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Complex geology and tectonics of the NW Iran, the Caucasus region, and Eastern Turkey, are responsible for the present‐day landscapes of the region. The Aras drainage basin located in Iran, Azerbaijan and Armenia borders, provides an appropriate geographical environment for systematically studying the landforms produced or modified by active tectonic processes. Several morphometric indices were calculated for 114 sub‐basins to assess relative tectonic activity levels. Results were evaluated using two different methods; Index of Active Tectonics (IAT) and Analytical Hierarchy Process (AHP) methods. IAT results show that 2% of the sub‐basins belong to very high, 25% to high, 46% to moderate and 27% to low tectonic activity classes. AHP results, display that 12% of the sub‐basins belong to very high, 25% to high, 43% to moderate, and 20% to low tectonic activity classes. Results of both methods show approximate consistency and indicate that the tectonic activity along the Aras drainage basin is moderate to high and decreases from southwest to the northwest which is probably due to terminating fault branches in young unconsolidated deposits or strain partitioning processes. The major fault zones (e.g., Aras, Pambak–Sevan–Sunik, Akera, and Moghan fault zones) include areas with very high and high tectonic activity classes. Accordingly, the uplift rates have been estimated as >0.5 mm/yr for central and western parts, whereas the uplift rates are relatively less in the eastern part (<0.5 mm/yr). The Aras fault zone includes five active structural segments that the main Aras and Horadiz segments of them show relatively higher tectonic activity. [ABSTRACT FROM AUTHOR]

As one of the most well-known metal nanoparticles, gold nanoparticles (AuNPs) have attracted much attention for the biological applications. This great interest in AuNPs can be attributed to their outstanding physical and chemical properties, such as special optical and electrochemical characteristics, high X-ray attenuation ability, strong X-ray absorption, photothermal effect, stability and biocompatibility. In addition, due to the ease of synthesis and modification of the surface of AuNPs, it is possible to control their shape, size and surface characteristics. All these features suggest that AuNPs can be used for biosensing strategies, drug delivery, photothermal therapy, nanobrachytherapy, enhanced radiotherapy and CT imaging. In addition, they can be used as antibacterial and antifungal agents. This minireview focuses on the key principles, research achievements and new opportunities in the synthesis of AuNPs as well as their biological applications. In fact, the growing progress in the use of AuNPs for the diagnostic and therapeutic applications is described in this survey. Overall, a better understanding of the key aspects of the synthesis methodologies will lead to the development of new protocols that can provide ideas for more cost-effective and reliable approaches to the production of AuNPs. [ABSTRACT FROM AUTHOR]

The aim of this study is to develop a nucleic acid sensor based on piezoelectric crystal microbalance system (QCM) for following hybridization. Piezoelectric quartz crystal surfaces were first treated in a glow–discharge apparatus with ethylene diamine (EDA) plasma at 15 W (discharge power), 2.5 min (incubation time) and 35 ml/min (monomer flow rate) to create amino groups on the crystal surfaces. The thickness of the EDA–plasma film formed was about 43±24 A˚. Then, the amino groups on the crystal surfaces were converted to aldehyde groups by reacting the amino groups with glutaraldehyde (GA) at different conditions. A GA concentration of 2.5% and an incubation time of 2 h were selected as optimal values at this step, corresponding to a GA surface concentration of about 270 ng/cm2. A double strand Oligonucleotides, having one extra base on 5′-end of one of the complementary strands, were immobilized through the amino groups of this base onto the GA-modified crystals. Optimal immobilization conditions were as follows: oligonucleotide concentration: 1 μg/ml; time: 3 h; pH: 9.2 carbonate buffer; ionic strength: 0.1; and temperature: 20 °C. The QCM sensor carrying the covalently bound strand was used in the hybridization experiments, which showed that equilibrium is achieved in about 5 min, and the frequency shift measured is related to the concentration of the target strand to be measured within the medium. [Copyright &y& Elsevier]

