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Effect of feeding of cyclopoid copepods (Eucyclop sp.) exposed to engineered titanium dioxide nanoparticles (nTiO2) and Lead (Pb2+) on Clarias gariepinus growth and metabolism



The application of Lead (Pb2+) and titanium dioxide nanoparticles (nTiO2) in commercial products is on the rise since the development of nanotechnology. The increasing usage of products containing these compounds had led to the rise of their concentration in aquatic environment, but information on the potential risk of co-exposure of these compounds in aquatic environment is still limited. In this study, the effect of feeding Clarias gariepinus with cyclopoid copepods exposed to engineered Pb2+ and nTiO2 on growth performance, and proximate composition of Clarias gariepinus was investigated.


A chronic (28 days) laboratory bioassay was carried out by feeding C. gariepinus fries with cyclopoid copepods exposed to nTiO2 (7.5, 16.5 μg L−1) and Pb2+ (6.5, 15 μg L−1) alone as well as binary mixtures through dietary uptake.


Our results indicate negative allometric growth (b < 3), while the highest condition factor (1.74) was recorded in the control. A significant decreased of specific growth rate (SGR) compared to the control was observed in exposed fish. Some parameters of proximate composition (crude protein, ash, moisture, total lipid) from the fish decreased significantly (P < 0.05) with synergistic effect on binary mixture. In contrast, carbohydrate content increased significantly (P < 0.05) with synergistic effect on binary mixture.


The present study clearly indicates that the chronic exposure of nTiO2 and Pb2+ mixtures caused the delay in the growth performance and changes in the proximate compositions of the fish. This findings raise concern regarding the fate of higher trophic level feeding on primary consumers inhabiting freshwater ecosystems contaminated with nTiO2 and Pb2+.


Nanomaterials are defined as engineered materials having nanostructured surface and topography of at least one dimension equal or less than 100 nm (Hagens, Oomen, de Jong, Cassee, & Sips, 2007). All nanomaterials have specific physical, chemical, optical, electrical, catalytical, and mechanical properties. In addition, particles size, number, surface area, charge, shape, and mass determine their biological interactions with consequences on the behavior and responses in the body of organisms (Hagens et al., 2007).

However, nanomaterials such as titanium dioxide have the peculiarity of having unique physicochemical properties including a bright white color, ability to block UV light, and antimicrobial activity (Smijs & Pavel, 2011). TiO2 nanoparticles exist in three different crystalline structures (anatase, rutile, and brookite) and are widely used as a pigment (in paint, plastic, and paper), in personal care products (sunscreens and toothpastes), and in food such as (ice cream) (Weir, Westerhoff, Fabricius, Hristovski, & Von Goetz, 2012).

Piccinno, Gottschalk, Seeger, and Nowack (2012) documented the estimated worldwide production of titanium dioxide nanoparticles (nTiO2) at approximately 5000 t/year in 2006–2010 and 10,000 t/year in 2011–2014; with an estimated production by 2025 expected to reach 2.5 million metric tons.

Since the application of nTiO2 has increased in recent years, it is expected that this nanomaterials will find their way into the aquatic environment (Gottschalk, Sonderer, Scholz, & Nowack, 2009). Based on toxicological studies, the predicted environmental concentration of nTiO2 in Switzerland waters was reported as 0.7–16 μg L−1(Mueller & Nowack, 2008). Despite increased usage of product containing nTiO2, there is very little data reported on their toxicological effects in aquatic environments in Sub-Sahara Africa. Recent research showed evidence of trophic transfer of nTiO2 via dietary exposure from freshwater Daphnia to Zebrafish without biomagnifications of the nanoparticles (Zhu, Chang, & Chen, 2010). Toxic effects of nTiO2 on aquatic organisms have been well documented in many in vivo and in vitro studies (Iavicoli, Leso, & Bergamaschi, 2012; Liu, Lin, & Zhao, 2013; Tassinari, La Rocca, Stecca, Tait, De Berardis, Ammendolia, Iosi, Di Virgilio, Martinelli, & Maranghi, 2015), but studies on the toxicity of nTiO2 and heavy metals mixtures are currently sparse (Hartmann, Legros, Von der Kammer, Hofmann, & Baun, 2012; Liu et al., 2013; Zhang, Niu, Li, Zhao, Song, Li, & Zhou, 2010). Although, it is possible that both compounds enter the aquatic systems differently, mixtures formed can demonstrate synergistic adverse effect on fish more than that of each compound alone.

Lead (Pb2+) has received critical attention as a major source of pollution worldwide (Tchounwou, Yedjou, Patlolla, & Sutton, 2012). This non-essential metal has been used for more than 800 decades in the manufacturing of glass, pigments, fuel additives, batteries, electronic components, cosmetics, and wine and has been detected in cooking, agricultural, urban, and industrial wastes (United Nation Environmental Programme, 2010). Lead (Pb2+) is known to affect growth, development, and reproduction in humans and animals. Lead (Pb2+) pollution has become an environmental problem worldwide especially in aquatic environment in which it may reach high-risk levels for aquatic organisms and their consumers including humans (Soto-Jimenez, Arellano-Fiore, Rocha-Velarde, Jara-Marini, & Ruelas-Inzunza, 2011).

