International Journal of Food Science

International Journal of Food Science / 2013 / Article

Review Article | Open Access

Volume 2013 |Article ID 585931 |

Alina Błaszczyk, Aleksandra Augustyniak, Janusz Skolimowski, "Ethoxyquin: An Antioxidant Used in Animal Feed", International Journal of Food Science, vol. 2013, Article ID 585931, 12 pages, 2013.

Ethoxyquin: An Antioxidant Used in Animal Feed

Academic Editor: Ángel Medina-Vayá
Received15 Jan 2013
Accepted02 Apr 2013
Published30 Apr 2013


Ethoxyquin (EQ, 6-ethoxy-1,2-dihydro-2,2,4-trimethylquinoline) is widely used in animal feed in order to protect it against lipid peroxidation. EQ cannot be used in any food for human consumption (except spices, e.g., chili), but it can pass from feed to farmed fish, poultry, and eggs, so human beings can be exposed to this antioxidant. The manufacturer Monsanto Company (USA) performed a series of tests on ethoxyquin which showed its safety. Nevertheless, some harmful effects in animals and people occupationally exposed to it were observed in 1980’s which resulted in the new studies undertaken to reevaluate its toxicity. Here, we present the characteristics of the compound and results of the research, concerning, for example, products of its metabolism and oxidation or searching for new antioxidants on the EQ backbone.

1. Introduction

During storage of animal feed many different processes may occur which alter their initial natural proprieties. First of all, lipids undergo peroxidation, the process during which they are deteriorated in a free radical autocatalytic oxidation chain reaction with atmospheric oxygen. Lipid autooxidation is a cascade phenomenon ensuring continuous delivery of free radicals, which initiate continuous peroxidation. This process results in food rancidity which manifests itself as the change of taste, scent, and color as well as decrease in shelf life of the product. Natural or synthetic antioxidants are usually used to slow down or stop lipid peroxidation and in consequence to preserve freshness of the product. Many natural antioxidants, such as tocopherols, vitamin C, flavonoids, for a short period, may be effective in food preserving, but in many cases such protection is not sufficient. Therefore synthetic antioxidants are widely used, among which BHT (butylated hydroxytoluene), BHA (butylated hydroxyanisole), and EQ (ethoxyquin) are the most frequent. However, some effects of synthetic antioxidants are not always beneficial for our health. Antioxidants such as BHA or BHT have been widely used for many years to preserve freshness, flavor, and colour of foods and animal feeds as well as to improve the stability of pharmaceuticals and cosmetics. There are many controversies about the use of these two antioxidants in foods. Some experimental studies have reported that both BHT and BHA have tumour-promoting activity [1, 2]. On the other hand, there were reports on anticarcinogenic properties of these antioxidants when they are used at low concentrations [3]. Human exposures are at least 1000-fold below those associated with any neoplastic actions in laboratory animals thus it is assumed that they are not harmful for human beings [3, 4].

The third compound, EQ, is one of the best known feed antioxidants for domestic animal and fish. Its unquestionable advantage is its high antioxidant capacity and low production costs. However, some of the authors have suggested that it is responsible for a wide range of health-related problems in dogs as well as in humans [59]. Due to the increased use of this antioxidant it was nominated by FDA (US Food and Drug Administration) for carcinogenicity testing [10]. The tests were carried out by Monsanto Company (USA), EQ producer, and after that in 1977 FDA requested for optional lowering of the maximum level of EQ in complete dog foods from allowed 150 ppm (0.015%) to 75 ppm (0.0075%). At the same time new studies were started by the Pet Food Institute to determine whether even lower EQ levels (between 30 and 60 ppm) would provide antioxidant protection for dog food [11].

Ethoxyquin is also known as Santoquin, Santoflex, Quinol. It was originally developed in rubber industry to prevent rubber from cracking due to oxidation of isoprene [12]. The Monsanto Company (USA) taking into account its high antioxidant efficiency and stability as well as low costs of synthesis refined it later for use as a preservative in animal feeds because it protects against lipid peroxidation and stabilizes fat soluble vitamins (A, E). Presently, ethoxyquin is used primarily as an antioxidant in canned pet food and in feed intended for farmed fish or poultry.

The use of ethoxyquin is not permitted in foods intended for human, except preserving powdered paprika and chili colour and using it as an antiscald agent in pears and apples (inhibition of “brown spots” development). However, because EQ is used as a feed antioxidant it can be also found in other products intended for human consumption like fish meal, fish oils, and other oils, fats, and meat (Table 1). An acceptable daily intake (ADI) of EQ for human (0–0.005 mg kg−1 bw) based on the results obtained from studies on dogs was established in 1998 [13, 14].

ProductDose [ppm]

Animal feed150
Uncooked fat of meat from animals (except poultry)5
Uncooked liver and fat of poultry3
Uncooked muscle meat of animals0.5
Poultry eggs0.5

According to the Code of Federal Regulations (CFR), Title 21, Parts 573.380, 573.400, 172.140.

This paper presents characteristics of ethoxyquin with regard to its properties, metabolism, toxicity, possible carcinogenicity, and antioxidant activity.

2. Physical and Chemical Properties of Ethoxyquin (EQ)

For the first time EQ was synthesized in 1921 by Knoevenagel [15]. The synthesis was based on condensation of aniline with molecules of acetone or its analogues [15, 16]. Błaszczyk et al. [16] synthesized EQ from p-phenetidine (4-ethoxyaniline) and diacetone alcohol in the presence of p-toluenesulfonic acid or iodine. Pure ethoxyquin (EQ; 6-ethoxy-1,2-dihydro-2,2,4-trimethylquinoline; CAS number 91-53-2; Figure 1) is a light yellow liquid, but it changes color to brown if it is exposed to oxygen [12]. It also tends to polymerize on exposure to light and air. The scent of EQ is described as mercaptan like. As a nonpolar substance EQ is soluble only in organic solvents. Some of the additional properties of EQ are presented in Table 2.

Properties of EQ

Molecular formulaC14H19NO
Molecular mass217.34 [g mol−1]
IUPAC name1,2-dihydro-2,2,4-trimethylquinolin-6-yl ethyl ether
CAS name6-ethoxy-1,2-dihydro-2,2,4-trimethylquinoline
Chemical classQuinoline
Melting point0°Ca
Boiling point123–125°C at 2 mm Hga
SolubilityInsoluble in water, soluble in fat and animal and plant oils, and soluble in ethanol, methanol, DMSO, and DMF
Vapor density7.48 (AIR = 1)a
StabilityStable under ordinary conditions, storage temp. 0–6°C
Spectral propertiesIndex of refraction: 1.569–1.672 at 25°Ca
Max absorption: 354 nm. Intense mass spectral peaks: 202 m/z (100%), 108 m/z (53%), 174 m/z (48%), and 137 m/z (36%)a
13C NMR in CDCl3 EQ (8% solution) in ppm: 151.2 (EQ-C-6); 137.6 (EQ-C-4); 129.5 (EQ-C-3); 128.5 (EQ-C-9); 122.8 (EQ-C-10); 114.6 (EQ-C-8); 113.6 (EQ-C-7); 111.1 (EQ-C-5); 64.2 (EQ-CH2-O); 51.6 (EQ-C-2); 30.4 (EQ-CH3-4); 18.5 (EQ-CH3-4); 15.0 (EQ-CH3-CH2-O-)b

According to the National Library of Medicine HSDB Database (last revision date: 2003) [18].
bAccording to Błaszczyk and Skolimowski [19].
DMSO: dimethyl sulfoxide, DMF: N,N-dimethylformamide.

