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Search Results (1,744)

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17 pages, 9133 KiB  
Article
Comparative Analysis of Piezoelectric Transducers for Low-Power Systems: A Focus on Vibration Energy Harvesting
by Iusley S. Lacerda, Antonio A. Silva, Eisenhawer M. Fernandes, Richard Senko, Andersson G. Oliveira, João M. P. Q. Delgado, Diego D. S. Diniz, Maria J. Figueiredo and Antonio G. B. Lima
Appl. Sci. 2024, 14(20), 9451; https://doi.org/10.3390/app14209451 (registering DOI) - 16 Oct 2024
Abstract
With advances in technology, the generation of electrical energy through the harvesting of energies dissipated in the form of mechanical vibration, known as power harvesting, has received increasing attention in recent decades. It is undoubtedly an interesting means to power systems with low [...] Read more.
With advances in technology, the generation of electrical energy through the harvesting of energies dissipated in the form of mechanical vibration, known as power harvesting, has received increasing attention in recent decades. It is undoubtedly an interesting means to power systems with low energy consumption. This research aims to evaluate an energy generation system based on the piezoelectric effect activated by mechanical excitation and develop a system capable of powering devices and sensors for temperature monitoring in a practical situation, such as in an engine room, aiming to ensure its safe operation. Two transducers subjected to vibrational excitation were evaluated, and then an energy generation system using a buck DC-DC converter circuit was assessed. The transducer was connected to the input of the board, the microcontroller to the output, and the LM35 temperature sensor along with the battery was used to ensure the circuit’s autonomy. Additionally, the Attiny85 microcontroller was programmed to perform temperature monitoring tasks in a continuous low-energy-consumption mode. The obtained spectral analysis results showed a maximum generation power of 8.88 mW for the PZT-5H transducer and 3.3 mW for the P5-13B transducer. The use of LTC3588-1 increased the autonomy of the monitoring system by 64.3% and reduced the system’s usage time in cases of temperature anomalies by 50%. Full article
(This article belongs to the Topic Power System Protection)
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<p>System models and output: system models. (<b>a</b>) Electromechanical collection system, (<b>b</b>) electric power harvesting circuit, and (<b>c</b>) system behavior at resonance.</p>
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<p>General model of the buck DC-DC circuit.</p>
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<p>Typical scheme of an energy harvester’s system.</p>
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<p>Diagram of the experimental setup.</p>
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<p>Schematic of the circuits: (<b>a</b>) Case I—resistive and (<b>b</b>) Case II—bridge rectifier circuit.</p>
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<p>Validation of the natural frequencies of PZTs: (<b>a</b>) analytical and (<b>b</b>) experimental.</p>
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<p>Resistance vs. voltage curves—resistive circuit; (<b>a</b>) PZT-5H and (<b>b</b>) P5-13B.</p>
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<p>Resistance vs. power curves—resistive circuit: (<b>a</b>) PZT-5H and (<b>b</b>) P5-13B.</p>
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<p>Resistance vs. voltage curves—bridge rectifier circuit: (<b>a</b>) PZT-5H and (<b>b</b>) P5-13B.</p>
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<p>Resistance vs. power curves—bridge rectifier circuit: (<b>a</b>) PZT-5H and (<b>b</b>) P5-13B.</p>
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<p>Frequency vs. power curves—DC-DC buck circuit: (<b>a</b>) PZT-5H and (<b>b</b>) P5-13B.</p>
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<p>Assembly of the monitoring system.</p>
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<p>Operation of the temperature monitoring system. (<b>a</b>) Temperature of LM35 and (<b>b</b>) state of ATtiny85.</p>
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<p>Autonomy of the monitoring system.</p>
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12 pages, 1754 KiB  
Article
Validation of a Remote Sampling Sensor for Measuring Urine Volume and Nitrogen Concentration in Grazing Dairy Cattle
by Mancoba C. Mangwe, Nigel Beale, Paige Beckett, Lucas Tey, Jeffery Curtis, Riki Burgess and Racheal H. Bryant
Animals 2024, 14(20), 2977; https://doi.org/10.3390/ani14202977 (registering DOI) - 15 Oct 2024
Viewed by 219
Abstract
The purpose of this research was to validate a urine sensor (Lincoln University PEETER V2.0, Canterbury, New Zealand) that records the time and volume of urination events for dairy cows in addition to collecting a proportional urine sample from all urination events. Sixteen [...] Read more.
