Paraben

Parabens are a class of widely used preservatives in cosmetic and pharmaceutical products. Chemically, they are a series of parahydroxybenzoates or esters of parahydroxybenzoic acid (also known as 4-hydroxybenzoic acid). Parabens are effective preservatives in many types of formulas. These compounds, and their salts, are used primarily for their bactericidal and fungicidal properties. They are found in shampoos, commercial moisturizers, shaving gels, personal lubricants, topical/parenteral pharmaceuticals, suntan products, makeup,[1] and toothpaste. They are also used as food preservatives.

General chemical structure of a paraben
(a para-hydroxybenzoate)
where R = an alkyl group

No effective direct links between parabens and cancer have been established.[2]

Mode of action

Parabens are active against a broad spectrum of microorganisms. However, their antibacterial mode of action is not well understood. They are thought to act by disrupting membrane transport processes[3] or by inhibiting synthesis of DNA and RNA[4] or of some key enzymes, such as ATPases and phosphotransferases, in some bacterial species.[5] Propylparaben is considered more active against more bacteria than methylparaben. The stronger antibacterial action of propylparaben may be due to its greater solubility in the bacterial membrane, which may allow it to reach cytoplasmic targets in greater concentrations. However, since a majority of the studies on the mechanism of action of parabens suggest that their antibacterial action is linked to the membrane, it is possible that its greater lipid solubility disrupts the lipid bilayer, thereby interfering with bacterial membrane transport processes and perhaps causing the leakage of intracellular constituents.[6]

Chemistry

Parabens are esters of para-hydroxybenzoic acid, from which the name is derived. Common parabens include methylparaben (E number E218), ethylparaben (E214), propylparaben (E216), butylparaben and heptylparaben (E209). Less common parabens include isobutylparaben, isopropylparaben, benzylparaben and their sodium salts. The general chemical structure of a paraben is shown at the top right of this page, where R symbolizes an alkyl group such as methyl, ethyl, propyl or butyl.[7]

Synthesis

All commercially used parabens are synthetically produced, although some are identical to those found in nature. They are produced by the esterification of para-hydroxybenzoic acid with the appropriate alcohol, such as methanol, ethanol, or n-propanol. para-Hydroxybenzoic acid is in turn produced industrially from a modification of the Kolbe-Schmitt reaction, using potassium phenoxide and carbon dioxide.

Health considerations

Most of the available paraben toxicity data are from single-exposure studies, meaning one type of paraben in one type of product. According to paraben research this is relatively safe, posing only a negligible risk to the endocrine system. However, since many types of parabens in many types of products are used commonly, further assessment of the additive and cumulative risk of multiple paraben exposure from daily use of multiple cosmetic and/or personal care products is needed.[8] FDA states that they have no information that use of parabens in cosmetics has any effect on health. They continue to consider certain questions and evaluate data about parabens' possible health effects.[9]

Allergic reactions

Parabens are, for the most part, non-irritating and non-sensitizing. Among people with contact dermatitis or eczema, less than 3% of patients were found to have a sensitivity to parabens.[10] At least one case has been reported of an allergic reaction to parabens.[11]

Breast cancer

The American Cancer Society mentioned a 2004 study that found parabens in the breast tissue of mastectomy patients but did not find parabens to be a cause of the cancers. Michael Thun of ACS stated that the effects of parabens would be minuscule compared to other risks "such as taking hormones after menopause and being overweight".[12] A 2005 review concluded "it is biologically implausible that parabens could increase the risk of any estrogen-mediated endpoint, including effects on the male reproductive tract or breast cancer" and that "worst-case daily exposure to parabens would present substantially less risk relative to exposure to naturally occurring endocrine active chemicals in the diet such as the phytoestrogen daidzein."[2]

Estrogenic activity

Animal experiments have shown that parabens have weak estrogenic activity, acting as xenoestrogens.[13] In an in vivo study, the effect of butylparaben was determined to be about 1/100,000th that of estradiol, and was only observed at a dose level around 25,000 times higher than the level typically used to preserve products.[14] The study also found that the in vivo estrogenic activity of parabens is reduced by about three orders of magnitude compared to in vitro activity.