3. Biotransformation of EQ

3.1. Animals

Ethoxyquin is rapidly absorbed from gastrointestinal tract of laboratory animals like rats and mice. Peak blood concentration of the compound is observed within 1 h. Distribution of EQ in animal body is similar when it is administered orally and intravenously. Small amounts of parent EQ were detected in liver, kidney, and adipose tissue and fish muscles [2024]. It is excreted predominantly as metabolites via urine. Metabolism of EQ was studied in rats, mice, dogs, chickens, and fish, as well as in plants [13, 21, 25]. It is not fully described but some metabolites were identified (Table 3). The most important EQ metabolites observed in rat urine and bile result from O-deethylation at position 6-C, and then conjugation with sulphate or glucuronide residues. The other metabolic pathways include hydroxylation and glucuronidation at position 8-C, deethylation at 6-C and epoxidation between positions 3-C and 4-C [21]. The main metabolites observed may be different depending on animal species. In mice mainly glucuronide metabolites were detected while in rats those result from conjugation of EQ with sulfate.

EQ metabolite/degradation productOrganism

585931.table.003a1,2-Dihydro-6-hydroxy-2,2,4-trimethylquinoline sulphateRats1
585931.table.003b1,2-Dihydro-6-hydroxy-2,2,4-trimethylquinoline glucuronideMice1
585931.table.003c1,2,3,4-Tetrahydro-3,6-dihydroxy-4-metylene-2,2-dimethylquinoline sulphateRats1
585931.table.003d1,2-Dihydro-6-ethoxy-8-hydroxy-2,2,4-trimethylquinoline glucuronideRats1  
585931.table.003g2,6-Dihydro-2,2,4-trimethyl-6-quinolone (quinone imine (QI))Rats1  
Atlantic salmon2
585931.table.003h6-Hydroxy-2,2,4-trimethyl-1,2-dihydroquinoline (deethylated EQ (DEQ))Atlantic salmon2
585931.table.003i1,8′-Di(1,2-dihydro-6-ethoxy-2,2,4-trimethylquinoline) or 6,6′-diethoxy-2,2,2′,2′,4,4′-hexamethyl-1′,2′-dihydro-2H-1,8′-biquinoline (ethoxyquin dimer (EQDM))
*Instead of the hydrogen atom there is a methyl group, it gives methyl C-N ethoxyquin dimer,
Atlantic salmon2  
585931.table.003jN-N Ethoxyquin dimer,
1,1′-di(1,2-dihydro-6-ethoxy-2,2,4-trimethylquinoline) or
methylethoxyquin (MEQ)
585931.table.003l6-Ethoxy-2,4-dimethylquinoline, dehydrodemethylethoxyquin (DHMEQ)Pears3,4
585931.table.003m6-Ethoxy-2,2,4-trimethyl-1,2,3,4-tetrahydroquinoline, dihydroethoxyquin (DHEQ)Pears3,4
demethylethoxyquin (DMEQ)

Glu: glucuronide, G: glutathione, Et: ethyl group (C2H5).
1Burka et al. [21], Berdikova Bohne et al. [26], 3Gupta and Boobis [14], 4JMPR [25].

In the studies of Bohne et al. [23, 26] parent EQ, dem-ethylated EQ (DEQ), quinone imine (QI), and EQ dimer (EQDM) were observed in salmonid fish after long-term dietary exposure to EQ. It was in agreement with the results obtained earlier by Skaare and Roald [27]. EQ is considered as a model inducer of phase II enzymes involved in the metabolism of xenobiotics, but influence of EQ on phase I enzyme gene transcript levels was also observed [28, 29]. The key role in mediating phase I reactions (e.g., oxidation or reduction) producing more hydrophilic compounds is played by the CYP (cytochrome P450) enzyme family. Bohne et al. [28, 29] observed the alteration of CYP3A gene expression; an increase in the amount of CYP3A transcripts was detected in salmon after feeding them with the diet containing EQ at the highest dose used (1800 mg kg−1). The authors speculate that EQ may regulate CYP3 gene expression by interaction, for example, with pregnane X nuclear receptor (PXR) whose function is to sense the presence of toxic xenobiotics and in response enhance the expression of proteins involved in their detoxification. On the other hand, CYP1A1 gene expression, which was described as an exposure biomarker to both endogenous and exogenous compounds [30], was not increased after dietary exposure of salmonid fish to EQ and during the depuration period a trend toward downregulation was noted [28, 29]. Such an effect was observed despite the increase in the expression of AhR mRNA (AhR, cytosolic transcription factor responsible for changes in gene transcription). This effect can be explained in several ways. For example, the parent EQ may bind CYP1A1 protein and as a result may inhibit the gene expression and activity of protein [31]. Hepatic antioxidant response elements (ARE) or AhR repressor (AhRR) together with basic-helix-loop-helix-PAS (Per-AhR/ARNT-Sim homology sequence) of transcription factor usually associated with each other to form heterodimers (AhR/ARNT or AhRR/ARNT) may be also involved in the CYP1A1 downregulation process. These heterodimers can influence gene expression by binding ARE sequences in the gene promoter regions [32].

However, EQ as other phenolic antioxidants, first of all causes induction of phase II xenobiotic-metabolizing enzymes. Bohne et al. [28, 29] observed elevated dose-related uridine diphosphate glucuronosyl-transferase (UDPGT) mRNA expression after dietary exposure to EQ. As UDPGT reacts with the compounds that have the hydroxyl group (-OH) parent EQ cannot be the potential substrate for glucuronidation, only its metabolites, for example DEQ (6-hydroxy-2,2,4-trimethyl-1,2-dihydroquinoline; Table 3), the metabolite identified by Berdikova Bohne et al. [26] in Atlantic salmon. Changes in the expression of glutathione S-transferase (GST) gene were also observed after feeding animals with EQ containing feed. The alterations in GST activity caused by EQ were documented in Atlantic salmon [28, 29], in rodents [33, 34], and in nonhuman primates [35]. In addition to UDPGT and GST, some other enzymes are involved in phase II metabolism of EQ, for example, NADP(H) : quinone oxidoreductase and epoxide hydrolase [36].

The expression pattern of both phase I and II enzymes involved in EQ metabolism may vary in different animals and should be considered in relation to the ratio of parent EQ and its metabolites (first of all DEQ, QI, and EQDM) in the liver [29, 37]. The research concerning this issue is currently in progress.

3.2. Plants

Ethoxyquin is also registered as an antioxidant to control scald (browning) in apples and pears. The EQ plant metabolites/degradation products were detected, and it was shown that in general they are different from those observed in animals (Table 3). In pears treated with ring-labeled [14C]ethoxyquin the following compounds were detected: N–N and C–N dimers, demethylethoxyquin (DMEQ), dehydrodemethylethoxyquin (DHMEQ), and dihydroethoxyquin (DHEQ) [14, 25]. It was shown that ethoxyquin was rapidly degradated or metabolized but itself it was not translocated into the pulp of fruit where the residues were detected (less than 0.5% of total radioactive residue was EQ). Toxicity of EQ metabolites, MEQ, DHMEQ, and DHEQ was studied in dogs (oral administration, single doses of 50 to 200 mg kg−1 bw), and it was found that they did not show any significant toxicity. In the report of Gupta and Boobis [14] the rank order of toxic potency for the plant metabolites and EQ is MEQ   EQ   DHEQ   DHMEQ (the least toxic first). MEQ, DHMEQ, and DHEQ were also evaluated for genotoxicity in in vitro and in vivo tests. The compounds did not cause gene mutations in Salmonella typhimurium and Escherichia coli strains, but they induced chromosomal aberrations or/and endoreduplication in Chinese hamster ovary cells. On the other hand, plant metabolites/degradation products did not exhibit genotoxic potential in vivo. ADI intake for humans for MEQ, DHMEQ, and DHEQ was estimated at the same level as for EQ (0–0.005 mg kg−1 bw).

