The novel procedure of few-layer black phosphorus (FLBP) stabilization and functionalisation was here proposed. The cationic polymer PLL and non-ionic PEG have been involved into encapsulation of FLBP to allow sufficient time for further nanofabrication process and overcome environmental degradation. Two different spacer chemistry was designed to bind polymers to tumor-homing peptides. The efficiency of functionalisation was examined by RP-HPLC, microscopic (TEM and SEM) and spectroscopic (FT-IR and Raman) techniques as well supported by ab-initio modelling. The cell and dose dependent cytotoxicity of FLBP and its bioconjugates was evaluated against HB2, MCF-7 and MDA-MB-231 cell lines. Functionalisation allowed not only for improvement of environmental stability, but also enhances therapeutic effect by abolished the cytotoxicity of FLBP against HB2 cell line. Moreover, modification of FLBP with PLL caused increase of selectivity against highly aggressive breast cancer cell lines. Results indicate the future prospect application of black phosphorus nanosheets as nanocarrier, considering its unique features synergistically with conjugated polymeric micelles.

Ecotoxicology is essential for the evaluation and comprehension of the effects of emergency pollutants (EP) such as heavy metal ions on the natural environment. EPs pose a substantial threat to the health of humans and the proper functioning of the global ecosystem. The primary concern is the exposure of humans and animals to heavy metal ions through contaminated water. The presence of heavy metal ions in drinking water ought to be monitored in accordance with World Health Organization regulations. Among the numerous harmful metal ions, copper ions are responsible for a variety of human diseases. This study investigates the application of phage display as a screening method for heavy metal toxicological targets, with copper served as the main focus. To identify a variety of Cu-binding M13 phage clones with unique peptides and to assess their affinity for metal ions, the study utilized Escherichia coli as a factories producing recombinant bacteriophages, modified biopanning procedure and an ELISA assay. The research highlights the increasing importance of phage display as a screening tool in ecotoxicology. We synthesized and modified the selected peptide to enable the rapid optical detection of Cu(II) ions in aqueous solutions. By incorporating the dansyl group into a designated peptide sequence, we implemented fluorescence detection assays for real-time measurements. The Cu2+- binding peptide’s efficacy was confirmed through spectroscopic measurements, which allowed for real-time detection with rapid response times with high selectivity. The phage display technique was successfully applied to develop the fluorescent peptide-based chemosensor that exhibited high selectivity and sensitivity for Cu2+.

The global market increasingly demands alternative rapid diagnostic tools, such as disposable biosensors, to meet the growing need for point-of-care clinical testing of infectious diseases. Bacterial vaginosis (BV), a common infection caused by Gardnerella vaginalis, requires efficient and accurate detection methods to improve patient outcomes and prevent complications. However, existing diagnostic approaches often lack sensitivity, specificity, or rapid response times, highlighting the need for innovative biosensing solutions. In response to this challenge, we developed a peptide-based electrochemical biosensor for the specific detection of Gardnerella vaginalis. The sensor was designed to achieve high sensitivity, selectivity, and stability, with detection performed through electrochemical techniques. Cyclic voltammetry (CV) was employed to monitor electron transfer kinetics at the electrode surface, while electrochemical impedance spectroscopy (EIS) provided insights into changes in resistance and capacitance during peptide binding. The sensor fabrication involved covalently bonding anti-Gardnerella vaginalis peptides to a gold nanoparticle (AuNP)-modified graphene electrode, significantly enhancing bioreceptor immobilization stability and increasing the surface area for target binding interactions. The incorporation of AuNPs improved signal amplification due to their high surface-to-volume ratio and excellent conductivity, leading to enhanced sensor performance. The biosensor demonstrated a low detection limit (LOD) of 0.02305 μg/mL, with a rapid response time of 5 min across various concentrations of the target Gardnerella vaginalis antigen. The results confirmed specific and selective binding to the pathogen marker, with minimal interference from non-target species, ensuring high accuracy. The combination of graphene, AuNPs, and peptide bioreceptors resulted in robust signal enhancement, making this biosensor a promising tool for fast and reliable point-of-care diagnostics in clinical settings.

The study reports a methodology of selecting the optimal receptor to create an electrochemical immunosensor for equine arteritis virus (EAV) protein detection. The detection was based on antigen recognition by antibodies immobilized on gold electrodes. Modification steps were controlled by electrochemical impedance spectroscopy and cyclic voltammetry measurements. In order to obtain the impedance immunosensor with the best parameters, seven different receptors complementary to equine arteritis virus protein were used. In order to make the selection, a rapid screening test was carried out to check the sensor’s response to blank, extremely low and high concentrations of target EAV protein, and negative sample: M protein from Streptococcus equi and glycoprotein G from Equid alphaherpesvirus 1. F6 10G receptor showed the best performance.

This publication presents the results of work on the development of a quick and cheap electrochemical immunosensor for the diagnosis of infections with the pathogen Streptococcus agalactiae. The research was carried out on the basis of the modification of the well-known glassy carbon (GC) electrodes. The surface of the GC (glassy carbon) electrode was covered with a film made of nanodiamonds, which increased the number of sites for the attachment of anti-Streptococcus agalactiae antibodies. The GC surface was activated with EDC/NHS (1-Ethyl-3-(3-dimethylaminopropyl)carbodiimide/N-Hydroxysuccinimide). Determination of electrode characteristics after each modification step, performed using cyclic voltammetry (CV) and electrochemical impedance spectroscopy (EIS).