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The presence of several organic contaminants in the environment and aquatic compartments has been a matter of great concern in the recent years. To tackle this problem, new sustainable and cost-effective technologies are needed. Herein we describe magnetic biosorbents prepared from trimethyl chitosan (TMC), which is a quaternary chitosan scarcely studied for environmental applications. Core@shell particles comprising a core of magnetite (Fe3O4) coated with TMC/siloxane hybrid shells (Fe3O4@SiO2/SiTMC) were successfully prepared using a simple one-step coating procedure. Adsorption tests were conducted to investigate the potential of the coated particles for the magnetically assisted removal of the antibiotic sulfamethoxazole (SMX) from aqueous solutions. It was found that TMC-based particles provide higher SMX adsorption capacity than the counterparts prepared using pristine chitosan. Therefore, the type of chemical modification introduced in the chitosan type precursors used in the surface coatings has a dominant effect on the sorption efficiency of the respective final magnetic nanosorbents.

Water pollution threatens environment and human health. Common polymer-based sorbents are used to trap pollutants by these sorbents are difficult to separate from treated water and, in turn, their application is limited. Alternatively, nanomaterials with magnetic features offer the advantage of fast and easy magnetically-assisted separation. Moreover, the surface modification of magnetic nanoparticles with biopolymers enhances their adsorptive capabilities. We review recent developments on magnetic biosorbents for water treatment. We present chemical strategies for the surface modification of magnetic nanoparticles with biopolymers to obtain highly effective, robust and reusable biosorbents. This can be done by two strategies: in situ functionalization and post-synthesis functionalization. Post-synthesis functionalization is done in two distinct stages, the synthesis of the magnetic nanoparticles and the surface functionalization, thus allowing better control of each stage individually. Surface functionalization involves either simple coating or the covalent attachment of the biopolymer chains to the surface. Overall, covalent immobilization of the biopolymer onto the particle’s surface is recommended to ensure successful recycling and reuse of the biosorbents without significant loss of adsorption capacity. Finally, we discuss the performance of several magnetic biosorbents in the uptake of heavy metal species and organic pollutants from water.

Functionality in nanoengineered materials has been usually explored on structural and chemical compositional aspects of matter that exist in such solid materials. It is well known that the absence of solid matter is also relevant and the existence of voids confined in the nanostructure of certain particles is no exception. Indeed, over the past decades, there has been great interest in exploring hollow nanostructured materials that besides the properties recognized in the dense particles also provide empty spaces, in the sense of condensed matter absence, as an additional functionality to be explored. As such, the chemical synthesis of hollow nanostructures has been driven not only for tailoring the size and shape of particles with well-defined chemical composition, but also to achieve control on the type of hollowness that characterize such materials. This review describes the state of the art on late developments concerning the chemical synthesis of hollow nanostructures, providing a number of examples of materials obtained by distinct strategies. It will be apparent by reading this progress report that the absence of solid matter determines the functionality of hollow nanomaterials for several technological applications.

Clean and accessible water for all has been defined by the United Nations as a major goal to promote sustainability in a planet with improved life quality. However, the growth of population and global industry processes are having a massive impact on the water quality. The presence of organic pollutants in water and wastewater, such as pharmaceuticals, organic dyes and by-products of industrial processes, is a major issue. Conventional wastewater treatments are still limited, and, consequently, it is crucial to design innovative cleaning technologies such as heterogeneous photocatalysis with nanomaterials. Here we review mechanisms and applications of carbon-based nanostructures for heterogeneous photocatalysis applied to water purification. In particular, we present recent developments in synthetic routes and surface modification of carbon nanostructures aiming at their use under visible light irradiation. As such, carbon-based nanostructures decorated with distinct phases have been investigated, such as semiconductor compounds and polyoxometalates. The photocatalytic efficiency of hybrid nanocomposite materials is attributed to improved light harvesting and reduced recombination of photo-generated charge carriers. Furthermore, the recovery of photocatalysts by using assisted magnetic separation is presented as a promising strategy of reusability.

Doxorubicin is one of the most widely used anti-cancer drugs, but side effects and selectivity problems create a demand for alternative drug delivery systems. Herein we describe a hybrid magnetic nanomaterial as a pH-dependent doxorubicin release carrier. This nanocarrier comprises magnetic iron oxide cores with a diameter of 10 nm, enveloped in a hybrid material made of siliceous shells and ĸ-carrageenan. The hybrid shells possess high drug loading capacity and a favorable drug release profile, while the iron oxide cores allows easy manipulation via an external magnetic field. The pH responsiveness was assessed in phosphate buffers at pH levels equivalent to those of blood (pH 7.4) and tumor microenvironment (pH 4.2 and 5). The nanoparticles have a loading capacity of up to 12.3 wt.% and a release profile of 80% in 5 h at acidic pH versus 25% at blood pH. In vitro drug delivery tests on human breast cancer and non-cancer cellular cultures have shown that, compared to the free drug, the loaded nanocarriers have comparable antiproliferative effect but a less intense cytotoxic effect, especially in the non-cancer cell line. The results show a clear potential for these new hybrid nanomaterials as alternative drug carriers for doxorubicin.