The aim of this study is to investigate complexation of metallothionein (MT) with cadmium and zinc ions. An oligopeptide (i.e. Lys-Cys-Thr-Cys-Cys-Ala), a fragment of MT was covalently immobilized onto piezoelectric crystals, which were first treated with ethylene diamine plasma in a glow-discharge apparatus, and then were chemically reacted with glutaraldehyde. Complexation of the immobilized MT with Zn(II) and Cd(II) ions in aqueous media was followed by recording the changes of the frequency shifts of the piezoelectric quartz crystals. The amount of Cd(II) ions interacted with the immobilized MT molecules was the highest at pH 7.4, and decreased with an increase in the pH of the medium, in parallel to the decrease in the amount of immobilized MT. The number of Zn(II) ions interacted with the immobilized MT molecules was higher than the number of Cd(II) ions when the adsorption was from solutions containing a single-metal ion with the same ion concentrations. In consecutive adsorption studies, we observed that the type of metal ions used in the first interaction is important. These experiments showed also that there is an exchange between the metal ions, and competition provokes adsorption of both ions due to synergistic–antagonistic effects. [Copyright &y& Elsevier]

The aim of this study is to develop an immunoaffinity sensor based on piezoelectric crystals for human serum albumin (HSA) detection in aqueous media. Quartz crystals were treated with ethylene diamine (EDA) plasma in a glow-discharge apparatus in order to substitute amino groups on their surfaces. Then anti-HSA antibodies were immobilized via these amino groups by using glutaraldehyde (GA) as cross-linker. Immobilization of the antibody on the quartz crystal was examined for different pH, antibody concentration and treatment time. The optimum conditions for anti-HSA immobilization were evaluated by the measurements of the activity of the surface against HSA. The optimum values of pH, antibody concentration and treatment time were found 6.2, 0.15 mg/ml and 2 h, respectively. For detection of HSA into the solution, two methods were used. In the first (dip and dry) method, the frequency shifts were measured in air after the 1 h interaction of the anti-HSA immobilized crystals with HSA solution. In the other (direct) method, the frequency shifts were followed continuously for 60 min. while the probe was immersed in the HSA solution. An increase for the frequency shifts was observed with increasing of HSA concentration of 16–128 μg/ml. Both the immobilization and antibody-interaction conditions were found important on the extend of these specific interaction. The relations between the HSA concentrations and frequency shifts were exponential in both methods. [Copyright &y& Elsevier]

The outbreak rate of human coronaviruses (CoVs) especially highly pathogenic CoVs is increasing alarmingly. Early detection of these viruses allows treatment interventions to be provided more quickly to people at higher risk, as well as helping to identify asymptomatic carriers and isolate them as quickly as possible, thus preventing the disease transmission chain. The current diagnostic methods such as RT-PCR are not ideal due to high cost, low accuracy, low speed, and probability of false results. Therefore, a reliable and accurate method for the detection of CoVs in biofluids can become a front-line tool in order to deal with the spread of these deadly viruses. Currently, the nanomaterial-based sensing devices for detection of human coronaviruses from laboratory diagnosis to point-of-care (PoC) diagnosis are progressing rapidly. Gold nanoparticles (AuNPs) have revolutionized the field of biosensors because of the outstanding optical and electrochemical properties. In this review paper, a detailed overview of AuNP-based biosensing strategies with the varied transducers (electrochemical, optical, etc.) and also different biomarkers (protein antigens and nucleic acids) was presented for the detection of human coronaviruses including SARS-CoV-2, SARS-CoV-1, and MERS-CoV and lowly pathogenic CoVs. The present review highlights the newest trends in the SARS-CoV-2 nanobiosensors from the beginning of the COVID-19 epidemic until 2022. We hope that the presented examples in this review paper convince readers that AuNPs are a suitable platform for the designing of biosensors. [ABSTRACT FROM AUTHOR]