The purpose of this research was to validate a urine sensor (Lincoln University PEETER V2.0, Canterbury, New Zealand) that records the time and volume of urination events for dairy cows in addition to collecting a proportional urine sample from all urination events. Sixteen multiparous Holstein × Jersey mid-lactating cows (101 ± 5 days in milk, 498 ± 24.2 kg body weight, 26.2 ± 3.07 kg/d milk yield; mean ± standard deviation) were allocated herbage diets ranging in protein and sodium content to generate a range of urine volumes and urine nitrogen (UN) concentrations. Total collection of individual urination events occurred during a 72-h measurement period where PEETER V2.0 sensors were attached to cows. A mixed model ANOVA using lme4 package (version 1.1-35.5) in R (version 4.3.3) were used to compare the means. The average urine event size was 2.65 ± 1.1 L for total collection by observers and 2.68 ± 1.1 L as recorded by the sensor (mean ± standard deviation; p = 0.730). The urine nitrogen concentration was 5.76 ± 1.2 g N/L for samples collected by observers and 5.85 ± 1.3 g N/L for the samples collected by the sensor (p = 0.583). The calculated UN excretion was 156 ± 45.1 g/day for direct measurements and 162 ± 40.0 g/day for the sensor (p = 0.539. Contrasts with simultaneously measured data were undertaken using Lin’s Concordance Correlation Coefficient (CCC) and a Pearson correlation coefficient (r). Correlations between the actual values and sensor values were strong, with little to moderate variability in the urine volume (CCC = 0.936, r = 0.937; n = 222), UN concentration (CCC = 0.840, r = 0.837, n = 48) and total UN excretion (CCC = 0.827, r = 0.836, n = 24). Considering the findings, the PEETER V2.0 urine sensor has the potential to reliably measure urine volumes and UN concentrations for estimations of the UN excretion of dairy cattle under grazing systems. Full article
(This article belongs to the Section Cattle)
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<p>PEETER V2.0 urine sensor.</p>
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<p>Set up and attachment of sensors to animals during the validation experiment.</p>
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<p>The regression line comparing the urinary nitrogen (UN) concentration (g N/L) of PEETER’s V2.0 acidified and non-acidified urine samples. Each back dot represents one paired UN concentration. The blue solid line is the regression line (y = 0.141 + 0.988x, R<sup>2</sup> = 0.93), with the 95% CI being shown by the shaded band. Each data point represents one paired UN concentration.</p>
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<p>Regression analysis comparing the urine nitrogen (UN) concentration (g N/L) from the PEETER V2.0 urine sensors and the first, middle and final third of the actual urine volume. Each back dot represents one paired UN concentration. The blue solid line is the regression line (first third; y = 1.43 + 0.791x, R<sup>2</sup> = 0.67; second third; y = 2.09 + 0.629x, R<sup>2</sup> = 0.40; y = 2.80 + 0.545x, R<sup>2</sup> = 0.39), with the 95% confidence interval being shown by the shaded band.</p>
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16 pages, 2049 KiB  
Article
Potentiometric Electronic Tongue for the Evaluation of Multiple-Unit Pellet Sprinkle Formulations of Rosuvastatin Calcium
by Patrycja Ciosek-Skibińska, Krzysztof Cal, Daniel Zakowiecki and Joanna Lenik
Materials 2024, 17(20), 5016; https://doi.org/10.3390/ma17205016 - 14 Oct 2024
Viewed by 358
Abstract
Sprinkle formulations represent an interesting genre of medicinal products. A frequent problem, however, is the need to mask the unpleasant taste of these drug substances. In the present work, we propose the use of a novel sensor array based on solid-state ion-selective electrodes [...] Read more.
