Chemosphere 66 (2007) 2159–2165
www.elsevier.com/locate/chemosphere
Toxicity of HC Orange No. 1 to Daphnia magna, Zebrafish
(Brachydanio rerio) embryos, and goldfish (Carassius auratus)
Hongling Liu a, Hongxia Yu a,*, John P. Giesy
Xiaorong Wang a
a
a,b,c
, Yuanyuan Sun
a,d
,
State Key Laboratory of Pollution Control and Resource Reuse, School of the Environment, Nanjing University,
Nanjing 210093, China
b
Department of Zoology, Institute of Environmental Toxicology, Center for Integrative Toxicology,
Michigan State University, East Lansing, MI 48824, USA
c
Department of Biology and Chemistry, City University of Hong Kong, Kowloon, SAR, Hong Kong, China
d
School of Chemistry and Environmental Science, Nanjing Normal University, Nanjing 210097, China
Received 19 January 2006; received in revised form 4 September 2006; accepted 4 September 2006
Available online 3 November 2006
Abstract
HC Orange No. 1 (HCO1; 2-nitro-4 0 -hydroxydiphenylamine) (CAS No. 54381-08-7) is used as a color additive in hair dyes and can be
released into aquatic environments in wastewater. In this paper, the effects of HCO1 on aquatic organisms were studied using a battery of
toxicological tests. These included measuring immobilization of Daphnia magna, inhibition of zebrafish embryo development, and acute
lethality in zebrafish and goldfish, which are different species belonging to different trophic levels. HCO1 was toxic to all of the organisms
studied. In our experiments, HCO1 remarkably restrained the mobility of D. magna, which may cause subsequent death. The EC50 value
for restrained the mobility of D. magna at 48 h was 1.54 mg HCO1 l1. In addition, HCO1 showed toxicity in zebrafish and goldfish,
where LC50 values at 96 h were 4.04 and 5.37 mg l1, respectively. The results also indicated that HCO1 remarkably retarded the development of zebrafish embryos, which may cause embryo abnormality and even lethality. The most sensitive toxicological endpoint in the
development of the embryos was failure to hatch, which had an EC50 of 0.19 mg HCO1 l1. These results indicated that HCO1 is a potential teratogen to zebrafish embryos. In addition, as HCO1 concentrations increased, the outcomes of each of these toxicity tests changed
in a concentration-dependent manner. Together, the results revealed that HCO1 appears to be toxic to multiple different species of aquatic organisms. The EC50 (LC50) values contain sufficient discriminatory power for risk assessment of HCO1 in aquatic environments.
Based on the present results, more efficient risk assessment procedures for HCO1 will be designed in the future, integrating more flexible
testing methods into the testing schemes that employ only the necessary tools for each case.
2006 Elsevier Ltd. All rights reserved.
Keywords: HCO1; Toxicology; Aquatic organisms; Battery of tests
1. Introduction
The use of hair dyes can be traced back to 4000 years
BC, when the hair on Egyptian mummies was dyed with
henna (Nohynek et al., 2004). Currently, synthetic organic
compounds are used for coloration in commercial hair
dyes. The majority of young women and an increasing pro*
Corresponding author. Tel.: +86 25 83592912; fax: +86 25 83707304.
E-mail address: [email protected] (H. Yu).
0045-6535/$ - see front matter 2006 Elsevier Ltd. All rights reserved.
doi:10.1016/j.chemosphere.2006.09.005
portion of men in industrialized countries regularly use hair
dyes. For example, the natural hair color of the Chinese is
black, but dying hair with other colors has also become
fashionable. Unfortunately, the chemical components of
these dyes can then be released into the aquatic environment, especially in some Asian countries where wastewater
treatment is not always available.
Some hair dye products have been found to contain
mutagenic and carcinogenic compounds (Ames et al.,
1975; Flamm, 1985). Thus, it is not surprising that
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H. Liu et al. / Chemosphere 66 (2007) 2159–2165
potential carcinogenic effects of hair dye products have
been observed in recent epidemiological studies (Rodstein
et al., 1994; La Vecchia and Tavan, 1995; Cook et al.,
1999; Gago-Dominguez et al., 2001).
