With the rapid development of nanotechnology and widespread use of nanoproducts, concerns have arisen regarding the ecotoxicity of these materials. In this paper, the photosynthetic toxicity and oxidative damage induced by nano Fe<sub>3</sub>O<sub>4</sub> on a model organism, <i>Chlorella vulgaris (C. vulgaris)</i> in aquatic environment, were studied. The results showed that Nano-Fe<sub>3</sub>O<sub>4</sub> was toxic to <i>C. vulgaris</i> and affected its content of chlorophyll a, malonaldehyde and glutathione, CO<sub>2</sub> absorption, net photosynthetic rate, superoxide dismutase activity and inhibition of hydroxyl radical generation. At higher concentrations, compared with the control group, the toxicity of nano-Fe<sub>3</sub>O<sub>4</sub> was significantly different. It suggested that nano-Fe<sub>3</sub>O<sub>4</sub> is ecotoxic to <i>C. vulgaris</i> in aquatic environment.
Nanomaterials have unique physicochemical properties, high strength, and good magnetic properties, which has led to their use in electronic, magnetic, optical, biomedical, pharmaceutical, cosmetic, energy, sensor, and catalytic applications. Rapid development of nanotechnology and nanomaterials, and continual expansion of their applications have resulted in widespread biosafety concerns [
Compared with bulk Fe3O4, nano-Fe3O4 has unique characteristics as superparamagnetism, size and quantum tunnel effects, and so on [2-6]. As an important member of the spinel ferrite family, Fe3O4 is among the most widely used soft magnetic materials. It is commonly used as a recording material, pigment, magnetic fluid material, catalyst, and in magnetic polymer microspheres and electronic materials. It also has wide applications in biotechnology and medicine.
There are concerns about potential pollution of the aquatic environment through mass leakage of nanomaterials during their production, transportation, use, or disposal. Nanomaterials may also be released to the environment through pharmaceuticals, cosmetics and sunscreens that end up in the sewage treatment system from patient’s feces, laundry or bathing [
As excellent aquatic models, microalgae are prevalent in lakes and seas, easy to culture and propagate, and sensitive to pollutants. Chlorella vulgaris (C. vulgaris) is distributed widely in freshwater and seawater and has a short growth cycle, which make it ideal for aquatic ecotoxicity studies and it can be used to directly observe toxicity at the cellular level [
In this study, C. vulgaris was used to study the photosynthetic toxicity and oxidative damage induced by nano-Fe3O4. This preliminary data could be used to support a thorough ecological safety assessment of nanomaterials.
C. vulgaris (
Louis, MO). Malonaldehyde (MDA) and superoxide dismutase (SOD) kits were supplied by Nanjing Jiancheng Bioengineering Institute, Nanjing, China. Glutathione (GSH) and hydroxyl radical (·OH) kits were supplied by Nanjing KeyGen Biotech. Co., Ltd., Nanjing, China. The instruments used in this study included a high-speed refrigerated centrifuge (AVANTI J-30I, Beckman Coulter, Brea, CA), microplate reader (BioTek, Winooski, VT), 96 well polystyrene microtiter plates, fluorescence microscope (DM4000B, Lecia, Solms, Germany), light incubator (LRH-250-GII, Yiheng Instruments Co., Lit., Shanghai, China), ultrasonic homogenizer for cell disruption (UP200S, Hielscher Ultrasonics, Teltow, Germany), and light oscillation incubator (HZQF, Nanjing Ascent Technology Development Co., Ltd., Nanjing, China).
1) Inoculation and cultivation of C. vulgaris Under sterile conditions, C. vulgaris was inoculated into SE medium and cultured for a week. The incubation was continued under a 12:12 h light-dark cycle with an illumination intensity of 3000 lx at 25 ± 1˚C until the logarithmic growth phase reached. The C. vulgaris test solution was prepared using an established method [14-16]. The initial density of C. vulgaris was adjusted to OD540 = 0.1 - 0.2, then cultured in a light incubator with shaking three times a day at regular intervals until the optical density of C. vulgaris reached OD540 = 1.0.