Timely diagnosis and appropriate antitumoral treatments remain of utmost importance, since cancer remains a leading cause of death worldwide. Within this context, nanotechnology offers specific benefits in terms of cancer therapy by reducing its adverse effects and guiding drugs to selectively target cancer cells. In this comprehensive review, we have summarized the most relevant novel outcomes in the range of 2010–2023, covering the design and application of nanosystems for cancer therapy. We have established the general requirements for nanoparticles to be used in drug delivery and strategies for their uptake in tumor microenvironment and vasculature, including the reticuloendothelial system uptake and surface functionalization with protein corona. After a brief review of the classes of nanovectors, we have covered different classes of nanoparticles used in cancer therapies. First, the advances in the encapsulation of drugs (such as paclitaxel and fisetin) into nanoliposomes and nanoemulsions are described, as well as their relevance in current clinical trials. Then, polymeric nanoparticles are presented, namely the ones comprising poly lactic-co-glycolic acid, polyethylene glycol (and PEG dilemma) and dendrimers. The relevance of quantum dots in bioimaging is also covered, namely the systems with zinc sulfide and indium phosphide. Afterwards, we have reviewed gold nanoparticles (spheres and anisotropic) and their application in plasmon-induced photothermal therapy. The clinical relevance of iron oxide nanoparticles, such as magnetite and maghemite, has been analyzed in different fields, namely for magnetic resonance imaging, immunotherapy, hyperthermia, and drug delivery. Lastly, we have covered the recent advances in the systems using carbon nanomaterials, namely graphene oxide, carbon nanotubes, fullerenes, and carbon dots. Finally, we have compared the strategies of passive and active targeting of nanoparticles and their relevance in cancer theranostics. This review aims to be a (nano)mark on the ongoing journey towards realizing the remarkable potential of different nanoparticles in the realm of cancer therapeutics.

Modern societies depend strongly on electronic and electric equipment (EEE) which has a side effect result on the large production of electronic wastes (e-waste). This has been regarded as a worldwide issue, because of its environmental impact—namely due to non-adequate treatment and storage limitations. In particular, EEE is dependent on the availability of rare earth elements (REEs), considered as the “vitamins” of modern industry, due to their crucial role in the development of new cutting-edge technologies. High demand and limited resources of REEs in Europe, combined with potential environmental problems, enforce the development of innovative low-cost techniques and materials to recover these elements from e-waste and wastewaters. In this context, sorption methods have shown advantages to pre-concentrate REEs from wastewaters and several studies have reported the use of diverse nanomaterials for these purposes, although mostly describing the sorption of REEs from synthetic and mono-elemental solutions at unrealistic metal concentrations. This review is a one-stop-reference by bringing together recent research works in the scope of the application of carbon nanomaterials for the recovery of REEs from water.

The design of cheap and safe antibacterial materials for widespread use has been a challenge in materials science. The use of copper nanostructures combined with abundant biopolymers such as cellulose offers a potential approach to achieve such materials though this has been less investigated as compared to other composites. Here, nanocomposites comprising copper nanofillers in cellulose matrices have been prepared by in situ and ex situ methods. Two cellulose matrices (vegetable and bacterial) were investigated together with morphological distinct copper particulates (nanoparticles and nanowires). A study on the antibacterial activity of these nanocomposites was carried out for Staphylococcus aureus and Klebsiella pneumoniae, as pathogen microorganisms. The results showed that the chemical nature and morphology of the nanofillers have great effect on the antibacterial activity, with an increase in the antibacterial activity with increasing copper content in the composites. The cellulosic matrices also show an effect on the antibacterial efficiency of the nanocomposites, with vegetal cellulose fibers acting as the most effective substrate. Regarding the results obtained, we anticipate the development of new approaches to prepare cellulose/copper based nanocomposites thereby producing a wide range of interesting antibacterial materials with potential use in diverse applications such as packaging or paper coatings.

The widespread use of gadolinium (Gd) in medical and industrial applications, especially as a contrast agent in magnetic resonance imaging (MRI), has led to its increasing presence in surface waters, disrupting natural geochemical cycles and posing risks to aquatic ecosystems. Addressing this challenge, recent studies have explored the potential of magnetic materials, such as spinel ferrite nanoparticles, in the removal of Gd from contaminated water sources. The present study specifically focused on the use of MnFe2O4 nanoparticles to remove Gd from contaminated solutions, employing response surface methodology (RSM) to optimize sorption conditions. Key variables evaluated included salinity (0–30 g/L), initial Gd concentration (1–5 μmol/L), and sorbent dose (20–180 mg/L), at a fixed pH of 6. The results revealed that salinity had a minimal impact on Gd sorption, likely due to the high sorbent mass used. Optimal conditions were identified as a sorbent dose of 165 mg/L, an initial Gd concentration of 1.3 μmol/L, and a salinity level of 13.4 g/L, at pH 6. The process was efficient and rapid, achieving over 90% Gd removal within 1 h in both freshwater and saline conditions, and over 75% removal in mineral water within 3 h. The high efficiency and celerity of this method suggest that MnFe2O4 nanoparticles are a promising solution for treating Gd-contaminated hospital effluents. Future research should focus on validating these results in real-world effluent matrices and addressing the environmental and economic aspects of large-scale implementation, thereby contributing to sustainable water remediation strategies.

The increased applications of engineered nanoparticles (NPs) may lead to environmental release and transport to estuarine environments where NPs are expected to aggregate/agglomerate with increasing ionic strength. However, more stable NPs that may be resistant to high ionic strength media and more dispersed in the aquatic environment are being synthesized. Thus, understanding colloidal NPs’ behavior in different ionic strength media is crucial for the assessment of the consequences of their environmental release. This work assessed the behavior of gold nanoparticles (AuNPs), with diverse sizes and coatings, in media with different ionic strengths (from biological buffers to artificial seawater). Overall, in biological buffers and artificial seawater, citratecoated AuNPs were unstable, displaying significantly increased sizes (between 100 and 400 nm), whereas no significant alterations (less than 5 % oscillation) were found for AuNPs with other coatings (bovine serum albumin, polyvinylpyrrolidone, and polyethylene glycol). Data suggest that coated AuNPs, and probably other NPs, may be dispersed in the environment from freshwater to estuarine systems.