Bismuth Tungstate Nanoplates-Vis Responsive Photocatalyst for Water Oxidation.

The development of visible-light-responsive (VLR) semiconductor materials for effective water oxidation is significant for a sustainable and better future. Among various candidates, bismuth tungstate (Bi2WO6; BWO) has attracted extensive attention because of many advantages, including efficient light-absorption ability, appropriate redox properties (for O2 generation), adjustable morphology, low cost, and profitable chemical and optical characteristics. Accordingly, a facile solvothermal method has been proposed in this study to synthesize two-dimensional (2D) BWO nanoplates after considering the optimal preparation conditions (solvothermal reaction time: 10-40 h). To find the key factors of photocatalytic performance, various methods and techniques were used for samples' characterization, including XRD, FE-SEM, STEM, TEM, HRTEM, BET-specific surface area measurements, UV/vis DRS, and PL spectroscopy, and photocatalytic activity was examined for water oxidation under UV and/or visible-light (vis) irradiation. Famous commercial photocatalyst-P25 was used as a reference sample. It was found that BWO crystals grew anisotropically along the {001} basal plane to form nanoplates, and all properties were controlled simultaneously by tuning the synthesis time. Interestingly, the most active sample (under both UV and vis), prepared during the 30 h solvothermal reaction at 433 K (BWO-30), was characterized by the smallest specific surface area and the largest crystals. Accordingly, it is proposed that improved crystallinity (which hindered charge carriers' recombination, as confirmed by PL), efficient photoabsorption (using the smallest bandgap), and 2D mesoporous structure are responsible for the best photocatalytic performance of the BWO-30 sample. This report shows for the first time that 2D mesoporous BWO nanoplates might be successfully prepared through a facile template-free solvothermal approach. All the above-mentioned advantages suggest that nanostructured BWO is a prospective candidate for photocatalytic applications under natural solar irradiation.

Correction: Novel sensor for the determination of CA 15-3 in serum of breast cancer patients based on Fe-gallic acid complex doped in modified cellulose polymer thin films.

[This corrects the article DOI: 10.1039/D3RA02495D.].

A comprehensive study for the potential removal of 152+154Eu radionuclides using a promising modified strontium-based MOF.

A facile modification of a strontium-based MOF using oxalic acid was carried out to prepare MTSr-OX MOF, which was used as a potential substance for eliminating 152+154Eu radioisotopes. Various analytical techniques were used to characterize MTSr-OX-MOF. The prepared MOF had a rod-like structure with a BET surface area of 101.55 m2 g-1. Batch sorption experiments were used to investigate the sorption performance of MTSr-OX-MOF towards 152+154Eu radionuclides where different parameters like pH, contact time, initial 152+154Eu concentration, ionic strength, and temperature were scrutinized to determine the optimum conditions for 152+154Eu removal. MTSr-OX-MOF showed superior effectiveness in the elimination of 152+154Eu with a maximum sorption capacity of 234.72 mg g-1 at pH 3.5. Kinetics fitted with the pseudo-second-order model and the Langmuir model correctly described the sorption mechanism. The thermodynamic variables were carefully examined, demonstrating that the 152+154Eu sorption was endothermic as well as spontaneous. The MTSr-OX-MOF has been found to be a significantly more effective sorbent towards 152+154Eu than that of many other adsorbents. When applied to real active waste, MTSr-OX-MOF demonstrated excellent removal performance for a wide range of radionuclides. As a result, the MTSr-OX-MOF can be recognized as an attractive solution for the 152+154Eu purification from active waste.

Recent progress in high-performance environmental impacts of the removal of radionuclides from wastewater based on metal-organic frameworks: a review.