The estrogenic activity of parabens increases with the length of the alkyl group. It is believed that propylparaben is estrogenic to a certain degree as well,[15] though this is expected to be less than butylparaben by virtue of its less lipophilic nature. Since it can be concluded that the estrogenic activity of butylparaben is negligible under normal use, the same should be concluded for shorter analogs due to estrogenic activity of parabens increasing with the length of the alkyl group.

Exposure during pregnancy

A 2020 study, published by scientists at the Helmholtz Centre for Environmental Research (UFZ) in Leipzig (Germany) finds, that maternal paraben exposure may trigger childhood overweight development.[16]

Regulation

The European Scientific Committee on Consumer Safety (SCCS) reiterated in 2013 that methylparaben and ethylparaben are safe at the maximum authorized concentrations (up to 0.4% for one ester or 0.8% when used in combination). The SCCS concluded that the use of butylparaben and propylparaben as preservatives in finished cosmetic products is safe to the consumer, as long as the sum of their individual concentrations does not exceed 0.19%.[17] Isopropylparaben, isobutylparaben, phenylparaben, benzylparaben and pentylparaben were banned by Commission Regulation (EU) No 358/2014.[18]

Controversy

Concerns about endocrine disruptors have led consumers and companies to search for paraben-free alternatives.[19] A common alternative has been phenoxyethanol, but this has its own risks and has led to an FDA warning on inclusion in nipple creams.[20]

Environmental considerations

Release into the environment

Paraben discharge into the environment is common due to its ubiquitous usage in cosmetic products. A 2010 study on consumer available personal care products revealed that 44% of the tested products contain parabens.[21] When washing these products off the human body, they flow down the drain and into community wastewater. Once this occurs, the potential for parabens to accumulate within aqueous and solid mediums materializes. Some of the most common paraben derivatives found in the environment include methylparaben, ethylparaben, propylparaben, and butylparaben.[22] Parabens flow from wastewater to wastewater treatment plants (WWTP) as influent where they are either removed, chemically altered, or released into the environment through sludge or tertiary effluent.[22]

General flow of parabens as they make their way through wastewater treatment plants.

In one New York WWTP, mass load of all parent paraben derivatives (methylparaben, ethylparaben, propylparaben, butylparaben, etc.) from influent wastewater was found to be 176 mg/day/1000 people.[23] When this value is used to estimate the amount of parabens entering WWTPs from the 8.5 million people currently residing in New York City for an entire year, a value of approximately 546 kg of parabens is calculated. Therefore, levels of paraben accumulation prove significant upon long-term observance. WWTPs eliminate between 92–98% of paraben derivatives; however, much of this removal is due to the formation of degradation products.[23] Despite their reputed high elimination through WWTPs, various studies have measured high levels of paraben derivatives and degradation products persisting in the environment.[24]

Formation of degradation products

Chlorinated products
Reaction of a general paraben with hypochlorous acid (HClO) to form mono- and di- chlorinated products.
Arrow pushing mechanism of the formation of a mono-chlorinated paraben.
Chlorination of propylparaben over time in water at 20 °C containing 0.5 μM propylparaben and 50 μM free chlorine.

In addition to parent parabens, paraben degradation products that form throughout WWTP stages present a concern to the environment, including mono- and di- chlorinated parabens. When paraben-containing products are washed down the drain, parabens have the potential to undergo chlorination reactions.[25] This reaction can occur with free chlorine present in tap water or with sodium hypochlorite, which is often used in WWTPs as a final disinfectant step.[26] In neutral water, Raman spectroscopy has confirmed that chlorine is predominantly present as hypochlorous acid (HClO).[27] Parabens can react with HClO to form mono- and di- chlorinated products through electrophilic aromatic substitution.[25] The electrophilic attack of the chlorine forms a carbocation that is stabilized by donated electron density from the hydroxyl group of the paraben.[28] This step is endergonic due to the loss of aromaticity, though the hydroxyl group acts as an activating group that increases the rate.[25] A base can then abstract a proton from the carbon containing the chlorine, which is followed by subsequent restoration of aromaticity by the involved pi electrons. Since the hydroxyl group is more activating than the ester group of the paraben, the reaction will direct in both ortho positions, as the para position is already blocked.[28]

