Currently, nanotechnology and nanoparticles have quickly emerged and have gained the attention of scientists due to their massive applications in environmental sectors. However, these environmental applications of silver nanoparticles potentially cause serious effects on terrestrial and aquatic organisms. In the current study, freshwater fish C. carpio were exposed to blood-mediated silver nanoparticles for toxicity, mortality, bioaccumulation, and histological alterations. Silver nanoparticles were fabricated using animal blood serum and their toxic effect was studied against common carp fish at different concentrations levels (0.03, 0.06, and 0.09 mg/L).
The findings have revealed a little influence of blood-induced silver nanoparticles on fish behavior at the highest concentration (0.09 mg/L). However, bioaccumulation of blood-mediated silver nanoparticles was reported in different organs of fish. Maximum bioaccumulation of silver nanoparticles was reported in the liver, followed by the intestine, gills, and muscles. Furthermore, the findings have shown that the bioaccumulation of silver nanoparticles led to histopathological alterations; including damaged structure of gill tissue and have caused necrosis. It is summarized that histopathological alteration in gill and intestine mostly occurred by the highest concentration of blood-induced silver nanoparticles (0.09 mg/L).
This study provides evidence of the silver nanoparticles influence on aquatic life; however, further systematic studies are crucial to access the effects of AgNPs on aquatic life.
Nanotechnology (NT) and nanoscience is one of the remarkable areas of science dealing with using the structure of nanoscale , and tremendously developed in the last decade . Due to their wide range of applications, NT is playing a beneficial role in water treatment, food industry, household equipment, biomedical, and health care . Nanoparticles (NPs) are a special kind of nanosized materials with unique properties due to their small size and dispersal . Among all the nanoparticles, silver nanoparticles (AgNPs) are well known for their commercialization worldwide [5, 6], due to their sole biological activities , and are being utilized widely in medicine . Despite the biological activities and a wide range applications of AgNPs, there is a lack of information regarding human health and environmental toxicity . The extensive use of AgNPs in the world, release into the aquatic environment, has raised concern  for a high impact on aquatic life .
The rare knowledge of AgNPs regarding aquatic toxicity and their linkage with living components have raised concerns in the last decade . It has been hypothesized and suggested that the concentration of AgNPs in an aquatic ecosystem is in µg L−1 or mg L−1 , however, these concentrations are yet toxic to any environment . It has been reported that mutable properties and the small size of AgNPs are toxic and dangerous to the ecosystems [15, 16]. Silver is found in four different oxidation states (Ag, Ag+, Ag2+, and Ag3+) in the aquatic environment [15, 17], though the exact estimates of AgNPs toxicity are still hindered due to lack of acquaintance . It has been accepted that the toxicity caused by AgNPs is due to the release of Ag+ into the environment and finally absorbed by living organisms . Silver nanomaterials are the most producing nanoparticles and release extensively to both terrestrial and aquatic environments , which is very toxic to fish fauna, and therefore it is very important to establish the toxicity of nanosilver .
Common carp fish (Cyprinus carpio) is one of the most important fish species of freshwater , distributed in the Asia and Europe . It has been estimated that the production of common carp fish is about 4.32 million tons . When fish is exposed to any kind of toxin, it could lead to changes in biochemical, hematological parameters, histological alteration, and gut microbial dysbiosis . Nowadays, NT is rapidly used as targeted specific drugs to control fish diseases , because of its broad antibacterial activity  and anti-protozoal activity , but the exposure of AgNPs to fish led to the multiplicity of effects, even mortality , organ dysfunction, other lesions and gene mutation . The small nanomaterials can easily penetrate inside the tissues of fish, such as the liver, gills, brain, and muscles . Fish, being a healthy food source for humans, hence, nanosilver could migrate from fish to human, which might lead to silver contamination in human.