HC Orange No. 1 (HCO1; 2-nitro-4 0 -hydroxydiphenylamine) (CAS No. 54381-08-7) is used as a colorant in
semi-permanent hair dyes (Pang and Fiume, 1998). The
product formulation data submitted to the US Food and
Drug Administration (USFDA) in 1996 reported that
HCO1 was used in a total of 95 hair dyes and colors
(USFDA, 1996). The concentration reported to be used is
approximately 0.15%, but information from manufacturers
suggested that higher concentrations might be used in the
future (Pang and Fiume, 1998). The effects of HCO1 on
mammals have been investigated and there is no indication
that semi-permanent hair dye formulations containing
0.15% HCO1 are carcinogenic in mice or rats (Burnent
et al., 1976; Pang and Fiume, 1998).
With rapid development of the dyestuff industry in
China, a relatively large amount of HCO1 has the potential
to reach aquatic environments where it may have adverse
effects. Furthermore, if HCO1 is not removed by sewage
treatment due to inefficiency or a complete lack of sewage
treatment in some rural locations, sewage could be a source
of potential toxic materials. However, there are few published studies on the effects of HCO1, especially in aquatic
life. Therefore, we conducted a study to determine the
potential effects of HCO1 in aquatic organisms.
One approach to assess the potential harmful effects of
chemicals in the aquatic environment is to use a set of global physical–chemical and biochemical parameters to predict the potential environmental fate and toxicity of the
chemicals (Denis, 2003). However, chemical–physical
properties alone cannot provide sufficient information on
the potential harmful effects of chemicals in the aquatic
environment (Vyryan et al., 1999). Acute and chronic toxicity, including subtle effects such as deformities and cancer, can also have long-term effects on populations. Thus,
bioassays have been used to evaluate risk assessment of
new registered chemicals as well as to investigate their
effects (Repetto et al., 2001). Due to the diversity of aquatic
organisms and differences in these possible endpoints, use
of a single bioassay may not provide sufficient information
for environmental protection. An alternative cost-effective
approach is to apply a battery of simple tests (Isooma
and Lilius, 1995; Bierkens et al., 1998; Repetto et al., 2001).
The aim of this study was to apply a battery of tests and
endpoints to assess the potential effects of HCO1 on the
aquatic environment. D. magna is a typical aquatic species
in toxicity tests (USEPA, 1991). The fish acute toxicity test
was also used to determine the toxicity of chemicals to
aquatic vertebrates (Anon, 1991). The zebrafish (Brachydanio rerio) (Vittozzi and De Angelis, 1991) was selected as a
model for homeostasis because of its similarity with mammals (Driever and Fishman, 1996). Moreover, to further
provide ecotoxicological information, fish embryos were
employed in place of mammals to study the potential
harmful effects of HCO1. These are useful because chemical cytotoxicity can replace the toxicity for individual
mammals, and chemical concentrations in water can be
directly compared with concentrations in culture medium
(Castaño et al., 1995; Repetto et al., 2001). Other characteristics of the zebrafish embryo make it the best model
for teratogenesis and toxicity studies. These include its ability to be handled with ease, its transparency, and its availability over the whole year (Strehlow and Gilbert, 1993).
The zebrafish embryo test was deemed to be a suitable
assay to minimize the number of fish used (Schulte and
Nagel, 1994). The goldfish (Carassius auratus) (Vittozzi
and De Angelis, 1991) was included in the battery of tests
because it is abundant in the freshwater of China (Masahiro et al., 1999). Such a battery of test systems and indicators would be not only representative of a wide range of
organisms but also simple and rapid, making it convenient
for routine environmental monitoring. The endpoints studied include immobilization of the D. magna, inhibition of
zebrafish embryo development, and acute lethality of adult
zebrafish and goldfish.