Sprinkle formulations represent an interesting genre of medicinal products. A frequent problem, however, is the need to mask the unpleasant taste of these drug substances. In the present work, we propose the use of a novel sensor array based on solid-state ion-selective electrodes to evaluate the taste-masking efficiency of rosuvastatin (ROS) sprinkle formulations. Eight Multiple Unit Pellet Systems (MUPSs) were analyzed at two different doses (API_50) and (API_10), as well as pure Active Pharmaceutical Ingredient (API) as a bitter standard. Calcium phosphate-based starter pellets were coated with the mixture containing rosuvastatin. Some of them were additionally coated with hydroxypropyl methylcellulose, which was intended to separate the bitter substance and prevent it from coming into contact with the taste buds. The sensor array consisted of 16 prepared sensors with a polymer membrane that had a different selectivity towards rosuvastatin calcium. The main analytical parameters (sensitivity, selectivity, response time, pH dependence of potential, drift of potential, lifetime) of the constructed ion-selective electrodes sensitive for rosuvastatin were determined. The signals from the sensors array recorded during the experiments were processed using Principal Component Analysis (PCA). The results obtained, i.e., the chemical images of the pharmaceutical samples, indicated that the electronic tongue composed of the developed solid-state electrodes provided respective attributes as sensor signals, enabling both of various kinds of ROS pellets to be distinguished and their similarity to ROS bitterness standards to be tested. Full article
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<p>Rosuvastatin((3R,5S,6E)-7-[4-(4-fluorophenyl)-2-(N-ethylmethanesulfonamido)-6-(propan-2-yl)pyrimidin-5-yl]-3,5-dihydroxyhept-6-ene acid).</p>
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<p>Schematic presentation of ISE and potentiometric sensor array.</p>
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<p>Dynamic response for electrodes no. 5, 6, 10 (<b>a</b>) and for electrodes no. 11 and 12 (<b>b</b>).</p>
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<p>Potential drift of the selected electrodes in 2 × 10<sup>−4</sup> mol L<sup>−1</sup> rosuvastatin solution during one hour.</p>
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<p>Effect of the pH on the potential response of the selected electrodes in 2 × 10<sup>−4</sup> mol L<sup>−1</sup> of rosuvastatin solution.</p>
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<p>Stability of sensitivity of the electrode no. 11 in time.</p>
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<p>PCA score plot of electronic tongue results for the studied formulations (A–H). and pure API (API_10 and API_50).</p>
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<p>PC1 values of the electronic tongue results showing gradually changing characteristics of the studied formulations (A–H), compared to pure API standards (API_10 and API_50).</p>
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<p>HCA showing the discrimination of ROS samples. Dashed lines represent a division into 2 groups at variance weighted distance &gt; 30, and 3 groups at variance weighted distance ~20.</p>
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24 pages, 5046 KiB  
Article
Ultrasensitive Electrochemical Detection of Salmonella typhimurium in Food Matrices Using Surface-Modified Bacterial Cellulose with Immobilized Phage Particles
by Wajid Hussain, Huan Wang, Xiaohan Yang, Muhammad Wajid Ullah, Jawad Hussain, Najeeb Ullah, Mazhar Ul-Islam, Mohamed F. Awad and Shenqi Wang
Biosensors 2024, 14(10), 500; https://doi.org/10.3390/bios14100500 - 14 Oct 2024
Viewed by 548
Abstract
The rapid and sensitive detection of Salmonella typhimurium in food matrices is crucial for ensuring food safety. This study presents the development of an ultrasensitive electrochemical biosensor using surface-modified bacterial cellulose (BC) integrated with polypyrrole (Ppy) and reduced graphene oxide (RGO), further functionalized [...] Read more.
