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Accumulating studies in animals have shown that nanoparticles could cause unusual rapid lung injury and extrapulmonary toxicity. Whether exposure of workers to nanoparticles may result in some unexpected damage as seen in animals is still a big concern. We previously reported findings regarding a group of patients exposed to nanoparticles and presenting with an unusual disease. The reported disease was characterized by bilateral chest fluid, pulmonary fibrosis, pleural granuloma, and multiorgan damage and was highly associated with the nanoparticle exposure. To strengthen this association, further information on exposure and the disease was collected and discussed. Our studies show that some kinds of nanomaterials, such as silica nanoparticles and nanosilicates, may be very toxic and even fatal to occupational workers exposed to them without any effective personal protective equipment. More research and collaborative efforts on nanosafety are required in order to prevent and minimize the potential hazards of nanomaterials to humans and the environment.
With the development and wide use of nanomaterials, concerns and fears have been expressed regarding potential risks of nanoparticles to worker's safety, human health, and environment contamination . Due to their unique physicochemical properties such as extremely small size, large surface area, and functional coating, nanomaterials may exhibit nonclassic bioactivity and interact with cellular or subcellular structures. And accumulating research data using animal or cultured cell models have shown nanoparticles could cause unusual rapid lung injury and extrapulmonary toxicity [2, 3]. It is possible theoretically that long-term exposure to nanoparticles may cause some unexpected damage to humans as seen in animals.
We previously reported findings regarding a group of patients, who worked at the same workplace in a print plant for 5–13 months exposing to nanoparticles . These workers presented with dyspnea on exertion pericardial and pleural effusions and rash with intense itching. The symptoms seen in these patients were similar to those seen in animals exposed to nanoparticles. In addition, considering particle size and deposition model, the damage in lungs was highly associated with the nanoparticle exposure. To strength this association, further information on exposure and disease was collected. In this paper, we will discuss these unusual diseases and their nanoexposure.
Our seven patients, 18–47 years old female workers, were all previously in good health and nonsmokers. They were found in almost the same time frame with the same symptoms of shortness of breath and the same clinical findings such as pleural effusion, progressive pulmonary fibrosis, and pleural damage. In addition, multiorgan damage was observed including disorders of haematotoxicity, cardiotoxicity, hepatotoxicity, and dermal toxicity. And a two-year follow-up revealed that two patients died of pulmonary failure and five were disabled with severe pulmonary dysfunction.
In the early disease stage [4, 5], the pathological examination showed the effusion of inflammatory cells in tunica mucosa bronchiorum, aggregations of macrophages and inflammatory cells, proteinaceous effusions in the alveolar space, swollen and widened alveolar septums with scattered neutrophil leukocytes, and pulmonary fibrosis. And pathological study of pleura exhibited fibrinous and inflammatory cells, foreign-body granulomas, and haemorrhage. In the late stage, damage to pulmonary tissue was similar to but more prominent than that in the early stage. Pulmonary alveoli were partly emphysematous with aggregations of macrophages and type II alveolar epithelial cell proliferations, and the alveolar septum was widened with blood vessel dilatation and congestion. Notably, damage to alveolar epithelial cells, macrophages, vascular endothelial cells, and the blood-gas barrier was also observed.
All the patients are characterized with pleural effusions. Some common causes of pleural effusions are lung infections, tuberculosis, pulmonary embolism, breast cancer, lung cancer, or autoimmune diseases. However, clinical examinations and long-term follow-up have eliminated the possibility of above diseases in our patients.
The coating material used in the workplace, an ivory white soft paste (polyacrylic ester stated by the paste producer), was analyzed by gas chromatography/mass spectrometry (GC/MS), and was found containing the following components : butanoic acid, butyl ester, N-butyl ether, acetic acid, toluene, di-tert-butyl peroxide, 1-butanol, acetic acid ethenyl ester, isopropyl alcohol, and ethylene dioxide. Unfortunately, these patients exhibited none of the signs and symptoms related to these irritant or asphyxiant gases, such as coughing, eye irritation, dizziness/headaches, drowsiness, nausea, or vomiting. In addition, the powder component in the raw materials used in the workplace was determined by inductively coupled plasma atomic emission spectrometry (ICP-AES) and was found containing (%): Si 0.016, Ba 0.069, Ca 0.20, Mg 0.051, Cu 0.0090, Fe 0.098, K 0.015, Na 0.82, Zn 0.0085, and P 0.048 [5, 6].
