems. Talanta 1992, 39, 1531–1535. [Google Scholar] [CrossRef]
  50. Berger, T.; Mathurin, F.A.; Gustafsson, J.P.; Peltola, P.; Åström, M.E. The Impact of Fluoride on Al Abundance and Speciation in Boreal Streams. Chem. Geol. 2015, 409, 118–124. [Google Scholar] [CrossRef]
  51. Romar, A.; Gago, C.; Fernández-Marcos, M.L.; Álvarez, E. Influence of Fluoride Addition on the Composition of Solutions in Equilibrium with Acid Soils. Pedosphere 2009, 19, 60–70. [Google Scholar] [CrossRef]
  52. Wamalwa Wambu, E.; Jerop Kurui, A. Fluoride Adsorption onto Soil Adsorbents: The Role of PH and Other Solution Parameters. In Soil pH for Nutrient Availability and Crop Performance; IntechOpen: London, UK, 2019. [Google Scholar]
  53. Khandare, A.L. Comparison of Fluoride Levels (Total and Extracted) in Young, Old Tea Leaves and Market Tea Samples along with Impact of Tea Infusion on Dental Fluorosis in Fluoride Endemic Villages of Nalgonda District, India. Adv. Dent. Oral Health 2019, 10, 555793. [Google Scholar] [CrossRef]
  54. Peng, C.; Xu, X.; Ren, Y.; Niu, H.; Yang, Y.; Hou, R.; Wan, X.; Cai, H. Fluoride Absorption, Transportation and Tolerance Mechanism in Camellia Sinensis, and Its Bioavailability and Health Risk Assessment: A Systematic Review. J. Sci. Food Agric. 2021, 101, 379–387. [Google Scholar] [CrossRef]
  55. Lung, S.-C.C.; Cheng, H.-W.; Fu, C.B. Potential Exposure and Risk of Fluoride Intakes from Tea Drinks Produced in Taiwan. J. Expo. Sci. Environ. Epidemiol. 2008, 18, 158–166. [Google Scholar] [CrossRef]
Figure 1. Selected physicochemical properties of black teas depending on form (leaf, bag, and pyramid bag) and region of origin. Bar plots (AD) show statistically significant differences between different tea forms, while chart (E) presents differences based on origin. * p < 0.05, ; *** p < 0.001.
Figure 1. Selected physicochemical properties of black teas depending on form (leaf, bag, and pyramid bag) and region of origin. Bar plots (AD) show statistically significant differences between different tea forms, while chart (E) presents differences based on origin. * p < 0.05, ; *** p < 0.001.
Foods 14 02452 g001
Figure 2. Correlation analysis of selected physicochemical properties. Each dot refers to a distinct tea type. Black lines show overall trend. (A) correlation plot for F and Ca. (B) inorganic P and F. (C) titratable acidity and F. (D) Ca and inorganic P. (E) titratable acidity and Ca. (F) inorganic P and titratable adicity.
Figure 2. Correlation analysis of selected physicochemical properties. Each dot refers to a distinct tea type. Black lines show overall trend. (A) correlation plot for F and Ca. (B) inorganic P and F. (C) titratable acidity and F. (D) Ca and inorganic P. (E) titratable acidity and Ca. (F) inorganic P and titratable adicity.
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Table 1. Types of teas included into the study.
Table 1. Types of teas included into the study.
Tea Name (Brand)FormOrigin
Assam Irish Breakfast (Ronnefeldt)BagsIndia
Classic Black Tea (Tetley)BagsIndia
Classic Earl Grey (Tetley)BagsIndia
Darjeeling (Ronnefeldt)BagsIndia
Earl Grey (Ronnefeldt)BagsIndia
Yellow Label (Lipton)BagsIndia