TiO2 nanoparticles can co-occur simultaneously with other heavy metal such as cadmium (Cd+), with consequent harmful effects on non-aquatic organisms (Zhang et al., 2010). However, engineered nanoparticles are capable of absorbing and separating metals from aqueous or organic solution (Mashhadizadeh & Karami, 2011; Tavallali, 2011). The higher surface area to volume of engineered nTiO2 NPs relative to that of traditional TiO2 NPs particles allows the NPs to absorb heavy metal and modify their toxicity (Sun, Zhang, Zhang, Chen, & Crittenden, 2009).

A careful review of available literature indicates inadequate attention given to the concomitant exposure of nTiO2 and Pb2+ on aquatic organisms via food uptake. Therefore, evaluating the interactive effects of nTiO2 after addition of Pb2+ through food intake is critical for safety concerns in the usage of products containing these compounds. We hypothesize that co-exposure of nTiO2 and Pb2+ impairs the growth and metabolism of aquatic organisms.

This study was therefore aimed at assessing the interactive effects of nTiO2 after addition of Pb2+ via food intake (contaminated zooplankton) on growth and proximate composition of Clarias gariepinus. Clarias gariepinus was selected as the model animal in the present study because of its advantages over other freshwater species for their rapid growth and their availability in most freshwater bodies in Africa.


Preparation and characterization of nTiO2

Titanium (IV) oxide-anatase-rutile nanoparticles (particle size < 21 nm) and PbNO3 were purchased from Sigma-Aldrich (St. Louis, MO, USA) and further characterization of the metals was done using X-ray diffraction using an Empyrean XRD (Panalytical, The Netherlands) equipped with filtered Cu Kα radiation operated at 40 Kv and 40 mA. The XRD patterns were recorded from 10 to 80 2θ° with a scanning speed of 0.526° per minute. X-ray diffraction analysis was used to confirm the chemical composition and crystal structure of the nTiO2.

TiO2 nanoparticles were rigorously mixed with magnetic stirrer on a plate (VWR Scientific 370, Radnor, PA, USA) using a 1-in bar for 15 min (30° C, 1400 rpm, 50 kHz). In addition, the morphology of nTiO2 aggregates in the test solutions was observed using a scanning electron microscope (Xpert Pro). Particles aggregation of nTiO2 after 24 h was also observed in 10 mg L−1 of nTiO2.

Culture of cyclopoid copepods sp.

Test organism

Cyclopoid copepods sp. were obtained from the National Institute of freshwater and Fisheries Research, (NIFFR), New Bussa, Nigeria and continuously cultured in the Limnology laboratory of the Institute. The culture medium was kept static for 48 h and the cyclopoid copepods sp. were fed daily with cultured Chlorella ellipsoidea contaminated with nTiO2, Pb2+ alone, and in combination. The culture was maintained at a constant temperature (25 ± 2 °C) with a natural light-dark cycle.

nTiO2 and Pb accumulation in cyclopoid copepods sp.

Cyclopoid copepods sp. were fed for 2 days (ad libitum) with contaminated C. ellipsoidea at a concentration of 1.106 cells mL−1 with the following concentrations of 0 (control), 6.5 μg L−1, and 15 μg L−1 of Pb; 7.5 μg L−1, 16.5 μ gL−1 TiO2 NPs and four couples of mixtures of (6.5, 7.5); (6.5, 16.5); (15, 7.5); (15, 16.5) μg L−1. In this experiment, 35 cyclopoid copepods sp. were placed in each container (1000 mL glass beakers containing 250 mL test solution), and each treatment had 3 replicates. Test containers were monitored every 24 h.

After 48 h of exposure, they were harvested, rinsed with fresh culture medium, and transferred immediately to Clarias gariepinus larvae tanks as fish food.

Acclimatization and training of C. gariepinus

Clarias gariepinus larvae (3 days old; 0.33 ± 0.09 g) were hatched at the Hatchery laboratory of NIFFR. The fish were kept in glass aquaria of 50 cm × 50 cm (25 fish per tank) filled with 10 L of freshwater. Before the experiment, fish were acclimatized to the experimental conditions (25 ± 2 °C; 12:12 h light:dark; with daily water change) for at least 1 week. At the same time, C. gariepinus larvae were trained to eat live cyclopoid copepods sp. During acclimatization and training, the health of the fish was observed and recorded. Only healthy fish were selected for the examination described below. All animal protocols in this study were conducted under the supervision and approval of the Ethical Committee of the University of Ilorin, Ilorin, Nigeria.

Trophic transfer of TiO2 NPs and Pb from cyclopoid copepods to Clarias gariepinus

Trophic transfer experiments consisting of a 28-day uptake period were conducted to determine if the transfer of nTiO2 and Pb from cyclopoid copepods sp. to C. gariepinus can occur.

