Fate Of Nanoparticles Research Articles

Nanoparticle delivery in vivo: A fresh look from intravital imaging.

Nanomedicine has proven promising in preclinical studies. However, only few formulations have been successfully translated to clinical use. A thorough understanding of how nanoparticles interact with cells in vivo is essential to accelerate the clinical translation of nanomedicine. Intravital imaging is a crucial tool to reveal the mechanisms of nanoparticle transport in vivo, allowing for the development of new strategies for nanomaterial design. Here, we first review the most recent progress in using intravital imaging to answer fundamental questions about nanoparticle delivery in vivo. We then elaborate on how nanoparticles interact with different cell types and how such interactions determine the fate of nanoparticles in vivo. Lastly, we discuss ways in which the use of intravital imaging can be expanded in the future to facilitate the clinical translation of nanomedicine.

Comprehensive study of stability of copper oxide nanoparticles in complex biological media

In response to the rapid development of nanomaterials in the biomedical field, especially in advanced cancer therapy, more comprehensive studies regarding the safety of nanomaterials are continuously required. Currently, several fundamental studies concerning the fate of nanoparticles in the biological media are needed, especially before in vivo studies. Inspired by these approaches, and the wide variation on result in the literature regarding copper (I) oxide nanoparticles (Cu2O NPs), in this article we modified sulfobetaine-stabilzed Cu2O NPs with glutathione (GSH) and hyaluronic acid (HA) tumor targeting ligands to investigate the effects of nanoparticles design on their stability in four different biological fluids: simulated saliva, human blood plasma, gastric and intestinal fluids. In addition, we examined the kinetics of copper ions release under physiological conditions, and according to mathematical models, we proposed the most probable mechanism of mass transport. The GSH- and HA-modified, as well as unmodified sulfobetaine-stabilized Cu2O NPs suspended in all tested biological fluids, formed agglomerates with sizes varying from 150 to 700 nm. The highest copper ions content was observed for Cu2O NPs in simulated gastric fluid. The formation of aggregates and copper ions release in contact with biological fluids influenced the Cu2O NPs cytotoxicity. The results indicated that cancer cells were more susceptible to HA-modified copper oxide NPs action.

Simultaneous screening of the stability and dosimetry of nanoparticles dispersions for in vitro toxicological studies with static multiple light scattering technique

To evaluate the nanoparticle (NP) toxicity, much efforts have been devoted for developing methods to accurately disperse NPs into aqueous suspensions prior to in vitro toxicological studies. As NP toxicity is strongly dependent on their physicochemical properties, NP characterization is a key step for any in vitro toxicological study. This study demonstrates that the static multiple light scattering (SMLS) technique allows for the simultaneous screening of the NP size, agglomeration state, stability and dosimetry in biological media. Batch dispersions of TiO2 P25 NPs in water with various bovine serum albumin (BSA) mass fractions (from 0% to 0.5%) and dilutions of these dispersions into cell culture media were characterized with SMLS. In the batch dispersions, TiO2 NPs are stable and well dispersed for BSA mass fraction lower than 0.2% while agglomeration and rapid settling is observed for higher BSA mass fractions. Paradoxically, when diluted in cell culture media, TiO2 NPs are well dispersed and stable for BSA mass fractions higher than 0.2%. The TiO2 NP dosimetry of these dilutions was evaluated experimentally with SMLS and confronted with numerical approaches. The TiO2 NP bottom concentration evolves far more slowly in the case of the higher BSA mass fraction. Such measurements give valuable insights on the NP fate and transport in biological media to obtain in fine reliable size and dose-cytotoxicity responses.