2) Treatment of C. vulgaris Appropriate amounts of nano-Fe3O4 powders (
3) Determination of photosynthetic toxicity a) Determination of the chlorophyll a content Phytoplankton biomass is an important indicator in aquatic ecosystems. As can be quickly estimated from the phytoplankton biomass, the phytoplankton chlorophyll a content is often used as an important index of phytoplankton biomass [
used to determine the chlorophyll a content. The chlorophyll a content was calculated using the ethanol extraction method [
where Chla refers to the chlorophyll a concentration (mg·m–3), Vethanol is the constant volume of the extract (mL), Vwater is the volume of filtered water (L), A665 is the absorbance of the samples in 665 nm wave, similar to A750. E665 indicates the absorbance of the samples acidified with 1 mol/L HCl in 665 nm wave, similar to E750.
b) Determination of the net photosynthetic rate The CO2 absorption rate of plants during photosynthesis can be quantitatively determined using an infrared gas analyzer. The net photosynthetic rate of plants (Pn) is usually expressed using the amount of absorbed CO2 (mg·dm–2·h–1). In the present study, flasks containing C. vulgaris were placed in a closed bell with a known volume. The CO2 levels were recorded at 0, 2, 4, 6, 8, 10 min, and the net photosynthetic rate (Pn) was calculated as follows:
where Pn is the net photosynthetic rate [CO2 absorption (mg·dm–2·h–1)]; C1 is the CO2 content in the air (ppm); C2 is the CO2 content of discharged air after photosynthesis (ppm); F is the gas flow rate (L·h–1), which was fixed in this experiment and equal to the bell volume (3 L·h–1); D is the CO2 density at the experimental temperature (mg·L–1); K is the pressure correction factor, which was equal to 1; A is the leaf area (dm2), which corresponds to the area of the base of the conical flask (1 dm2) used in this experiment.
4) Determination of oxidative damage Kit instructions were followed to determine the MDA and GSH contents, SOD activity, and inhibition of ·OH generation.
The data were analyzed by one-way analysis of variance using SPSS 13.0 (IBM, Endicott, NY), and the LSD test package. Statistical significance was evaluated using significance levels of 0.01 and 0.05.
equals the initial concentration of CO2 minus the final concentration of CO2. Compared with the control, in all exposure groups, the CO2 absorption decreased as the nano-Fe3O4 concentration increased over the 10 min that samples were analyzed.
Nanomaterials are new type of pollutant, and they can affect organisms at all levels in aquatic ecosystems. Many
studies have investigated the toxicity of nanomaterials on mammals, fish and other higher forms of life [19-21]. Toxicity of nano-Fe3O4 and photosynthetic effects of nanomaterials have also been reported [
As primary producers in aquatic ecosystems, algae can utilize solar energy for photosynthesis. Chloroplasts in the algae use the solar energy to covert CO2 and water into glucose while generating oxygen.
This process is crucial for the survival of almost all organisms in aquatic ecosystems. If the photosynthetic balance is upset, both the oxygen supply and nutrient balance of carbon in aquatic ecosystems are directly affected. Therefore, photosynthesis is essential to the stability of the entire aquatic environment.
Chlorophyll is an important participant in the photosynthetic reaction. The main chlorophyll species involved in phytoplankton photosynthesis are chlorophyll a, b and c. Chlorophyll a is present in all types of phytoplankton, and its concentration is related to the level of photosynthesis and is an important indicator of phytoplankton biomass. The amount of chlorophyll a is routinely determined in biological monitoring of lakes, reservoirs, and other water bodies.
In this study, the chlorophyll a content was observed to decrease as the nano-Fe3O4 concentration increased. However, among exposure groups with nano-Fe3O4 concentrations > 100 mg·L–1 the changes were relatively flat. These results show when the concentrations are higher than a certain level (100 mg·L–1), nano-Fe3O4 has a significant toxic effect on the chlorophyll a content in C. vulgaris. And as the concentration (200 mg·L–1) increase, the toxicity change is relatively flat.