4. Antioxidant Activity of EQ

EQ possesses high-antioxidative activity. It is very efficient in protecting lipids which are present in food against oxidization [38, 39]. Specifically it is used to retard oxidation of carotene, xanthophylls, and vitamins (like vitamins A or E). In animals treated with ethoxyquin three times higher level of vitamins A and E in blood plasma was observed [40]. This finding suggests that an organism is using EQ instead of natural antioxidants. High efficiency of this antioxidant results not only from chemical features of EQ itself but also from the fact that products of its oxidation also possess antioxidative properties [12, 39, 41].

Studies on EQ antioxidant properties were performed by Taimr [39] with the use of alkylperoxyls, and it was shown that the reaction rate of EQ with them is very high. In the presence of high oxygen concentrations EQ reacts with alkylperoxyl molecule to form aminyl radical (6-ethoxy-2,2,4-trimethyl-1,2-dihydroquinolin-1-yl) which subsequently may enter various pathways. In nonoxidizing conditions it can be stabilized both by the loss of methyl group and aromatization of heterocycle to form 2,4-dimethyl-1,2-dihydroquinoline (dehydrodemethylethoxyquin (DHMEQ)) and through dimerization to form EQ dimer (EQDM) [39, 42]. On the other hand, in an oxidizing medium other molecules can be formed, for example, 2,6-dihydro-2,2,4-trimethyl-6-quinolone (QI) or nitroxide radical (6-ethoxy-2,2,4-trimethyl-1,2-dihydroquinolin-N-oxyl) which is also a strong antioxidant [39, 42].

Products of EQ oxidation were detected by different authors in fish oil and meal [22, 4345]. According to He and Ackman [46] the following oxidization products of EQ dominate in fish meal and fish feed: 2,6-dihydro-2,2,4-trimethyl-6-quinolone (QI) and 1,8′-di(1,2-dihydro-6-ethoxy-2,2,4-trimethylquinoline) (EQDM). At high storage temperature neither QI nor EQDM accumulates; however, another product of EQ oxidation, 2,4-dimethyl-6-ethoxyquinoline, is stable [41]. As it was pointed out earlier, ethoxyquin oxidization products also possess antioxidative properties. The EQDM and QI show 69% and 80% of EQ efficacy, respectively (studies on fish meal) [12]. On the other hand, in the studies of Thorisson et al. [45] quinone imine (QI) and EQ nitroxide were also powerful antioxidants, while EQDM, the main product of EQ oxidation, showed little or no antioxidant behavior.

Antioxidant activity of EQ was also demonstrated in experiments performed both in vivo and in vitro. Antimutagenic effect of this antioxidant was observed in mice, rats, and Chinese hamsters treated with cyclophosphamide, an agent widely used in cancer chemotherapy [4749]. During cyclophosphamide bioactivation reactive oxygen species are formed which can cause damage of genetic material [50, 51]. EQ reduced the number of chromosome aberrations, micronuclei, and dominant lethal mutations induced by the anticancer drug [4749]. There were also some reports that EQ can modify carcinogenic response to different carcinogens [35, 52, 53]. EQ given to Fischer 344 rats in diet completely prevented the formation of aflatoxin B1-induced preneoplastic liver lesions [52, 53].

In in vitro experiments with human lymphocytes, antioxidant activity of EQ was observed in the comet assay (the method used to detect single- and double-strand DNA breaks, cross-links, and alkaline labile sites) and in micronucleus test (the method for the detection of micronuclei induced by clastogens or aneugens). EQ used at the concentrations ranging from 1 μM to 10 μM protected human lymphocytes against DNA damage caused by hydrogen peroxide (H2O2, 10 μM) [17]. This antioxidant also reduced the number of micronuclei caused by H2O2 used at concentration of 75 μM. However, the significant reduction was evident only in the case of lower EQ concentrations (5 μM, 10 μM) with no effect at higher concentration [17].

5. Adverse Effects of EQ: In Vivo and In Vitro Studies

Different phenolic antioxidants may be used in animal feed, such as BHA (butylated hydroxyanisole), BHT (butylated hydroxytoluene), and the most efficacious EQ. The levels of the antioxidants in finished feed should not be higher than 150 ppm for EQ and 200 ppm for BHT and BHA (U.S. Food and Drug Administration permissions). The fact that efficient antioxidants work optimally when they are used at low concentrations is their remarkable characteristic. On the other hand, when antioxidants are used at high concentrations they act as prooxidants. The impact of these compounds depends on their concentration as well as on other factors such as metal-reducing potential, chelating behaviour, solubility, and pH. The effect of antioxidants on living organisms also depends on their bioavailability and stability in tissues [54, 55]. Phenolic antioxidants under favorable conditions may be converted to phenoxyl radicals with prooxidant activity [55]. It was shown that dissolved EQ may exist partly in the free radical form which it was also detected in the compound itself [56]. Therefore, ethoxyquin nitroxide which is produced by EQ oxidation similarly as other nitroxide molecules (e.g., tempol) may also show prooxidative properties [57]. Formation of free oxygen species as a result of using too high EQ concentrations can cause adverse health effects in animals fed with EQ containing feed or in people consuming meat from farmed animals, for example, different fishes.

The studies on EQ prooxidant activity and toxicity associated with it were performed both in vivo and in vitro. Dogs are most susceptible to the harmful effects of EQ, and first reports of such effects were received by FDA in 1988. The symptoms observed by dog owners and veterinarians were liver, kidney, thyroid and reproductive dysfunction, teratogenic and carcinogenic effects, allergic reactions, and a host of skin and hair abnormalities [7]. According to the studies on dogs and laboratory animals it was shown that ethoxyquin had little acute toxicity, except when it is administered parenterally. Values of LD50 for EQ are 1700 mg kg−1 bw (rats, oral gavage), 2000 mg kg−1 bw (rats, dermal treatment, 24 h), 900 mg kg−1 bw (mice, intraperitoneal administration), and 180 mg kg−1 bw (mice, intravenous administration) [13]. Despite species differences in the majority of animals treated with EQ at the concentrations higher than those permitted in animal feed, the same characteristic symptoms and pathologies appeared such as weight loss, liver, and kidney damage, alterations of alimentary duct (Table 4). The concentration of 100 ppm (equivalent to 2.5 mg kg−1 bw per day) was considered to be a minimal-effect level for clinical signs of toxicity and liver effects in dogs, the most susceptible animals [13, 14].

The harmful effectAnimals

Loss of weightMarmosets1, rats2, dogs2, mice2, rabbits3
Changes in liverMarmosets1, rats1,4, dogs2, mice2, broiler chickens2, tilapia5
Changes in kidneyMarmosets1, rats2,6,7, dogs2, broiler chickens2,8
Changes in alimentary ductMarmosets1, dogs2, mice2, broiler chickens2,8
Changes in urinary bladderRats2
Changes in mitochondriaRats2
Colored urine, skin, or furDogs2, rats2
Increase in mortalityBroiler chickens2,8
Effect on immunity Tilapia5
Condition factor: the final body weight in relation to body length of fishLarge yellow croaker9
Allergy (contact exposure)Humans10,11,12

McIntosh et al. [58], 2Drewhurst [13], 3Little [10],4Ito et al. [59], 5Yamashita et al. [60], 6Neal et al. [61], 7Manson et al. [53], 8Leong and Brown [62], 9Wang et al. [63], 10Rodríguez-Trabado et al. [9], 11Brandao [5], 12Savini et al. [6].

