Unclear biological fate hampers the clinical translation of nanoparticles for biomedical uses. In recent years, it is documented that the formation of protein corona upon nanoparticles is a critical factor leading to the ambiguous biological fate. Efforts have been made to explore the protein corona forming behaviors on nanoparticles, and rearrangement of the relevant studies will help to understand the current trend of such a topic. In this work, the publications about protein corona of nanoparticles in Science Citation Index Expanded database of Web of Science from 2007 to 2020 (1417 in total) were analyzed in detail, and the bibliometrics landscape of them was showcased. The basic bibliometrics characteristics were summarized to provide an overall understanding. Citation analysis was performed to scrutinize the peer interests of these papers. The research hotspots in the field were evaluated, based on which some feasible topics for future studies were proposed. In general, the results demonstrated that protein corona of nanoparticles was a prospective research area, and had attracted global research interests. It was believed that this work could comprehensively highlight the bibliometrics landscape, inspire further exploitation on protein corona of nanoparticles, and ultimately promote the clinical translation of nanoparticles.
Regarding the increasing number of cancer patients, the global burden of this disease is continuing to grow. Despite a considerable improvement in the diagnosis and treatment of various types of cancer, new diagnosis and treatment strategies are required. Nanotechnology, as an interesting and advanced field in medicine, is aimed to further advance both cancer diagnosis and treatment. Gold nanocages (AuNCs), with hollow interiors and porous walls, have received a great deal of interest in various biomedical applications such as diagnosis, imaging, drug delivery, and hyperthermia therapy due to their special physicochemical characteristics including the porous structure and surface functionalization as well as optical and photothermal properties. This review is focused on recent developments in therapeutic and diagnostic and applications of AuNCs with an emphasis on their theranostic applications in cancer diseases.
Nanotoxicology has become the subject of intense research for more than two decades. Thousands of articles have been published but the space in understanding the nanotoxicity mechanism and the assessment is still unclear. Recent researches clearly show potential benefits of nanomaterials (NMs) in diagnostics and treatment, targeted drug delivery, and tissue engineering owing to their excellent physicochemical properties. However, these NMs display hazardous health effect then to the greater part of the materials because of small size, large surface area-to-volume ratio, quantum size effects, and environmental factors. Nowadays, a large number of NMs are used in industrial products including several medical applications, consumer, and healthcare products. However, they came into the environment without any safety test. The measurement of toxicity level has become important because of increasing toxic effects on living organisms. New realistic mechanism-based strategies are still needed to determine the toxic effects of NMs. For the assessment of NMs toxicity, reliable and standardized procedures are necessary. This review article provides systematic studies on toxicity of NMs involving manufacturing, environmental factors, eco-toxic and genotoxic effects, some parameters which have been ignored of NMs versus their biological counterparts, cell heterogeneity, and their current challenges and future perspectives.
A reliable and efficient solution to the current energy crisis and its associated environmental issues is provided by fuel cells, metal–air batteries and overall water splitting. The heart reactions for these technologies are oxygen reduction reaction (ORR), oxygen evolution reaction (OER) and hydrogen evolution reaction (HER). Different supporters such as graphene, carbon nanotube, and graphitic carbon nitride have been used to avoid agglomeration of active materials and provide maximum active surface for these reactions. Among all the supporters, boron nitride (BN) gains extensive research attention due to its analogue with graphene and excellent stability with good oxidation and chemical inertness. In this mini-review, the well-known strategies (exfoliation, annealing, and CVD) used in the synthesis of BN with different morphologies for HER, OER and ORR applications have been briefly debated and summarized. The comparative analysis determines that the performance and stability of state-of-the-art electrocatalysts can be further boosted if they are deposited on BN. It is revealed that BN-based catalysts for HER, OER and ORR are rarely studied yet especially with non-noble transition metals, and this research direction should be studied deeply in future for practical applications.
Developing chemotherapy drugs with high efficacy and few side effects has been a bottleneck problem that requires an efficient solution. The active cancer treatment ingredient disulfiram (DSF), inspired by the copper(II) diethyldithiocarbamate complex (CuET), can be used in a one-pot synthesis method to construct a CuET delivery nanosystem (CuET-ZIFCu@HA). Due to the high biocompatibility, targeting of CD44 overexpressed cancer cells, and acid response of zeolitic imidazolate framework (ZIF) materials of hyaluronic acid (HA), we realized that CuET-ZIFCu@HA could become an effective and highly selective cancer treatment. Both in vivo and in vitro experiments have demonstrated that CuET-ZIFCu@HA has robust anti-tumor properties without evident side effects. This research provided a promising strategy for DSF nanosystems that involves simple preparation and high efficacy, both of which are key to reusing DSF in cancer treatment.
Interface engineering is an efficient strategy to modify electronic structure and further improve electrocatalytic activity. Herein, crystalline/amorphous heterostructured Co3O4–SmMn2O5 nanosheets (Co3O4–SMO NSs) have been synthesized by coupling of SMO (electron acceptor) with higher Fermi-level Co3O4 (electron donor), via a one-step hydrothermal method followed by calcination. The resulting Co3O4–SMO NSs display higher half-wave potential and specific activity than those of pure SMO or Co3O4. In addition, Co3O4–SMO NSs exhibit superior stability and methanol tolerance. The crystalline/amorphous heterostructure and the electron interaction between SMO and Co3O4 result in interfacial charge transfer. This leads to more active valence states and more oxygen vacancies, optimizing the adsorption energy of O species and expediting electron migration, thus boosting oxygen reduction reaction (ORR) catalytic performance. This study provides a promising strategy to design efficient ORR electrocatalysts by interfacial engineering.