Elucidating the fate of nanoparticles among key cell components of the tumor microenvironment for promoting cancer nanotechnology

Successful integration of nanotechnology into the current paradigm of cancer therapy requires proper understanding of the interface between nanoparticles (NPs) and cancer cells, as well as other key components within the tumor microenvironment (TME), such as normal fibroblasts (FBs) and cancer-associated FBs (CAFs). So far, much focus has been on cancer cells, but FBs and CAFs also play a critical role: FBs suppress the tumor growth while CAFs promote it. It is not yet known how NPs interact with FBs and CAFs compared to cancer cells. Hence, our goal was to elucidate the extent of NP uptake, retention, and toxicity in cancer cells, FBs, and CAFs to further understand the fate of NPs in a real tumor-like environment. The outcome of this would guide designing of NP-based delivery systems to fully exploit the TME for a better therapeutic outcome. We used gold nanoparticles as our model NP system due to their numerous applications in cancer therapy, including radiotherapy and chemotherapy. A cervical cancer cell line, HeLa, and a triple-negative breast cancer cell line, MDA-MB-231 were chosen as cancer cell lines. For this study, a clinically feasible 0.2 nM concentration of GNPs was employed. According to our results, the cancer cells and CAFs had over 25- and 10-fold higher NP uptake per unit cell volume compared to FBs, respectively. Further, the cancer cells and CAFs had over 30% higher NP retention compared to FBs. There was no observed significant toxicity due to GNPs in all the cell lines studied. Higher uptake and retention of NPs in cancer cells and CAFs vs FBs is very important in promoting NP-based applications in cancer therapy. Our results show potential in modulating uptake and retention of GNPs among key components of TME, in an effort to develop NP-based strategies to suppress the tumor growth. An ideal NP-based platform would eradicate tumor cells, protect FBs, and deactivate CAFs. Therefore, this study lays a road map to exploit the TME for the advancement of “smart” nanomedicines that would constitute the next generation of cancer therapeutics.

Uptake, translocation, and physiological effects of hematite (α-Fe2O3) nanoparticles in barley (Hordeum vulgare L.)

There has been a growing concern with the environmental influences of nanomaterials due to recent developments in nanotechnology. This study investigates the impact and fate of hematite nanoparticles (α-Fe2O3 NPs) (∼14 nm in size) on a crop species, barley (Hordeum vulgare L.). For this purpose, hematite NPs (50, 100, 200, and 400 mg/L) were hydroponically applied to barley at germination and seedling stages (three weeks). Inductively coupled plasma mass spectrophotometry (ICP-MS) along with vibrating sample magnetometer (VSM) techniques were used to track the NPs in plant tissues. The effects of NPs on the root cells were observed by scanning electron microscopy (SEM) and confocal microscopy. Results revealed that α-Fe2O3 NPs significantly reduced the germination rate (from 80% in control to 30% in 400 mg/L), as well as chlorophyll (36–39%) and carotenoid (37%) contents. Moreover, the treatment led to a significant decline in the quantum yield of photosystem II (Fv/Fm). Leaf VSM analysis indicated a change in magnetic signal for NPs-treated samples compared with untreated ones, which is mostly attributed to the iron (Fe) ions incorporated within the leaf tissue. Besides, Fe content in the roots and leaf had gradually increased by the increasing doses of NPs, which was confirming NPs’ translocation to the aerial parts. Microscopic observations revealed that α-Fe2O3 NPs altered root cell morphology and led to the injury of cell membranes. This study, in the light of our findings, shows that α-Fe2O3 NPs (∼14 nm in size) are taken up by the roots of the barley plants, and migrate to the plant leaves. Besides, NPs are phytotoxic for barley as they inhibit germination and pigment biosynthesis. This inhibition is probably due to the injury of the cell membranes in the roots. Therefore, the use of hematite NPs in agriculture and thereby their environmental diffusion must be addressed carefully.

Subcellular Imaging of Localization and Transformation of Silver Nanoparticles in the Oyster Larvae.

To accurately assess the behavior and toxicity of silver nanoparticles (AgNPs), it is essential to understand their subcellular distribution and biotransformation. We combined both nanoscale secondary ion mass spectrometry (NanoSIMS) and electron microscopy to investigate the subcellular localization of Ag and in situ chemical distribution in the oyster larvae Crassostrea angulata after exposure to isotopically enriched 109AgNPs. Oyster larvae directly ingested particulate Ag, and in vivo dissolution of AgNPs occurred. The results collectively showed that AgNPs were much less bioavailable than Ag+, and the intracellular Ag was mainly originated from the soluble Ag, especially those dissolved from the ingested AgNPs. AgNPs absorbed on the cell membranes continued to release Ag ions, forming inorganic Ag-S complexes extracellularly, while Ag-organosulfur complexes were predominantly formed intracellularly. The internalized Ag could bind to the sulfur-rich molecules (S-donors) in the cytosol and/or be sequestered in the lysosomes of velum, esophagus, and stomach cells, as well as in the digestive vacuoles of digestive cells, which could act as a detoxification pathway for the oyster larvae. Ag was also occasionally incorporated into the phosphate granules, rough endoplasmic reticulum, and mitochondria. Our work provided definite evidence for the partial sulfidation of AgNPs after interaction with oyster larvae and shed new light on the bioavailability and fate of nanoparticles in marine environment.