The rapid and sensitive detection of Salmonella typhimurium in food matrices is crucial for ensuring food safety. This study presents the development of an ultrasensitive electrochemical biosensor using surface-modified bacterial cellulose (BC) integrated with polypyrrole (Ppy) and reduced graphene oxide (RGO), further functionalized with immobilized S. typhimurium-specific phage particles. The BC substrate, with its ultra-fibrous and porous structure, was modified through in situ oxidative polymerization of Ppy and RGO, resulting in a highly conductive and flexible biointerface. The immobilization of phages onto this composite was facilitated by electrostatic interactions between the polycationic Ppy and the negatively charged phage capsid heads, optimizing phage orientation and enhancing bacterial capture efficiency. Morphological and chemical characterization confirmed the successful fabrication and phage immobilization. The biosensor demonstrated a detection limit of 1 CFU/mL for S. typhimurium in phosphate-buffered saline (PBS), with a linear detection range spanning 100 to 107 CFU/mL. In real samples, the sensor achieved detection limits of 5 CFU/mL in milk and 3 CFU/mL in chicken, with a linear detection range spanning 100 to 106 CFU/mL, maintaining high accuracy and reproducibility. The biosensor also effectively discriminated between live and dead bacterial cells, demonstrating its potential in real-world food safety applications. The biosensor performed excellently over a wide pH range (4–10) and remained stable for up to six weeks. Overall, the developed BC/Ppy/RGO–phage biosensor offers a promising tool for the rapid, sensitive, and selective detection of S. typhimurium, with robust performance across different food matrices. Full article
(This article belongs to the Special Issue Advancements in Biosensors for Foodborne Pathogens Detection)
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<p>Fabrication of BC/Ppy/RGO composite. Immobilization of the <span class="html-italic">S. typhimurium</span>-specific phages to develop a BC/Ppy/RGO-phage biointerface for the electrochemical detection of <span class="html-italic">S. typhi</span> in milk and chicken samples using DPV.</p>
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<p>FE-SEM investigation of pristine BC before and after modification with Ppy, RGO, and immobilized phages. (<b>A</b>,<b>B</b>) Pristine BC at different magnifications, (<b>C</b>) Ppy polymerization on BC, (<b>D</b>,<b>E</b>) BC/Ppy/RGO at different magnifications, and (<b>F</b>,<b>G</b>) show the immobalized phages on BC/Ppy/RGO biointerface and red color arrows represent the individual phage particles. (<b>H</b>) Magnified image of the phage particles attached to the BC/Ppy/RGO shown in rectangular and the yellow circles represent individual phage particle. Elemental mapping images of BC/Ppy/RGO (<b>I</b>), carbon (<b>J</b>), oxygen (<b>K</b>), and nitrogen (<b>L</b>).</p>
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<p>Characterization of modified BC composites and BC-phage biointerfaces. (<b>A</b>) XRD patterns of GO, RGO, BC, Ppy, BC/Ppy, and BC/Ppy/RGO and physiological changes of GO in RGO; (<b>B</b>) FT-IR spectra of BC, BC/Ppy, BC/Ppy/RGO; (<b>C</b>) BC/MWCNT-COOH/Ppy; (<b>D</b>) BC/MWCNT-COOH/Ppy-phage. (<b>C</b>) Selected magnified area in (<b>B</b>) FT-IR-fingerprint of BC/Ppy, BC/Ppy/RGO, and BC/Ppy/RGO-phage ranging from 1800 to 800 cm<sup>−1</sup>. (<b>D</b>) XPS wide-scan patterns of BC, BC/Ppy, BC/Ppy/RGO, and BC/Ppy/RGO–phage. (<b>E</b>) N 1s core-level spectra of BC/MWCNTS-COOH/Ppy-phage biointerface.</p>
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<p>Plaque assays for anti-<span class="html-italic">Salmonella</span> potential of BC-based biointerfaces. (<b>A</b>–<b>E</b>) Plaque formation of materials such as BC, BC/Ppy, and BC/Ppy/RGO (I–III). (<b>F</b>–<b>J</b>) Plaque formation after immobilization of phages on different BC-based bio-interfaces such as BC, BC/Ppy, and BC/Ppy/RGO (I–III)–phage. (<b>K</b>–<b>O</b>) Sonicated interfaces with immobilized phages and their lytic activity.</p>