Cyclopoid copepods sp. exposed to 6.5 μg L−1 and 15 μg L−1 of Pb; 7.5 μg L−1, 16.5 μg L−1 nTiO2 and the 4 couples of mixtures of (6.5, 7.5); (6.5, 16.5); (15, 7.5); (15, 16.5) μg L−1 for 48 h (as mentioned above) were harvested with a plastic net, rinsed three times using fresh culture medium, and transferred into C. gariepinus aquaria as fish food.

Clarias gariepinus were fed with cyclopoid copepods sp. (ad libitum) in the uptake period and uncontaminated cyclopoid copepods in the depuration period.

Twice daily (6 am and 6 pm), the water (in which neither nTiO2 nor Pb2+ was added) was renewed; in most cases, the C. gariepinus would consume the entire cyclopoid copepods sp. This static renewal system was used to ensure that the C. gariepinus ate all the food provided and so that none would be washed away.

Assessment of length-weight relationship and condition factor

Fish samples were collected for a period of 7 weeks, standard length of the fish was measured to the nearest centimeter, using measuring board. The fish were also weighed to the nearest gram on a sensitive balance. The length-weight relationship and Fulton’s condition factor were calculated according to Le Cren’s, (1951) equations:

  1. (1)

    W = alb. Then the data were transformed into logarithms prior to calculations. The equation became LogW = Loga + bLogL


    • W = weight of fish (g)

    • L = standard length of fish (cm)

    • a = constant or intercept

    • b = an exponent or slope.

  2. (2)

    Fulton’s condition factor: K = 100 W/L3 where

    • K = condition factor

    • W = weight of fish (g)

    • L = standard length of fish (cm)

    The percentage of survival of C. gariepinus within the duration of the experiment was calculated according to the formula of Zhu et al. (2007) and Wang, Long, Cheng, Liu, & Yan (2015).

    Percentage survival rate = number of fry that survived × 100 / total number of fry that start the treatment in each aquarium.

  3. (3)

    Specific growth rate (% per week) = (final ln weight-initial ln weight) × 100/experimental days.

Proximate composition

Fish was subjected to several procedures for determination of crude protein, ash, moisture, total lipid (fat), and carbohydrate.

Total crude protein was measured according to Lowry, Rosebrough, Farr and Randall (1951). A stock of Lowry reagent was compounded in a 48:1:1 ratio of Lowry reagents (2% (w/v) anhydrous Na2CO3 in 0.1 N NaOH); (1% (w/v) NaK Tartrate tetrahydrate) and (0.5% (w/v) CuSO4.5H2O in H2O), respectively. Samples were then incubated for 10 min at room temperature, absorbance was read at 600 nm, and concentration was determined using standard curve: total protein content = wt. of protein (from BSA curve) × 100 / dry cell mass (g).

Ash content was determined by incinerating 5 g of fish sample in a muffle furnace according to (Helrick, 1990).

To determine the moisture, the sample was dried to a constant weight in a vacuum oven at 100 °C (Helrick, 1990). The moisture loss was determined gravimetrically.

Lipid was extracted according to the method of Bligh and Dyer (1959). A mixture of 2 mL of methanol and 1 mL of chloroform was made and added to 1 g fish biomass. The lower layer was pipetted out and weighed: lipid content (%) = wt. of lipid (g) × 100 / wt. of culture (g).

For carbohydrate determination, 50 μL of 80% phenol and 5 mL of 95% sulfuric acid was added to 1 mL culture supplemented with 1 mL of filtered distilled water, following the method of Dubois, Gilles, Hamilton, Roberts and Smith (1956) using glucose as standard.

DNA isolation, purification, and quantification

Total deoxyribonuclease (DNA) was purified from C. gariepinus tissues using EZNA, tissue DNA kit (OMEGA, USA). The purified DNA was subjected to spectrometry using a Nanodrop 1000. The absorbance of extracted DNA was read at A280nm.

Statistical analysis

All experiments were done in triplicates, and data were recorded as the mean and standard deviation (SD). One-way analysis of variance with Tukey’s multiple comparisons was used to detect significant differences among groups. In all data analyses, a P value < 0.05 was considered statistically significant.


Fish fed with contaminated copepods for 4 weeks showed the lowest survival (50%) in combined compounds (Pb (15) + nTiO2 (16.5)). However, the lowest mean weight (0.15 g) was recorded in nTiO2 (7.5), while a decrease in mean weight was observed in exposed fish compared to the control; the lowest weight gain (0.15) was concentration dependent (Pb (15)) for single Pb (Table 1).

Table 1 Growth response and survival of C. gariepinus fries fed with contaminated zooplankton of Pb and nTiO2

Weight gain significantly (P < 0.05) decreased compared to the control; the lowest weight gain (0.25 g) was recorded in fish exposed to Pb (15) and the highest (0.42 g) was recorded in fish exposed to Pb (15) + nTiO2 (16.5). Furthermore, the specific growth rate (SGR) was lowest (3) in fish exposed to Pb (15) and highest (3.8) in fish exposed to Pb (6.5) + nTiO2 (16.5) (Table 1).