Tracing the In Vivo Fate of Nanoparticles with a “Non-Self” Biological Identity

Nanoparticles can acquire a biomolecular corona with a species-specific biological identity. However, "non-self" incompatibility of recipient biological systems is often not considered, for example, when rodents are used as a model organism for preclinical studies of biomolecule-inspired nanomedicines. Using zebrafish embryos as an emerging model for nanobioimaging, here we unravel the in vivo fate of intravenously injected 70 nm SiO2 nanoparticles with a protein corona preformed from fetal bovine serum (FBS), representing a non-self biological identity. Strikingly rapid sequestration and endolysosomal acidification of nanoparticles with the preformed FBS corona were observed in scavenger endothelial cells within minutes after injection. This led to loss of blood vessel integrity and to inflammatory activation of macrophages over the course of several hours. As unmodified nanoparticles or the equivalent dose of FBS proteins alone failed to induce the observed pathophysiology, this signifies how the corona enriched with a differential repertoire of proteins can determine the fate of the nanoparticles in vivo. Our findings thus reveal the adverse outcome triggered by incompatible protein coronas and indicate a potential pitfall in the use of mismatched species combinations during nanomedicine development.

Role of Physicochemical Properties of Protein in Modulating the Nanoparticle-Bio Interface.

Nanoparticles, on exposure to the biological milieu, tend to interact with macromolecules to form a biomolecular corona. The biomolecular corona confers a unique biological identity to nanoparticles, and its protein composition plays a deterministic role in the biological fate of nanoparticles. The physiological behavior of proteins stems from their physicochemical properties, including surface charge, hydrophobicity, and structural stability. However, there is insufficient understanding about the role of physicochemical properties of proteins in biomolecular corona formation. We hypothesized that the physicochemical properties of proteins would influence their interaction with nanoparticles and have a deterministic effect on nanoparticle-cell interactions. To test our hypothesis, we used model proteins from different structural classes to understand the effect of secondary structure elements of proteins on the nanoparticle-protein interface. Further, we modified the surface of proteins to study the role of protein surface characteristics in governing the nanoparticle-protein interface. For this study, we used mesoporous silica nanoparticles as a model nanoparticle system. We observed that the surface charge of proteins governs the nature of the primary interaction and the extent of subsequent secondary interactions causing structural rearrangements of the protein. We also observed that the secondary structural contents of proteins significantly affected both the extent of secondary interactions at the nanoparticle-protein interface and the dispersion state of the nanoparticle-protein complex. Further, we studied the interactions of different protein-coated nanoparticles with different cells (fibroblast, carcinoma, and macrophage). We observed that different cells internalized the nanoparticle-protein complex as a function of secondary structural components of the protein. The type of model protein had a significant effect on their internalization by macrophages. Overall, we observed that the physicochemical characteristics of proteins had a significant role in modulating the nanoparticle-bio-interface at the level of both biomolecular corona formation and nanoparticle internalization by cells.

To-Do and Not-To-Do in Model Studies of the Uptake, Fate and Metabolism of Metal-Containing Nanoparticles in Plants.

Due to the increasing release of metal-containing nanoparticles into the environment, the investigation of their interactions with plants has become a hot topic for many research fields. However, the obtention of reliable data requires a careful design of experimental model studies. The behavior of nanoparticles has to be comprehensively investigated; their stability in growth media, bioaccumulation and characterization of their physicochemical forms taken-up by plants, identification of the species created following their dissolution/oxidation, and finally, their localization within plant tissues. On the basis of their strong expertise, the authors present guidelines for studies of interactions between metal-containing nanoparticles and plants.