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<p>Infectious dynamics of phages immobilized on surface-modified BC against <span class="html-italic">S. typhimuruim</span> and their density under confocal microscopy. (<b>A</b>) Growth reduction curves in terms of optical density (OD<sub>600</sub>) of <span class="html-italic">S. typhi</span>, with free phages and phages immobilized on BC, BC/Ppy, BC/Ppy/RGO (I-III), (<b>B</b>) pristine BC, and (<b>C</b>) immobilized phages on BC (in-focus). (<b>D</b>–<b>F</b>) Density of stained phage particles (in-focus), while the composite is out of focus; (<b>D</b>) immobilized phages on pristine BC, (<b>E</b>) immobilized phages on BC/Ppy, and (<b>F</b>) immobilized phages on BC/Ppy/RGO.</p>
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<p>Electrochemical characterization of the surface BC-based modified electrodes for <span class="html-italic">S. typhi</span> detection. CV curves of different BC and BC-modified electrodes in cyclic voltammograms of the Fe(CN)<sub>6</sub><sup>3−</sup>/Fe(CN)<sub>6</sub><sup>4−</sup> redox system, such as BC/Ppy, and different concentrations of RGO and immobilized phages, including (<b>A</b>) BC/Ppy/RGO (I)-phage, (<b>B</b>) BC/Ppy/RGO (II)-phage, and (<b>C</b>) BC/Ppy/RGO (III)-phage. DPV-based current responses of different concentrations of RGO with Ppy and phages (<b>D</b>) BC/Ppy/RGO (I)-phage, (<b>E</b>) BC/Ppy/RGO (II)-phage, and (<b>F</b>) BC/Ppy/RGO (III)-phage.</p>
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<p>Specificity, live/dead cell discrimination, and practical applications of the BC/Ppy/RGO-phage biosensor for electrochemical detection of <span class="html-italic">S. typhi</span>. (<b>A</b>) DPV current response towards detected <span class="html-italic">S. typhi</span> in PBS, (<b>B</b>) linear range of <span class="html-italic">S. typhi</span> detection in PBS, (<b>C</b>) specificity of the biosensor, (<b>D</b>) biosensor discrimination for live, dead, and mixture of live/dead <span class="html-italic">S. typhi</span>, (<b>E</b>) DPV curves of the detected <span class="html-italic">S. typhi</span> in milk, (<b>F</b>) linear range of <span class="html-italic">S. typhi</span> in milk, (<b>G</b>) detection of <span class="html-italic">S. typhi</span> in chicken samples at different concentrations, and (<b>H</b>) linear range of detection in chicken. The standard deviations of triplicate analyses for each experiment are indicated by error bars.</p>
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15 pages, 6318 KiB  
Article
Snowflake Iron Oxide Architectures: Synthesis and Electrochemical Applications
by Anna Kusior, Olga Waś, Zuzanna Liczberska, Julia Łacic and Piotr Jeleń
Molecules 2024, 29(20), 4859; https://doi.org/10.3390/molecules29204859 - 14 Oct 2024
Viewed by 441
Abstract
The synthesis and characterization of iron oxide nanostructures, specifically snowflake architecture, are investigated for their potential applications in electrochemical sensing systems. A Raman spectroscopy analysis reveals phase diversity in the synthesized powders. The pH of the synthesis affects the formation of the hematite [...] Read more.
The synthesis and characterization of iron oxide nanostructures, specifically snowflake architecture, are investigated for their potential applications in electrochemical sensing systems. A Raman spectroscopy analysis reveals phase diversity in the synthesized powders. The pH of the synthesis affects the formation of the hematite (α-Fe2O3) and goethite (α-FeOOH). Scanning electron microscopy (SEM) images confirm the distinct morphologies of the particles, which are selectively obtained through recrystallization during the elongated reaction time. An electrochemical analysis demonstrates the differing behaviors of the particles, with synthesis pH affecting the electrochemical activity and surface area differently for each shape. Cyclic voltammetry measurements reveal reversible dopamine detection processes, with snowflake iron oxide showing lower detection limits than a mixture of snowflakes and cube-like particles. This research contributes to understanding the relationship between iron oxide nanomaterials’ structural, morphological, and electrochemical properties. It offers practical insights into their potential applications in sensor technology, particularly dopamine detection, with implications for biomedical and environmental monitoring. Full article