The effect of surface modification on enhancing the magnetic heating behavior of magnetic nano fluids were investigated, for this purpose Fe3O4 nanoparticles were synthesized using co-precipitation method and surface modification was done using citric acid, ascorbic acid, tetraethyl orthosilicate (TEOS), polyvinyl alcohol (PVA) and polyethylene glycol (PEG). Experimental heating tests using AC magnetic field were done in the frequency of 100 kHz and different magnetic field (H) intensities. Theoretically the specific absorption rate (SAR) in magnetic nano fluids is independent of nanoparticles concentration but the experimental results showed different behavior. The theoretical SAR value @ H = 12kA.m–1 for Nano fluids containing bare Fe3O4 nanoparticles was 11.5 W/g but in experimental tests the obtained value was 9.72 W/g for nano fluid containing 20,000 ppm of dispersed nanoparticles. The experimental SAR calculation was repeated for sample containing 10,000 ppm of nanoparticles and the results showed increase in experimental SAR that is an evidence of nanoparticles agglomeration in higher concentrations. The surface modification has improved the dispersion ability of the nanoparticles. The Ratio of SAR, experimental, 20000ppm to SAR, experimental, 10000ppm was 0.85 for bare Fe3O4 nanoparticles dispersion but in case of surface modified nanoparticles this ratio has increased up to 0.98 that shows lower agglomeration of nanoparticles as a result of surface modification, although on the other hand the surface modification agents were magnetically passive and so it is expected that in constant concentration the SAR for bare Fe3O4 nanoparticles to be higher than this variable for surface modified nanoparticles. At lower concentrations the dispersions containing bare Fe3O4 nanoparticles showed higher SAR values but at higher concentrations the surface modified Fe3O4 nanoparticles showed better results although the active agent amount was lower at them. Finally, it should be noted that the nanoparticles that were surface modified using polymeric agents showed the highest decrease in experimental SAR amounts comparing theoretical results that was because of the large molecules of polymers comparing other implemented surface modification agents. [ABSTRACT FROM AUTHOR]

Abstract In this work, a novel simple and sensitive electrochemical immunosensor was developed based on lactate oxidase as a single electrochemical probe for the detection of carcinoma antigen 125 (CA125). Chitosan-gold nanoparticle/multiwall carbon nanotube/graphene oxide (CS-AuNP/MWCNT/GO) was used as the electrode substrate to increase the electrode specific surface area and improve the protein immobilization and the electrochemical performance of the electrode in terms of oxidation of H 2 O 2. Due to the peroxidase-like function of CS-AuNP, the oxidation peak of H 2 O 2 was observed at a very low potential (0.034 V). The lactate oxidase is used, for the first time, as the single-enzyme label in a sandwich type immunosensor. In the optimum condition, the designed immunosensor exhibited two linear ranges (0.01–0.5 U/mL and 0.5–100 U/mL) by chronoamperometry (CHA). The limit of detection (LOD) was estimated to be 0.002 U/mL. The immunosensor displayed excellent reproducibility and stability with remarkable selectivity in terms of the detection of CA125 even in the human serum samples as compared to the ELISA. In conclusion, the engineered immunosensor is proposed as an ultra-sensitive tool for the detection and monitoring of CA125 in the human serum. Graphical abstract fx1 Highlights • A novel sandwich immunosensor based on lactate oxidase as a single-enzyme label was developed for the detection of CA125. • Gold nanoparticles were synthesized using chitosan as the reducing and capping agent. • The potential of hydrogen peroxide oxidation was reduced to 0.034 V by the chitosan-Au nanoparticles. • CA125 was detected with a low limit of detection of 0.002 U/mL and a linear range of 0.01–100 U/mL. [ABSTRACT FROM AUTHOR]