Detrimental effects of EQ were also seen when the experiments were performed at the cell metabolism level. Hernandez et al. [64] and Reyes et al. [65] analysed the impact of EQ on the metabolic pathways of rat renal and hepatic cells, as well as on mitochondria and submitochondrial particles obtained from bovine heart and kidney. They observed influence of EQ on energy processes in cells. EQ inhibited renal Na+, K+-ATPase activity involved in ion transport [64]. The authors suggested that EQ interacted with site I of the mitochondrial respiratory chain, and it resulted in inhibition of oxygen consumption in the mitochondria of kidney and liver cells when glucose was a respiratory substrate. The effect was dose dependent.

More than 30 years ago when EQ began to be more commonly used in animal feed research started to assess its mutagenicity with the use of Ames test which is performed on different Salmonella typhimurium strains. The results were equivocal as some results were negative [6668], but the positive effects were also observed [69, 70]. It was also shown that EQ enhanced the mutagenic activity of DMBA (3,2′-dimethyl-4aminobiphenyl), a compound having carcinogenic properties [70]. Ethoxyquin was reported to both enhance and inhibit genetic changes induced by known carcinogens; on the other hand it can also lead to cancer in exposed animals. Manson et al. [53] observed in Fischer 344 rats that EQ caused severe damage in kidney. Many hyperplastic and putative preneoplastic tubules were found which suggested that EQ may be exerting a carcinogenic effect. Similar effects were observed earlier by Ito et al. [59] in relation not only to the kidney but also to the urinary bladder.

Possible carcinogenicity of EQ is probably connected with its prooxidant activity and induction of reactive oxygen radicals which cause DNA damage. DNA damage is usually repaired by cellular repair system, but if it is severe or there are too many lesions, this leads to programmed cell death (apoptosis). Sometimes, however, the programmed cell death pathway is damaged so when the defense mechanisms fail there is no way to stop a cell from becoming a cancer cell. Some in vitro studies showed both cytotoxic effects of EQ leading to cell apoptosis or necrosis and damage of genetic material at DNA or chromosome levels. Cytotoxic effects of pure EQ (purity   97%) were studied in vitro with the use of human lymphocytes. The IC50 value (the concentration causing 50% growth inhibition) for EQ determined after 72-hour treatment of the cells in the MTT assay was 0.09 mM [71]. This antioxidant significantly reduced viability of lymphocytes detected with trypan blue exclusion method after 24-hour treatment at the concentrations of 0.25 and 0.5 mM (cell divisions were stimulated by phytohemagglutinin, (PHA)) [19] or of 0.05 mM and higher when 1-hour treatment was performed [72]. EQ-induced apoptosis by observed in in vitro cultured human lymphocytes starting from 0.05 mM concentration and the detected number of apoptotic cells depended on the treatment time [71]. Ethoxyquin caused also DNA damage in the comet assay [72] however, most lesions could be repaired by cellular DNA repair systems [73]. On the other hand, the results obtained with the use of chromosome aberration test showed that unrepaired DNA damage induced by EQ could lead to permanent changes in genetic material [16, 74]. Błaszczyk et al. [16] and Gille et al. [74] showed that this antioxidant induced chromosome aberrations such as breaks, dicentrics, atypical translocated chromosomes, or chromatid exchanges in human lymphocytes and Chinese hamster ovary cells. These aberrations are known to have serious biological consequences [75].

6. Analogues and Derivatives of EQ

Because of adverse health effects caused by EQ it is reasonable to search for new antioxidants as effective in scavenging free radicals as EQ which produce no such problems. In the paper of de Koning [12] nine analogues of EQ prepared to compare their antioxidant efficacy with that of the parent chemical are presented. The compounds have been tested in a refined fish oil and subsequently some of the most promising ones have been also tested in fish meal. It was noted that the results obtained in fish oil were not always the same as in fish meal, for example, hydroxyquin (1,2-dihydro-6-hydroxy-2,2,4-trimethylquinoline; Figure 1) was 3.5 times as effective as EQ in fish oil, while only of its efficacy was observed in fish meal. In the case of another compound—hydroquin (1,2-dihydro-2,2,4-trimethylquinoline; Figure 1) antioxidant efficacy in relation to EQ was 101% in fish oil and 52% in fish meal. Despite the lower efficiency of this compound in fish meal the author stated that hydroquin can compete with EQ as an antioxidant of choice [12]. The reason is that preparation of hydroquin based on aniline and acetone is more cost-effective than that of EQ whose production requires p-phenetidine (more expensive than aniline). Hydroquin was earlier patented as an antioxidant in animal feeds in 1997 [76]. The 2-year dermal research with the use of F344/N rats and B6C3F1 mice conducted under the National Toxicology Program [77] showed that the compound was not carcinogenic, but the studies performed by Sitarek and Sapota [78] showed its teratogenic properties.

In 2000 Dorey et al. [15] presented the report concerning the synthesis and biological properties of a new class of antioxidants based on the EQ backbone. The studies were performed to search for new quinolinic derivatives with radical scavenging activity, potential candidates for central nervous system protection. EQ is not suitable for that as it has been shown to exhibit significant hypothermic effect, probably as a result of an inhibition of electron transport in the mitochondrial respiratory chain [65]. Dorey et al. [15] synthesized and studied many 1,2-dihydro and 1,2,3,4-tetrahydroquinolines and then selected for further evaluation a group of antioxidants (5 compounds) with high radical scavenging capacities, relatively low toxicity, and moderate hypothermia. The compounds belonging to the group of 1,2,3,4-tetrahydroquinolines (e.g., 6-ethoxy-2,2,5,7-tetramethyl-1,2,3,4-tetrahydroquinoline, characterized with the lowest toxicity and high radical scavenger capacity) are structurally similar to 2,2,4,7-tetramethyl-1,2,3,4-tetrahydroquinoline synthesized and tested in our laboratory (Figure 1) [17]. The latter compound also had promising features: its antioxidant activity was comparable to that of EQ, but its cytotoxicity and genotoxicity studied with the use of human lymphocytes in vitro were significantly lower. We believe that this chemical is worth of detailed studies to confirm its usefulness as a food preservative. Some other EQ derivatives and salts were also studied for cytotoxicity, genotoxicity, and antioxidant activity, namely, the complexes of ethoxyquin with flavonoids (rutin or quercetin), ethoxyquin hydrochloride, ethoxyquin phosphate, ethoxyquin L-ascorbate, ethoxyquin n-hexanoate, ethoxyquin salicylate, and ethoxyquin salt of Trolox C [19, 7982]. The biological properties of the compounds were analysed with the use of MTT, TUNEL, and trypan blue staining methods (cytotoxicity testing), comet assay (genotoxicity testing), and micronucleus test (mutagenicity testing). From among the compounds tested ethoxyquin phosphate (EQ-F) was the least toxic (Table 5)—its cytotoxic and genotoxic activities in comparison with those of EQ were reduced positively (  mM versus 0.09 mM for EQ) [71]. On the other hand, antioxidant activity of EQ-F was observed, but it was the lowest of the tested compounds [82]. The studies showed that all the tested compounds were less toxic to human lymphocytes than EQ, and the antioxidant activity of four of them (ethoxyquin n-hexanoate, ethoxyquin complex with quercetin, ethoxyquin L-ascorbate, and ethoxyquin salicylate) was comparable with that of EQ [7982]. The results obtained indicate that their use as antioxidants may be considered.