The b value accounting for the allometric growth was negative and less than 3 (b < 3) in all exposed fish indicating disproportionate growth between the size and the weight of fish. However, the maximum b value of 2.09 was recorded from the control indicating that the absence of the compounds in the food was responsible for moderate negative allometric growth (b < 3). The b values in this study were fitted into respective correlation coefficient (r) levels and transformed into linear equations (Table 2). The result showed significant correlation (P < 0.05) of no allometric growth throughout the treatments except for fish fed contaminated copepods nTiO2 (7.5), Ti (16.5), and Pb (6.5) + nTiO2 (16.5) (Table 2).

Table 2 Estimated parameters of total length-body weight relationships and condition factor for C. gariepinus

Clarias gariepinus post fries in this study had relatively low allometric growth rate in fish fed with contaminated copepods with b values between − 13 and − 0.12.

Condition factor (K) of contaminated fish ranged between 0.99 and 1.74 (Table 2); these values were lower than the ideal level of 2.9–4.8 for fish water quality.

Proximate composition of C. gariepinus fed with cyclopoid copepods exposed to Pb and nTiO2 showed that the protein content significantly (P < 0.05) decreased in exposed fish to contaminated dietary food. A decrease of 83.9%, 82%, 88.5%, 84.37%, 82.38%, 81.75%, 80.98%, and 80.88% was recorded for Pb (6.5), Pb(15), nTiO2 (7.5), nTiO2 (16.5), Pb(6.5) + nTiO2 (7.5), Pb(6.5) + nTiO2 (16.5), Pb(15) + nTiO2 (7.5), Pb(15) + nTiO2 (16.5) μg L−1 respectively. The results showed that there was a synergistic decrease of protein content in binary compounds (Fig. 1a).

Fig. 1
figure 1

Proximate composition of Clarias gariepinus fed contaminated copepods after 28 days. a Protein content, F (8, 27) = 2580, P < 0.0001. b Ash content, F (8, 18) = 8454, P < 0.0001. c Moisture content, F (8, 18), P < 0.0001. d Total lipid content, F (8, 18) = 1144, P < 0.0001. e Carbohydrate content, F (8, 18), P < 0.0001. Threshold replicate were included (n = 3). Errors bars indicate Standard deviation (SD). Ti ie nTiO2

Ash content was lowest in binary mixture compared to the control 96.97%, 95.97%, 95.4%, 95.30% for Pb(6.5) + nTiO2 (7.5), Pb(6.5) + nTiO2 (16.5), Pb(15) + nTiO2 (7.5), Pb(15) + nTiO2 (16.5) μg L−1 respectively. This result showed that there was significant (P < 0.05) decrease of ash content compared to the control (Fig. 1b).

Moisture content in fish significantly (P < 0.05) decreased in single and combined compounds compared to the control, 94.44%, 93.82%, 97.53%, 96.91%, 93.82%, 97.53%, 96.91%, 93.82%, 91.97%, 91.35%, 91.11% for Pb (6.5), Pb(15), nTiO2 (7.5), Ti(16.5), Pb(6.5) + nTiO2 (7.5), Pb(6.5) + nTiO2 (16.5), Pb(15) + nTiO2 (7.5), Pb(15) + nTiO2 (16.5) μg L−1 respectively. The moisture content decreased with the increase of concentrations when the compound was used alone. This result showed synergistic effect of binary compounds for moisture content (Fig. 1c).

Decrease of total lipid content of exposed fish was concentration dependent when both compounds were used separately with percentages 83.46%, 73.50%, 86.25%, 83.86% for Pb (6.5), Pb(15), nTiO2 (7.5), and nTiO2 (16.5) respectively. After addition of nTiO2 to Pb2+, the combination of both compounds further decreased the total lipid content in fish; however, this decrease was highly significant (P < 0.001) compared to the control (Fig. 1d).

Figure 1e shows a significant (P < 0.05) increase of carbohydrate content in all treated fish compared to the control. The increase were 1.12-, 1.14-, 1.10-, 1.14-, 1.15-, 1.16-, 1.166-, and 1.169-fold higher than the control for treated fish Pb (6.5), Pb(15), nTiO2 (7.5), nTiO2 (16.5), Pb(6.5) + nTiO2 (7.5), Pb(6.5) + nTiO2 (16.5), Pb(15) + nTiO2 (7.5), Pb(15) + nTiO2 (16.5) μg L−1 respectively. The binary mixture showed higher increase and synergistic effect compared to single treated compound. Furthermore, two-way ANOVA showed that there was significant interaction between both compounds.

DNA extracted was quantified using a spectrophotometer Gene Quant. Table 3 showed that the variation of DNA concentration due to treatment of fish was irrespective of the concentration of the compound of the fed fish. The highest (91.85) DNA concentration was recorded in nTiO2 (7.5) and the lowest (21.2) was recorded in nTiO2 (16.5). The mixture of both compounds had the highest concentration (90.3) for Pb(6.5) + nTiO2 (7.5) exposed fish compared to the control. There was no synergistic effect of the compounds recorded in the present study. However, there was significant (P < 0.05) difference between DNA concentration and the exposed fish compared to the control.