Herein, aptamer-modified self-propelled nanomotors were used for transportation of human promyelocytic leukemia cells (HL-60) from a human serum sample. For this purpose, the fabricated manganese oxide nanosheets-polyethyleneimine decorated with nickel/gold nanoparticles (MnO 2 -PEI/Ni/Au) as nanomotors were added to a vial containing thiolated aptamer KH1C12 solution as a capture aptamer to attach to the gold nanoparticles on the surface of nanomotors covalently. The aptamer-modified self-propelled nanomotors (aptamer KH1C12 /nanomotors) were then separated by placing the vial in a magnetic stand. The aptamer-modified self-propelled nanomotors were rinsed three times with water to remove the non-attached aptamers. Then, the resulting aptamer KH1C12 /nanomotors were applied for the on-the-fly” transporting of HL-60 cancer cell from a human serum sample. To release of the captured HL-60 cancer cells, the complementary nucleotide sequences of KH1C12 aptamer solution (releasing aptamer) that has a with capture aptamer was added to phosphate buffer solution (1 M, pH 7.4) containing HL-60/aptamer KH1C12 /nanomotors. Because of the high affinity of capture aptamer to complementary nucleotide sequences of aptamer KH1C12 , the HL-60 cancer cells released on the surface of aptamer KH1C12 /nanomotors into the solution. The second goal of the present work was determining the concentration of HL-60 cancer cell in the human serum samples. The electrochemical impedance spectroscopy technique (EIS) was used for the determination of HL-60 cancer cell. The concentration of separated cancer cell was determined by aptamer/gold nanoparticles-poly(3,4-ethylene dioxythiophene) modified GC electrode (GC/PEDOT-Au nano /aptamer KH1C12 ). The proposed aptasensor exhibited a good response to the concentration of HL-60 cancer cells in the range of 2.5 × 10 1 to 5 × 10 5 cells mL -1 with a low limit of detection of 250 cells mL -1 . [ABSTRACT FROM AUTHOR]

Herein, for the first time a visible-light-driven photoelectrochemical (PEC) aptasensor for shrimp tropomyosin determination was fabricated by using graphitic carbon nitride (g-C 3 N 4 ) and titanium dioxide (TiO 2 ) as photoactive nanomaterials, ascorbic acid (AA) as electron donor and ruthenium (III) hexaammine (Ru(NH 3 ) 6 3+ ) as signal enhancer. The surface of an ITO electrode was first modified with g-C 3 N 4 , TiO 2 , and polyethyleneimine (PEI) and then the amine terminal aptamer TROP probe was attached to PEI by the use of glutaraldehyde (GA) as cross-linker. After that, Ru(NH 3 ) 6 3+ was adsorbed on aptamer to enhance the photocurrent signal. The principle of proposed PEC aptasensor is based on the formation of a selective complex between tropomyosin and immobilized aptamer TROP probe on the surface of ITO/g-C 3 N 4 -TiO 2 /PEI/aptamer TROP -Ru(NH3) 6 +3 . After the incubation of tropomyosin with TROP aptamer probe, the photocurrent signal decreased due to releasing adsorbed Ru(NH 3 ) 6 3+ on aptamer and preventing AA from scavenging photogenerated holes to the photoactive modified electrode. Under the optimized conditions, the fabricated PEC aptasensor was used for the determination of shrimp tropomyosin in the concentration range of 1–400 ng mL −1 with a limit of detection of 0.23 ng mL −1 . The proposed PEC aptasensor exhibited high selectivity, sensitivity, and good stability. [ABSTRACT FROM AUTHOR]

Background: Recently, some studies have focused on dendrimer nanopolymers as a magnetic resonance imaging (MRI) contrast agent or a vehicle for gene and drug delivery. Considering the suitable properties of these materials, they are appropriate candidates for coating iron-oxide nanoparticles which are applied in magnetic hyperthermia. To the best of our knowledge, the novelty of this study is the investigation of fourth-generation dendrimer-coated iron-oxide nanoparticles (G4@IONPs) in magnetic hyperthermia and MRI.Methods: IONPs were synthesized via co-precipitation and coated with the fourth generation (G4) of polyamidoamine dendrimer. The cytotoxicity of G4@IONPs with different concentrations was assessed in a human breast cancer cell line (MCF7) and human fibroblast cell line (HDF1). Hemolysis and stability of G4@IONPs were investigated, and in addition, the interaction of these particles with MCF7 cells was assessed by Prussian blue staining. Heat generation and specific absorption rate (SAR) were calculated from measurement and simulation results at 200 and 300 kHz. MCF7 and HDF1 cells were incubated with G4@IONPs for 2 h and then put into the magnetic coil for 120 min. Relaxometry experiments were performed with different concentrations of G4@IONPs with T1- and T2-weighted MR images.Results: The TEM results showed that G4@IONPs were 10 ± 4 nm. The in vitro toxicity assessments showed that synthesized nanoparticles had low toxicity. The viability of MCF7 cells incubated with G4@IONPs decreased significantly after magnetic hyperthermia. In addition, MR imaging revealed that G4@IONPs improved transverse relaxivity (r2) significantly.Conclusions: Our results encouraged the future application of G4@IONPs in magnetic hyperthermia and MR imaging. [ABSTRACT FROM AUTHOR]