The Arrhenius equation was used in a study to calculate activation energies for the chlorination of four parent parabens (methyl-, ethyl-, propyl-, and butylparaben) and was found to range from 36–47 kJ/mol.[25] In another study, tap water at 20 °C (68 °F) containing 50–200 μM free chlorine was spiked with 0.5 μM propylparaben and the composition of the mixture was monitored over 40 minutes to determine if chlorination occurs under conditions found in tap water.[26] Results from the study confirm the disappearance of propylparaben after 5 minutes, the appearance of both 3-chloro-propylparaben and 3,5-dichloro-propylparaben paraben by 5 minutes, and the persistence of 3,5-dichloro-propylparaben as the main species remaining in the reaction.[26] A similar, though more rapid, trend was found in a study in which the reaction temperature was increased to 35 °C.[25]

4-Hydroxybenzoic acid (PHBA)
Overall reaction showing the degradation of a parent paraben to 4-hydroxybenzoic acid through base-catalyzed hydrolysis of the ester bond.
Arrow pushing mechanism showing the degradation of a parent paraben into PHBA through base-catalyzed hydrolysis of the ester bond

Another significant paraben degradation product is 4-hydroxybenzoic acid (PHBA). There are two mechanisms in which parabens can degrade to PHBA. The first degradation route occurs chemically. Parent parabens readily undergo base-catalyzed hydrolysis of the ester bond, forming PHBA. The reaction occurs under moderately alkaline conditions, specifically when the pH is ≥ 8.[25] This reaction is quite prevalent in household environments due to the pH range of household wastewater being 6–9[29] and the prevalent existence of parabens in cosmetic products. When paraben-containing cosmetic products are discharged into community wastewater influent, they become exposed to an environment where the pH ≥ 8, and the base-catalyzed hydrolysis of the parent paraben ensues, forming PHBA.

In the electron transfer mechanism, the pi electrons in the double bond between the oxygen and carbonyl carbon resonate to the oxygen, leaving a negative charge on the oxygen and a positive charge on the carbonyl carbon. A hydroxide ion, acting as a nucleophile, attacks the now electrophilic carbonyl carbon, yielding sp3 hybridization on the carbonyl carbon. The electrons resonate back to form the double bond between the oxygen and the carbonyl carbon. In order to retain the original sp2 hybridization, the –OR group will leave. The –OR group acts as a better leaving group than the –OH group due to its ability to maintain a negative charge with greater stability. Lastly, the –OR-, acting as a base, will deprotonate the carboxylic acid to form a carboxylate anion.

The second way in which parabens can degrade into PHBA occurs biologically within WWTPs. During the secondary clarifier phase of Wastewater treatment, sludge accumulates at the bottom of the secondary clarifier. Upon separation of the liquid and solid phases of the incoming influent, parabens have a greater tendency accumulate in the sludge. This is due to its moderate hydrophobicity, as quantified by a log Kow value of approximately 1.58.[30] This sludge is concentrated in organic nutrients; consequently, a proliferation of microorganisms becomes common within the sludge. One organism is Enterobacter cloacae, which biologically metabolizes the sludge parabens into PHBA.[31]

Accumulation of degradation products in the environment

Through various analytical techniques such as gas chromatography and high-performance liquid chromatography, the exact levels of accumulation of paraben derivatives and degradation products in the environment have been quantified.[22][26] These levels have been accurately measured in tertiary effluent and sewage sludge, as these are the primary avenues for which parabens and their degradation products reach the environment upon discharge from WWTPs.[22]

Concentrations of parabens in tertiary effluent water samples in μg/L (left). Concentrations of parabens in sewage sludge samples in μg/g (right).