Thermal analysis of a nanofluid free jet impingement on a rotating disk using volume of fluid in combination with discrete modelling

The objective of this research is to analyse the heat transfer characteristics of air/nanofluid jet cooling flow on a hot circular rotating disk and track the possible fate of nanoparticles. Computational methods are employed to initially solve the air and liquid multiphase flow in ANSYS Fluent 19.3 by considering the importance of surface tension between two phases through the volume of fluid model. Subsequently, the nanoparticles are injected through the nozzle into the jet liquid to calculate nanoparticles distribution via pre-defined user functions. The impacts of parameters such as nanoparticles volume fraction and disk rotation are evaluated. The patterns of the jet flow from inlet until steady-state condition shows that there exist six stages of fluid flow for a stationary hot disk, while splattering of droplets disappears when the disk starts rotating. In spite of the positive impact of nanoparticles for rotating disk, larger torque is required for higher nanofluid volume fraction to enhance heat transfer due to increase in viscosity. Also, the trend for heat transfer coefficient identifies five flow regions from the stagnation point to the edge of the rotating disk.

A REVIEW OF VARIOUS METHODS OF SYNTHESIZING NANOPARTICLES AND THEIR APPLICATIONS

There is an increasing interest and need to develop a deeper understanding of the nature, fate and behavior of nanoparticles in the environment. This is driven by the increased use of engineered nanoparticles and the increased pressure to commercialize this growing technology. Nanoparticles are different from bulk particles in terms of their physical, chemicals and biological properties. Nanoparticles in their different size acts differently. Nanotechnology in recent years has had numerous applications in different fields such as industry, biotechnology, energy and environment. This paper presents a review of recent journals on the different methods of synthesizing nanoparticles and their various applications. Metallic nanoparticles of gold, silver, manganese, zinc oxide and cadmium sulfide were synthesized using different methods which ranges from sol gel, precipitation, hydrothermal, chemical reduction to green synthesis. It was concluded that these synthesized nanoparticles have immense applications in the medical, environmental, agricultural and industrial sector.

Transport behaviour of different metal-based nanoparticles through natural sediment in the presence of humic acid and under the groundwater condition

The production of nanoparticles (NPs) has increased significantly, given that they have numerous commercial and medical applications. There might have some risk associated with the release of these NPs in the environment. To assess the possible risk of releases of NPs in the groundwater, it is important to evaluate the fate and transport behaviour of NPs through porous media. The objective of this study is, therefore, to evaluate the transport behaviour of widely used NPs [i.e., silver (Ag), iron oxide (FexOy), titanium dioxide (TiO2) and zinc oxide (ZnO)] through porous media in the presence and/or absence of organic matter [i.e., humic acid (HA)] under controlled de-ionized and natural groundwater condition. To achieve the objective, first, the detailed characterizations of NPs are carried out in the presence and absence of HA. Column transport experiments were performed using a 1-D sand-packed column. Different NPs were injected from one end of the column with a flow rate of 0.0054 cm/sec. The result suggests that nAg, nTiO2, and nZnO particles are colloidal stable in the suspension, while nFexOy particles tend to aggregate and settle down very rapidly. However, in the presence of HA, the colloidal stability of nFexOy in the suspension increases significantly. Evaluation of transport behaviour of different metal NPs suggests that a high amount of nFexOy (C/C0=0.01) and nZnO (C/C0=0.09) particles are retained in the porous media. However, in the presence of HA, the transport efficiency of nFexOy (C/C0=0.64) increases significantly. The extensively high amount of nAg and nTiO2 particles are transported in the absence/presence of HA. The surface charge of particles and thus the interaction energy between the NPs and the sand is the main factor controlling the deposition of NPs. Overall, it could be stated that there is a risk of migration of nAg and nTiO2 particles irrespective of the presence of organic matter or of nFexOy particles in the presence of organic matter through the aquifer porous media. However, in the natural groundwater system, when the different ion is present, the extent of transport of NPs is expected to be less, and the risk associated with releasing of NPs in the groundwater would be comparatively low than that is predicted under the controlled de-ionized water condition. However, the nTiO2 particles always have a high risk of release into the groundwater.