2. Materials and methods
2.1. Toxicant exposure
HCO1 (purity > 99%) was purchased from Nanjing
King-Pharm Co., Ltd., Nanjing. A stock solution of
HCO1 was prepared in methanol and maintained in darkness at 0 C. Before each bioassay, stock solutions were
warmed to room temperature and used to prepare the final
test concentrations, which were sterilized by filtration
through a 0.22 lm filter (Millipore, Beijing). The methanol
concentration in the medium containing the solvent control
was less than 0.1%. One control group and one solvent
control group were designated for each exposure test, with
the total mortality of test organisms near zero. Results of
the preliminary studies indicated that HCO1 was stable
enough that nominal concentrations changed less than
20% in a week. Reported concentrations are nominal.
Before experiments, the test organisms were acclimatized
in aquariums for two weeks under conditions similar to
those under which the tests were performed.
2.2. Model systems
2.2.1. D. magna
Acute toxicity test conditions (48 h) conformed to the
guidelines developed by the Organization for Economic
Cooperation and Development (OECD, 1984). Specifically,
eight groups (0.60, 1.00, 1.50, 2.50, 3.00, 3.50, 4.00, and
5.00 mg l1 of HCO1) of five neonates each were kept for
48 h in 20 ml of water contained in 50-ml glass beakers.
Result of preliminary studies indicated that 6.00 mg
HCO1 l1 restrains all D. magna from moving in response
to stimulus within a few hours. Experiments were conducted in quadruplicate for each concentration. D. magna
H. Liu et al. / Chemosphere 66 (2007) 2159–2165
2.2.2. Zebrafish embryos
The test design (72 h) conformed to the guidelines developed by the Organization for Economic Cooperation and
Development (OECD, 1996). Adult zebrafish were maintained in groups of four females and eight males (Nagel,
1986). Fertilized eggs were used to investigate the acute
toxicity of HCO1. The eggs were collected by a plastic
box (12 · 24 cm) placed at the bottom of each tank before
the light was turned on. The group mating occur during the
first 30 min of the light period. The fertilized eggs were
exposed to different concentrations (0.01, 0.05, 0.10, 0.20,
0.40, 0.80, 1.20, 1.60, 2.00, 4.00, and 8.00 mg l1) of
HCO1 within 1 h of collecting and washing them and then
incubated at 26.5 C in embryo medium (Cheng et al.,
2001). Twenty-four-well culture plates with 3 ml volume
in each well were prepared with 2 ml test solution. In each
plate, 20 wells contained a single concentration of the test
solution and four wells were internal controls containing
embryo medium. To exclude mutual influences, only one
fertilized egg was placed in each well. The fertilized eggs
collected for each well of a single plate were taken from
the vessel with the same concentration of HCO1. In order
to keep the concentration constant, the wells were covered
with foil. The development of the eggs was not affected by
this procedure (Schulte and Nagel, 1994).
Developmental stages of embryos are described as hours
post-fertilization (hpf) and classified according to the morphological characteristics described in a study by Chen
et al. (2004). Embryos were examined under an inverted
stereomicroscope. Only those embryos that developed normally were selected for the subsequent experiments.
Embryo viability was determined for each level of HCO1
at different developmental stages (4, 8, 12, 24, 48 and
72 hpf). All groups of eggs were observed and differences
in the chosen parameters were documented (Table 1).
2.2.3. Adult zebrafish
Zebrafish were purchased from a local supplier and had
an average body length and weight of 2.8 cm and 2.5 g,
respectively. Before exposure, fish were acclimated to the
water with a total mortality of one fish in 500. Fish were
fed 0.2 g frozen brine shrimp (Artemia salina) per fish each
day and were subjected to a 14 h light 10 h dark photoperiod. During the experiment, aerated water had a pH of
7.3 ± 0.3 (95%CI) and a temperature of 26.5 C. The water
hardness was approximately 100 mg CaCO3 l1, and the
Table 1
The chosen toxicological endpoints at different stages of development of
zebrafish embryos (hpf)
Coagulated eggs
Completion of gastrulation
Extension of the tail
Spontaneous movements within 20 s
Development of the eye
Heartbeat
Circulation
Heart-rate
Development of the otolith
Development of melanocytes
Rate of malformed egg
Rate of hatched
4
8
12
24
48
72
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
‘‘+’’ indicates that the morphological changes parameters are selected as
toxicological endpoints at different stages of development.