Among all aquatic organisms, fish is one of the most used aquatic organism for assessing environmental toxicity and toxic effects . Therefore, this study was designed to evaluate the acute, chronic, and sublethal toxicity of three different concentrations of blood-mediated AgNPs in common carp fish for a long-time exposure of twenty days’ period. In vivo, the studies regarding toxicity and toxic effects of AgNPs are principally lacking; especially in aquatic systems where ecologically significant and diverse organisms are affected. The current study was aimed to expose freshwater fish C. carpio to novel fabricated silver nanoparticles for toxicity, mortality, bioaccumulation, and histological alterations. Primarily the tissues exposed to various foreign pollutants in an aquatic fish are gills, muscles, intestine, and liver, hence these tissues were studied.
Materials and methods
Sheep's (Ovis aries) blood was collected from the slaughterhouse, Xiao Xihu Gonglin Road, Lanzhou (longitudes of 102°30″ to 104°30″ and latitudes of 35°5″ to 38°), Gansu, China. The blood was collected in a closed container in the presence of a buffer solution, which keeps maintaining the proteins and other biological molecules of blood serum. The blood was stored at room temperature for serum separation and then centrifuged three times at 12,000 rpm for 30 min. The serum was separated and stored at 4 ℃ for further analysis. Pure silver nitrate (99.99%) solution (Sigma Aldrich Beijing, China) of 10 mL was mixed with 90 mL distilled water (10 mM AgNO3 solution). Subsequently, 100 mL of serum was added to 100 mL of silver nitrate solution (10 mM) in a 500-mL Erlenmeyer flask and incubated for 24 h at 37 ℃ at 150 rpm. The synthesized B-AgNPs were purified and separated through repeated centrifugation at 12,000 rpm for 20 min and stored for further use.
Characterization of nanoparticles
The synthesis of blood serum mediated silver nanoparticles (B-AgNPs) was indicated by the color change of the solution from reddish to brownish after incubation. However, UV–Vis spectrometry was used and plasmon bands were recorded at 422 nm that verify the B-AgNPs formation. The obtained B-AgNPs were characterized for their shape and size. The phase purity and crystalline structure of the obtained B-AgNPs were analyzed by X-ray diffraction (XRD) using Bruker D2 Phaser with graphite monochromator operated at 30 kV and 15 mA. Transmission electron microscopy (TEM) Tecnai G2 Bio-Twin and scanning electron microscope (SEM) Hitachi S-3400N was used to characterize the detailed morphology, size, and distribution of synthesized B-AgNPs. The size of the synthesized B-AgNPs was measured by ImageJ software.
Fish species and their laboratory maintenance
The juvenile common carp fish (C. carpio) (length: 12.3 ± 1.28 cm, weight: 9.59 ± 1.83 g) were brought from the Yantan local market, Chengguan district (36,007°N 103,082°E; Lanzhou, Gansu). The present study was conducted from August to October 2020. These fish were allowed to adapt in tap water under a natural photoperiod of 14:10 h light–dark period for one week. After acclimation, the healthy fish were selected for further studies, which were confirmed through physical appearance (skin luster, eyes, color, and behavior). All fishes were kept at ambient temperature, pH, and dissolved oxygen (DO2) given in Additional file 1: Fig. S1. Fish were fed with a commercial food diet two times a day (9:00 AM and 9:00 PM), manufactured by JK. Aquarium, China (algae powder, shrimp meal, wheat gluten, soya bean, crude protein, and fresh fishmeal). The overall experiment was conducted in 10:14 dark and light cycles. In the whole experiment, 20% of water was changed daily for avoiding bacterial or fungal infection while 100% of water was changed once a week.
The current study was conducted according to the requirements of the Organization for Economic Cooperation and Development  for long-time exposure to B-AgNPs. There were four experimental groups as follows: a control group and three B-AgNPs (different concentrations) treatment groups. The fish in the water tanks were exposed to B-AgNPs 0.03 mg/L (LC50), 0.06 mg/L (LC50), and 0.09 mg/L (LC50). Each group comprised 20 fish. Fish were not fed for 24 h before starting the experiment. After every 48 h, the fish were sampled from every group of studies. The collected fish were anesthetized and dissected for different organs (muscles, gills, intestine, and liver) collection. The collected organs were stored at − 80 °C for further studies.