Agronomic providences of surface functionalized CuO nanoparticles on Vigna radiata

In recent years, the unique physiochemical properties and non-toxicity of these CuO NPs open up new pathways in crop science. However, the detailed responses of CuO NPs on physiological and molecular factors responsible for conquering plant stress are mainly unexplored. The current work highlighted the agronomic fate of CuO NPs as a nano-nutrient for enhancing the stress tolerance in Vigna radiata during seedling emergence and germination. The economically feasible microwave assisted methodology was chosen to fabricate CuO NPs with average size ranges between 10−12 nm. A variety of laboratory experiments have shown that the root (37 %) and shoot (13 %) growth was appreciably improved in presence of 50 mg/l of CuO NPs at 15 °C. The presence of CuO has the ability to maximize the germination index at 35/25 °C and minimum was at 45 °C/35 °C. The variation of 12 h light and dark exposure was sufficient to enhance the germination rate. The stress marker level was reduced to 20.4 % for dark, 17.4 % for light and 29.6 % for light/dark (12/12 h) exposure in presence of 50 mg/l of CuO@DOP NPs. The enzymatic antioxidant was significantly affected at higher concentration of CuO@DOP NPs with 15 °C and 45 °C and minima was observed at 35 °C. However, lower concentration of CuO NPs (50 mg/l) has enhanced antioxidant enzyme activity and diminishes the stress markers level respectively. The outcomes of the current work deduce the secure and sustainable impact of nanoparticles in farming. The agronomic fate of nanoparticles has brought a bright future to enhance the crop productivity and brings revolutionary changes in the agriculture sector.

Investigation of the Fate of Silver and Titanium Dioxide Nanoparticles in Model Wastewater Effluents via Selected Area Electron Diffraction.

The increasing use of manufactured nanomaterials (MNMs) and their inevitable release into the environment, especially via wastewater treatment plants (WWTPs), poses a potential threat for aquatic organisms. The characterization of MNMs with analytical tools to comprehend their fate and effect on the ecosystem is hence of great importance for environmental risk assessment. We herein report, for the first time, the investigation of physicochemical transformation processes during artificial wastewater treatment of silver (Ag-NPs) and titanium dioxide nanoparticles (TiO2-NPs) via selected area electron diffraction (SAED). TiO2-NPs with an anatase/rutile ratio of ∼80/20 were found to not undergo any physicochemical transformation, as shown via previous energy-dispersive X-ray analysis (EDX) elemental mapping and crystal structure analysis via SAED. In contrast, Ag-NPs were colocalized with substantial amounts of sulfur (Ag/S ratio of 1.9), indicating the formation of Ag2S. SAED ultimately proved the complete transformation of face-centered cubic (fcc) Ag-NPs into monoclinic Ag2S-NPs. The size distribution of both nanomaterials remained virtually unchanged. Our investigations show that cloud point extraction of NPs and their subsequent crystal structure analysis via SAED is another valuable approach toward the comprehensive investigation of wastewater-borne MNMs. However, the extraction procedure needs optimization for environmentally low NP concentrations.

Controlling evolution of protein corona: a prosperous approach to improve chitosan-based nanoparticle biodistribution and half-life

Protein corona significantly affects in vivo fate of nanoparticles including biodistribution and half-life. Without manipulating the physicochemical properties of nanoparticles with considering their biointerference, attaining effective treatment protocols is impossible. For this reason, protein corona evolution and biodistribution of different chitosan (Ch)-based nanoparticles including Ch and carboxymethyl dextran (CMD)/thiolated dextran (TD) polyelectrolyte complexes (PECs) were studied using highly precious and sensitive methods such as liquid chromatography-mass/mass (LC-MS/MS) spectroscopy and positron emission tomography/computed tomography (PET/CT) scan. The importance of serum presence/absence in culture medium with different pH and corona effect on cellular uptake of PECs investigated by in vitro study. Designed PECs have low amounts of proteins in corona mostly enriched by Apolipoproteins, protein C, hemoglobin subunits, and inter-alpha- trypsin inhibitor that beside improving uptake of nanoparticles, they have low liver uptake and notable heart blood pool accumulation that confirmed the long circulation time of the nanoparticles which is favorable for delivery of nanoparticles to the site of action and achieving required therapeutic effect.