ActivitityActivity from the lowest (left) to the highest (right) one

CytotoxicityEQ-F < EQ-HCl < EQ-C < EQ-S < EQ-T < EQ-Q < EQ-R < EQ-H < EQ
GenotoxicityEQ-F < EQ-C < EQ-H < EQ-HCl < EQ-Q < EQ-T < EQ-S < EQ-R < EQ
Antioxidant activityEQ-F < EQ-HCl < EQ-R < EQ-T < EQ-S < EQ-C < EQ-Q < EQ < EQ-H

EQ-F: ethoxyquin phosphate; EQ-HCl: ethoxyquin hydrochloride; EQ-C: ethoxyquin L-ascorbate; EQ-S: ethoxyquin salicylate; EQ-T: ethoxyquin salt of Trolox C; EQ-Q: ethoxyquin complex with quercetin; EQ-R: ethoxyquin complex with rutin; EQ-H: ethoxyquin -hexanoate; EQ: ethoxyquin.

7. Food Safety Aspect

EQ safety has been under consideration for many years. The level of this antioxidant in animal feeds should not be higher than 150 ppm (U.S. Food and Drug Administration permissions). The approved uses of ethoxyquin in animal feeds are addressed in the Code of Federal Regulations (CFR), Title 21, Parts 573.380 and 573.400, and established tolerances are in Part 172.140. On the one hand, the observed adverse health effects (firstly in dogs) could be caused by the fact that the animals ate a lot of feed containing EQ, but on the other hand, it could also be the result of its excessive amounts in the feed. Ethoxyquin is added to animal feed either directly or indirectly as a component of an ingredient. From time to time FDA reminds industry about labeling and safe use requirements for ethoxyquin, but if it is added at the ingredient level this is not always indicated.

Another important safety issue is the presence of EQ oxidation and EQ metabolism products in animal feed or in foods prepared from farmed animal meat. de Koning [12] described main products of EQ oxidation which can be observed in stored feeds or in fish meal: EQ dimer (EQDM, 1,8′-di(1,2-dihydro-6-ethoxy-2,2,4-trimethylquinoline) and quinone imine (QI, 2,6-dihydro-2,2,4-trimethyl-6-quinolone). Both compounds were shown to be potent antioxidants, but they can also have detrimental effect, especially so because the half-life of the dimer was considerably greater than that of EQ [26, 28]. In the recent studies no adverse toxicological effects of EQDM, in terms of kidney and liver function, were observed in in vivo experiments with F344 rats exposed for 90 days to the compound [37]. On the other hand, Augustyniak et al. [83] showed that EQDM, similarly as EQ, was cytotoxic and genotoxic to human lymphocytes. Toxicity of QI has not been studied yet, but the results obtained by the authors indirectly indicated that the compound could be cytotoxic to human cells.

The levels of the parent compound (EQ) in meat of farmed animals are usually lower than MRL (Maximum Residue Level) [20, 84], but EQ oxidation products are usually not controlled. It was shown that EQDM and other EQ residues can be present in different animal tissues [23, 24, 26, 28, 37]. In the studies of Bohne et al. [23] in which Atlantic salmons were fed for 12 weeks with the feed containing this antioxidant, four compounds were identified in their muscles: parent EQ (6-ethoxy-1,2-dihydro-2,2,4-trimethylquinoline), deethylated EQ (6-hydroxy-2,2,4-trimethyl-1,2-dihydroquinoline), quinone imine (2,6-dihydro-2,2,4-trimethyl-6-quinolone, QI), and EQ dimer (1,8′-di(1,2-dihydro-6-ethoxy-2,2,4-trimethylquinoline, EQDM). It was also shown that the concentration of EQ in fish muscle was proportional to the duration of exposure and the level of EQ in the feed [23]. The same linear increase was seen for EQDM, the main metabolite of EQ, and the sum of EQ and EQDM. Bohne et al. [23] found that the level of EQ and its metabolites in fish muscle could be predicted from the level of dietary EQ and then controlled, but because it is not the only factor which may affect the levels of EQ and its metabolites in the salmon tissue (others for example are fish size and age), the concentration of EQ and EQDM in fish ready for consumption may be higher than that observed in their studies. In their experiments it was shown that the elimination of EQ from salmon was concurrent with significant increase in the level of EQDM, and they concluded that mandatory 14 days of depuration were not sufficient for elimination of EQ residues—it is mainly because EQDM is characterized by the considerably longer half-life than that of EQ. Moreover, EQDM accounted for 99% of the sum of the two compounds (EQ and EQDM), and its toxicological effects in animals and humans are unknown. EQ and EQ dimer were also detected in similar amounts not only in Atlantic salmon, but also in other commercially important species of farmed fishes (halibut, rainbow trout) by Lundebye et al. [24]. They found that in Atlantic salmon, halibut, and rainbow trout the concentration of EQDM was more than 10-fold higher than that of EQ. The authors estimated that consumer exposure to EQ from a single portion (300 g) of skinned-fillets of different species of farmed fish could amount up to 15% of the ADI. In the light of data concerning the presence of EQDM in the body of farmed fishesand providing that EQ dimer was included in the ADI, the EQ and EQDM intake from a single portion of Atlantic salmon would be close to ADI [24]. Farmed fish is probably the major source of EQ and its residues for European consumers (its use as a food additive is forbidden). In our opinion, however, both fish and other farmed animals, for example, chickens, should be controlled for the presence of not only EQ, but also EQDM, its main oxidation product.

8. Conclusion

Ethoxyquin has been used as an antioxidant in animal feed for several decades and despite the search for new compounds that could be used as free radical scavengers, it is still the most effective antioxidant. The negative health effects in domestic animals fed with EQ containing feed were observed some years ago, but the presence of its approved doses should not be hazardous. Toxicity and mutagenicity of EQ were observed in in vivo and in vitro studies showing its potential harmful effects. This makes it very important to label all products and ingredients to which EQ is added and to comply with the recommended doses. Additionally, the results of the studies on products of EQ oxidation, especially EQDM, detected in farmed animal tissues indicate that it should be under control and some regulations should be introduced.

Conflict of Interests

The authors declare that there is no conflict of interests.