Lethal concentration (LC50)
The mortality and acute toxicity were carried out according to the Organization for Economic Cooperation and Development . The mortality rates were recorded every 24 h for 20 days.
Tissue silver contents
The collected organs were washed and properly dried. Dried organs were kept inside the muffle furnace at 450 ℃ for 2 h for digestion. Further 10 mL HCl of 6 mM was added to 1 g of ash. After the complete absorption of ash in HCl, the solution was allowed for filtration following the protocol of .
Analytical detection of AgNPs in tissue
The filtered solution was analytically analyzed by inductively coupled plasma atomic emission spectroscopy (ICP-OES) (Agilent Technologies, 5100) for the bioaccumulation of AgNPs in different tissues of common carp fish.
Tissue preparation for light microscopy
Tissues were observed for histopathological alteration under a light microscope. The dissected tissues were fixed in a 9% formaldehyde solution. After the fixation, the tissues were dehydrated in gradient alcohol solutions and implanted with paraffin wax. The tissue of 4 μm thickness was prepared by a rotary microtome Leica-2016 Germany and placed on a glass slide and stained with eosin and hematoxylin. The prepared samples were visualized with digital trinocular camera microscope BA210Digital.
Tissue extracts for antioxidant enzyme measurements were obtained from gills and liver by homogenizing the tissues using 0.1 M sodium phosphate buffer, pH 6.5 containing 20% glycerol, I mM EDTA, and 1.4 mM dithioerythritol. The glutathione S-transferase (GST) activity was conducted using 1-chloro-2,4-dinitrobenzene substrate. Glutathione reductase activity (GR) was conducted using homogenizing the tissues in 0.1 M K-phosphate, 5 mM ascorbate. Catalase assay (CAT) mixture of 3 mL consisted of 0.05 mL tissue extract, 1.6 mL phosphate buffer (100 mM buffer, pH 7.0), 0.5 mL H2O2, and 0.95 mL distilled water.
In the overall experiment, the median lethal concentrations (LC50) were obtained using the trimmed Spearman–Karber method. All the experimental data were tested for normality and presented as means with standard deviation. The data were tested for time (days) and treatment effects by two-way analysis (ANOVA) followed by post hoc Duncan. p value < 0.05 was considered statistically significant.
Characterization of B-AgNPs
In this study, stable, spherical, small size, and well-dispersed AgNPs were obtained by using animal blood. The synthesis of B-AgNPs was initially confirmed from the color change of the solution, however, the maximum absorption of UV–Vis spectrometry at 422 nm (Fig. 1a) further confirmed the B-AgNPs synthesis. The X-ray diffraction analysis showed peaks 111, 200, 220, and 311 that indicate the crystalline structure of the obtained B-AgNPs (Fig. 1b). The other peaks lower than 30, is due to residue of organic components present in the blood serum. The size of the obtained B-AgNPs was a small-sized range from 20 to 50 nm (Fig. 2a). Moreover, the SEM analysis showed spherical and well-dispersed AgNPs at 2.0 μm (Fig. 2b).
Toxicity of B-AgNPs against fish
The obtained B-AgNPs were applied in vitro for their mortality and toxicity in fish fauna. C. carpio was very prone to B-AgNPs absorption and caused damage at the tissue level, but with very little mortality. In the present study, the behavior of fish was studied and the fish group (0.09 mg/L) has shown very less abnormal behavior while exposed to B-AgNPs as given in Table 1. Therefore, B-AgNPs could be an appropriate indicator for further use in any fisheries department. The mortality potential or lethal effect of any application materials is the first parameter of any application study. The fish mortality in the lethal concentration of B-AgNPs was dose-dependent, e.g., the highest mortality was found at the highest dose (0.09 mg/L) given in (Table 2; Fig. 3). There was no mortality found in the other three groups (control, 0.03 mg/L, 0.06 mg/L) of the study. In the overall experiment, the mortality was observed on days 2, 6, 13, and 19 while no mortality has occurred on other days of the experiment. Median lethal concentration (LC50) values for 2, 6, 13, and 19 days are given in Table 2.