Table 3 Quantified DNA of C. gariepinus fed contaminated copepods


The result of the present study suggests that Lead (Pb2+) and nTiO2 nanoparticles have negative impact on the survivability and growth of C. gariepinus which is evidence by numerous other studies indicating the negative effect of heavy metals and nanoparticles on fish (Asharani, Wu, Gong, & Valiyaveettil, 2008; Kim & Kang, 2015; Zhou, Wang, Gu, & Li, 2009). The interaction between the highest concentrations of binary mixture observed in the present study was more prominent for fish that demonstrated low survival rate (50%) indicating that post fries were unable to cope with their hyperactivity due to stress leading to depletion of energy and causing death.

Chojnacki and Sliwinski (2013) reported that the growth of Leuciscus idus fish was positively affected by silver nanoparticles served through dietary means. The growth rate is generally retarded in response to exposure to toxicant because the allocation of energy for growth is used to compensate for repair (Kim & Kang, 2015). The specific growth rate (SGR) of fish contaminated with single and combined compounds, in this study decreased compared to the control. The effect on growth of fish in the study was not concentration-dependent. This implies that the fish fed with contaminated zooplankton continued its growth though not significant (P > 0.05). This result agreed with findings of Chojnacki and Sliwinski (2013) who also documented higher SGR in contaminated fodder with titanium dioxide nanoparticles fed to fish. This was probably related to the initiation of detoxification processes and reduction of the integrity of the cell membrane (Chojnacki & Sliwinski, 2013).

The negative allometric growth between the length and weight of fish in the present study may be due to the presence of single and combined nanoparticles of Pb and TiO2 in the fish diets. These compounds might have caused the disproportionate growth of fish given that dietary Lead (Pb) exposure has been shown to generate a significant inhibition of growth in rockfish (Kim & Kang, 2015). In addition, hazardous effect of nanoparticles induced growth restriction in Mystusvittatus (Chatterjee, Bhattacharjee, & Lu, 2014). Similar observation was found in the present study for nTiO2; furthermore, the combination of binary compounds also showed relatively low allometric values suggesting that the addition of nTiO2 to Pb causes retardation of growth.

Condition factors (K) values in this study ranged between 0.99 and 1.74 and were lower than the ideal level 2.9–4.8 reported by Bagenal (1978) for maximum growth of freshwater fish. The low (K) values recorded might have been caused by the rapid decrease of biological dissolve oxygen demand in the flow through water system in cultured fries.

Protein levels in the present study decreased in all other treated fish compared to the control. Protein content below 15% is considered low (FAO, 2007); however, it is worthy to note that the protein composition in this study was above 15% in all samples. The result of the present study agrees with protein levels between 16.30 and 18.73% in black sprat (Sprattus sprattus) and Goby (Neogobius melanostonus) reported by Stancheva, Merdzhanova, Petrova, and Petrova (2013).

Decrease of crude fat or total lipid in this study was observed in all treatment compared to the control. Ackman (1989) documented that fish species can be classified into four categories: high fat (up to 8.0 g.100 g−1 w.w); medium fat (4–8 g.100 g−1 w.w); low fat (2–4); and lean (< 2 g−1 w.w).

In this study, the total lipid varied between 10.04 and 6.09% suggesting that C. gariepinus that consumed contaminated copepods with these compounds experienced an alteration of lipid composition possibly due to stress. The fish in this study could be classified to be of high fat and medium fat content despite the consumption of compounds. This finding differ with findings of Stancheva et al. (2013) who reported lipid contents of between 1.60 and 4.30% in black sea spat and goby fish after exposure to Pb2+.

However, the decrease of protein and lipid observed in C. gariepinus proximate composition may be due to their utilization as energy source for detoxification and maintenance of homeostasis during intake of stressors (Wang et al., 2015). In this study, protein content and lipid content decreased with an increase in concentration of Pb2+ and nTiO2 used alone and subjected to C. gariepinus, indicating that Pb2+ were less harmful to energy stores. The addition of nTiO2 to Pb2+ shows further synergistic decrease of protein content and lipid content suggesting the presence of nTiO2 might have increased the bioavailability of Pb2+ thereby being critically deleterious to energy storage.

Moisture content consistently decreased and varied between 16.2 and 14.76% which was not between the 60 and 80% acceptable levels of moisture content in fish (Gallagher, Harrell, & Rulifson, 1991). In this study, the concentration of compounds used influenced fish moisture level, higher in nTiO2 than Pb2+ that, however, synergistically decreased in combined mixture. The size of the fish (post larvae) could be responsible for the low moisture level as observed in the control. The moisture level in the present study was not in agreement with the 70% moisture content reported by Stanchevaet al. (2013).

Ash content in food could be defined as the measure of the total amount of minerals content present in food item. In this study, ash content decreased in all exposed fish, but further decrease in binary mixtures was also observed probably because of the reduction of minerals levels in the fish. However, the range of ash was between 5.96 and 5.68% indicating low ash content compared to Pseudotolithus elongates and Pseudotolithus typus from the Cameroonian Coast which recorded ash content between 7.7 and 54% (Njinkoue et al., 2016).