Black with Ginger and Turmeric (Remsey)BagsKenya
Classic Black (Remsey)BagsKenya
Earl Grey (Lord Nelson)BagsKenya
Earl Grey Strong Tempting Bergamot Flavour (Remsey)BagsKenya
Earl Grey with a Hint of Lemon Bergamot Flavour (Remsey)BagsKenya
English Breakfast (Lipton)BagsKenya
English Teatime (Lipton)BagsKenya
Yellow Label (Lipton)BagsKenya
Classic Black (Lord Nelson)BagsOutside EU
Black Tea “Minutka” (Minutka)BagsSri Lanka
Black Tea (Minutka)BagsSri Lanka
Black Tea Earl Grey Full-Bodied (Vintage Teas)BagsSri Lanka
Ceylon (Loyd)BagsSri Lanka
Ceylon Black (Remsey)BagsSri Lanka
Ceylon Black Tea (Big-Active)BagsSri Lanka
Ceylon Earl Grey (Remsey)BagsSri Lanka
Ceylon Gold (Sir William’s Tea)BagsSri Lanka
Ceylon Premium Tea (Dilmah)BagsSri Lanka
Classic Earl Grey (Exclusive) (Lipton)BagsSri Lanka
Earl Grey (Ahmad Tea)BagsSri Lanka
Earl Grey (Akbar)BagsSri Lanka
Earl Grey (Loyd)BagsSri Lanka
Earl Grey (Loyd)BagsSri Lanka
Earl Grey (Sir William’s Tea)BagsSri Lanka
Earl Grey (Teekane)BagsSri Lanka
English Breakfast (Ahmad Tea)BagsSri Lanka
English Breakfast (Ronnefeldt)BagsSri Lanka
English Breakfast (Sir William’s Tea)BagsSri Lanka
English Breakfast Tea (Remsey)BagsSri Lanka
English Tea No. 1 (Ahmad Tea)BagsSri Lanka
Finest Black Tea (Eternal)BagsSri Lanka
Gold (Tekkane)BagsSri Lanka
Gold Tea (Loyd)BagsSri Lanka
Intense Black (Lipton)BagsSri Lanka
Lemon Black (Minutka)BagsSri Lanka
Royal Elixir Tea (Impra Tea)BagsSri Lanka
Eternal Finest (Eternal)GranulateIndia
Golden Assam (Golden Assam)GranulateIndia
Yellow Label (Lipton)GranulateKenya
Black Tea (Yunnan)LeavesChina
China Black Golden Silk Missing (Five o’clock)LeavesChina
China Panyong Golden Needle (Five o’clock)LeavesChina
Earl Grey with Lemon Zest (Lord Nelson)LeavesChina
Formosa Lapsang Souchong (Five o’clock)LeavesChina
Golden Yunan (Five o’clock)LeavesChina
Golden Yunan Superior (Five o’clock)LeavesChina
Keemun (Five o’clock)LeavesChina
Yunan Black Tea (ZAS)LeavesChina
Yunnan (Loyd)LeavesChina
Yunnan (ZAS)LeavesChina
Georgian Black Wild Op (Five o’clock)LeavesGeorgia
Assam (Lord Nelson)LeavesIndia
Assam (ZAS)LeavesIndia
Assam Halmari GTGFBOP (Five o’clock)LeavesIndia
Assam Halmari GTGFOP1CL (Five o’clock)LeavesIndia
Assam Satrupa (Five o’clock)LeavesIndia
Assam Singlijan (Five o’clock)LeavesIndia
Assam Tea (Ahmad Tea)LeavesIndia
Assam Tonganagaon (Five o’clock)LeavesIndia
Ceylon Lumbini (Five o’clock)LeavesIndia
Darjeeling Flower Balasun (Five o’clock)LeavesIndia
Darjeeling Gielle (Five o’clock)LeavesIndia
Darjeeling Liza Hill DJ5/21 (Five o’clock)LeavesIndia
Darjeeling Musk Puttabang (Five o’clock)LeavesIndia
Darjeeling Nagr DJ2 (Five o’clock)LeavesIndia
Darjeeling Shree Dwarika (Five o’clock)LeavesIndia
Darjeeling Teesta Valley DJ11 (Five o’clock)LeavesIndia
Madras (Loyd)LeavesIndia
Madras (ZAS)LeavesIndia
Pure Ceylon Tea (Akbar)LeavesIndia
South India Nilgiri Kukicha Roasted (Five o’clock)LeavesIndia
Japan Black Tea (Five o’clock)LeavesJapan
Safari (Astra)LeavesKenya
Yellow Label (Lipton)LeavesKenya
Laos Black Saylom (Five o’clock)LeavesLaos
Nepal Arubote (Five o’clock)LeavesNepal
Nepal Yun Chiyabari Himalayan Imperial (Five o’clock)LeavesNepal