CO2 is a raw material in photosynthesis, and its concentration and amount absorbed directly affect the efficiency of photosynthesis. The net photosynthetic rate (Pn) is an important index in plant photosynthesis research, and is usually expressed as the amount of CO2 absorbed by the plant during photosynthesis per unit area and unit time (mg·dm–2·h–1). In this study, as the nano-Fe3O4 concentration increased, both the amount of CO2 absorbed over a certain period and the net photosynthetic rate decreased in C. vulgaris. These results illustrate that nanoFe3O4 has a significant toxic effect on CO2 absorption and the net photosynthetic rate. These results agree with the chlorophyll a results on the toxic effect of nanoFe3O4 in C. vulgaris.
It was noted that when the nano-Fe3O4 concentration was only 50 mg·L–1, the photosynthetic toxicity of nanoFe3O4 in C. vulgaris was not significant. Therefore, we propose that 50 mg·L–1 is a safe concentration for nanoFe3O4 to avoid photosynthetic toxicity.
One of the commonly accepted mechanisms of nanomaterial toxicity is through induced reactive oxygen species (ROS) generation [
Oxidative stress can be quantitatively evaluated using three types of markers. The first category includes ROS such as superoxide anions (O2–), ·OH, and hydrogen peroxide (H2O2). In our study, ·OH was selected as a marker for quantitative evaluation of oxidative stress. The Fenton reaction produces ·OH from H2O2, and the amount of H2O2 used in the reaction is proportional to the amount of ·OH produced. The second category includes lipid peroxidation products such as ketones and other carbonyl compounds, hydroxyl compounds, and malondialdehyde (MDA). MDA is an important marker of lipid peroxidation and cellular oxidative damage. Lipid peroxidation turns ROS into the active chemical agents by non-free radical decomposition products of lipids, and amplifies the role of ROS by chain or branched chain reactions. ROS induces cell damage by peroxidation of polyunsaturated fatty acids in the biomembrane, and through the decomposition products of lipid hydroperoxide. Determination of the MDA content can reflect the extent of lipid peroxidation and indirectly reflect the degree of cell damage. The third category includes enzymes that are active in the ROS elimination system and non-enzymatic and enzymatic antioxidants. Non-enzymatic antioxidants include vitamin C, vitamin E, and glutathione (GSH). GSH is a low molecular weight scavenger for species such as the O2– and H2O2. GSH is a major non-protein thiol and a substrate for erythrocyte glutathione peroxidase and glutathione Stransferase, indispensable for their decomposition of hydrogen peroxide. GSH can also stabilize thiol-containing enzymes. Therefore, it is important to determine the GSH content when evaluating the antioxidant capacity. Superoxide dismutases (SODs) are important enzymatic antioxidants that catalyze the reaction of superoxide with hydrogen ions to generate H2O2 and O2. SODs scavenge superoxide anion radicals to prevent cell damage, and play a vital role in the balance between oxidation and antioxidation. Under normal conditions, antioxidants will eliminate excess oxygen free radicals and achieve a dynamic balance. However, under external stress, the level of oxygen free radicals in the cell will increase, which will in turn increase enzyme activity in the antioxidation system to effectively remove the excess harmful substances. Once the oxygen free radical content exceeds a certain level, the free radicals are not efficiently removed by the antioxidation system, and excess free radicals accumulate and decrease the enzyme activity in antioxidation [
The MDA content in C. vulgaris gradually increased as the nano-Fe3O4 concentration increased, and the MDA content was significantly different to that in the control group with >400 mg·L–1 nano-Fe3O4. These results indicate that nano-Fe3O4 stress increases the MDA content in C. vulgaris, exacerbates lipid peroxidation of C. vulgaris, and leads to membrane damage in the algal cells.