Carbohydrate serves as the instant energy source during stress, so it is expected that during exposure, glycogen content in the muscles was broken down to carbohydrate (glucose) via glycogenolysis (Javed & Usmani, 2015). Carbohydrate content in the present study varies between 46.28 and 54.09% and was higher than in the control. This result suggests that carbohydrate level in treated C. gariepinus increased due to chronic stress. The result in this study was in line with the result reported by Javed and Usmani (2015) who reported depletion of glycogen in the liver and muscle of Channa punctatus inhabiting river polluted by thermal power plant effluents.

During stress conditions, fish need more energy to detoxify the pollutants and overcome stress (Amza et al., 2006). In this study, decrease of basic metabolic compounds (protein, lipid, carbohydrate) was observed. This may be due to the need for energy to meet the increasing demand for energy due to stress. The observed depletion of protein, lipid, and ash may have been due to their degradation and probably possible utilization of degraded products for metabolic purpose (Amza et al., 2006).

Assessment of DNA concentration and damage was studied by using several methods. One of the methods is the quantification of DNA that has been carried out using a UV absorbance at 280 with spectrophotometer (Georgiou, Papapostolou, & Grintzalis, 2009). Characterizing the structural integrity of genomic DNA is very important in a variety of biological application (Georgiou et al., 2009). The genomic DNA product derived in this study stem from the exposure of post fries C. gariepinus to Pb and nTiO2 alone and in combination with values ranging between 21.2 and 102.45 ng/μL. The present study indicated low DNA concentrations in exposed fish in comparison with control; DNA concentrations however, were not dose dependent. In addition, fish exposed to lower concentration of nTiO2 alone and after addition to the lowest concentration of Pb induced high DNA damage. This is probably due to the impairment of mitochondria function, causing alteration of mitochondrial membrane permeability (Teodoro et al., 2011). Repairable or non-repairable DNA damage can originate from oxidative attack on reactive oxygen species (ROS) DNA (Georgiou et al., 2009). This result was in agreement with the findings of Sayed, Mahmoud, and Mekkawy (2013) who also reported DNA concentration of 12.03–181.47 ng/μL of adults and embryo of C. gariepinus exposed to 4-Nonylphenol.


The result obtained from this study indicated a synergistic effect of Pb and nTiO2 on the proximate composition of C. gariepinus. The growth and DNA concentration of C. gariepinus were influenced by exposure of Pb and nTiO2, a phenomenon that can be used as biomarker for stress in polluted aquatic ecosystems. The role of nTiO2 in binary mixture with heavy metal in relation to food uptake in food chain and their physiological and metabolic effects on fish need further investigations.


C. ellipsoisea:

Chlorella ellipsoidea

C. gariepinus:

Clarias gariepinus




Nigeria Freshwater and Fisheries research

nTiO2 :

Titanium dioxide nanoparticles




Specific growth rate


X-ray diffraction


  • Ackman, R. G. (1989). Nutritional composition of fats in seafoods. Progress in Food & Nutrition Science, 13(3–4), 161–289.

    CAS  Google Scholar 

  • Amza, H., Ngu, T., & Wanda, I. (2006). Stressor impacts on fish energetics and stress. Journal of Biosafety, 7, 98–104.

    Google Scholar 

  • Asharani, P. V., Wu, Y. L., Gong, Z., & Valiyaveettil, S. (2008). Toxicity of silver nanoparticles in zebrafish models. Nanotechnology, 19(25), 255102.

    Article  CAS  Google Scholar 

  • Bagenal, T. B. (1978). Age and growth. Methods for assessment of fish production in fresh waters, (3rd ed., pp. 101–136). Oxford: Blackwell scientific publication.

    Google Scholar 

  • Bligh, E. G., & Dyer, W. J. (1959). A rapid method of total lipid extraction and purification. Canadian Journal of Biochemistry and Physiology, 37(8), 911–917.

    Article  CAS  Google Scholar 

  • Chatterjee, N., Bhattacharjee, B., & Lu, C.-H. (2014). Hazardous effect of ZnS nanoparticles on the feeding behaviour, growth and maturation process of the Asian striped catfish, Mystus vittatus (Bloch, 1794). International Aquatic Research, 6(3), 113–125.

    Article  Google Scholar 

  • Chojnacki, M., & Sliwinski, J. (2013). The effects of exposure of ide's larvae and juvenile Leuciscus idus (L.) to silver nanoparticles via the digestive tract. Annales Universitatis Mariae Curie-SkÅ odowska Sectio EE: Zootechnica, 31(4), 42–54.

    Google Scholar 

  • Dubois, M., Gilles, K. A., Hamilton, J. K., Roberts, P. A., & Smith, F. (1956). Phenol sulphuric acid method for carbohydrate determination. Annal of Chemistry, 28, 350–359.

    Article  CAS  Google Scholar 

  • FAO. (2007). Protein and amini acid requirement in human nutrition. WHO Technical Report series 935. United Nation University and World health organization, p. 284.

  • Gallagher, M. L., Harrell, M. L., & Rulifson, R. A. (1991). Variation in lipid and fatty acid contents of Atlantic croakers, striped mullet, and summer flounder. Transactions of the American Fisheries Society, 120, 614–619.