We prepared porous Fe-doped nickel cobaltate (Fe-NiCo2O4) hollow hierarchical nanospheres through a facile self-templated synthetic strategy. Due to the porous hollow structure and composition, the Fe-NiCo2O4 presented vastly superior electrocatalytic activity for the oxygen evolution reaction (OER), compared with NiCo2O4 and the majority of other OER catalysts. With an aim of stimulating a current density of 10 mA·cm−2, the Fe-NiCo2O4 catalyst needs an overpotential of 210 mV, which is on a par with the general properties of commercial IrO2. In addition, the Fe-NiCo2O4 catalyst performed stably in long-term testing. The excellent activity and long-term stability showed that such catalysts have great promise for widespread application in the field of water splitting.
WO3(H2O)0.333/CdS (WS) nanocomposites are obtained via a rapid microwave hydrothermal method, and they are served as visible light-driven photocatalysts for the H2 generation. By using Pt as the cocatalyst, the WS nanocomposite with 70 wt.% CdS reaches the H2 evolution rate of 10.32 mmol·g−1·h−1, much quicker than those of WO3(H2O)0.333 and CdS. The cycling test reveals the good photocatalytic stability of the WS nanocomposite. The carrier transfer mechanism of WS nanocomposites can be explained by the Z-scheme mechanism. The existence of the Z-scheme heterojunction greatly helps to separate photogenerated carriers and thus improves the photocatalytic activity. The present work provides a rapid synthesis method for preparing Z-scheme heterojunction photocatalysts, and may be helpful for the green production of hydrogen.
Water–solid triboelectric nanogenerators (TENGs), as new energy collection devices, have attracted increasing attention in ocean energy harvesting and self-powered sensing. Polyacrylic acid (PAA) coating, usually used on the surface of marine equipment, has the property of anti-aging and anti-wear but limits triboelectrical output when used with TENGs. In this paper, polyacrylic acid coating was modified with fluorinated polyacrylate resin (F-PAA) to increase its triboelectrical output, by 6 times, and also to increase its anti-corrosion property. In addition, the corrosion resistance property can be further enhanced by cathodic protection using the electrical output generated by the water-flow triboelectrical energy transfer process. Given their easy fabrication, water-flow energy harvesting, and corrosion resistance, PAA/F-PAA coating-based TENGs have promising applications in river and ocean energy collection and corrosion protection.
To construct supercapacitors (SCs) with high-efficient electrochemical properties, the morphology and structure of applied electrode materials are the key factors. Herein, three-dimensional (3D) sea urchin-like MnCo2O4 nanoarchitectures grown on Ni foam (NF) were successfully synthesized via a simple solvothermal method and subsequent annealing treatment. Electrochemical tests revealed that the area specific capacitances of the MnCo2O4 electrode and the corresponding assembled asymmetric device can achieve 1634 and 522 mF·cm−2, respectively. When the power density of the assembled asymmetric supercapacitor (ASC) is 2.25 mW·cm−2, the maximum energy density can reach 0.163 mW·h·cm−2. After 5500 cycles of long-term stability test, the capacity retention rate maintains 91.7%. The excellent electrochemical performance can be mainly ascribed to the unique nanostructure of the material, which provides a great quantity of electroactive sites for Faraday redox reactions as well as accelerates the process of the ions/electrons transport. This work provides a certain reference value for the preparation of MnCo2O4 electrode with novel structure and excellent electrochemical performance for SCs.
Realizing the real-time detection of CH4 is important for the safety of human life. A facile hydrothermal method was used to synthesize Ag nanoparticles-decorated ZnO porous nanoflakes (PNFs) in this study. The characterization results confirmed that Ag nanoparticles had been decorated in ZnO nanoflakes with the thickness of ~10 nm. The gas-sensing properties of Ag-decorated ZnO nanoflakes were also investigated. While the gas-sensing performances of ZnO were remarkably improved by decorating Ag nanoparticles on the surface of ZnO nanoflakes, the response of the Ag-decorated ZnO sensor to 3000 ppm CH4 is almost 1.3 times as high as that of pristine ZnO sensor. The obtained Ag/ZnO sensor exhibits better long-term stability and shorter response recovery time (5/38 s) in the comparison with pristine ZnO, demonstrating the possibility for the actual detection of CH4. The enhanced CH4 sensing performance can be attributed to the synergism between the unique hierarchical porous structure and the sensitizing actions utilized by the Ag nanoparticles.
Solar thermal desalination (STD) is a promising and sustainable techno- logy for extracting clean water resources. Whereas recent studies to improve STD performance primarily focus on interfacial solar evaporation, a non-traditional bottom heating method was designed in this study. Herein, we prepared the polyvinyl alcohol/graphene oxide (PVA-GO) composite membrane and adhered to the bottom of a beaker using crystallized PVA. The GO was loaded on a non-woven fabric and different concentrations of PVA were compared for their effect on the evaporation efficiency. The results showed that the addition of PVA increased the evaporation rate. The surface characteristic of GO membrane without PVA was a fibrous filamentous structure as observed by SEM, whereby the fibers were clearly visible. When the PVA concentration reached 6%, the non-woven fiber was completely wrapped by PVA. Under the action of a fixed light intensity, the photothermal conversion rates of GO, 2% PVA-GO, 4% PVA-GO and 6% PVA-GO membrane device could reach 39.93%, 42.61%, 45.10% and 47.00%, respectively, and the evaporation rates were 0.83, 0.88, 0.94 and 0.98 kg·m−2·h−1, respectively. In addition, the PVA-GO composite membrane showed an excellent stability, which has significance for industrial application.