Tradeoff between risks through ingestion of nanoparticle contaminated water or fish: Human health perspective

This study proposed a framework (termed as “nanoHealthRisk” hereafter) for incorporating i) interaction of nanoparticles (NPs) with fishes, ii) availability of NPs to the human digestive system, and iii) estimation of health risk due to fish consumption and inadvertent ingestion of NP-contaminated surface water, for the first time as per the literature review. The framework was applied for estimating health risks due to hypothetical exposures of pristine ZnO, CuO, and TiO2 NPs (without any surface functionalization) from fish tissues. Values of bio- concentration factors (BCF) of ZnO, CuO, and TiO2 NPs in fish and model distributions of bio-assimilation factor of ZnO, CuO and TiO2 NPs in the human digestive system were incorporated explicitly in the risk assessment of NPs for the first time. ZnO NP was observed to be transferred more to the human digestive system from aqueous matrix than the other two NPs. Maximum allowable values of NP posing no risk were found to be 0.115 mg/L, 0.152 mg/L, and 1.77 × 107 mg/L for pristine ZnO, CuO and TiO2 NP, respectively. At the environmental concentration range, exposures of studied NPs from aquatic environment under the assumptions used did not pose any health risk under the conditions studied in this study. More work is required to (1) Estimate bio-concentration factors of a mixture of NPs with other constituents in fish tissues, (2) Estimate dissolution of NP from fish tissue in human digestive media, (3) Generate new data to develop reference dose of NP for human health risk assessment, and (4) Study effect of NP fate in the water on health risk through fish consumption pathway. Until all above-mentioned aspects are not explicitly incorporated in the risk assessment framework, risk estimates do not represent the risk from environment completely. Thus, continuous monitoring of these NPs in the environment is required to protect health due to chronic exposure of small concentrations of NPs from an aqueous matrix.

Responses of freshwater biofilm formation processes (from colonization to maturity) to anatase and rutile TiO2 nanoparticles: Effects of nanoparticles aging and transformation

Most of the current studies on the toxicology of pristine nanoparticles (NPs) are environmentally irrelevant, because their ‘‘aging’’ process accompanied by the physicochemical transformation is inevitable in the environment. Considering aging phenomenon will gain a better understanding of the toxicity and fate of NPs in the environment. Here, we focused on the physicochemical transformation of anatase-NPs (TiO2-A) and rutile-NPs (TiO2-R) after 90 days of aging and investigated the responses of freshwater biofilm formation to the stress changes of naturally aged TiO2-NPs (aTiO2-NPs). We found that after aging, the TiO2-NPs underwent sophisticated physicochemical transformations in the original morphology and microstructure owing to organic and crystal salts inclusions, such as energy band changes and the formation of Ti3+ on the NPs surfaces. These comprehensive transformations increased the stability of NPs in the exposed suspension. However, the physicochemical transformations were crystal-forms-dependent, and aging did not change the crystal structure and crystallinity. Interestingly, compared to pristine NPs, aTiO2-NPs showed much lower cytotoxicity and had the weaker ability to promote or inhibit the biofilm formation (p < 0.05) owing to the passivation of photoactivity caused by the comprehensive effect of the inclusions, especially for aTiO2-A. Regardless of aging or not of crystal forms, responses of biofilm formation were exposure-concentration-dependent, namely low concentration promotion (0.1 mg/L) and high concentration inhibition (10 mg/L), e.g., role transition of the pioneers (algae or bacteria) in initial colonization, extracellular polymeric substances (EPS) secretion and compositions of development stages with polysaccharide (PS)-rich and protein (PRO)-rich stages, and biomass and cell activity at different depths of mature biofilms. The reactive oxygen species (ROS) induced by TiO2-NPs showed typical hormesis. The changing trends of the autoinducers (c-di-GMP and quorum sensing signals including AHL and AI-2) were highly consistent with the growth stages of biofilms and were stimulated or suppressed by TiO2-NPs. The NPs crystal-dependently changed the microorganism community structures, while the UPGMA clustering of bacteria was based on the growth stages of the biofilms. The toxic mechanisms revealed that photoactivity and nanoscale retention of particles are the main reasons for the differences in the ecological stress capacity of four kinds of TiO2-NPs. Aging reduced characteristic differences of two pristine NPs and even reversed their relative stresses levels (p > 0.05). However, the toxicity of high-concentration aTiO2-NPs (10 mg/L) remained serious in a water environment. This study provides a better understanding for the water environmental risks evaluation and policy control of nanoparticles, that is, the effect of time aging has to be considered.