    Article  CAS  Google Scholar 

  • Georgiou, C. D., Papapostolou, I., & Grintzalis, K. (2009). Protocol for the quantitative assessment of DNA concentration and damage (fragmentation and nicks). Nature Protocols, 4, 125–131.

    Article  CAS  Google Scholar 

  • Gottschalk, F., Sonderer, T., Scholz, R. W., & Nowack, B. (2009). Modeled environmental concentrations of engineered nanomaterials (TiO2, ZnO, Ag, CNT, fullerenes) for different regions. Environmental Science & Technology, 43, 9216–9222.

    Article  CAS  Google Scholar 

  • Hagens, W. I., Oomen, A. G., de Jong, W. H., Cassee, F. R., & Sips, A. J. M. (2007). What do we (need to) know about the kinetic properties of nanoparticles in the body? Regulatory Toxicology and Pharmacology, 49, 217–229.

    Article  CAS  Google Scholar 

  • Hartmann, N. B., Legros, S., Von der Kammer, F., Hofmann, T., & Baun, A. (2012). The potential of TiO2 nanoparticles as carriers for cadmium uptake in Lumbriculus variegatus and Daphnia magna. Aquatic Toxicology, 118, 1–8.

    Article  CAS  Google Scholar 

  • Helrick, K. (1990). Official methods of analysis of the association of official analytical chemists. Fifteen edition published by the association of official analytical chemist, Inc, Arlinton Virginia USA. 77 Pp.

  • Iavicoli, I., Leso, V., & Bergamaschi, A. (2012). Toxicological effects of titanium dioxide nanoparticles: a review of in vivo studies. Journal of Nanomaterials, 964381, 36.

    Google Scholar 

  • Javed, M., & Usmani, N. (2015). Stress response of biomolecules (carbohydrate, protein and lipid profiles) in fish Channa punctatus inhabiting river polluted by thermal power plant effluent. Saudi Journal of Biological Sciences, 22, 237–242.

    Article  CAS  Google Scholar 

  • Kim, J.-H., & Kang, J.-C. (2015). The lead accumulation and hematological findings in juvenile rock fish Sebastes schlegelii exposed to the dietary lead (II) concentrations. Ecotoxicology and Environmental Safety, 115, 33–39.

    Article  CAS  Google Scholar 

  • Le Cren, E. D. (1951). The length-weight relationship and seasonal cycle in gonad weight and condition in the perch (Perca fluviatilis). The Journal of Animal Ecology, 20, 201–219.

    Article  Google Scholar 

  • Liu, K., Lin, X., & Zhao, J. (2013). Toxic effects of the interaction of titanium dioxide nanoparticles with chemicals or physical factors. International Journal of Nanomedicine, 8, 2509–2520.

    PubMed  PubMed Central  Google Scholar 

  • Lowry, O. H., Rosebrough, N. J., Farr, A. L., & Randall, R. J. (1951). Protein measurement with the Folin phenol reagent. Journal of Biological Chemistry, 193, 265–275.

    PubMed  CAS  Google Scholar 

  • Mashhadizadeh, M. H., & Karami, Z. (2011). Solid phase extraction of trace amounts of Ag, Cd, Cu, and Zn in environmental samples using magnetic nanoparticles coated by 3-(trimethoxysilyl)-1-propantiol and modified with 2-amino-5-mercapto-1, 3, 4-thiadiazole and their determination by ICP-OES. Journal of Hazardous Materials, 190, 1023–1029.

    Article  CAS  Google Scholar 

  • Mueller, N. C., & Nowack, B. (2008). Exposure modeling of engineered nanoparticles in the environment. Environmental Science & Technology, 42, 4447–4453.

    Article  CAS  Google Scholar 

  • Njinkoue, J. M., Gouado, I., Tchoumbougnang, F., Ngueguim, J. H. Y., Ndinteh, D. T., Fomogne-Fodjo, C. Y., & Schweigert, F. J. (2016). Proximate composition, mineral content and fatty acid profile of two marine fishes from Cameroonian coast: Pseudotolithus typus (Bleeker, 1863) and Pseudotolithus elongatus (Bowdich, 1825). NFS Journal, 4, 27–31.

    Article  Google Scholar 

  • Piccinno, F., Gottschalk, F., Seeger, S., & Nowack, B. (2012). Industrial production quantities and uses of ten engineered nanomaterials in Europe and the world. Journal of Nanoparticle Research, 14, 1109.

    Article  Google Scholar 

  • Sayed, A. H., Mahmoud, U. M., & Mekkawy, I. A. (2013). Genotoxicity induced by 4-Nonylphenol in adult and embryos of Clarias gariepinus. Global Advanced Research Journal of Environmental Science and Toxicology, 2, 107–118.

    Google Scholar 

  • Smijs, T. G., & Pavel, S. (2011). Titanium dioxide and zinc oxide nanoparticles in sunscreens: focus on their safety and effectiveness. Nanotechnology, Science and Applications, 4, 95–112.