Abstract An early on-time detection of breast cancer can effectively affect the outcome of the treatment. Here, we developed an ultrasensitive, simple and reliable immunosensor to detect the lowest alteration of CA 15-3, the standard biomarker of breast cancer patients. The proposed immunosensor was achieved by modification of gold electrode by streptavidin to immobilize the biotinylated anti-CA 15-3 monoclonal antibody (mAb). Bovine serum albumin was used to prevent nonspecific binding. To improve the sensitivity of modified immunosensor, the sandwich signal enhancer consisting of streptavidin-coated magnetic beads conjugated with biotinylated horseradish peroxidase (HRP) and anti-CA 15-3 biotinylated mAb was applied. The electrochemical measurements were obtained in the presence of hydroquinone as a redox agent and H 2 O 2 as the activating agent of HRP. Under optimized condition and using square wave voltammetry, the lower limit of quantification was obtained as 15 × 10−6 U/mL and the linear CA 15-3 concentration range was 50–15 × 10−6 U/mL. While showing significant stability, the immunosensor displayed an excellent sensitivity and specificity for the detection of CA 15-3 even in the human serum as compared to the enzyme-linked immunosorbent assay (ELISA) as a gold standard method. Based on our findings, the engineered immunosensor is proposed as a robust diagnostic tool for the clinical determination of CA 15-3 and other cancer biomarkers. Highlights • An ultrasensitive and reliable immunosensor was developed for the detection of CA 15-3. • An enzymatic sandwich approach was applied to enhance the signals of the biosensor. • A significant lower limit of quantification was achieved. • An excellent performance of proposed immunosensor was observed compared to ELISA as the reference method. [ABSTRACT FROM AUTHOR]

The sensitive quantification of Human Epidermal growth factor Receptor 2 (HER2), as a key prognostic tumor marker, plays a critical role in screening, early diagnosis and management of breast cancer. This paper describes a sandwich-type immunoassay with silver signal enhancement strategy for highly sensitive detection of HER2. For this purpose, the target capturing step was designed by functionalization of 3-aminopropyltrimethoxysilane coated magnetite nanoparticles with antibody (antiHER2/APTMS-Fe 3 O 4 ), as a platform bioconjugate (PB), and immobilized at a bare GCE. Then, in the presence of label-free immunosensor, the PB was covered by magnetic gold nanoparticles self-assembled with thiolated antibodies (antiHER2/Hyd@AuNPs-APTMS-Fe 3 O 4 ) containing chemically reduced silver ions, as a label bioconjugate (LB). Under optimum conditions, a linear relationship between the differential pulse voltammetric (DPV) stripping signal of silver and the logarithm of HER2 concentrations was obtained in the range of 5.0 × 10 −4 -50.0 ng mL −1 (R 2 = 0.9906) with a detection limit of 2.0 × 10 −5 ng mL −1 . The effectiveness of this protocol was evaluated experimentally through employing of designed immunosensor for detection of the serum level of tumor marker. The good consistency of the results with those obtained by the enzyme-linked immunosorbent assay (ELISA) conventional method ( p- value of < 0.05) showed that this immunosensor can be applied for the testing of HER2 in clinical samples of breast cancer patients. [ABSTRACT FROM AUTHOR]