  1. H. Babich, “Butylated hydroxytoluene (BHT): a review,” Environmental Research, vol. 29, no. 1, pp. 1–29, 1982. View at: Publisher Site | Google Scholar
  2. R. Kahl, “Synthetic antioxidants: biochemical actions and interference with radiation, toxic compounds, chemical mutagens and chemical carcinogens,” Toxicology, vol. 33, no. 3-4, pp. 185–228, 1984. View at: Google Scholar
  3. G. M. Williams, M. J. Iatropoulos, and J. Whysner, “Safety assessment of butylated hydroxyanisole and butylated hydroxytoluene as antioxidant food additives,” Food and Chemical Toxicology, vol. 37, no. 9-10, pp. 1027–1038, 1999. View at: Publisher Site | Google Scholar
  4. A. A. M. Botterweck, H. Verhagen, R. A. Goldbohm, J. Kleinjans, and P. A. van den Brandt, “Intake of butylated hydroxyanisole and butylated hydroxytoluene and stomach cancer risk: results from analyses in the Netherlands cohort study,” Food and Chemical Toxicology, vol. 38, no. 7, pp. 599–605, 2000. View at: Publisher Site | Google Scholar
  5. F. M. Brandao, “Contact dermatitis to ethoxyquin,” Contact Dermatitis, vol. 9, no. 3, article 240, 1983. View at: Google Scholar
  6. C. Savini, R. Morelli, E. Piancastelli, and S. Restani, “Contact dermatitis due to ethoxyquin,” Contact Dermatitis, vol. 21, no. 5, pp. 342–343, 1989. View at: Publisher Site | Google Scholar
  7. D. A. Dzanis, “Safety of ethoxyquin in dog foods,” Journal of Nutrition, vol. 121, no. 11, pp. S163–164, 1991. View at: Google Scholar
  8. K. Alanko, R. Jolanki, T. Estlander, and L. Kanerva, “Occupational 'multivitamin allergy' caused by the antioxidant ethoxyquin,” Contact Dermatitis, vol. 39, no. 5, pp. 263–264, 1998. View at: Google Scholar
  9. A. Rodríguez-Trabado, J. Miró I Balagué, and R. Guspi, “Hypersensitivity to the antioxidant ethoxyquin,” Actas Dermo-Sifiliograficas, vol. 98, no. 8, p. 580, 2007. View at: Publisher Site | Google Scholar
  10. A. D. Little, “Ethoxyquin, national toxicology program, executive summary of safety and toxicity information,” Chemical Committee Draft Report, Ethoxyquin CAS Number 91-53-2, 1990, View at: Google Scholar
  11. U.S Food and Drug Administration, Animal and Veterinary, “FDA requests that ethoxyquin levels be reduced in dog foods,” 1997, View at: Google Scholar
  12. A. J. de Koning, “The antioxidant ethoxyquin and its analogues: a review,” International Journal of Food Properties, vol. 5, no. 2, pp. 451–461, 2002. View at: Publisher Site | Google Scholar
  13. I. Drewhurst, “Ethoxyquin. JMPR Evaluations,” 1998, View at: Google Scholar
  14. P. K. Gupta and A. Boobis, “Ethoxyquin (Addendum),” 2005, View at: Google Scholar
  15. G. Dorey, B. Lockhart, P. Lestage, and P. Casara, “New quinolinic derivatives as centrally active antioxidants,” Bioorganic & Medicinal Chemistry Letters, vol. 10, no. 9, pp. 935–939, 2000. View at: Publisher Site | Google Scholar
  16. A. Błaszczyk, R. Osiecka, and J. Skolimowski, “Induction of chromosome aberrations in cultured human lymphocytes treated with ethoxyquin,” Mutation Research, vol. 542, no. 1-2, pp. 117–128, 2003. View at: Publisher Site | Google Scholar
  17. A. Błaszczyk and J. Skolimowski, “Comparative analysis of cytotoxic, genotoxic and antioxidant effects of 2,2,4,7-tetramethyl-1,2,3,4-tetrahydroquinoline and ethoxyquin on human lymphocytes,” Chemico-Biological Interactions, vol. 162, no. 1, pp. 70–80, 2006. View at: Publisher Site | Google Scholar
  18. National Library of Medicine HSDB Database, “Ethoxyquin CASRN: 91-53-2,” 2003, View at: Google Scholar
  19. A. Błaszczyk and J. Skolimowski, “Synthesis and studies on antioxidants: ethoxyquin (eq) and its derivatives,” Acta Poloniae Pharmaceutica—Drug Research, vol. 62, no. 2, pp. 111–115, 2005. View at: Google Scholar
  20. A. Hobson Frohock, “Residues of ethoxyquin in poultry tissues and eggs,” Journal of the Science of Food and Agriculture, vol. 33, no. 12, pp. 1269–1274, 1982. View at: Google Scholar
  21. L. T. Burka, J. M. Sanders, and H. B. Matthews, “Comparative metabolism and disposition of ethoxyquin in rat and mouse. II. Metabolism,” Xenobiotica, vol. 26, no. 6, pp. 597–611, 1996. View at: Google Scholar
  22. P. He and R. G. Ackman, “Residues of ethoxyquin and ethoxyquin dimer in ocean-farmed salmonids determined by high-pressure liquid chromatography,” Journal of Food Science, vol. 65, no. 8, pp. 1312–1314, 2000. View at: Google Scholar
  23. V. J. B. Bohne, A. K. Lundebye, and K. Hamre, “Accumulation and depuration of the synthetic antioxidant ethoxyquin in the muscle of Atlantic salmon (Salmo salar L.),” Food and Chemical Toxicology, vol. 46, no. 5, pp. 1834–1843, 2008. View at: Publisher Site | Google Scholar
  24. A. K. Lundebye, H. Hove, A. Måge, V. J. B. Bohne, and K. Hamre, “Levels of synthetic antioxidants (ethoxyquin, butylated hydroxytoluene and butylated hydroxyanisole) in fish feed and commercially farmed fish,” Food Additives and Contaminants A Chemistry, Analysis, Control, Exposure and Risk Assessment, vol. 27, no. 12, pp. 1652–1657, 2010. View at: Publisher Site | Google Scholar
  25. JMPR, “Pesticide residues in food—2005. Report of the Joint Meeting of the FAO Panel of Experts on Pesticide Residues in Food and the Environment and the WHO Core Assessment Group on Pesticide Residues,” JMPR Report, Ethoxyquin 035, 2005, View at: Google Scholar
  26. V. J. Berdikova Bohne, H. Hove, and K. Hamre, “Simultaneous quantitative determination of the synthetic antioxidant ethoxyquin and its major metabolite in atlantic salmon (Salmo salar, L), ethoxyquin dimer, by reversed-phase high-performance liquid chromatography with fluorescence detection,” Journal of AOAC International, vol. 90, no. 2, pp. 587–597, 2007. View at: Google Scholar
  27. J. U. Skaare and S. O. Roald, “Ethoxyquin (EMQ) residues in Atlantic salmon measured by fluorimetry and gas chromatography (GLC),” Nordisk Veterinaermedicin, vol. 29, no. 4-5, pp. 232–236, 1977. View at: Google Scholar
  28. V. J. B. Bohne, K. Hamre, and A. Arukwe, “Hepatic biotransformation and metabolite profile during a 2-week depuration period in Atlantic Salmon fed graded levels of the synthetic antioxidant, ethoxyquin,” Toxicological Sciences, vol. 93, no. 1, pp. 11–21, 2006. View at: Publisher Site | Google Scholar
  29. V. J. B. Bohne, K. Hamre, and A. Arukwe, “Hepatic metabolism, phase I and II biotransformation enzymes in Atlantic salmon (Salmo Salar, L) during a 12 week feeding period with graded levels of the synthetic antioxidant, ethoxyquin,” Food and Chemical Toxicology, vol. 45, no. 5, pp. 733–746, 2007. View at: Publisher Site | Google Scholar