Paraben stability in sewage sludge is relatively high due to their ability to bind with organic matter. Soil adsorption coefficient values were calculated by the U.S. Environmental Protection Agency as 1.94 (methylparaben), 2.20 (ethylparaben), 2.46 (propylparaben), and 2.72 (butylparaben),[32] all of which suggest that parabens have the ability to adhere to the organic portion of sediment and sludge, and thus, persist environmentally.[33]

Chlorinated parabens are removed from WWTPs with only 40% efficiency in comparison to 92–98% efficiency of parent parabens.[22] The decrease in removal efficiency can be attributed to the decreased biodegradability of chlorinated parabens, their increased overall stability throughout WWTPs, and their relatively low sorption to the sludge phase due to low log Kow values.[22]

Higher levels of PHBA are found in tertiary effluent in comparison to paraben derivatives, and PHBA exists in the highest concentration in sewage sludge. There are two reasons for these levels of accumulation. The first reason is PHBA's tendency to sorb to solid particles, which can be approximated by benzoic acid's high Kd value of approximately 19. The pKa of PHBA is 2.7, but it is in an environment of a pH between 6–9.[29][34] Since the pKa is less than the pH, the carboxylic acid will be deprotonated. The carboxylate allows it to act as a sorbent on solid environmental matrices, thus promoting its aggregation in tertiary effluent, but especially sewage sludge, which acts as the solid matrix itself. The second reason is due to the intermediate increase in levels of PHBA during the secondary clarifier phase of the WWTP through biological processes.

Environmental concerns with paraben degradation products

Multiple studies have linked chlorinated parabens to endocrine disrupting functions, specifically mimicking the effects of estrogen, and chlorinated parabens are believed to be 3–4 times more toxic than their parent paraben.[35][36] In Daphnia magna, general toxicity conferred by chlorinated parabens occurs through non-specific disruption of cell membrane function.[36] The potency of the chlorinated parabens correlates with the propensity of the compound to accumulate in cell membranes.[36] Thus, chlorinated parabens generally increase in toxicity as their ester chains increase in length due to their increased hydrophobicity.[36]

The implications of PHBA's environmental accumulation also warrants attention. If the tertiary effluent is re-used for community use as greywater, it poses a hazard to humans. These hazards include, but are not limited to, abnormal fetal development, endocrine disrupting activity, and improper estrogen-promoting effects.[37] If the tertiary effluent is released to the environment in rivers and streams or if the sludge is used as fertilizer, it poses as a hazard to environmental organisms. It is especially toxic to those organisms on lower trophic levels, particularly various algal species. In fact, it has been shown that the LC50 for a specific algal species, Selenastrum capricornutum, is 0.032 micrograms per litre (μg/L).[38] This is less than the natural abundance of PHBA in tertiary effluent at a level of 0.045 μg/L, thus indicating that current levels of PHBA in tertiary effluent can potentially eradicate more than 50% of Selenastrum capricornutum it comes in contact with.

Removal of parabens through ozonation
Arrow pushing mechanism of the ozonation of parabens.

Ozonation is an advanced treatment technique that has been considered as a possible method to limit the amount of parabens, chlorinated parabens, and PHBA that are accumulating in the environment.[22] Ozone is an extremely powerful oxidant that oxidizes parabens and makes them easier to remove once subsequently passed through a filter.[39] Due to the electrophilic nature of ozone, it can easily react with the aromatic paraben ring to form hydroxylated products.[39] Ozonation is generally regarded as a less dangerous method of disinfection than chlorination, though ozonation requires more cost considerations.[39] Ozonation has demonstrated great efficacy in the removal of parabens (98.8–100%) and a slightly lower efficacy of 92.4% for PHBA.[22] A moderately lower rate of removal, however, is observed for chlorinated parabens (59.2–82.8%).[22] A proposed reaction mechanism for the removal of parabens by ozonation is detailed mechanistically.[39]