Fate of Fe3O4@NH2 in soil and their fixation effect to reduce lead translocation in two rice cultivars.

The fate of nanoparticles in the ecological chain of agriculture has been concerned as their potential pollution and biological effect to humans with rapid development and massive emission of nanomaterials. Here, we found that two rice cultivars (Oryza sativa L) have different heavy metal accumulation results in the roots and shoots after 15 days growth. Two rice cultivars (Oryza sativa L), grown in soil containing magnetite (Fe3O4@NH2) nanoparticles and heavy metal simultaneous, showed less Pb uptake in the roots and shoots, compared with that without Fe3O4@NH2 added. The shape and magnetic properties of Fe3O4@NH2 have no obvious change; however, the transmission electron microscope (TEM) results showed the shell of Fe3O4@NH2 could be broken in the process of interaction with soil. These results suggested that magnetite nanoparticles, such as Fe3O4@NH2, could potentially be used as the recyclable heavy metal fixation materials for alleviating heavy metal poisoning to plant.

In vivo phytotoxicity, uptake, and translocation of PbS nanoparticles in maize (Zea mays L.) plants

PbS nanomaterials are of great concern because of their potential toxicity and unavoidable releases of multiple commercial applications of nanoparticles (NPs). Commercial NPs act as mediators of damage to plant cells and pose potential toxicity to plants and human health. The mechanisms involved in the toxicity, uptake, and biotranslocation of PbS NPs in plants are poorly understood. We synthesize 15 ± 6 nm PbS nanoparticles (NPs) and report the phytotoxicology, uptake, and translocation of PbS NPs in maize (Zea mays L.) plants under various hydroponic treatments (5 mg/L, 10 mg/L, 20 mg/L, 30 mg/L, 40 mg/L, 50 mg/L of PbS NPs, 1.5 mg/L Pb2+ ion and controls) for 15 days. The findings indicate that PbS NPs has phytotoxic effects on seeds germination and similar effects in root elongation. The PbS NPs significantly inhibites the biomass of shoots and roots, as well as root morphology compared with the controls. The PbS NPs can penetrate the epidermis of maize roots and bioaccumulate in shoots at higher concentrations than controls treated with Pb2+ ions. The observations are consistent with indices of biotranslocation factor and confirmed by STEM-EDS mapping. The results illustrate PbS NPs can enter the cell wall and exist in intercellular space and cytoplasm of the cortical cell of maize seedlings by apoplastic and symplastic pathways. This study highlights the importance of the uptake, phytotoxicity, and biotranslocation of PbS NPs in maize crops and demonstrates the possible transfer into human food as an outcome of the fate of PbS NPs in plants.

The Influence of Nanoparticle Shape on Protein Corona Formation.

Nanoparticles have become an important utility in many areas of medical treatment such as targeted drug and treatment delivery as well as imaging and diagnostics. These advances require a complete understanding of nanoparticles' fate once placed in the body. Upon exposure to blood, proteins adsorb onto the nanoparticles surface and form a protein corona, which determines the particles' biological fate. This study reports on the protein corona formation from blood serum and plasma on spherical and rod-shaped nanoparticles. These two types of mesoporous silica nanoparticles have identical chemistry, porosity, surface potential, and size in the y-dimension, one being a sphere and the other a rod shape. The results show a significantly larger amount of protein attaching from both plasma and serum on the rod-like particles compared to the spheres. Interrogation of the protein corona by liquid chromatography-mass spectrometry reveals shape-dependent differences in the adsorption of immunoglobulins and albumin proteins from both plasma and serum. This study points to the need for taking nanoparticle shape into consideration because it can have a significant impact on the fate and therapeutic potential of nanoparticles when placed in the body.