A novel electrochemical sensor with a dual-template molecular imprinting technology was fabricated for the simultaneous detection of paracetamol (PAR) and isoniazid (INZ). The sensor was constructed using nitrogen and sulfur co-doped molybdenum carbide (N, S@Mo₂C) and a thin layer of electro-polymerized methylene blue was applied onto the surface of the N, S@Mo₂C. The electrochemical sensor demonstrated remarkable analytical efficiency for the concurrent PAR and INZ quantification under optimal circumstances. The system achieved an exceptionally low limit of detection (S/N = 3) of  3.7 nM for PAR, with a concentration range  of  0.013 and 140 µM.  A LOD of 7.6 nM was attained for INZ, with a linear range  between 0.025 and 140 µM. Furthermore, the platform’s selectivity was evaluated using differential pulse voltammetry  (DPV). The designed platform successfully detected PAR and INZ in authentic samples with recoveries varying between 98.3% and 104.9%. The relative standard deviations (RSD) for these measurements ranged from 2.7 to 4.0%, demonstrating that the proposed sensor is extremely stable, repeatable, and reproducible. These promising results suggest that the sensor holds potential for the detection of various (bio) molecules, paving the way for future applications in sensing fields.

Graphical abstract

Accurate determination of glutathione (GSH) levels in biological fluids and food supplements is paramount. To address this need, we developed a near-infrared (NIR) fluorescent probe with high sensitivity and selectivity for GSH detection. This probe comprises thioctic acid-functionalized silver and gold nanoclusters (ThA@Ag/Au NCs), emitting red light at 720 nm upon excitation at 310 nm. In the presence of Fe³⁺ ions, which form complexes with ThA, the fluorescence of ThA@Ag/Au NCs is quenched due to aggregation. However, upon addition of GSH, a potent chelator for Fe³⁺, the fluorescence of the probe is restored, leading to enhanced emission. Under optimized conditions, the fluorescence response (F/F°) exhibits a linear relationship with increasing GSH concentration within the range of 0.03–95 µM, achieving a limit of detection (LOD) of 9.0 nM. This designed scheme demonstrates excellent selectivity, sensitivity, and accuracy for GSH detection. Furthermore, the NIR fluorescent probe effectively estimated GSH levels in various matrices, including capsules, serum, urine, and saliva samples, yielding recoveries % ranging from 97.2 % to 103.2 %, with RSD % below 4.34 %. Due to its NIR properties, this fluorescent probe holds promise for diagnosing various diseases and potential in vivo applications.

Graphical abstract

Terbium and nitrogen co-doped carbon dots (Tb@N-CDs), combined with α-lipoic acid-functionalized copper nanoclusters (LA@CuNCs), were proposed for the ratiometric detection of quinolone (QA) antibiotics. In this system, Tb@N-CDs facilitate the aggregation of LA@CuNCs, enhancing its fluorescence emission at 670 nm via aggregation-induced emission enhancement (AIEE). Meanwhile, the fluorescence emission of Tb@N-CDs at 460 nm diminishes due to Förster resonance energy transfer (FRET). Upon the introduction of QA, the binding between Tb³⁺ ions and N-CDs weakens, disrupting both AIEE and FRET processes. This disruption results in a reduction in fluorescence emission at 670 nm and a concurrent increase at 460 nm. The fluorescence response ratio (F₄₆₀/F₆₇₀) increases with higher concentrations of ciprofloxacin (CFX), demonstrating a linear range from 0.008 to 120 μmol L⁻¹ and LOD of 1.6 nmol L⁻¹. The method successfully detected CFX in milk and urine samples, achieving recoveries between 97.7 % and 103.8 %, RSD of less than 3.79 %.

Melamine, often used as an adulterant in infants’ formula due to its high protein content, can be harmful when ingested in large amounts, leading to the formation of cyanurate-melamine co-crystals in infants and potentially causing kidney damage. In this study, we introduce a fluorescent method for the selective and reliable detection of melamine in milk and infants’ formula. The fluorescent probe comprises copper nanoclusters (Cu NCs) functionalized with thiosalicylic acid (TSA) and polyvinylpyrrolidone (PVP) as double-protecting ligands. Upon the addition of Hg²⁺, the fluorescence emission of TSA-PVP@Cu NCs is diminished due to static quenching. Subsequently, the fluorescence emission of the TSA-PVP@Cu NCs + Hg²⁺ probe is restored upon the introduction of melamine, facilitated by the coordination interaction between melamine and Hg²⁺ and the formation of a stable chelate between them. Under optimized conditions, the fluorescence emission was recorded initially for the TSA-PVP@Cu NCs + Hg²⁺ probe (F°) and after melamine addition (F). The (F/F°) ratio increased with rising melamine concentrations within the range of 0.025–65 µM. The detection limit, calculated using a signal-to-noise ratio of 3, was determined to be 8.0 nM. The TSA-PVP@Cu NCs + Hg²⁺ probe was successfully employed to detect melamine in milk and infants’ formula, yielding acceptable recovery percentages and relative standard deviations. These results underscore the reliability and efficacy of the proposed probe for the fluorometric detection of melamine in real-world samples.

Background

Levels of heavy metal pollution are increasing due to industrial activities and urban expansion. While cobalt (Co) can be toxic to plants at high levels and isn’t considered essential, it plays a beneficial role in many enzymes and is critical for various biological functions. We conducted experiments to determine how Adhatoda vasica proliferated shoots react to exposure to various Co concentrations (50–1000 µM). We employed physiological and biochemical markers to elucidate the response mechanisms of this medicinal plant. The experiment was conducted in two replicates per treatment. The statistical analysis was based on data from four biological replicates per treatment.

Results

Interestingly, the lowest Co concentration (50 µM) increased proliferated shoot growth by 41.45%. In contrast, higher Co concentrations (100–1000 µM) had detrimental effects on proliferated shoot development, water content, and photosynthetic pigment concentrations. As Co concentration increased, proliferated shoots produced excessive concentrations of reactive oxygen species (ROS). This ROS overproduction is believed to be the primary cause of oxidative damage, as evidenced by the elevated concentrations (18.46%-72.84%) of malondialdehyde (MDA) detected. In response to Co stress, non-enzymatic antioxidants were activated in a concentration-dependent manner. Co administration significantly increased the concentrations of different stress-protective compounds in shoots, including total antioxidants (133.18%), ascorbic acids (217.94%), free and bound phenolics (97.70% and 69.72%, respectively), proline (218.59%), free amino acids (206.96%), soluble proteins (65.97%), and soluble carbohydrates (18.52%). FTIR analysis further corroborated changes in the chemical composition of proliferated shoots. The analysis revealed variations in the peaks associated with major macromolecules, including phenolic compounds, lipids, proteins, carbohydrates, cellulose, hemicellulose, and sugars.

Conclusions

Our study offers the first comprehensive investigation into mechanisms by which Co stress triggers oxidative damage and alters functional groups in the medicinal plant, Adhatoda vasica.