Size-tunable platinum nanoparticles (PtNPs) prepared by a facile method in an aqueous environment without the use of catalyst-poisoning reagents are used here in the electrocatalytic detection of hydrogen peroxide. Spherical nanoparticles with sizes as small as 4 and 20 nm are obtained as shown by transmission electron microscopy (TEM) analysis only using small easy-to-remove molecules such as sodium citrate. PtNPs are freed from the citrate capping agent at the surface by changing the pH to basic values and then deposited on a glassy carbon electrode by a very simple and rapid drop-casting method, achieving high cleanliness of the nanoparticle surface without the need for further treatments. The superior quality of nanoparticles on the glassy carbon is further investigated by scanning electron microscopy (SEM) analysis, which shows a highly homogeneous distribution of well-dispersed nanoparticles on the electrode surface, as well as by X-ray photoelectron spectroscopy (XPS) analysis, which confirms a drastic decrease of the citrate content, providing useful information about the citrate–platinum interaction, and evidences a related remarkable increase of conductivity of capping-free washed nanoparticles. Due to such key features, PtNPs possess excellent electrocatalytic properties, which have been tested in hydrogen peroxide electroreduction, a well-known catalytic reaction of nanostructured platinum materials. The size effect on PtNPs electrocatalytic properties is demonstrated, achieving higher performances with smaller NPs in the amperometric detection of hydrogen peroxide at −0.1 V in the concentration range of 25–750 μM, with a detection limit of 10 μM. Good sensing results toward hydrogen peroxide have also been obtained in terms of sensitivity, selectivity, repeatability, stability, and in tests performed in tap water samples. In addition, the strong adhesion of nanoparticles to the electrode surface has been verified and ascribed to their coating-free surface.

Herein we report the electropolymerization of a scopoletin based molecularly imprinted polymer (MIP) for the detection of lysozyme (Lyz), an enzymatic marker of several diseases in mammalian species. Two different approaches have been used for the imprinting of lysozyme based, respectively, on the use of a monomer-template mixture and on the covalent immobilization of the enzyme prior to polymer synthesis. In the latter case, a multi-step protocol has been exploited with preliminary functionalization of gold electrode with amino groups, via 4-aminothiophenol, followed by reaction with glutaraldehyde, to provide a suitable linker for lysozyme. Each step of surface electrode modification has been followed by cyclic voltammetry and electrochemical impedance spectroscopy, which has been also employed to test the electrochemical responses of the developed MIP. The sensors show good selectivity to Lyz and detect the enzyme at concentrations up to 292 mg/L (20 μM), but with different performances, depending on the used imprinting approach. An imprinting factor equal to 7.1 and 2.5 and a limit of detection of 0.9 mg/L (62 nM) and 2.1 mg/L (141 nM) have been estimated for MIPs prepared with and without enzyme immobilization, respectively. Competitive rebinding experiment results show that this sensing material is selective for Lyz determination. Tests were performed using synthetic saliva to evaluate the potential application of the sensors in real matrices for clinical purposes.

Looking at the literature focused on molecularly imprinted polymers (MIPs) for protein, it soon becomes apparent that a remarkable increase in scientific interest and exploration of new applications has been recorded in the last several years, from 42 documents in 2011 to 128 just 10 years later, in 2021 (Scopus, December 2021). Such a rapid threefold increase in the number of works in this field is evidence that the imprinting of macromolecules no longer represents a distant dream of optimistic imprinters, as it was perceived until only a few years ago, but is rapidly becoming an ever more promising and reliable technology, due to the significant achievements in the field. The present critical review aims to summarize some of them, evidencing the aspects that have contributed to the success of the most widely used strategies in the field. At the same time, limitations and drawbacks of less frequently used approaches are critically discussed. Particular focus is given to the use of a MIP for protein in the assembly of electrochemical sensors. Sensor design indeed represents one of the most active application fields of imprinting technology, with electrochemical MIP sensors providing the broadest spectrum of protein analytes among the different sensor configurations. Graphical abstract

A new sustainable route to nanodispersed and functionalized carbon black in water phase (W-CB) is proposed. The sonochemical strategy exploits ultrasounds to disaggregate the CB, while two selected functional naturally derived compounds, sodium cholate (SC) and rosmarinic acid (RA), act as stabilizing agents ensuring dispersibility in water adhering onto the CB nanoparticles’ surface. Strategically, the CB-RA compound is used to drive the AuNPs self-assembling at room temperature, resulting in a CB surface that is nanodecorated; further, this is achieved without the need for additional reagents. Electrochemical sensors based on the proposed nanomaterials are realized and characterized both morphologically and electrochemically. The W-CBs’ electroanalytical potential is proved in the anodic and cathodic window using caffeic acid (CF) and hydroquinone (HQ), two antioxidant compounds that are significant for food and the environment. For both antioxidants, repeatable (RSD ≤ 3.3%; n = 10) and reproducible (RSD ≤ 3.8%; n = 3) electroanalysis results were obtained, achieving nanomolar detection limits (CF: 29 nM; HQ: 44 nM). CF and HQ are successfully determined in food and environmental samples (recoveries 97–113%), and also in the presence of other phenolic classes and HQ structural isomers. The water dispersibility of the proposed materials can be an opportunity for (bio) sensor fabrication and sustainable device realization.

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