Nanostructured rhodamine B/aluminosilicate extracted sugarcane bagasse modified with tobacco-derived carbon quantum dot as ratiometric fluorescence probe for determination of tetracycline.

Tetracycline (TC), as a widely used antibiotic, is very useful in treating bacterial infections. However, its residues in animal foodstuffs can enter the human body through the food cycle and causes severe and chronic diseases. On the other hand, due to its weak non-biodegradability, it is considered a threat to the environment. In this regard, the development of sensing methods to detect and measure TC is need of the hour. Herein, a dual-emission fluorescence sensor based on porous aluminosilicate structure (ASS) with rough surface hexagonal shape morphology and pore diameter less than 2 nm was prepared. The porous AAS was modified by post-modification method with blue carbon dots (CDT) and rhodamine B (RB) as two fluorophores to develop the ratiometric fluorescence (RF) sensor (CDT-AAS/RB). Nanostructured CDT-AAS/RB emitted two resolved peaks at 445 and 585 nm , which were dramatically quenched in the presence of TC. The RF sensor, with excellent sensitivity, was able to measure TC over the linear range of 0.001-150 µM with a limit of detection of 5.4 nM in the aqueous phosphate buffer. Moreover, the AAS component granted high selectivity and anti-interference ability to the sensor. In addition, the stability of the sensor was greatly improved due to the non-accumulation of CDT nanoparticles and RB molecules in the presence of the AAS. The proposed method was able to determine TC in complex real samples with satisfactory recovery, and the obtained results were validated with standard high-performance liquid chromatography technique.

Orange peel-derived carbon dots/Cu-MOF nanohybrid for fluorescence determination of l-ascorbic acid and Fe3.

Recycling and reuse of biomass waste in synthesis of nanomaterials have recently received much attention as an effective solution for environmental protection and sustainable development. Herein, nitrogen-doped carbon dots (N-CDs) with blue emission were synthesized from the orange peels as a precursor through a simple hydrothermal method and then, modified with ethylenediamine tetraacetic acid (N-CD@EDTA). The N-CD@EDTA was embedded as a fluorophore in Cu-based metal-organic framework (MOF-199) structure (N-CD@EDTA/MOF-199) to construct fluorescence sensor toward l-ascorbic acid (L-AA) determination. The N-CD@EDTA/MOF-199 nanohybrid significantly and selectively turned on toward L-AA determination during the fluorimetric experiments. Under optimal conditions, the probe showed a suitable linear response in the concentration range of 10 nM-100 µM with a low limit of detection (LOD) of 8.6 nM and high sensitivity of 0.201 µM-1. The possible mechanism of recognition and adsorption, including the reduction of Cu 2+ nodes in the MOF-199 structure in the presence of L-AA and the release of trapped N-CD@EDTA into the solution, was explored. Moreover, the N-CD@EDTA/MOF-199/L-AA (100 µM) system was further applied as a fluorescent "on-off" sensor for Fe3+ determination with a LOD of 1.15 µM. The proposed probe was successfully used in orange juice and water samples to determine L-AA and Fe3+ with satisfactory recovery, which displays the promising capability of sensor in real samples. The recoveries obtained by suggested method are consistent with that obtained from high performance liquid chromatography (HPLC) and atomic absorption spectroscopy which confirm the favorable characteristic of the sensor for accurate determination of L-AA and Fe3+ in practical applications.

Förster resonance energy transfer-based molecularly imprinted polymer /amine-functionalized metal-organic framework nanocomposite for trace level detection of 4-nitrophenol.

Herein, luminescent metal-organic framework (LMOF) is modified with molecularly imprinted polymer (MIP) and employed as an efficient and cost-effective nanoprobe for the determination of 4-nitrophenol (4-NP). Amine-UiO-66 support with unique luminescence property is chosen for creating the template of 4-NP using MIP to construct a highly selective LMOF-based sensor (amine-UiO-66/MIP nanocomposite). The imprinted sites formed at the surface of LMOF significantly enhance the selectivity of the probe for 4-NP over its analogs. 4-NP can effectively quench the fluorescent intensity of the optical sensor via the Förster resonance energy transfer (FRET) mechanism. Amine-UiO-66/MIP sensor provided the linear range of 0.05-50 µM and low limit of detection of 0.009 µM for sensing of 4-NP. The application of probe for the fluorometric analysis of real samples, including drinking and environmental water, provided satisfactory recovery results with low relative standard deviation (RSD).

Design of turn-on luminescent sensor based on nanostructured molecularly imprinted polymer-coated zirconium metal-organic framework for selective detection of chloramphenicol residues in milk and honey.

Herein, an optical sensor based on nanostructured molecularly imprinted polymer (MIP) coated on a luminescent zirconium metal-organic framework (MIP/Zr-LMOF) is introduced, and its performance is investigated for the fluorescent determination of chloramphenicol (CAP) antibiotic residues in milk and honey. To fabricate the sensor, the surface of Zr-LMOF is modified with MIP in the presence of CAP template, resulting in the introduction of recognition sites for antibiotic molecules. The porous structure of Zr-LMOF with specific binding sites for CAP recognition benefiting from coated MIP leads to selective and sensitive detection of antibiotic. The probe yields a linear range for detection of CAP in trace concentrations (0.16-161.56 µg.L-1) and provides a detection limit of 0.013 µg.L-1. Acceptable recoveries are achieved for antibiotic in real samples, which are consistent with that obtained from liquid chromatography-tandem mass spectrometry (LC-MS/MS), confirm the favorable performance of sensor for accurate determination of CAP in practical applications.

Gold-copper bimetallic nanoparticles supported on nano P zeolite modified carbon paste electrode as an efficient electrocatalyst and sensitive sensor for determination of hydrazine.

In this report, a facile, efficient and low cost electrochemical sensor based on bimetallic Au-Cu nanoparticles supported on P nanozeolite modified carbon paste electrode (Au-Cu/NPZ/CPE) was constructed and its efficiency for determination of hydrazine in trace level was studied. For this purpose, agro waste material, stem sweep ash (SSA) was employed as the starting material (silica source) for the synthesis of nano P zeolite (NPZ). After characterization of the synthesized NPZ by analytical instruments (scanning electronic microscopy (SEM), transmission electron microscopy (TEM), X-ray diffraction (XRD) and Fourier transform infrared (FT-IR) spectroscopy), construction of Au-Cu/NPZ/CPE was performed by three steps procedure involving preparation of nano P zeolite modified carbon paste electrode (NPZ/CPE), introducing Cu+2 ions into nano zeolite structure by ion exchange and electrochemical reduction of Cu+2 ions upon applying constant potential. This procedure is followed by partial replacement of Cu by Au due to galvanic replacement reaction (GRR). The electrochemical properties of hydrazine at the surface of Au-Cu/NPZ/CPE was evaluated using cyclic voltammetry (CV), amperometry, and chronoamperometry methods in 0.1 M phosphate buffer solution (PBS). It was found that the prepared sensor has higher electrocatalytic activity at a relatively lower potential compared to other modified electrodes including Au/NPZ/CPE, Cu/NPZ/CPE, Au-Cu/CPE and etc. Moreover, the proposed electrochemical sensor presented the favorable analytical properties for determination of hydrazine such as low detection limit (0.04 µM), rapid response time (3 s), wide linear range (0.01-150 mM), and high sensitivity (99.53 µA mM-1) that are related to the synergic effect of bimetallic of Au-Cu, porous structure and enough surface area of NPZ. In addition, capability of Au-Cu/NPZ/CPE sensor was successfully tested in real samples with good accuracy and precision.