Nanoparticles found in the patients' pulmonary tissues and chest effusions were the same raw materials used by these workers. Element of silica of nanoparticles was identified in biopsies and chest fluid by using transmission electron microscopy and energy dispersive X-ray analysis. They were largely found in macrophages (cytoplasm, mitochondria, lysosomes, and nuclei), pulmonary microvascular vessels, vascular endothelial cells, microlymphatic vessels, and pleural effusions. We also observed silica nanoparticles accumulated in alveolar epithelial cells and pulmonary interstitial tissue but to a less extent [4, 5]. In addition, nanosilicates, as well as microscale silicates, were also observed in a patient pleural effusion and contained elements of Si, Ca, Mg, K, Na, Ba, Al, P, S, Cl, and O .
The concordance of the components of powder in the raw material and nanomaterials in patients' biopsies indicated that the powder in the raw material was made of silica nanoparticles and silicates, a mixture used to obtain some special coating quality, such as abrasive resistant, flame retardant, or adherent. Thus, a rough sketch can be made of the coatings used at these patients' workplace: filters and additives of silica nanoparticles and nano- and microscale silicates, a film-forming polyacrylate agent, and various solvents, including butanoic acid, butyl ester, acetic acid, and toluene.
Coatings usually have several components of binders, pigments, solvents, fillers, and additives . Fillers and additives are generally composed of natural or synthetic minerals, such as silicon dioxide, barium sulfate, silicates, or a complex mixture of the above materials, to produce special and improved functions, such as water resistance, transparency, and flame retardation [7, 8]. Due to their small size, large specific surface area, and more alkyl groups in different bonding states, silica nanoparticles in coatings can markedly improve the suspension stability, weatherability, tensile strength, and the washing, infrared, abrasion, heat, and radiation resistances of a coating and even yield the coating clear at the same time [8, 9]. However, microsilica can only increase the hardness and abrasion resistance . Similarly, Layered silicates, another very popular coating nanomaterial ingredient, play an important role as adsorbents, catalysts, and ionic exchangers in the production of nanocoatings and could greatly increase thermal stability and act as fire retardants in the form of nanocomposites .
Nanosilicates, often characterized by only one dimension in the nanometer range, are a group of very complex chemical substances in which there is a copolymerization of silicic acid with hydroxides of other metals drawn from almost the entire periodic table , while silicates isolated in our patients contain 13–15 different elements and widely varying O/Si ratios. Their structure consists of layers made up of two tetrahedrally coordinated silicon atoms fused to an edge-shared octahedral sheet of either aluminum or magnesium hydroxide. Using layered nanosilicates in nanomaterials, several structural types may be obtained, including intercalated nanocomposites in which polymer chains are sandwiched between silicate layers and exfoliated nanocomposites in which separated, individual, silicate layers are more or less uniformly dispersed in a polymer matrix. These nanocomposites exhibit markedly improved mechanical, thermal, optical, and physicochemical properties compared with pure polymers or conventional (microscale) composites .
Given the benefits of silica nanoparticles and nanosilicates, they are usually utilized concurrently in varying ratios to each other in the production of nanocomposite coatings. And this may be the very reason that amorphous silica and silicates in nanoscale were found in the raw materials that these workers exposed to.
Occupational exposures to inhaled pathogenic particles and fibers such as silica and silicate have been associated with the development of lung inflammation and occupational disease. These diseases include silicosis, interstitial fibrosis, industrial bronchitis, small airway disease, emphysema, and vascular diseases as well as immunologic reactions [12, 13]. Even though amorphous silica appears less toxic than the crystalline form, toxicological studies about amorphous silica nanoparticles have exhibited that they increase reactive oxygen species (ROS) concentrations, reduce glutathione levels, and induce pro-inflammatory, inflammatory, and oxidative stress responses both in vivo and in vitro [14, 15]. Amorphous silica nanoparticles can enter cell nuclei where reducing aberrant clusters of topoisomerase I and protein aggregates in the nucleoplasm . In vitro studies also show that amorphous silica nanoparticles disturb mitochondrial function and lower cell survival via decreasing cell survival signaling in human neural cells . Furthermore, amorphous nanosilica has been shown to accumulate in the lung, liver, kidney, gut, bone marrow, and brain in animal experiments and cause multiorgan damage .