dissolved oxygen (DO) concentration was greater than
6.0 mg l1. The test concentrations were selected based on
data obtained from the preceding acute toxicity tests and
preliminary test results. Exposure of fish to the higher concentration of HCO1 (10.00 mg l1) in the preliminary test
caused a rapid loss of equilibrium, associated with a spiral
swimming behaviour. Fish then became hypoactive and all
died within a 4 h exposure period. Standard conditions
included test containers containing 10 organisms each, with
nine nominal concentrations of HCO1 (1.00, 2.00, 3.00,
4.00, 5.00, 5.40, 6.00, 7.00 and 8.00 mg l1) (each in triplicate). Fish were not fed during the 4 d acute toxicity tests.
Mortality was recorded hourly during the first 4 h of exposure and daily thereafter.
2.2.4. Goldfish
The average length and weight of goldfish were approximately 9.8 cm and 30.8 g, respectively. During experiments, the aerated water temperature was 22.0 ± 2.0 C,
and lighting was 12 h light and 12 h dark. Prior to the
experiments, the fish were acclimated with a total mortality
of zero. In the preliminary test, 15.00 mg HCO1 l1 caused
*
100
90
80
70
60
50
40
30
20
10
0
24h
48h
*
*
*
*
*
Mortality (%)
(clone A) were maintained at 20.0 C in aerated water at a
pH of 7.3 ± 0.3 (95%CI). The water had a hardness of
approximately 100 mg l1 CaCO3 and a dissolved oxygen
(DO) concentration greater than 6.0 mg l1. The D. magna
were subjected to a 12 h light 12 h dark cycle and fed with
green alga (Chlorella vulgaris). Adults were separated from
neonates 24 h before the initiation of the test so that neonates less than 24 h old would be available for testing.
The measured effect was death, which was defined as
immobilization for 15 s after stimulation by a bright light.
2161
*
*
*
*
*
0.6
1
*
*
*
1.5
2.5
3
3.5
Concentration (mg l -1)
4
5
Fig. 1. Daphnia magna immobilization after exposure to different
concentrations of HCO1 for 24 h and 48 h. Data were expressed as mean
values ± SD from one representative experiment (n = 4). Significant
difference from control value was at P < 0.05.
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H. Liu et al. / Chemosphere 66 (2007) 2159–2165
all goldfish to die within a 4 h exposure period. For subsequent experiments, nominal concentrations of 4.00, 5.00,
6.00, 6.40, 7.00, 8.00, and 10.00 mg HCO1 l1 were used.
The goldfish were tested in triplicate in groups of eight
goldfish in 50 l fishbowls containing 30 l of aerated water
under a static test.
fidence limits were determined using Trimmed Spearman–
Karber method version 1.5 (USEPA, 1990).
2.3. Calculations and statistical analysis
The results of this study demonstrated that D. magna is
moderately sensitive to HCO1, showing a dose-dependent
curve of immobilization with an EC50 of 4.47 mg l1 at
24 h and of 1.54 mg l1 at 48 h (Fig. 1).
All the tests were considered valid if control mortality
was 65%. All experiments were performed at least three
times and at least in triplicate for each concentration.
The EC50 (50% effect concentration) values for zebrafish
embryos and the respective 95% confidence limits were
determined by probit analysis (version 4.0). LC50 (EC50)
values for the other test species and the respective 95% con-
3. Results
3.1. D. magna
3.2. Zebrafish embryo
HCO1 caused both deformities and lethality of zebrafish
embryos. The developing embryo of zebrafish offers a sys-
Fig. 2. Morphological images changes at development stages of zebrafish embryos exposed to HCO1. Bar is 50 lm. (a) Coagulated egg. (b) Gastrulation
(8 h). (c) Completion of gastrulation (12 h). (d) Normally developed embryo (48 h) with apparent pigmentation. (e) Abnormally developed embryo (48 h).
(f) Delayed hatch (72 h).