Kivu Lake Selected (HAYB)LeavesRwanda
Rwanda Rukei Op (Five o’clock)LeavesRwanda
Black Tropical Tea (Sir Adalbert’s Tea)LeavesSri Lanka
Ceylon (Big-Active)LeavesSri Lanka
Ceylon Ahinsa (Five o’clock)LeavesSri Lanka
Ceylon Gold (Dilmah)LeavesSri Lanka
Ceylon Premium Tea (Dilmah)LeavesSri Lanka
Ceylon Supreme (Dilmah)LeavesSri Lanka
Ceylon Tea (Ahmad Tea)LeavesSri Lanka
Ceylon Vithanakande (Five o’clock)LeavesSri Lanka
Dimbula (Vintage Teas)LeavesSri Lanka
Earl Grey (Ahmad Tea)LeavesSri Lanka
Earl Grey (Akbar)LeavesSri Lanka
Earl Grey (Loyd)LeavesSri Lanka
Earl Grey (Sir Adalbert’s Tea)LeavesSri Lanka
Earl Grey (Vintage Teas)LeavesSri Lanka
English Breakfast (Ahmad Tea)LeavesSri Lanka
English Breakfast (DilmahLeavesSri Lanka
English Royal Tea (Chelton)LeavesSri Lanka
English Tea No. 1 (Ahmad Tea)LeavesSri Lanka
Finest Top (Eternal)LeavesSri Lanka
Gourmet Earl Grey Tea (Dilmah)LeavesSri Lanka
Kandy (Vintage Teas)LeavesSri Lanka
Nuwara Eliya (Vintage Teas)LeavesSri Lanka
Organic Black Tea (Vintage Teas)LeavesSri Lanka
Royal Elixir Tea (Gold) (Impra Tea)LeavesSri Lanka
Ruhuna (Vintage Teas)LeavesSri Lanka
Sabaragamuwa (Vintage Teas)LeavesSri Lanka
Darjeeling Tea (Teapigs)Pyramid bagsIndia
English Breakfast (Teapigs)Pyramid bagsIndia
Earl Grey (English Teashop Organic)Pyramid bagsSri Lanka
Earl Grey (Vintage Teas)Pyramid bagsSri Lanka
Earl Grey Strong (Teapigs)Pyramid bagsSri Lanka
Elegant Earl Grey (Dilmah)Pyramid bagsSri Lanka
English Breakfast (Dilmah)Pyramid bagsSri Lanka
English Breakfast (English Teashop Organic)Pyramid bagsSri Lanka
English Breakfast (Vintage Teas)Pyramid bagsSri Lanka
Maharaja Reserve Assam (Dilmah)Pyramid bagsSri Lanka
Organic Black Tea Broken Orange Pekoe KANDY (Vintage Teas)Pyramid bagsSri Lanka
Perfect Ceylon Tea (Dilmah)Pyramid bagsSri Lanka
Valley of Kings Ceylon Pekoe (Dilmah)Pyramid bagsSri Lanka
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Małyszek, A.; Zawiślak, I.; Kulus, M.; Watras, A.; Kensy, J.; Kotela, A.; Styczyńska, M.; Janeczek, M.; Matys, J.; Dobrzyński, M. Fluoride Content in Infusions of Selected Teas Available on the Polish Market—An In Vitro Study. Foods 2025, 14, 2452. https://doi.org/10.3390/foods14142452

AMA Style

Małyszek A, Zawiślak I, Kulus M, Watras A, Kensy J, Kotela A, Styczyńska M, Janeczek M, Matys J, Dobrzyński M. Fluoride Content in Infusions of Selected Teas Available on the Polish Market—An In Vitro Study. Foods. 2025; 14(14):2452. https://doi.org/10.3390/foods14142452

Chicago/Turabian Style

Małyszek, Agata, Ireneusz Zawiślak, Michał Kulus, Adam Watras, Julia Kensy, Agnieszka Kotela, Marzena Styczyńska, Maciej Janeczek, Jacek Matys, and Maciej Dobrzyński. 2025. "Fluoride Content in Infusions of Selected Teas Available on the Polish Market—An In Vitro Study" Foods 14, no. 14: 2452. https://doi.org/10.3390/foods14142452

APA Style

Małyszek, A., Zawiślak, I., Kulus, M., Watras, A., Kensy, J., Kotela, A., Styczyńska, M., Janeczek, M., Matys, J., & Dobrzyński, M. (2025). Fluoride Content in Infusions of Selected Teas Available on the Polish Market—An In Vitro Study. Foods, 14(14), 2452. https://doi.org/10.3390/foods14142452

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