The nuclear industry is rapidly developing and the effective management of nuclear waste and monitoring the nuclear fuel cycle are crucial. The presence of various radionuclides such as uranium (U), europium (Eu), technetium (Tc), iodine (I), thorium (Th), cesium (Cs), and strontium (Sr) in the environment is a major concern, and the development of materials with high adsorption capacity and selectivity is essential for their effective removal. Metal-organic frameworks (MOFs) have recently emerged as promising materials for removing radioactive elements from water resources due to their unique properties such as tunable pore size, high surface area, and chemical structure. This review provides an extensive analysis of the potential of MOFs as adsorbents for purifying various radionuclides rather than using different techniques such as precipitation, filtration, ion exchange, electrolysis, solvent extraction, and flotation. This review discusses various MOF fabrication methods, focusing on minimizing environmental impacts when using organic solvents and solvent-free methods, and covers the mechanism of MOF adsorption towards radionuclides, including macroscopic and microscopic views. It also examines the effectiveness of MOFs in removing radionuclides from wastewater, their behavior on exposure to high radiation, and their renewability and reusability. We conclude by emphasizing the need for further research to optimize the performance of MOFs and expand their use in real-world applications. Overall, this review provides valuable insights into the potential of MOFs as efficient and durable materials for removing radioactive elements from water resources, addressing a critical issue in the nuclear industry.

A novel test device and quantitative colorimetric method for the detection of human chorionic gonadotropin (hCG) based on Au@Zn-salen MOF for POCT applications.

The human chorionic gonadotropin (hCG) hormone is a biomarker that can predict tumors and early pregnancy; however, it is challenging to develop sensitive qualitative-quantitative procedures that are also effective, inventive, and unique. In this study, we used a novel easy in situ reaction of an organic nano-linker with Zn(NO3)2·6H2O and HAuCl4·3H2O to produce a gold-zinc-salen metal-organic framework composite known as Au-Zn-Sln-MOF. A wide variety of micro-analytical instruments and spectroscopic techniques were used in order to characterize the newly synthesized Au-Zn-Sln-MOF composite. Disclosure is provided for a novel swab test instrument and a straightforward colorimetric approach for detecting hCG hormone based on an Au-Zn-Sln-MOF composite. Both of these methods are easy. In order to validate a natural enzyme-free immunoassay, an Au-Zn-Sln-MOF composite was utilized in the role of an enzyme; a woman can use this gadget to determine whether or not she is pregnant in the early stages of the pregnancy or whether or not her hCG levels are excessively high, which is a symptom that she may have a tumor. This cotton swab test device is compatible with testing of various biological fluids, such as serum, plasma, or urine, and it can be easily transferred to the market to commercialize it as a costless kit, which will be 20-30% cheaper than what is available on the market. Additionally, it can be used easily at home and for near-patient testing (applications of point-of-care testing (POCT)).

Prostate-Specific Antigen Monitoring Using Nano Zinc(II) Metal-Organic Framework-Based Optical Biosensor.

BACKGROUND: The prostate-specific antigen (PSA) is an important cancer biomarker that is commonly utilized in the diagnosis of prostate cancer. The development of a PSA determination technique that is rapid, simple, and inexpensive, in addition to highly accurate, sensitive, and selective, remains a formidable obstacle. METHODS: In this study, we developed a practical biosensor based on Zn(II) metal-organic framework nanoparticles (Zn-MOFs-NPs). Many spectroscopic and microanalytical tools are used to determine the structure, morphology, and physicochemical properties of the prepared MOF. RESULTS: According to the results, Zn-MOFs-NPs are sensitive to PSA, selective to an extremely greater extent, and stable in terms of chemical composition. Furthermore, the Zn-MOFs-NPs did not exhibit any interferences from other common analytes that might cause interference. The detection limit for PSA was calculated and was 0.145 fg/mL throughout a wide linear concentration range (0.1 fg/mL-20 pg/mL). CONCLUSIONS: Zn-MOFs-NPs were successfully used as a growing biosensor for the monitoring and measurement of PSA in biological real samples.

Smart prototype for an electronic color sensor device for visual simultaneous detection of macrofuran based on a coated paper strip.