(This article belongs to the Special Issue Nanomaterials for Electrocatalytic Applications)
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<p>The SEM images of the obtained iron oxide nanostructures (S series) after 24, 48, and 72 h from the solution with 8.5 pH.</p>
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<p>The SEM images of the obtained iron oxide nanostructures (P series) after 24, 48, and 72 h from the solution with 12 pH.</p>
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<p>The XRD analysis of the iron oxide-based material obtained (<b>a</b>) at pH = 8.5 and (<b>b</b>) at pH = 12. Caption 1 is assigned to the tetrairon(III) hexacyanoferrate(II) 9.3-hydrate 4.7-(dideuriohydrate), and 2 to tetrairon(III) tris(hexacyanoferrate(II)) tetradecahydrate.</p>
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<p>The Raman spectra of the obtained iron oxide nanostructures (S series) after 24, 48, and 72 h from the solution with 8.5 pH. The scheme of the obtained structures at various synthesis times.</p>
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<p>The Raman spectra of the obtained iron oxide nanostructures (P series) after 24, 48, and 72 h from the solution with 12 pH. The scheme of the obtained structures at various synthesis times.</p>
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<p>Current–voltage dependence for the modified carbon electrodes (<b>a</b>) in the 0.1 M KCl + 3 mM [Fe(CN)<sub>6</sub>]<sup>3−/4−</sup>, and comparison with the SPE (<b>b</b>). Data were recorded at various scan rates from 10 to 2000 mVs<sup>−1</sup>.</p>
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<p>Current–voltage dependence for the modified carbon electrodes in the 0.1 M KCl + 3 mM [Fe(CN)<sub>6</sub>]<sup>3−/4−</sup> solution. Data were recorded at various scan rates from 10 to 2000 mVs<sup>−1</sup>.</p>
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<p>(<b>a</b>) The plot of the anodic peak current as a function of the square root of the scan rate ν<sup>0.5</sup> for modified electrodes with (<b>b</b>) electrochemically active surface area, EASA, compared to the SPE electrode.</p>
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<p>(<b>a</b>) Comparison of cyclic voltammograms in various dopamine concentrations (from 1 to 10 mM solution in PBS environment) for modified screen-printed electrodes by the obtained iron oxide powders. (<b>b</b>) The recorded data at 5 mM DA for the pure SPE and S2-modified electrode. Data were recorded at 50 mVs<sup>−1</sup>.</p>
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<p>(<b>a</b>) Calibration curves for series S modified screen-printed electrodes in the presence of various concentrations of dopamine (from 1 to 10 mM solution) with (<b>b</b>) LOD and LOQ parameters of the SPE-modified electrodes. The square, circle, and triangle symbols correspond to the dopamine changes for S1, S2, and S3 samples.</p>
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<p>Comparison of cyclic voltammograms in various dopamine concentrations (from 1 to 10 mM solution in PBS environment) for modified screen-printed electrodes by the obtained iron oxide powders. Data were recorded at 50 mVs<sup>−1</sup>.</p>
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25 pages, 9538 KiB  
Article
Internet of Things-Driven Precision in Fish Farming: A Deep Dive into Automated Temperature, Oxygen, and pH Regulation
by Md. Naymul Islam Nayoun, Syed Akhter Hossain, Karim Mohammed Rezaul, Kazy Noor e Alam Siddiquee, Md. Shabiul Islam and Tajnuva Jannat
Computers 2024, 13(10), 267; https://doi.org/10.3390/computers13100267 - 12 Oct 2024
Viewed by 518
Abstract
The research introduces a revolutionary Internet of Things (IoT)-based system for fish farming, designed to significantly enhance efficiency and cost-effectiveness. By integrating the NodeMcu12E ESP8266 microcontroller, this system automates the management of critical water quality parameters such as pH, temperature, and oxygen levels, [...] Read more.