Exposure to silica and/or silicate results in pneumoconiosis, what if exposure to silica and/or silicate in nanoscale? Given the well-documented toxicity of microscale silica in humans and findings of amorphous silica nanoparticles in animals, it is possible that these silica nanoparticles may have been contributed in part to these patients' disease and multiorgan damage, whatever they exerted toxicities directly or acted as carriers. These patients were found multiorgan damage, which may have been related to nanoparticle entry into the systematic circulation and multiorgan deposition. These silica nanoparticles in the nuclei may potentially bind to the DNA phosphate backbone, influence nuclear integrity, and trigger genotoxicity by physical-chemical interaction, forming intranuclear protein aggregates, and regulating redoxsensitive transcription factors and DNA-damage responsive signaling, as seen in animal-based nanotoxicological studies [16–18], and also, these silica nanoparticles in cytoplasm may exert cytotoxicity by increasing reactive oxygen species and by inducing proinflammatory, inflammatory, and oxidative stress responses, as seen both in vivo and in vitro [14, 15].
A hypothesis of the potential translocation pathways of nanoparticles and their potential damage was made as follows (Figure 1). When coatings were sprayed, heated, and dried in the workplace, nanosilica and nanosilicates in these coatings aired in the workplace as flocculi (condensation of the aerosol, containing nanosilica and nanosilicates from the volatilized material) and caused itching on the faces and arms of patients (dermal toxicity), while the workers used no personal protective equipment (PPE), because the nanomaterials were invisible and they knew nothing of the toxicity of the materials they were handling. When inhaled into the pulmonary respiratory tract, the nanomaterials deposited in the pulmonary alveoli were taken up by macrophages, crossed the lung epithelium, and entered the pulmonary interstitial tissue, blood, and lymph, finally reaching extrapulmonary organs of patients, as has been observed in animal experiments , and resulted in the haematotoxicity, hepatotoxicity, cardiotoxicity, and pulmonary and pleural injuries seen in these patients. The nanomaterials within pleural effusions may have come from visceral pleura through the pulmonary circulation and from partial pleura through the systemic circulation, or come from penetration through lung tissue to the pleural membrane, as small-sized nanomaterials like nanosilica can readily pass through lung tissue or behave like gases . Finally, chronic and repetitive exposure (5–13 months) to the nanomaterials may have resulted in these patients' illness and death.
In our patients, the initial and persistent symptoms were the recurring production of copious amounts of chest fluids. The likelihood of patients developing pleural effusion is a combined effect of nanosilicates and nanosilica, which can be obtained as an indication from the pleural effusions caused by silicosis or asbestosis . The occurrence of pleural effusion may have been caused not by the chemical compositions of the nanomaterials but by their nanosize. These nanomaterials are small enough to pass through the lung tissue into the pleural cavity but large enough to block proper lymphatic drainage of the pleural membrane. Furthermore, lymphatic flow under physiological conditions amounts to 3μL/min/mm2 and flow velocity in initial lymphatics is on the order of 2mm/min , which is much slower than blood flow velocity and thus prone to pleural lymphatic stomata blocking. Importantly, the draining role of parietal lymphatics in patients with asbestosis is demonstrated by the finding of the “black spots,” the accumulation of asbestos fibers around the parietal pleural lymphatic stomata due to the fibers being flow-driven towards the pleural fluid draining sites [22, 23]. Also, the presumption that pleural effusions in our patients may have been caused by nanomaterials blocking proper lymphatic drainage of the pleural cavity was confirmed by the observation of lymphangiectasis and lymphostasis in high-resolution CT scans of lungs and pathologic observation of lungs and pleural membranes.
Our findings of nanosilica in patients' biopsies and pleural effusions, together with our previous report, present a clue that these silica nanoparticles may have contributed in part to the illness reported in these workers. The reported disease was characterized by bilateral chest fluid, pulmonary fibrosis, and pleural damage and was featured by a concealed onset (a relatively long latency between initial exposure and disease emergence), rapid and progressive development, and multiorgan damage. These characteristics varied greatly from diseases such as silicosis or asbestosis which were caused by microscale silica or silicates. Thus, the disease related to nanomaterials produces new challenges and concerns in terms of how to prevent the potential risks of nanomaterial exposure to workers and the environment as nanomaterials are invisible.
In conclusion, our studies show that some kinds of nanomaterials, such as silica nanoparticles and nanosilicates, may be very toxic and even fatal to occupational workers exposed to but without any effective PPE. And the disease related to these nanomaterials produces new health and safety concerns on how to prevent the potential risks of nanomaterial exposure to workers and the environment as well as how to clinically diagnose and treat the disease or injury. More research and collaborative efforts on nanosafety, and more government funding and private investment in nanotoxicology are required in order to prevent and minimize the potential hazards of nanomaterials to humans and the environment.
The author sincerely thanks all the doctors and nurses for their hard work in the treatment of these patients. This work was supported in part by National Natural Science Foundation of China (Grant no. 81172614), Knowledge Innovation Project of Beijing Academy Science and Technology (PXM2011-178304-112365) and Beijing New Century Talents Projects (2009BJRS001).