Bioaccumulation of B-AgNPs in tissue
The result of bioaccumulation of B-AgNPs in different organs is given in Fig. 4. Overall the B-AgNPs were mostly bioaccumulated in the liver, followed by the intestine, gills, and muscles (p < 0.05). In all organs, the bioaccumulation of B-AgNPs was dose-dependent, e.g., the bioaccumulation of B-AgNPs was increased while the dose was increased. Comparatively the treatment groups consisted of different concentrations of B-AgNPs. The results revealed that the highest bioaccumulation of B-AgNPs was seen at the highest concentration of B-AgNPs (0.09 mg/L) while the lowest bioaccumulation was seen at the lowest concentration B-AgNPs (0.03 mg/L). The overall absorption of B-AgNPs in different organs is given in Fig S2 while the daily basis bioaccumulation of B-AgNPs in different organs of (Cyprinus carpio) is given in Aditional file (Table S3 = gills, S4 = intestine, S5 = muscle, and S6 = liver). The liver was the most bioaccumulated organ (Fig. 4a). The highest absorption of B-AgNPs was observed in a group (0.09 mg/L), i.e., 272.09 mg in the 20 days exposure. 299.15 mg B-AgNPs were absorbed in the intestine for 20 days exposure as shown in Fig. 4b. Gills have absorbed 225.99 mg of B-AgNPs for 20 days (Fig. 4c) while the lowest absorption of B-AgNPs was observed in the muscles of fish, i.e., 76.64 mg (p < 0.05) shown in Fig. 4d. However, the highest level of absorption of B-AgNPs was seen in the liver and intestine (p < 0.05). The bioaccumulation of B-AgNPs reported in this study was compared with previous studies (Table 3).
The histological investigation showed that exposure of fish fauna to B-AgNPs led to an alteration in tissue level in targeted organs (gills, intestine). Tissue alterations in the sense of damage, atrophy, shortening of secondary lamella, degeneration, and necrosis at different concentrations of B-AgNPs have been observed. The gill tissue structure was damaged and led to atrophy and necrosis while exposed to 0.03 mg/L of AgNPs shown in Fig. 5. Figure 6 shows that necrosis has occurred, which led to vacuolation, and the tissues are arranged disorderly. The shedding and degeneration have started in the tissues of gills at 0.06 mg/L concentration of B-AgNPs. At the highest concentration of B-AgNPs (0.09 mg/L), the reduction or shortening of lamella was observed as shown in Fig. 7. Not only the gills, but the AgNPs also caused histological alterations in intestinal tissues. In the current study, some intestinal villi mucosal epithelial cells are shaded and a small number of epithelial cells on the top are missing. Figure 8 shows that there is degeneration, shedding, and necrosis have been observed. The fish exposed to 0.03 mg/L B-AgNPs concentration shows that there is shedding and a small number of epithelial cells on the top of intestinal villi are missing. The fish exposed to 0.06 mg/L concentration led to necrosis and degeneration in the mucosal cell. The exposure of fish to 0.09 mg/L led to necrosis and cell lysis in the villi mucosal epithelial cells as shown in Figure 8c. So, it was summarized that lesions, degeneration, necrosis, and shedding even cell lysis were formed mostly at the highest concentration of B-AgNPs exposure given in Additional file 1: Table S1 and S2.