Nowadays, in the clinical, pharmaceutical, and environmental sectors, the development of facile and sensitive analytical methods and/or innovative devices for the follow-up and detection of antibiotics and pharmaceutical formulations, in general, are urgently needed and still challenging. This work declared three vital applications for broad-spectrum nitrofurantoin (macrofuran) antibiotic detection and quantification: A colorimetric method, a coated paper strip-based nano-lanthanum complex prototype and fabrication of smart electronic color sensor device-based coated paper strips. The colorimetric method showed a significant response upon increasing the concentration of the nitrofurantoin in a range between (1.0-100.0 ng/mL) via a visual color change from orange-yellow to red colors degree with detection and quantification limits of 0.175 and 0.53 ng/mL, respectively, whereas the nano-lanthanum complex coated paper strip prototype showed qualitative on-site sensing for nitrofurantoin via naked eye color changes which can be detected anywhere. Moreover, a smart prototype for detecting macrofuran in the means of paper color change in the RGB color component extraction algorithm and the grayscale projection value processing algorithm was fabricated. The change in RGB color on the coated paper strip was detected using an electronic color sensor device. The developed colorimetric method, coated paper strip, and the electronic color sensor device prototype exhibited fast, simple, costless, and selective towards macrofuran over the competing analyzed. As well as, showed good applicability in the different real samples spiked with different concentrations of macrofuran.

Visible-light-driven photodegradation of organic pollutants by simply exfoliated kaolinite nanolayers with enhanced activity and recyclability.

The need for abundant photocatalyst in wastewater treatment is currently a must. A simple intercalation process was utilized to exfoliate Kaolinite clay mineral structure Al2Si2O5(OH)4 into two-dimensional nanostructured separated layers operated in visible light range. The intercalating agents were hydrazine hydrate and urea. Detailed characterization confirmed the nanolayered structures of kaolinite hexagonal nanosheets (NK). In addition, Bandgap energy was reduced based on intercalating agents from 3.45 to 2.48 eV as revealed by light absorption spectra. The quenching of PL spectra for the nK has also been ascribed to the suppression of charge carrier recombination. The exfoliated nK was utilized to photodegrade Rhodamine B dye (RhB) and P-nitrophenol (PNP) as industrial pollutants in wastewater. The results showed 92.3% and 99.7% photodegradation of RhB and PNP within 180 min of visible-light irradiation utilizing the exfoliated NK by urea. We denote the boosted photocatalytic performance of this NK to the uncovered, low bandgap metal oxide inclusions on the exterior of NK besides the nitrogen doping due to exfoliation with urea. This simple exfoliation has modified abundant and stable clay nanolayers that are a promising alternative for the eminent nanostructured oxide photocatalysts to overcome the organic pollutants in wastewater at a high scale.

A novel strontium-based MOF: synthesis, characterization, and promising application in removal of 152+154Eu from active waste.

Removal of hazardous radioactive materials such as 152+154Eu from active waste using the batch approach has attracted attention nowadays. In this work, a novel melamine-terephthalic strontium metal-organic framework (MTSr-MOF) was prepared via a hydrothermal method. The MTSr-MOF was characterized by various analytical techniques such as FT-IR, 1H/13C-NMR, mass spectroscopy, XPS, XRD, TGA, BET, FE-SEM/EDX, TEM, and UV. The obtained data revealed that MTSr-MOF exhibited brick-like building blocks that were bridged together by the linkers, and each block had a thickness of ∼120 nm. The BET surface area was 74.04 m2 g-1. MTSr-MOF was used for the removal of 152+154Eu radionuclides from active waste. Further functionalization using various modifiers, including oxalic acid, EDTA, sulfuric acid, and sodium hydroxide was carried out to improve the sorption efficiency of MTSr-MOF towards 152+154Eu radionuclides. Among them, MTSr-MOF modified with oxalic acid (MTSr-OX-MOF) demonstrated a superior removal efficiency toward 152+154Eu radionuclides when compared to MTSr-MOF or other published reports, with a removal efficiency of more than 96%. The higher sorption efficiency of the MTSr-OX-MOF indicates that it could be a promising candidate for the removal of 152+154Eu radionuclides from radioactive waste.

Nanomaterials and metal-organic frameworks for biosensing applications of mutations of the emerging viruses.