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References
  1. Nutrition, Center for Food Safety and Applied. "Ingredients - Parabens in Cosmetics". www.fda.gov. Retrieved 2016-11-01.
  2. Golden R, Gandy J, Vollmer G (2005). "A review of the endocrine activity of parabens and implications for potential risks to human health". Critical Reviews in Toxicology. 35 (5): 435–58. doi:10.1080/10408440490920104. PMID 16097138.
  3. Freese, E; Sheu, CW; Galliers, E (2 February 1973). "Function of lipophilic acids as antimicrobial food additives". Nature. 241 (5388): 321–5. Bibcode:1973Natur.241..321F. doi:10.1038/241321a0. PMID 4633553.
  4. Nes, IF; Eklund, T (April 1983). "The effect of parabens on DNA, RNA and protein synthesis in Escherichia coli and Bacillus subtilis". The Journal of Applied Bacteriology. 54 (2): 237–42. doi:10.1111/j.1365-2672.1983.tb02612.x. PMID 6189812.
  5. Ma, Y; Marquis, RE (November 1996). "Irreversible paraben inhibition of glycolysis by Streptococcus mutans GS-5". Letters in Applied Microbiology. 23 (5): 329–33. doi:10.1111/j.1472-765x.1996.tb00201.x. PMID 8987716.
  6. Valkova N, Lépine F, Villemur R (2001). "Hydrolysis of 4-Hydroxybenzoic Acid Esters (Parabens) and Their Aerobic Transformation into Phenol by the Resistant Enterobacter cloacae Strain EM". Applied and Environmental Microbiology. 67 (6): 2404–09. doi:10.1128/AEM.67.6.2404-2409.2001. PMC 92888. PMID 11375144.
  7. "Parabens: A Review of Epidemiology, Structure, Allergenicity, and Hormonal Properties". Medscape. Retrieved Feb 29, 2016.
  8. Karpuzoglu E, Holladay SD, Gogal RM (2013). "Parabens: potential impact of low-affinity estrogen receptor binding chemicals on human health". Journal of Toxicology and Environmental Health Part B: Critical Reviews. 16 (5): 321–35. doi:10.1080/10937404.2013.809252. PMID 23909435.
  9. "Parabens". U.S. Food and Drug Administration. Retrieved 21 December 2018.
  10. Hafeez, F; Maibach, H (2013). "An overview of parabens and allergic contact dermatitis". Skin Therapy Letter. 18 (5): 5–7. PMID 24305662.
  11. Nagel JE, Fuscaldo JT, Fireman P (1977). "Paraben allergy". JAMA. 237 (15): 1594–5. doi:10.1001/jama.237.15.1594. PMID 576658.
  12. The American Cancer Society Archived 2004-08-16 at the Wayback Machine Antiperspirants and Breast Cancer Risk
  13. Byford JR, Shaw LE, Drew MG, Pope GS, Sauer MJ, Darbre PD (January 2002). "Oestrogenic activity of parabens in MCF7 human breast cancer cells". J Steroid Biochem Mol Biol. 80 (1): 49–60. doi:10.1016/S0960-0760(01)00174-1. PMID 11867263.
  14. Edwin J. Routledge; et al. (1998). "Some alkyl hydroxy benzoate preservatives (parabens) are estrogenic". Toxicology and Applied Pharmacology. 153 (1): 12–19. doi:10.1006/taap.1998.8544. PMID 9875295.
  15. Cashman AL, Warshaw EM (2005). "Parabens: a review of epidemiology, structure, allergenicity, and hormonal properties". Dermatitis. 16 (2): 57–66, quiz 55–6. doi:10.1097/01206501-200506000-00001. PMID 16036114.
  16. Maternal paraben exposure triggers childhood overweight development, published by Leppert, B.; Strunz, S.; Seiwert, B.; Schlittenbauer, L.; Schlichting, R.; Pfeiffer, C.; Röder, S.; Bauer, M.; Borte, M.; Stangl, G.I.; Schöneberg, T.; Schulz, A.; Karkossa, I.; Rolle-Kampczyk, U.E.; Thürmann, L.; von Bergen, M.; Escher, B.I.; Junge, K.M.; Reemtsma, T.; Lehmann, I.; Polte, T. in Nature Communication, 2020
  17. SCCS: Opinion on Parabens. Colipa No P82 3 May 2013.
  18. Commission Regulation (EU) No 358/2014 of 9 April 2014 amending Annexes II and V to Regulation (EC) No 1223/2009 of the European Parliament and of the Council on cosmetic products
  19. Lebovits SC (May 26, 2008). "Cosmetics firms heed calls for organics". The Boston Globe.
  20. Commissioner, Office of the. "2008 - FDA Warns Consumers Against Using Mommy's Bliss Nipple Cream". www.fda.gov. Retrieved 2015-10-31.