Graphene/cobalt nanocomposites are promising materials for theranostic nanomedicine applications, which are defined as the ability to diagnose, provide targeted therapy and monitor the response to the therapy. In this study, the composites were synthesized via chemical method, using graphene oxide as the source material and assembling cobalt nanoparticles of 15 nm over the surface of graphene sheets. Various characterization techniques were then employed to reveal the morphology, size and structure of the nanocomposites, such as X-ray diffraction analysis, X-ray photoelectron spectroscopy, Fourier transform infrared spectroscopy, high resolution transmission electron microscopy and ultraviolet visible spectroscopy. Using ion-coupled plasma optical emission spectroscopy, cobalt concentration in the nanocomposites was found to be 80%. In addition, cytotoxicity of graphene/cobalt nanocomposites were evaluated using 3-[4,5-dimethylthiazol-2yl]-2,5-diphenyltetrazolium bromide or MTT assay. MTT viability assay exhibited biocompatibility to L929 mouse fibroblasts cells, under a high dose of 100 μg/mL over 24 h. Hyperthermia results showed the superior conversion of electromagnetic energy into heat at 350 kHz frequency for 0.01 and 0.005 g/L of the nanocomposites solution. The measured heat generation and energy transfer results were anticipated by the finite element analysis, conducted for the 3D structure. Magnetic resonance imaging characteristics also showed that negatively charge graphene/cobalt nanocomposites are suitable for T 1 -weighted imaging. [ABSTRACT FROM AUTHOR]

The purpose of this work was to fabricate an electrochemical DNA biosensor for detecting hepatitis B virus. Gold nanorods (GNRs), which are known for their conductivity, were used to increase surface area and consequently increase the immobilization of single-stranded DNA (ss-DNA) on the modified gold electrode. The GNRs were characterized via transmission electron microscopy. The morphology of the gold electrode before and after modification with GNRs was characterized by scanning electron microscopy. Atomic-force microscopy was used to evaluate the morphology of the GNR electrode surface before and after interaction with ss-DNA. Cyclic voltammetry was used to monitor DNA immobilization and hybridization, using [Co(phen)] as an electrochemical indicator. The target DNA sequences were quantified at a linear range from 1.0 × 10 to 10.0 × 10 mol L, with a detection limit of 2.0 × 10 mol L by 3 σ. The biosensor had good specificity for distinguishing complementary DNA in the presence of non-complementary and mismatched DNA sequences. [ABSTRACT FROM AUTHOR]

The development of novel nanoparticles for diagnostic and therapeutic applications has been one of the most crucial challenges in cancer theranostics for the last decades. Herein, we functionalized iron oxide nanoparticles (IONPs) with the fourth generation (G4) of poly amidoamine (PAMAM) dendrimers (G4@IONPs) for magnetic hyperthermia treatment of breast cancer in Bagg albino strain C (BALB/c)mice. The survival of breast cancer cells significantly decreased after incubation with G4@IONPs and exposure to an alternating magnetic field (AMF) due to apoptosis and elevation of Bax (Bcl-2 associated X)/Bcl-2(B-cell lymphoma 2) ratio. After intratumoral injection of G4@IONPs, tumor-bearing BALB/c mice were exposed to AMF for 20 min; this procedure was repeated three times every other day. After the last treatment, tumor size was measured every three days. Histopathological and Immunohistochemical studies were performed on the liver, lung, and tumor tissues in treated and control mice. The results did not show any metastatic cells in the liver and lung tissues in the treatment group, while the control mice tissues contained metastatic breast cancer cells. Furthermore, the findings of the present study showed that magnetic hyperthermia treatment inhibited tumor growth by increasing cancer cell apoptosis, as well as reducing the tumor angiogenesis. [ABSTRACT FROM AUTHOR]