The world today lives in a state of terrible fear due to the mutation of the emerging COVID-19. With the continuation of this pandemic, there is an urgent need for fast, accurate testing devices to detect the emerging SARS-CoV-2 pandemic in terms of biosensors and point-of-care testing. Besides, the urgent development in personal defense tools, anti-viral surfaces and wearables, and smartphones open the door for simplifying the self-diagnosis process everywhere. This review introduces a quick COVID-19 overview: definition, transmission, pathophysiology, the identification and diagnosis, mutation and transformation, and the global situation. It also focuses on an overview of the rapidly advanced technologies based on nanomaterials and MOFs for biosensing, diagnosing, and viral control of the SARS-CoV-2 pandemic. Finally, highlight the latest technologies, applications, existing achievements, and preventive diagnostic strategies to control this epidemic and combat the emerging coronavirus. This humble effort aims to provide a helpful survey that can be used to develop a creative solution and to lay down the future vision of diagnosis against COVID-19.

Development of Sulfur-Doped Graphitic Carbon Nitride for Hydrogen Evolution under Visible-Light Irradiation.

Developing eco-friendly strategies to produce green fuel has attracted continuous and extensive attention. In this study, a novel gas-templating method was developed to prepare 2D porous S-doped g-C3N4 photocatalyst through simultaneous pyrolysis of urea (main g-C3N4 precursor) and ammonium sulfate (sulfur source and structure promoter). Different content of ammonium sulfate was examined to find the optimal synthesis conditions and to investigate the property-governed activity. The physicochemical properties of the obtained photocatalysts were analyzed by X-ray diffraction (XRD), field emission-scanning electron microscopy (FE-SEM), scanning transmission electron microscopy (STEM), specific surface area (BET) measurement, ultraviolet-visible light diffuse reflectance spectroscopy (UV/vis DRS), X-ray photoelectron spectroscopy (XPS), photoluminescence (PL) spectroscopy and reversed double-beam photo-acoustic spectroscopy (RDB-PAS). The as-prepared S-doped g-C3N4 photocatalysts were applied for photocatalytic H2 evolution under vis irradiation. The condition-dependent activity was probed to achieve the best photocatalytic performance. It was demonstrated that ammonium sulfate played a crucial role to achieve concurrently 2D morphology, controlled nanostructure, and S-doping of g-C3N4 in a one-pot process. The 2D nanoporous S-doped g-C3N4 of crumpled lamellar-like structure with large specific surface area (73.8 m2 g-1) and improved electron-hole separation showed a remarkable H2 generation rate, which was almost one order in magnitude higher than that of pristine g-C3N4. It has been found that though all properties are crucial for the overall photocatalytic performance, efficient doping is probably a key factor for high photocatalytic activity. Moreover, the photocatalysts exhibit significant stability during recycling. Accordingly, a significant potential of S-doped g-C3N4 has been revealed for practical use under natural solar radiation.

Selective and Fast Detection of Fluoride-Contaminated Water Based on a Novel Salen-Co-MOF Chemosensor.

The development of selective and fast optical sensitive chemosensors for the detection and recognition of different cations and anions in a domain is still a challenge in biological, industrial, and environmental fields. Herein, we report a novel approach for the detection and determination of fluoride ion (F-) sensing based on a salen-cobalt metal-organic framework (Co(II)-MOF). By a simple method, the Co(II)-MOF was synthesized and characterized using several tools to elucidate the structure and morphology. The photoluminescence (PL) spectrum of the Co(II)-MOF (100.0 nM/L) was examined versus different ionic species like F-, Br-, Cl-, I-, SO4 2-, and NO3 - and some cationic species like Mg2+, Ca2+, Na+, and K+. In the case of F- ions, the PL intensity of the Co(II)-MOF was scientifically enhanced with a remarkable red shift. With the increase of F- concentration, the Co(II)-MOF PL emission spectrum was also professionally enhanced. The limit of detection (LOD) for the Co(II)-MOF chemosensor was 0.24 µg/L, while the limit of quantification (LOQ) was 0.72 µg/L. Moreover, a comparison of the Co(II)-MOF optical approach with other published reports was studied, and the mechanism of interaction was also investigated. Additionally, the applicability of the current Co(II)-MOF approach in different real water samples, such as tap water, drinking water, Nile River water, and wastewater, was extended. This easy-to-use future sensor provides reliable detection of F- in everyday applications for nonexpert users, especially in remote rural areas.