H. Liu et al. / Chemosphere 66 (2007) 2159–2165
2163
Table 2
Toxic effect of HCO1 on the different models and bioindicators included in the proposed ecotoxicological battery
Model system
Origin
Indicator
Exposure period (h)
E(L)C50 (mg l1) (95%CI)
Daphnia magna
Daphnia magna
Embryos
Embryos
Embryos
Embryos
Embryos
Embryos
Embryos
Embryos
Embryos
Embryos
Zebrafish
Zebrafish
Goldfish
Goldfish
Goldfish
Clone A
Clone A
Zebrafish
Zebrafish
Zebrafish
Zebrafish
Zebrafish
Zebrafish
Zebrafish
Zebrafish
Zebrafish
Zebrafish
Immobilization
Immobilization
Coagulated egg
Coagulated egg
Gastrulation is not finished
No spontaneous movement
Coagulated egg
No development of melanocytes
No development of the otolith
Coagulated egg
All abnormality
Embryo does not hatch
Lethal
Lethal
Lethal
Lethal
Lethal
24
48
4
8
12
24
24
48
48
48
72
72
48
96
48
72
96
4.47
1.54
4.93
4.01
3.86
0.38
0.57
0.66
0.70
0.54
0.43
0.19
4.38
4.04
7.52
6.08
5.37
tem with natural interactions between cells. Fifty percent of
the eggs coagulated after 4 h of exposure at a concentration
of 4.93 mg HCO1 l1. Coagulated eggs were milky white
and appeared dark under the microscope (Fig. 2a) (OECD,
1996). After 8 h, the beginning of gastrulation was examined. In a process called epiboly the blastoderm spreads
over the yolk cell. The blastoderm margin, clearly seen as
a fold, should by this time have extended over the equatorial line of the egg (about 70%-epiboly stage; Fig. 2b)
(OECD, 1996). Completion of gastrulation is documented
after 12 h. At this time, the blastoderm has completely
enveloped the yolk cell (100%-epiboly stage). The blastoderm margin has disappeared due to fusion at vegetal pole
(Fig. 2c) (OECD, 1996). Embryogenesis in zebrafish is
completed within the first 72 h and major development of
most internal organs, including the cardiovascular system,
gut, liver and kidney, occurs in the first 24–48 h. Spontaneous myotomal contractions start after approximately 20 h.
After 24 h, side-to-side contractions involving the trunk
and tail should be discernible approximately every 20 s.
One endpoint in the development of the embryos that is
sensitive to HCO1 is a lack of spontaneous movement at
24 hpf, which occurs with an EC50 value of 0.38 mg
HCO1 l1. After 48 h, deviation of pigmentation from normal development was evaluated. At 48 h, the most sensitive
endpoint was a lack of melanocyte development, which
occurs with an EC50 of 0.66 mg HCO1 l1 (Fig. 2d)
(OECD, 1996) (Fig. 2e) (after HCO1 exposure). For
HCO1, the most sensitive endpoint in the development of
the embryos was failure to hatch (72 hpf), occurring with
an EC50 of 0.19 mg HCO1 l1. The concentration of
HCO1 causing 50% of embryos to express abnormalities
(72 hpf) was 0.43 mg l1. The most common deformity
was tail flexures (Fig. 2f) (after HCO1 exposure), which
suggests that HCO1 is a potential teratogen. The magnitude and severity of the effects increased with time of
exposure.
(4.00–5.00)
(1.27–1.86)
(4.80–5.09)
(3.91–4.12)
(3.70–3.99)
(0.32–0.46)
(0.40–0.82)
(0.55–0.80)
(0.32–1.54)
(0.40–0.72)
(0.31–0.60)
(0.11–0.35)
(3.94–4.87)
(3.61–4.52)
(7.35–7.69)
(5.06–6.55)
(4.92–5.87)
3.3. Adult zebrafish
In toxicity tests with adult zebrafish no lethality was
observed for exposures of 96 h to HCO1 at concentrations
of less than 2.00 mg l1. However, concentrations greater
than 7.00 mg l1 caused rapid lethality. Exposure of fish
to the higher concentration (8.00 mg l1) of HCO1 resulted
in a rapid loss of equilibrium, associated with a spiral
swimming behaviour. Fish then became hypoactive and
all died within a 24–48 h exposure period. LC50 values were
4.38 and 4.04 mg HCO1 l1, for 48 and 96 h, respectively
(Table 2).