Biomarker assay for enzymes
Antioxidant enzyme activities are summarized in Table 4. The different concentrations of B-AgNPs led to significant changes in the hepatic and gill enzymatic activities. With a reduction in the fish group exposed to (0.03 mg/L and 0.06 mg/L) and an increase in the highest concentration of B-AgNPs (p < 0.05). At the highest concentration (0.09 mg/L) of B-AgNPs, a rise in GST and decrease were noticed in GR in the case of the liver. But in the gills, GST and GR both have been decreased as compared to control. The CAT increased at 0.03 mg/L while decreased in both 0.06 mg/L and 0.09 mg/L in case of the gills and liver. The GR decreased at all the concentrations of B-AgNPs comparing to the control group gills while in the liver the GR has increased at 0.03 mg/L and 0.06 mg/L but has decreased at 0.09 mg/L.
The toxicity of AgNPs in the aquatic ecosystem is affected by the capability of uptake of aquatic organisms. We herein measured and evaluated the long-time exposure toxicity of newly synthesized B-AgNPs using animal blood in common carp fish (C. carpio). In the current study, the focus was on mortality, bioaccumulation in different organs, abnormal behavior, and the histopathological study of B-AgNPs. During the study period, the bioaccumulation of B-AgNPs in gills, liver, intestine, and muscles was observed. The results of the current study revealed that the B-AgNPs were mostly bioaccumulated in the liver, followed by the intestine, gills, and muscles. During the overall experiment, no abnormal behaviors were noticed. For instance, the fish properly moved toward the food. The food was not rejected by fish. The feces excretion was normal. No irregular operculum movement was found, but the fish movement toward the surface was normal. Moreover, the B-AgNPs also damage and cause necrosis, even cell lysis in intestinal villi.
It has been proved that the AgNPs are not much stable and able to be dissolved in aqueous solutions, so it releases Ag ions progressively . Though the toxic effects of the silver in nano-form have been widely reported the toxicity of AgNPs is seems to be primarily due to the Ag+ release [2, 33]. The high surface-to-volume ratio in metallic nanoparticles increases the probability of releasing ion form nanoparticles . According to , the toxicity of AgNPs in fish fauna is mostly because of Ag ions instead of nanoparticles.
To investigate the consequences of B-AgNPs, mortality (LC50) was measured in the current study. The results revealed that LC50 was dose-dependent. There was no mortality at 0.03, 0.06 mg/L concentration of B-AgNPs while 5/20 fish in the same group at the variant time died at the highest dose (0.09 mg/L) of B-AgNPs. The highest mortality (2/20) was noted on the 16th day of the experiment. In comparison, our results revealed the lowest mortality at the highest concentration of B-AgNPs. A study conducted by  revealed the mortality in every concentration even by the lowest concentration (0.01 mg/L) of AgNPs. Another conducted study exhibited that 7/21 fish died at 0.03 mg/L after 96 h of exposure to AgNPs , but in our study, there was no mortality at the lowest concentration (0.03 mg/L) till the end of the experiment.
It has been assumed that biological synthesized AgNPs are less toxic as compared to chemically synthesized nanoparticles . In the current study, the AgNPs were synthesized for the first time using animal blood serum and tested for the bioaccumulation in fish fauna. The results for the bioaccumulation revealed that the B-AgNPs were mostly accumulated in the liver, followed by the intestine, gills, and muscle (Fig. 4a–d). Similar results have been achieved by , in which the AgNPs were accumulated mostly in the liver and intestine. No doubt, there are few studies conducted on the fish toxicity of AgNPs. Based on the above results, it can be assumed or hypothesized that fish liver might play an important role in the metabolism of silver. Previously studies described that the silver first increase in blood when a fish is exposed to AgNPs, then the liver absorbs the silver, therefore bioaccumulation of silver NPs highly took place [37, 38]. In the current study, the fish were fed two times a day, so it can be assumed that while ingesting food particles, they also ingested silver nanoparticles, therefore the intestine is the second most bioaccumulated organ followed by the liver (Fig. 4a). Another previously conducted study also revealed that the intestine was the second most accumulated after the liver [39, 40]. The small finger-like projections (villi) present in the intestine increase the surface area for the absorption of any particles. Therefore,  concluded that the increased bioaccumulation of AgNPs perhaps due to the absorption from the liver by the intestine. In the present study, gills were the third most B-AgNPs bioaccumulated organ. This might be because of two reasons: (1) gills are highly exposed to the external environment; (2) due to large surface area, the gills have the capability to absorb more and more especially small-sized materials.  concluded that small-sized AgNPs were mostly absorbed as compared to large-sized AgNPs.