The GSH content in C. vulgaris decreased as the nano-Fe3O4 concentration increased, and GSH content was significantly different to that in the control group with >200 mg·L–1 nano-Fe3O4. In the low concentration of nano-Fe3O4 stress, small increases in GSH content were observed, which may be an adaptative response of C. vulgaris to the stress. By increasing formation of GSH, C. vulgaris enhances its resistance to ROS damage by increasing the efficiency of ROS scavenging. By contrast, the GSH content decreased in the high concentration of nano-Fe3O4 stress, which may be attributed to the consumption of a large amount of the GSH in a variety of detoxification processes. In the high concentration of nano-Fe3O4 stress, destruction of antioxidation structures and a decrease in the level of antioxidants probably occurs, which results in rapid accumulation of ROS.
As the nano-Fe3O4 concentration increased, the SOD activity change in a unimodal manner. When the nanoFe3O4 concentrations were <400 mg·L–1, the SOD activity significantly increased. This shows that at low nanoFe3O4 concentrations, production of SOD is induced in C. vulgaris to remove excess ROS and protect the organism. When the nano-Fe3O4 concentrations were >400 mg·L–1, the SOD activity decreased gradually. This indicates that at high nano-Fe3O4 concentrations, the C. vulgaris cell structure is destroyed because the self-protection systems of the organism cannot function at this level.
The curve for the change in inhibition of ·OH generation as the nano-Fe3O4 concentration increased was also unimodal. When the nano-Fe3O4 concentrations were <200 mg·L–1, the inhibition of ·OH generation slightly increased. This indicated that under stress of low concentrations of nano-Fe3O4, the self-scavenging capacity of C. vulgaris for ·OH improves to protect the organism. The changes in the inhibition of ·OH generation at nanoFe3O4 concentrations > 200 mg·L–1 were significant, which suggested that significant oxidative damage occured. This concentration (200 mg·L–1) can be taken as safe concentration to avoid oxidative damage of ·OH generation induced by nano-Fe3O4.
This is the first study to investigate the ecotoxicity of nano-Fe3O4 in a model organism, C. vulgaris. NanoFe3O4 was found to have a significantly effect on the contents of chlorophyll a, MDA and GSH, amount of CO2 absorbed, net photosynthetic rate, SOD activity and inhibition of ·OH generation in C. vulgaris. At higher concentrations, compared with the control group, the toxicity of nano-Fe3O4 was significantly different.
To date, most studies have focused on the toxicological effects of nanomaterials on fish, but studies on other aquatic organisms such as phytoplankton have been limited, and there have been no studies on the photosynthetic toxicity effects of nanomaterials. As primary producers in the aquatic environment, algae provide energy for the entire aquatic ecosystem. Adverse effects of nanomaterials on algal photosynthesis could directly damage the ecological balance in aquatic environments and negatively impact the entire ecosystem.
Because of rapid development in the nanotechnology industry, the use of nano-Fe3O4 has gradually become more common in catalysis, biomedicine, and microwave absorbing materials. However, there is a lack of data on the toxicological effects of nano-Fe3O4. A preliminary investigation of these effects was conducted in the present study, and it can be concluded that the ecotoxicity and environmental effects of nanomaterials cannot be ignored. Further studies of nanomaterial pollution are required to determine the pathway and extent of pollution, to systematically determine the ecotoxicity of nanomaterials, and to establish guidelines for evaluation of the ecological safety of nanomaterials. This will help reduce the environmental and health risks associated with widespread use of nanomaterials, and ultimately allow scientific and effective management of nanomaterial use. This will ensure that the development of nanotechnology can meet actual needs without undermining the principles of sustainable development.
This work was supported by the grants of the Chinese National Natural Science Foundation (21103059), the Chinese National Program for High Technology Research and Development (863 program) (2006AA03Z330) and Key Project of Chinese National Program for Fundamental Research and Development (973 program) (2010CB 933904).