  30. T. D. Bucheli and K. Fent, “Induction of cytochrome P450 as a biomarker for environmental contamination in aquatic ecosystems,” Critical Reviews in Environmental Science and Technology, vol. 25, no. 3, pp. 201–268, 1995. View at: Google Scholar
  31. A. Arukwe, L. Förlin, and A. Goksøyr, “Xenobiotic and steroid biotransformation enzymes in Atlantic salmon (Salmo salar) liver treated with an estrogenic compound, 4-nonylphenol,” Environmental Toxicology and Chemistry, vol. 16, no. 12, pp. 2576–2583, 1997. View at: Google Scholar
  32. T. M. Buetler, E. P. Gallagher, C. Wang, D. L. Stahl, J. D. Hayes, and D. L. Eaton, “Induction of phase I and phase II drug-detabolizing enzyme mRNA, protein, and activity by BHA, ethoxyquin, and oltipraz,” Toxicology and Applied Pharmacology, vol. 135, no. 1, pp. 45–57, 1995. View at: Publisher Site | Google Scholar
  33. J. D. Hayes, D. J. Pulford, E. M. Ellis et al., “Regulation of rat glutathione S-transferase A5 by cancer chemopreventive agents: mechanisms of inducible resistance to aflatoxin B1,” Chemico-Biological Interactions, vol. 111-112, pp. 51–67, 1998. View at: Publisher Site | Google Scholar
  34. K. L. Henson, G. Stauffer, and E. P. Gallagher, “Induction of glutathione S-transferase activity and protein expression in brown bullhead(Ameiurus nebulosus) liver by ethoxyquin,” Toxicological Sciences, vol. 62, no. 1, pp. 54–60, 2001. View at: Publisher Site | Google Scholar
  35. T. K. Bammler, D. H. Slone, and D. L. Eaton, “Effects of dietary oltipraz and ethoxyquin on aflatoxin B1 biotransformation in non-human primates,” Toxicological Sciences, vol. 54, no. 1, pp. 30–41, 2000. View at: Google Scholar
  36. R. Kahl, “Elevation of hepatic epoxide hydratase activity by ethoxyquin is due to increased synthesis of the enzyme,” Biochemical and Biophysical Research Communications, vol. 95, no. 1, pp. 163–169, 1980. View at: Google Scholar
  37. R. Ørnsrud, A. Arukwe, V. Bohne, N. Pavlikova, and A. K. Lundebye, “Investigations on the metabolism and potentially adverse effects of ethoxyquin dimer, a major metabolite of the synthetic antioxidant ethoxyquin in salmon muscle,” Journal of Food Protection, vol. 74, pp. 1574–1580, 2011. View at: Google Scholar
  38. L. Taimr, M. Prusikova, and J. Pospisil, “Antioxidants and stabilizers. 113. Oxidation-products of the antidegradant ethoxyquin,” Angewandte Makromolekulare Chemie, vol. 190, pp. 53–65, 1991. View at: Publisher Site | Google Scholar
  39. L. Taimr, “Study of the mechanism of the antioxidant action of ethoxyquin,” Angewandte Makromolekulare Chemie, vol. 217, pp. 119–128, 1994. View at: Publisher Site | Google Scholar
  40. C. Lauridsen, K. Jakobsen, and T. K. Hansen, “The influence of dietary ethoxyquin on the vitamin E status in broilers,” Archiv fur Tierernahrung, vol. 47, no. 3, pp. 245–254, 1995. View at: Google Scholar
  41. D. R. Brannegan, Analysis of ethoxyquin and its oxidation products using supercritical fluid extraction and high performance liquid chromatography with chemiluminescent nitrogen detection [thesis], Faculty of the Virginia Polytechnic, Institute and State University in Partial Fulfillment of the Requirements of the Degree of Master of Science in Chemistry, 2000,
  42. L. Taimr, M. Smelhausova, and M. Prusikova, “The reaction of 1-cyano-1-methylethyl radical with antidegradant ethoxyquin and its aminyl and nitroxide derivatives,” Angewandte Makromolekulare Chemie, vol. 206, pp. 199–207, 1993. View at: Publisher Site | Google Scholar
  43. A. J. de Koning and G. van der Merwe, “Determination of ethoxyquin and two of its oxidation products in fish meal by gas chromatography,” The Analyst, vol. 117, no. 10, pp. 1571–1576, 1992. View at: Google Scholar
  44. P. He and R. G. Ackman, “HPLC determination of ethoxyquin and its major oxidation products in fresh and stored fish meals and fish feeds,” Journal of the Science of Food and Agriculture, vol. 80, pp. 10–16, 2000. View at: Publisher Site | Google Scholar
  45. S. Thorisson, F. Gunstone, and R. Hardy, “The antioxidant properties of ethoxyquin and of some of its oxidation products in fish oil and meal,” Journal of the American Oil Chemists' Society, vol. 69, pp. 806–809, 1992. View at: Publisher Site | Google Scholar
  46. P. He and R. G. Ackman, “Purification of ethoxyquin and its two oxidation products,” Journal of Agricultural and Food Chemistry, vol. 48, no. 8, pp. 3069–3071, 2000. View at: Publisher Site | Google Scholar
  47. H. W. Renner, “Antimutagenic effect of an antioxidant in mammals,” Mutation Research, vol. 135, no. 2, pp. 125–129, 1984. View at: Google Scholar
  48. H. W. Renner and M. Knoll, “Antimutagenic effects on male germ cells of mice,” Mutation Research, vol. 140, no. 2-3, pp. 127–129, 1984. View at: Google Scholar
  49. D. Guyonnet, C. Belloir, M. Suschetet, M. H. Siess, and A. M. Le Bon, “Antimutagenic activity of organosulfur compounds from Allium is associated with phase II enzyme induction,” Mutation Research, vol. 495, no. 1-2, pp. 135–145, 2001. View at: Publisher Site | Google Scholar
  50. A. Stankiewicz, E. Skrzydlewska, and M. Makieła, “Effects of amifostine on liver oxidative stress caused by cyclophosphamide administration to rats,” Drug Metabolism and Drug Interactions, vol. 19, no. 2, pp. 67–82, 2002. View at: Google Scholar
  51. S. Ray, B. Pandit, S. D. Ray, S. Das, and S. Chakraborty, “Cyclophosphamide induced lipid peroxidation and changes in cholesterol content: protective role of reduced glutathione,” International Journal of PharmTech Research, vol. 2, no. 1, pp. 704–718, 2010. View at: Google Scholar
  52. J. R. P. Cabral and G. E. Neal, “The inhibitory effects of ethoxyquin on the carcinogenic action of aflatoxin B1 in rats,” Cancer Letters, vol. 19, no. 2, pp. 125–132, 1983. View at: Google Scholar
  53. M. M. Manson, J. A. Green, and H. E. Driver, “Ethoxyquin alone induces preneoplastic changes in rat kidney whilst preventing induction of such lesions in liver by aflatoxin B1,” Carcinogenesis, vol. 8, no. 5, pp. 723–728, 1987. View at: Google Scholar
  54. E. A. Decker, “Phenolics: prooxidants or antioxidants?” Nutrition Reviews, vol. 55, no. 11, pp. 396–398, 1997. View at: Google Scholar
  55. Y. Sakihama, M. F. Cohen, S. C. Grace, and H. Yamasaki, “Plant phenolic antioxidant and prooxidant activities: phenolics-induced oxidative damage mediated by metals in plants,” Toxicology, vol. 177, no. 1, pp. 67–80, 2002. View at: Publisher Site | Google Scholar
  56. J. U. Skaare and T. Henriksen, “Free-radical formation in antioxidant ethoxyquin,” Journal of the Science of Food and Agriculture, vol. 26, pp. 1647–1654, 1975. View at: Publisher Site | Google Scholar
  57. C. S. Wilcox and A. Pearlman, “Chemistry and antihypertensive effects of tempol and other nitroxides,” Pharmacological Reviews, vol. 60, no. 4, pp. 418–469, 2008. View at: Publisher Site | Google Scholar