    Article  CAS  Google Scholar 

  • Soto-Jimenez, M. F., Arellano-Fiore, C., Rocha-Velarde, R., Jara-Marini, M. E., Ruelas-Inzunza, J., & Páez-Osuna, F. (2011). Trophic transfer of lead through a model marine four-level food chain: Tetraselmis suecica, Artemia franciscana, Litopenaeus vannamei, and Haemulon scudderi. Archives of Environmental Contamination and Toxicology, 61, 280–291.

    Article  CAS  Google Scholar 

  • Stancheva, M., Merdzhanova, A., Petrova, E., & Petrova, D. (2013). Heavy metals and proximate composition of Black Sea sprat (Sprattus sprattus) and goby (Neogobius melanostomus). Bulgarian Journal of Agricultural Science, 19, 35–41.

    Google Scholar 

  • Sun, H., Zhang, X., Zhang, Z., Chen, Y., & Crittenden, J. C. (2009). Influence of titanium dioxide nanoparticles on speciation and bioavailability of arsenite. Environmental Pollution, 157, 1165–1170.

    Article  CAS  Google Scholar 

  • Tassinari, R., La Rocca, C., Stecca, L., Tait, S., De Berardis, B., Ammendolia, M. G., Iosi, F., Di Virgilio, A., Martinelli, A. Maranghi, F. (2015). In vivo and in vitro toxicological effects of titanium dioxide nanoparticles on small intestine. AIP Conference Proceedings, (vol. 1667, p. 020016).

  • Tavallali, H. (2011). Alumina-coated magnetite nanoparticles for solid phase extraction of Cd in water samples. Chemistry and Technology, 3, 1647–1651.

    CAS  Google Scholar 

  • Tchounwou, P.B., Yedjou, C.G., Patlolla, A.K., & Sutton, D.J. (2012). Heavy metal toxicity and the environment. EXS, 101: 133-164.

  • Teodoro, J. S., Simaues, A. M., Duarte, F. V., Rolo, A. P., Murdoch, R. C., Hussain, S. M., & Palmeira, C. M. (2011). Assessment of the toxicity of silver nanoparticles in vitro: a mitochondrial perspective. Toxicology In Vitro, 25, 664–670.

    Article  CAS  Google Scholar 

  • United Nation Environmental Programme. (2010). Chemicals and waste ensuring sound management of chemicals. Annual Report, Published by the United Nation Environmental Programme, p. 57.

  • Wang, T., Long, X., Cheng, Y., Liu, Z., & Yan, S. (2015). A comparison effect of copper nanoparticles versus copper sulphate on juvenile Epinephelus coioides: growth parameters, digestive enzymes, body composition, and histology as biomarkers. International Journal of Genomics, 2015, 783021.

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  • Weir, A., Westerhoff, P., Fabricius, L., Hristovski, K., & Von Goetz, N. (2012). Titanium dioxide nanoparticles in food and personal care products. Environmental Science & Technology, 46, 2242–2250.

    Article  CAS  Google Scholar 

  • Zhang, R., Niu, Y., Li, Y., Zhao, C., Song, B., Li, Y., & Zhou, Y. (2010). Acute toxicity study of the interaction between titanium dioxide nanoparticles and lead acetate in mice. Environmental Toxicology and Pharmacology, 30, 52–60.

    Article  CAS  Google Scholar 

  • Zhou, X., Wang, Y., Gu, Q., & Li, W. (2009). Effects of different dietary selenium sources (selenium nanoparticle and selenomethionine) on growth performance, muscle composition and glutathione peroxidase enzyme activity of crucian carp (Carassius auratus gibelio). Aquaculture, 291, 78–81.

    Article  CAS  Google Scholar 

  • Zhu, X., Chang, Y., & Chen, Y. (2010). Toxicity and bioaccumulation of TiO2 nanoparticle aggregates in Daphnia magna. Chemosphere, 78, 209–215.

    Article  CAS  Google Scholar 

  • Zhu, X., Zhu, L., Li, Y., Duan, Z., Chen, W., & Alvarez, P. J. J. (2007). Developmental toxicity in zebrafish (Danio rerio) embryos after exposure to manufactured nanomaterials: buckminsterfullerene aggregates (nC60) and fullerol. Environmental Toxicology and Chemistry, 26, 976–979.

    Article  CAS  Google Scholar 

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We acknowledge the efforts of Dr. Okaeme and Dr. Ovie, Executive Director and Director of Operation of the National Institute for Freshwater Fisheries Research (NIFFR) respectively, for providing necessary support throughout this research work. We also commend all the technologists in the Institute, for their guidance and tremendous assistance throughout the study. We are grateful to Mr. Ibrahim Maikaita for reviewing the manuscript prior to submission.

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Correspondence to Moise Matouke Matouke.

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Matouke Matouke, M., Mustapha, M. Effect of feeding of cyclopoid copepods (Eucyclop sp.) exposed to engineered titanium dioxide nanoparticles (nTiO2) and Lead (Pb2+) on Clarias gariepinus growth and metabolism. JoBAZ 79, 42 (2018).

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