Multifunctional Hydroxyapatite/Silver Nanoparticles/Cotton Gauze for Antimicrobial and Biomedical Applications.

Medical textiles have played an increasingly important protection role in the healthcare industry. This study was aimed at improving the conventional cotton gauze for achieving advanced biomedical specifications (coloration, UV-protection, anti-inflammation, and antimicrobial activities). These features were obtained by modifying the cotton gauze fabrics via in-situ precipitation of hydroxyapatite nanoparticles (HAp NP), followed by in-situ photosynthesis of silver (Ag) NPs with ginger oil as a green reductant with anti-inflammation properties. The HAp-Ag NPs coating provides good UV-protection properties. To further improve the HAp and Ag NPs dispersion and adhesion on the surface, the cotton gauze fabrics were modified by cationization with chitosan, or by partial carboxymethylation (anionic modification). The influence of the cationic and anionic modifications and HAp and Ag NPs deposition on the cotton gauze properties (coloration, UV-protection, antimicrobial activities, and water absorption) was thoroughly assessed. Overall, the results indicate that chemical (anionic and cationic) modification of the cotton gauze enhances HAp and Ag NPs deposition. Chitosan can increase biocompatibility and promotes wound healing properties of cotton gauze. Ag NP deposition onto cotton gauze fabrics brought high antimicrobial activities against Candida albicans, Gram-positive and Gram-negative bacteria, and improved UV protection.

A novel nano-lanthanum complex: synthesis, characterization and application as a macrofuran chemosensor in pharmaceutical, biological and environmental samples.

Macrofuran is widely used as an antibiotic for the treatment of urinary tract infections. Nevertheless, it is prohibited due to toxicity and environmental concerns. The development of a fast, simple, and cost-effective approach for the determination of macrofuran antibiotic (MFA) is still a challenge. Herein, we report a chemosensor based on a nano-lanthanum complex derived from phenylenediamine. The physicochemical properties and structure of the prepared complex were confirmed using different spectroscopic tools such as X-ray diffraction (XRD), scanning electron microscopy equipped with EDX, elemental analysis, Fourier transform-infrared (FT-IR) spectroscopy, UV-vis spectroscopy, mass spectroscopy and photoluminescence (PL). The nano-lanthanum complex was found to be chemically stable, highly sensitive and selective to MFA, without interference from other common antibiotics. The limit of detection for MFA was 0.025 ng mL-1, over a linear concentration range of 0.02-30.0 ng mL-1, with a correlation coefficient of 0.994. The nano-lanthanum complex can be used successfully as a promising chemosensor for MFA determination in pharmaceutical formulation and different biological samples (whole blood-serum-plasma). In addition, this approach will protect human beings from the environmental hazards of antibiotics through the detection of the low limit of MFA. Meanwhile, the mechanism of interaction between the nano-lanthanum complex and MFA was studied and investigated.

A novel nano copper complex: potentiometry, DFT and application as a cancer prostatic biomarker for the ultrasensitive detection of human PSA.

Worldwide, prostate cancer is considered to be one of the three most commonly occurring cancers amongst the male population. Clinically, early detection of diverse forms of cancer before they spread and become incurable plays an important role in treatment strategy. Therefore, the development of fast, accurate, sensitive, and low-cost analytical methodologies and techniques for the detection of cancer biomarkers is an attractive research area for scientists globally. Herein, a Schiff base ligand (A1) was prepared via the refluxing of 3-aminobenzoic acid with 1,2-phenylenediamine. After that, a nano Cu complex (N1) was synthesized by reacting A1 with copper chloride. The produced A1 and N1 were characterized using several techniques to determine their physicochemical properties. A density functional theory study was carried out to rationalize the experimental work and support the obtained results. Moreover, the nano Cu complex (N1) was used for the fabrication of a potentiometric membrane biosensor for the early detection of the prostate-specific antigen (PSA). The results reveal that the electrode displays a stable Nernstian response of 29.26 ± 0.87 mV per decade for PSA in a linear dynamic range of 5.0 pg mL-1-10.0 ng mL-1, in a pH range of 6.5-9.2, with a short response time of 25 ± 5 s. The lifetime was between 5-7 weeks under different storage conditions. The detection (LOD) and quantification (LOQ) limits were 0.098 and 0.297 pg mL-1, respectively. The presence of different interfering species on the potentiometric biosensor response against PSA was investigated. The sensing mechanism of N1 toward PSA and the applicability of the developed electrode for the screening and quantification of PSA in real serum samples were also studied.