  58. G. H. McIntosh, J. S. Charnock, P. H. Phillips, and G. J. Baxter, “Acute intoxication of marmosets and rats fed high concentrations of the dietary antioxidant "ethoxyquin 66",” Australian Veterinary Journal, vol. 63, no. 11, pp. 385–386, 1986. View at: Google Scholar
  59. N. Ito, S. Fukushima, and H. Tsuda, “Carcinogenicity and modification of the carcinogenic response by BHA, BHT and other antioxidants,” Critical Reviews in Toxicology, vol. 15, no. 2, pp. 109–150, 1985. View at: Google Scholar
  60. Y. Yamashita, T. Katagiri, N. Pirarat, K. Futami, M. Endo, and M. Maita, “The synthetic antioxidant, ethoxyquin, adversely affects immunity in tilapia (Oreochromis niloticus),” Aquaculture Nutrition, vol. 15, no. 2, pp. 144–151, 2009. View at: Publisher Site | Google Scholar
  61. G. E. Neal, D. J. Judah, G. G. Hard, and N. Ito, “Differences in ethoxyquin nephrotoxicity between male and female F344 rats,” Food and Chemical Toxicology, vol. 41, no. 2, pp. 193–200, 2003. View at: Publisher Site | Google Scholar
  62. V. Y. Leong and T. P. Brown, “Toxicosis in broiler chicks due to excess dietary ethoxyquin,” Avian Diseases, vol. 36, no. 4, pp. 1102–1106, 1992. View at: Google Scholar
  63. J. Wang, Q. Ai, K. Mai et al., “Effects of dietary ethoxyquin on growth performance and body composition of large yellow croaker Pseudosciaena crocea,” Aquaculture, vol. 306, no. 1–4, pp. 80–84, 2010. View at: Publisher Site | Google Scholar
  64. M. E. Hernandez, J. L. Reyes, C. Gomez-Lojero, M. S. Sayavedra, and E. Melendez, “Inhibition of the renal uptake of p-aminohippurate and tetraethylammonium by the antioxidant ethoxyquin in the rat,” Food and Chemical Toxicology, vol. 31, no. 5, pp. 363–367, 1993. View at: Publisher Site | Google Scholar
  65. J. L. Reyes, M. Elisabeth Hernández, E. Meléndez, and C. Gómez-Lojero, “Inhibitory effect of the antioxidant ethoxyquin on electron transport in the mitochondrial respiratory chain,” Biochemical Pharmacology, vol. 49, no. 3, pp. 283–289, 1995. View at: Publisher Site | Google Scholar
  66. P. E. Joner, “Butylhydroxyanisol (BHA), butylhydroxytoluene (BHT) and ethoxyquin (EMQ) tested for mutagenicity,” Acta Veterinaria Scandinavica, vol. 18, no. 2, pp. 187–193, 1977. View at: Google Scholar
  67. T. Ohta, M. Moriya, Y. Kaneda et al., “Mutagenicity screening of feed additives in the microbial system,” Mutation Research, vol. 77, no. 1, pp. 21–30, 1980. View at: Google Scholar
  68. E. Zeiger, “Mutagenicity of chemicals added to foods,” Mutation Research, vol. 290, no. 1, pp. 53–61, 1993. View at: Publisher Site | Google Scholar
  69. A. Rannug, U. Rannug, and C. Ramel, “Genotoxic effects of additives in synthetic elastomers with special consideration to the mechanism of action of thiurams and dithiocarbamates,” Progress in Clinical and Biological Research, vol. 141, pp. 407–419, 1984. View at: Google Scholar
  70. B. S. Reddy, D. Hanson, L. Mathews, and C. Sharma, “Effect of micronutrients, antioxidants and related compounds on the mutagenicity of 3,2'-dimethyl-4-aminobiphenyl, a colon and breast carcinogen,” Food and Chemical Toxicology, vol. 21, no. 2, pp. 129–132, 1983. View at: Google Scholar
  71. A. Błaszczyk and J. Skolimowski, “Apoptosis and cytotoxicity caused by ethoxyquin and two of its salts,” Cellular and Molecular Biology Letters, vol. 10, no. 1, pp. 15–21, 2005. View at: Google Scholar
  72. A. Błaszczyk, “DNA damage induced by ethoxyquin in human peripheral lymphocytes,” Toxicology Letters, vol. 163, no. 1, pp. 77–83, 2006. View at: Publisher Site | Google Scholar
  73. J. J. Skolimowski, B. Cieślińska, M. Zak, R. Osiecka, and A. Błaszczyk, “Modulation of ethoxyquin genotoxicity by free radical scavengers and DNA damage repair in human lymphocytes,” Toxicology Letters, vol. 193, no. 2, pp. 194–199, 2010. View at: Publisher Site | Google Scholar
  74. J. J. P. Gille, P. Pasman, C. G. M. van Berkel, and H. Joenje, “Effect of antioxidants on hyperoxia-induced chromosomal breakage in Chinese hamster ovary cells: protection by carnosine,” Mutagenesis, vol. 6, no. 4, pp. 313–318, 1991. View at: Google Scholar
  75. T. H. Rabbitts, “Chromosomal translocations in human cancer,” Nature, vol. 372, no. 6502, pp. 143–149, 1994. View at: Publisher Site | Google Scholar
  76. A. J. de Koning, “An antioxidant for fish meal,” Republic of South Africa Patent, 970894, 1997. View at: Google Scholar
  77. National Toxicology Program (NTP), Toxicology and Carcinogenesis Studies of 1,2-Dihydro-2,2,4-Trimethylquinoline (CAS no. 147-47-7) in F344/N Rats and B6C3DF1mice (Dermal Studies) and the Initiation/Promotion (Dermal Study) in Female Sencar Mice, Technical Report Series no. 456, U.S. Department of Health and Human Services, 1997,
  78. K. Sitarek and A. Sapota, “Maternal-fetal distribution and prenatal toxicity of 2,2,4-trimethyl-1,2-dihydroquinoline in the rat,” Birth Defects Research Part B—Developmental and Reproductive Toxicology, vol. 68, no. 4, pp. 375–382, 2003. View at: Publisher Site | Google Scholar
  79. A. Błaszczyk, J. Skolimowski, and A. Materac, “Genotoxic and antioxidant activities of ethoxyquin salts evaluated by the comet assay,” Chemico-Biological Interactions, vol. 162, no. 3, pp. 268–273, 2006. View at: Publisher Site | Google Scholar
  80. A. Błaszczyk and J. Skolimowski, “Apoptosis and cytotoxicity caused by ethoxyquin salts in human lymphocytes in vitro,” Food Chemistry, vol. 105, no. 3, pp. 1159–1163, 2007. View at: Publisher Site | Google Scholar
  81. A. Błaszczyk and J. Skolimowski, “Evaluation of the genotoxic and antioxidant effects of two novel feed additives (ethoxyquin complexes with flavonoids) by the comet assay and micronucleus test,” Food Additives and Contaminants, vol. 24, no. 6, pp. 553–560, 2007. View at: Publisher Site | Google Scholar
  82. A. Błaszczyk and J. Skolimowski, “Preparation of ethoxyquin salts and their genotoxic and antioxidant effects on human lymphocytes,” Arkivoc, vol. 2007, no. 6, pp. 217–229, 2007. View at: Google Scholar
  83. A. Augustyniak, A. Niezgoda, J. Skolimowski, R. Kontek, and A. Błaszczyk, “Cytotoxicity and genotoxicity of ethoxyquin dimers,” Bromatologia i Chemia Toksykologiczna, vol. 45, pp. 228–234, 2012. View at: Google Scholar
  84. Y. Aoki, A. Kotani, N. Miyazawa et al., “Determination of ethoxyquin by high-performance liquid chromatography with fluorescence detection and its application to the survey of residues in food products of animal origin,” Journal of AOAC International, vol. 93, no. 1, pp. 277–283, 2010. View at: Google Scholar

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