After the long period of exposure of C. carpio to sublethal concentrations of blood-induced silver nanoparticles, different lesions and alterations were observed in the intestine and gills (Figs. 5, 6, 7, 8). In detail, it has been observed that there was necrosis, degeneration, and cell lysis in the gills and intestine of fish at different concentrations of B-AgNPs given in Additional file 1: Tables S1 and S2. These kinds of changes in gills are the indications of a defense mechanism, subsequently, they increase the gap between the external environment and bloodstream, and prevent the penetration of pollution . In the current study, during exposure to AgNPs, the tissue damaging mostly depended on the concentration of B-AgNPs. At the highest concentration (0.09 mg/L) caused severe damage as compared to the lowest concentration (0.03 mg/L). Among all NPs, silver is the most powerful toxicant that affects the gills primarily . In the current study by comparison with other previously conducted studies. It has been observed that our study showed less toxicity in the sense of mortality, bioaccumulation, and histological alterations. Therefore, blood serum-mediated silver nanoparticles might be an alternative to the other biological synthesized AgNPs.
The current study aimed to investigate the toxicity and toxic effects of B-AgNPs. According to the results of the present study, it might be said that after the long-time exposure, the B-AgNPs were bioaccumulated in the targeted organs while the liver was the main target for bioaccumulation. Furthermore, the bioaccumulation of B-AgNPs has led to histological alterations in the gills and intestine. The surface capping, morphology, and size of AgNPs are the major difficulties while studying the nano-ecotoxicity. These properties of AgNPs are the main factors for causing toxicity in fish fauna. Therefore, it is concluded that the focus and attention should be given to all these factors while synthesizing the green AgNPs. This might help in the future to reduce the nano-toxicity in biodiversity.
Availability of data and materials
- µg L−1 :
Microgram per liter
- C. carpio :
Scanning electron microscopy
Transmission electron microscopy
- DO2 :
Organization for Economic Cooperation and Development
- LC50 :
Blood-induced silver nanoparticles
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The authors are very grateful to the Chinese Government Scholarship Council for the award of Doctoral studies in Lanzhou University. Finally, we are thankful to the School of Life Sciences, Lanzhou University, for providing a perfect environment in conducting studies.
This study was supported by the National Natural Science Foundation of China (No. 32060277, 32060258); Science and Technology Plan of Gansu Province (18JR3RA004), the "Light of West China" Program of the Chinese Academy of Sciences, and Project of Gansu Cultural Relics Bereau (GWJ202011).
Ethics approval and consent to participate
The current study was ethically approved by the committee of the School of life science, Lanzhou University, Lanzhou, Gansu, China.
Consent for publication
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. The daily basis bioaccumulation of B-AgNPs in gill of (Cyprinus carpio). Table S4. The daily basis bioaccumulation of B-AgNPs in intestine of (Cyprinus carpio). Table S5. The daily basis bioaccumulation of B-AgNPs in muscles of (Cyprinus carpio). Table S6. The daily basis bioaccumulation of B-AgNPs in liver of (Cyprinus carpio).
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Kakakhel, M.A., Wu, F., Sajjad, W. et al. Long-term exposure to high-concentration silver nanoparticles induced toxicity, fatality, bioaccumulation, and histological alteration in fish (Cyprinus carpio). Environ Sci Eur 33, 14 (2021). https://doi.org/10.1186/s12302-021-00453-7
- Novel Silver nanoparticles
- Histopathological alterations
- Enzymatic stress