A novel HCV electrochemical biosensor based on a polyaniline@Ni-MOF nanocomposite.

Hepatitis-C virus ribonucleic acid (HCV-RNA) recognition and quantification based on real-time polymerase chain reaction (RT-PCR) is key to infection control, management, and response to treatment due to its specificity, sensitivity, and quantification capabilities. However, the high cost, time requirements, and need for sophisticated laboratory infrastructure have limited the use of this method in rapid screening, blood banks, and point-of-care testing (POCT). In this work, a novel label-free electrochemical biosensor constructed using a polyaniline@nickel metal-organic framework (Ni-MOF) nanocomposite was developed for direct detection of unamplified HCV nucleic acid. A robust biosensor was fabricated using smooth layer-by-layer deposition of the polyaniline@Ni-MOF nanocomposite, deoxyribonucleic acid (DNA) probe, and bovine serum albumin (BSA) onto a glassy carbon electrode (GCE) and was subsequently monitored real-time via cyclic voltammetry (CV) and electrochemical impedance spectroscopy (EIS). The sensitivity and specificity of the newly developed biosensor were specifically examined using the EIS approach. The results revealed that the novel biosensor is highly efficient in quantitative sensing of the HCV target in the presence of nonspecific nucleic acids over the range of 1 fM-100 nM with a detection limit of 0.75 fM (at a S/N ratio of 3). To the best of the authors' knowledge, the proposed biosensor is superior to other MOF platforms. These research findings are expected to have a positive influence on the quantitative detection of HCV RNA and other nucleic acids by offering exceptional accuracy and cost effectiveness, especially in low resource countries. Moreover, this biosensor could be simply adopted for full automation and used in point-of-care testing.

Nucleic acids biosensors based on metal-organic framework (MOF): Paving the way to clinical laboratory diagnosis.

Development of ultra-sensitive, high specific and cost-effective nucleic acids (NAs) biosensors is critical for early diagnosis of cancer, genetic diseases and follows up response to treatment. Metal-organic frameworks (MOFs) as sensing materials underwent significant development in recent years due to their unique merits, such as structural diversity, tunable pore scale, large surface area, remarkable adsorption affinities, and good thermal stability. MOFs have shown potential contribution in nucleic acids biosensors research. Herein, a comprehensive overview on NAs biosensors state of the art based on MOFs has been discussed extensively, including different MOFs platforms sensing strategies (fluorescence, electrochemistry, electrochemiluminescence, and colorimetric techniques), their analytical performance and figures of merit in clinical diagnostics, with the future perspective in introducing MOFs in clinical laboratory diagnostics. Moreover, the different MOFs synthesis methods have been highlighted to serve as a guide for the researchers in selecting the appropriate platform that suits their research needs, and applications.

Photodegradation of Microcystin-LR Using Visible Light-Activated C/N-co-Modified Mesoporous TiO2 Photocatalyst.