In the current study, we report on the design and development of a novel electrochemical immunosensor for the detection of cancer antigen 125 (CA125) oncomarker. Polyamidoamine/gold nanoparticles (PAMAM/AuNPs) were used to increase the conductivity and enhance the number of antibodies (Abs) immobilized on the electrode surface. Three-dimensional reduced graphene oxide-multiwall carbon nanotubes (3DrGO-MWCNTs) were used to modify the glassy carbon electrode to improve the electrode conductivity and specific surface area. Ab and toluidine blue attached to O -succinyl-chitosan-magnetic nanoparticles (Suc-CS@MNPs) as a tracer. The poor solubility of chitosan (CS) was improved by succinic anhydride using a novel modification method. Under optimum condition, the developed immunosensor exhibited a wide linear range (0.0005–75 U/mL) and an excellent limit of detection around 6 μU/mL. The reliability of the engineered immunosensor in detecting CA125 was verified by standard addition recovery method, which was further compared to enzyme-linked immunosorbent assay (ELISA). The proposed immunosensor exhibited excellent stability, high selectivity and sensitivity, and good reproducibility. Based on the great performance of the engineered immunosensor, it is proposed as a robust and reliable diagnostic tool for the detection of CA125 in the clinic. Image 1 • An immunosensor was developed for detecting CA125 with a wide linear range (0.0005–75 U/mL) and an excellent LOD (6 μU/mL). • PAMAM/AuNPs were synthesized through a one-step method using PAMAM as a stabilizing and reducing agent. • Chitosan water solubility in natural pH was increased using a novel modification method. • Succinyl-chitosan-coated magnetic nanoparticles were synthesized with good dispersity and high surface functional groups. [ABSTRACT FROM AUTHOR]

• Use of reduced graphene oxide as a photothermal label for lateral flow assay. • Reduced graphene oxide shows higher photothermal properties than graphene oxide. • Sensitivity improvement of a lateral flow assay by photothermal quantification. Lateral flow immunoassay (LFA) is a well-known point-of-care technology for the detection of various analytes. However, low sensitivity and lack of quantitative results are some of its critical drawbacks. Here we report a photothermal enhanced lateral flow sensor on the basis of the photothermal properties of reduced graphene oxide (rGO) for the detection of E-coli O157:H7 as a model pathogen. The calibration curve of the photothermal method exhibited a linear range from 5 × 10⁵ to 5 × 10⁷ CFU/ml with a correlation coefficient of R2 = 0.96 and a regression equation of y = 8.1x-43 for standard bacteria solutions in phosphate buffer. The limit of detection was ∼5 × 10⁵ CFU/ml for standard bacteria solutions, which was a 10-fold enhancement in sensitivity compared to the qualitative results. Specificity experiments showed that the photothermal method can only detect the target bacteria among 6 types of bacteria strains. It was confirmed that the developed technique could be a highly potential method for the rapid detection field because it can provide fast quantitative results with improved sensitivity. [ABSTRACT FROM AUTHOR]

Objective: In recently air pollution is motivated by many agents and in the aerosol we can distinguish smallest airways, composed by biological particles, such as pollen grains and particulate of anthropogenic origin. During the last decade the size, shape, composition, sources and effect of these particle matters (PM) on human health have been studied by microscopic methods. Atomic force microscopy (AFM) is therefore a valuable complementary microscopy technique for the comparative study of the pollen grains surface morphology. The main goals of this research we investigated to characterize the elemental differences in the composition of the airborne ash pollen exine wall and to describe the particulate matter found adhered to this pollen in the Tehran, capital city of Iran, using an Energy Dispersive X-Ray analysis (EDX) on the SEM and Atomic force microscopy (AFM). Material and Methods: The first stage, pollen grains were collected in pollutant area (Tehran regions) and nonpollutant area (Parand city near the Tehran).Then used SEM/EDX for pollen grains analysis and advantages of two samples for AFM for the imaging of reside in the sticky PM on the ash pollen surface of the high spatial resolution, compared with SEM images, and the unique three-dimensional rendition of the exine surface topography, which avoids cross sectioning of the samples. Results: Images showed of exine units from the tectum of polluted and non- polluted pollen were done by AFM. These units of polluted sample showed were recorded adhered the PM in exine surface as being 250 to 300nm wide. This particle matter size is lower than PM2.5. We have obtained atomically resolved images on single aerosol particles in Tehran at the first on environmental biological samples. Conclusion: Our results showed AFM images method can be used for identifying pollen surface contamination and evaluation of PM size more exact and showed good agreement with light and electron microscopy micrographs. [ABSTRACT FROM AUTHOR]