3.4. Goldfish
Goldfish exposed to high concentrations of HCO1
(10.00 mg l1) died almost immediately, and mortality
was 100% within 48 h. LC50 values were 7.52, 6.08 and
5.37 mg HCO1 l1 for 48, 72 and 96 h, respectively (Fig. 3).
Fig. 3. Diagram of the concentration/response relationship for HCO1 in
goldfish for 48 h, 72 h and 96 h. Data were expressed as mean values ± SD
(n = 3). Significant difference from control value was at P < 0.05.
2164
H. Liu et al. / Chemosphere 66 (2007) 2159–2165
4. Discussion
There is no doubt that D. magna is an excellent test
organism for screening the relative toxicity of chemicals.
Invertebrates have been suggested to be sensitive species
that can serve as surrogates for mice and rats in ecotoxicity
studies. In support of this, LC50 values for D. magna when
exposed to some metals were found to correlate with the
corresponding LD50 values for the mouse and rat (Neuhauser et al., 1985). The predictive screening potentials of
some aquatic invertebrate tests for acute oral toxicity in
humans have been shown to be better than the rat LD50
test for some chemicals (Calleja and Persoone, 1992). The
major advantage of using invertebrate bioassays as a prescreening method is to reduce of the number of vertebrate
animals required for toxicity testing. Since these methods
are in vivo tests, biotransformation of chemicals is taken
into account, making these tests preferable to in vitro methods that have been used to evaluate human acute toxicity
(Ekwall et al., 1989, 1998). The association between the
acute toxicity to D. magna and the corresponding oral
LD50 values in the rat is further evidence of a strong relationship between the two species (Guilhermino et al., 2000).
The D. magna test seems to have a predictive capacity comparable to that of mammalian cytotoxicity tests. Since it is
an in vivo test taking into account the biotransformation of
toxicants and potential integrated effects that occur in the
organism as a whole, the toxicity data produced by this test
could be advantageous in many situations.
The toxic effects of HCO1 on the different models and
bioindicators included in the proposed ecotoxicological
battery are summarized in Table 2. D. magna was also relatively sensitive to the effects of HCO1 exposure. The toxicity of chemicals to D. magna can be predictive of effects
on both invertebrates and mammals. All of the features discussed above are interconnected. D. magna is vulnerable to
fish predation because of its large size. While D. magna is
an aquatic invertebrate, zebrafish and goldfish aquatic vertebrates. The different trophic levels of these species result
in the differences in their EC50 values. This suggests that
their tolerance to HCO1 is different. Their nutritional levels
increase gradually, resulting in the increase in their EC50
values, which suggests that their tolerance to HCO1
increases. The effect of HCO1 on fish is not very speciesspecific, with 96-h EC50 values for lethality goldfish of
5.37 mg l1 becoming appreciably higher than the corresponding values for zebrafish. On the other hand, it is
worth noting that EC50 values for zebrafish embryos
indicate the embryos cannot endure higher HCO1 concentrations.
If the concentrations of HCO1 in D. magna, embryos
and fish could be monitored, EC50 (LC50) values might
be greater than those observed in this study because of bioaccumulation. The relationship between toxicity and body
burden can be used to predict impact (Chapman, 1997). In
the future, tests including the chronic toxicity test, the long
term toxicity test in low dose exposure, and molecular tox-
icological tests will be used to assess the toxicology of
HCO1 more accurately. Because of the potential for
HCO1 to be released into aquatic environments, the discharge of sewage or effluent containing HCO1 should be
monitored and controlled.
Acknowledgements
This work was supported by the National Natural Science Foundation of China (Nos. 20237010 and 20375015)
and the Core University Program of the Japan Society
for Promotion of Science. The manuscript was significantly
improved by the comments of two anonymous reviewers.
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