Microcystin-LR (MC-LR), a potent hepatotoxin produced by the cyanobacteria, is of increasing concern worldwide because of severe and persistent impacts on humans and animals by inhalation and consumption of contaminated waters and food. In this work, MC-LR was removed completely from aqueous solution using visible-light-active C/N-co-modified mesoporous anatase/brookite TiO2 photocatalyst. The co-modified TiO2 nanoparticles were synthesized by a one-pot hydrothermal process, and then calcined at different temperatures (300, 400, and 500 °C). All the obtained TiO2 powders were analyzed by X-ray diffraction (XRD), Raman spectroscopy, transmission electron microscope (TEM), specific surface area (SSA) measurements, ultraviolet-visible diffuse reflectance spectra (UV-vis DRS), X-ray photoelectron spectroscopy (XPS), Fourier transform infrared (FTIR) spectroscopy, and photoluminescence (PL) analysis. It was found that all samples contained mixed-phase TiO2 (anatase and brookite), and the content of brookite decreased with an increase in calcination temperature, as well as the specific surface area and the content of non-metal elements. The effects of initial pH value, the TiO2 content, and MC-LR concentration on the photocatalytic activity were also studied. It was found that the photocatalytic activity of the obtained TiO2 photocatalysts declined with increasing temperature. The complete degradation (100%) of MC-LR (10 mg L-1) was observed within 3 h, using as-synthesized co-modified TiO2 (0.4 g L-1) at pH 4 under visible light. Based on the obtained results, the mechanism of MC-LR degradation has been proposed.

A novel optical approach for determination of prolactin based on Pr-MOF nanofibers.

The analytical quantification and follow-up of the hormone prolactin is very important in clinical diagnosis (e.g., in cases of breast cancer), treatment, and the medical laboratory. The development of a new simple, fast, and less costly method is of considerable importance. Novel praseodymium metal-organic framework nanofibers (Pr-MOF-NFs) were synthesized by a facile and simple method for the determination of human prolactin in serum samples. The Pr-MOF-NFs were well characterized with several spectroscopic tools, such as mass spectrometry, Fourier transform IR spectroscopy, UV-vis spectroscopy, elemental analysis, X-ray diffraction, field-emission scanning electron microscopy combined with energy-dispersive X-ray spectroscopy, and high-resolution transmission electron microscopy. The photoluminescence of Pr-MOF-NFs was investigated, and the results revealed that Pr-MOF-NFs could be used as a sensitive and selective nanofiber optical sensor for the detection of human prolactin. The calibration graph was studied over a wide prolactin concentration range of 0-200 ng/mL, with limits of detection and quantitation of 0.276 and 0.838 ng/mL, respectively, lower than the values mentioned in previous reports. The correlation coefficient was 0.9792. Moreover, the Pr-MOF-NFs were applied successfully for the detection of serum human prolactin at clinically applicable concentrations without interference from several types of hormones and various interfering analytes. Graphical abstract.

A novel, fast, high sensitivity biosensor for supporting therapeutic decisions and onset actions for chest pain cases.

In this work, a novel and promising organic nano linker (NL) was prepared via refluxing 5-aminoisophthalic acid and 1,2-phenylenediamine at 80 °C for 48 h. After that, this linker was reacted with manganese chloride to afford a novel manganese metal-organic framework (Mn-MOF). The produced materials were characterized using 1H-NMR, 13C-NMR, mass spectrometry, elemental analysis, UV, IR, FE-SEM, EDX, TEM, and thermal study. In addition to X-ray diffraction, XPS, magnetic properties and photoluminescence investigation for Mn-MOF. The study was extended to apply Mn-MOF as electroactive material for the preparation of a novel cardiac troponin I (cTn) potentiometric membrane biosensor. The biosensor, based on Mn-MOF with an optimized membrane composition, exhibits a fast, stable and linear-Nernstian response to cTn in the concentration range between 0.01 and 30.0 ng mL-1 with a pH range between 5.6 and 10.1 and a fast response time of 20 ± 5 s. The detection and quantification limits are 0.055 and, 0.168 ng mL-1, respectively. The lifetime of the electrode is between 3-12 week without a significant change in the membrane compositions and the performance characteristics based on the storage conditions. The electrode shows high selectivity towards cTn with respect to common interfering analytes. This approach of Mn-MOF-electrode could be addressed, facilitated and helped an emergency departments (EDs) decision-making in patients with chest pain and early myocardial infarction diagnosis. The future vision is converting the present approach to a small device with satisfactory results which will be used in term of point-of-care testing (POCT) for measuring the most important cardiac blood biomarkers.