  21. Yazar K., Johnsson S., Lind M. L., Boman A., Lidén, C. (2011). Preservatives and fragrances in selected consumer-available cosmetics and detergents. Contact Dermatitis. 64: 265–272.
  22. Li W., Shi Y., Gao L., Liu J., Cai Y. (2015). Occurrence, fate and risk assessment of parabens and their chlorinated derivatives in an advanced wastewater treatment plant. Journal of Hazardous Materials 300: 29–38.
  23. Wang W., Kannan K. (2016). Fate of Parabens and their Metabolites in two wastewater treatment plants in New York, United States. Environmental science & technology. 50: 1174–1181
  24. Haman C., Dauchy X., Rosin C., Munoz J. (2015). Occurrence, fate, and behavior of parabens in aquatic environments: A review. Water Research. 68: 1–11.
  25. Mao Q., Ji F., Wang W., Wang Q., Hu Z., Yuan S. (2016) Chlorination of parabens: reaction kinetics and transformation product identification. Environ. Sci. Polut. Res. 23, 23081–23091.
  26. Terasaki M., Takemura Y., Makino M. (2012). Paraben-chlorinated derivatives are found in river water. Environ Chem Lett 10: 401–406
  27. Cherney D. P., Durik S. E., Tarr J. C., Collette T. W. (2006) Monitoring the speciation of aqueous free chlorine from pH 1 to 12 with Raman spectroscopy to determine the identity of the potent low-pH oxidant. Appl. Spectrosc. 60(7), 764–772.
  28. Gowda B. T., Mary M. C. (2001) Kinetics and mechanism of chlorination of phenol and substituted phenols by sodium hypochlorite in aqueous alkaline medium. Indian Journal of Chemistry. 40, 1196–1202.
  29. Harashit M. (2014) Influence of Wastewater PH on Turbidity. International Journal of Environmental Research and Development. 4, 105–114.
  30. 4-HYDROXYBENZOIC ACID https://pubchem.ncbi.nlm.nih.gov/compound/4-hydroxybenzoic_acid#section=Color (accessed Nov 27, 2017).
  31. Nelly V., Francois L., Loredana V., Maryse D., Louisette L., Jean-Guy B., Rejean B., Francois S., Richard V. (2001) Hydrolysis of 4-Hydrobenzoic Acid Esters (Parabens) and Their Aerobic Transformation into Phenol by the Resistant Enterobacter cloacae Strain EM. Applied and Environmental Microbiology. 67, 2404–2409.
  32. Ferreira A. M., Möder M., Laespada M. E. (2011) Stir bar sorptive extraction of parabens, triclosan and methyl triclosan from soil, sediment and sludge with in situ derivatization and determination by gas chromatography-mass spectrometry. J. Chromatogr. 1218, 3837−3844.
  33. Chunyang L., Sunggyu L., Hyo-Bang M., Yamashita N., Kannan K. (2013) Parabens in Sediment and Sewage Sludge from the United States, Japan, and Korea: Spatial Distribution and Temporal Trends. Environmental Science & Technology. 47(19):10895–10902.
  34. Emmanuel A., Esi A., Lawrence D., Richard A., Gabriel O. (2013) Water quality assessment of wastewater treatment plant in a Ghanaian Beverage Industry. International Journal of Water Resources and Environmental Engineering. 5, 272–279.
  35. Vo T. T. B., Jeung E. B. (2009) An Evaluation of Estrogenic Activity of Parabens Using Uterine Calbindin-D9k Gene in an Immature Rat Model. Toxicological Sciences. 112, 68–77.
  36. Terasaki M., Makino M., Tatarazako N. (2009) Acute toxicity of parabens and their chlorinated by-products with Daphnia magna and Vibrio fischeri bioassays. J. Appl. Toxicol. 29, 242–247.
  37. Soni M., Carabin I., Burdock G. (2005) Safety assessment of esters of p-hydroxybenzoic acid (parabens). Food and Chemical Toxicology. 43, 985–1015.
  38. 4-HYDROXYBENZOIC ACID. SIDS Initial Assessment Report for 9th SIAM, UNEP, 1999, France.
  39. Tay K. S., Rahman N. A., Abas M. R. B. (2010) Ozonation of parabens in aqueous solutions: kinetics and mechanism of degradation. Chemosphere. 81, 1446–1453.
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