The research introduces a revolutionary Internet of Things (IoT)-based system for fish farming, designed to significantly enhance efficiency and cost-effectiveness. By integrating the NodeMcu12E ESP8266 microcontroller, this system automates the management of critical water quality parameters such as pH, temperature, and oxygen levels, essential for fostering optimal fish growth conditions and minimizing mortality rates. The core of this innovation lies in its intelligent monitoring and control mechanism, which not only supports accelerated fish development but also ensures the robustness of the farming process through automated adjustments whenever the monitored parameters deviate from desired thresholds. This smart fish farming solution features an Arduino IoT cloud-based framework, offering a user-friendly web interface that enables fish farmers to remotely monitor and manage their operations from any global location. This aspect of the system emphasizes the importance of efficient information management and the transformation of sensor data into actionable insights, thereby reducing the need for constant human oversight and significantly increasing operational reliability. The autonomous functionality of the system is a key highlight, designed to persist in adjusting the environmental conditions within the fish farm until the optimal parameters are restored. This capability greatly diminishes the risks associated with manual monitoring and adjustments, allowing even those with limited expertise in aquaculture to achieve high levels of production efficiency and sustainability. By leveraging data-driven technologies and IoT innovations, this study not only addresses the immediate needs of the fish farming industry but also contributes to solving the broader global challenge of protein production. It presents a scalable and accessible approach to modern aquaculture, empowering stakeholders to maximize output and minimize risks associated with fish farming, thereby paving the way for a more sustainable and efficient future in the global food supply. Full article
(This article belongs to the Section Internet of Things (IoT) and Industrial IoT)
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<p>A block diagram of the proposed system.</p>
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<p>An illustration of the circuit design of the envisioned system.</p>
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<p>The working process of the proposed system.</p>
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<p>A photograph of the prototype.</p>
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<p>Real-time pH value observation.</p>
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<p>Real-time temperature value observation.</p>
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<p>Real-time oxygen value observation.</p>
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<p>pH calibration steps.</p>
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<p>pH in normal water.</p>
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<p>pH in acidic water.</p>
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<p>Total data cycle process in different stages.</p>
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<p>Morning pH value observation.</p>
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<p>Morning temperature value observation.</p>
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<p>Morning oxygen value observation.</p>
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<p>pH value observation at noon.</p>
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<p>Temperature value observation at noon.</p>
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<p>Oxygen value observation at noon.</p>
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<p>pH value observation in the evening.</p>
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<p>Temperature value observation in the evening.</p>
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<p>Oxygen value observation in the evening.</p>
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<p>pH value observation at night.</p>
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<p>Temperature value observation at night.</p>
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<p>Oxygen value observation at night.</p>
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25 pages, 14822 KiB  
Review
Tear-Based Ocular Wearable Biosensors for Human Health Monitoring
by Arunima Rajan, Jithin Vishnu and Balakrishnan Shankar
Biosensors 2024, 14(10), 483; https://doi.org/10.3390/bios14100483 - 8 Oct 2024
Viewed by 824
Abstract
Wearable tear-based biosensors have garnered substantial interest for real time monitoring with an emphasis on personalized health care. These biosensors utilize major tear biomarkers such as proteins, lipids, metabolites, and electrolytes for the detection and recording of stable biological signals in a non-invasive [...] Read more.
Wearable tear-based biosensors have garnered substantial interest for real time monitoring with an emphasis on personalized health care. These biosensors utilize major tear biomarkers such as proteins, lipids, metabolites, and electrolytes for the detection and recording of stable biological signals in a non-invasive manner. The present comprehensive review delves deep into the tear composition along with potential biomarkers that can identify, monitor, and predict certain ocular diseases such as dry eye disease, conjunctivitis, eye-related infections, as well as diabetes mellitus. Recent technologies in tear-based wearable point-of-care medical devices, specifically the state-of-the-art and prospects of glucose, pH, lactate, protein, lipid, and electrolyte sensing from tear are discussed. Finally, the review addresses the existing challenges associated with the widespread application of tear-based sensors, which will pave the way for advanced scientific research and development of such non-invasive health monitoring devices. Full article
(This article belongs to the Special Issue Recent Advances in Wearable Biosensors for Human Health Monitoring)
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<p>Schematic illustration of tear-based biosensors showing contact lens, flexible eye patch, and eye glass-based biosensors coupled with the real time data acquisition through a smartphone camera.</p>
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<p>(<b>i</b>) Structure of three layered tear film constituting of inside mucin, intermediate aqueous, and exterior lipid layer (Reprinted with permission from [<a href="#B52-biosensors-14-00483" class="html-bibr">52</a>]), tear fluid collection steps using (<b>ii</b>) Schirmer’s test strip and (<b>iii</b>) microcapillary tube methods (Reprinted with permission from [<a href="#B53-biosensors-14-00483" class="html-bibr">53</a>]).</p>
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<p>(<b>a</b>) Preclinical evaluation of NovioSense tear glucose sensor in sheep, (<b>b</b>) clinical trial–phase II evaluation in human eye using tear glucose sensor, (<b>c</b>) NovioSense device relative response to physiological interferences and glucose at varying concentration (reprinted with permission from [<a href="#B119-biosensors-14-00483" class="html-bibr">119</a>]), (<b>d</b>) digital image of the sensor layer transferred onto a dome-shaped PDMS substrate, (<b>e</b>) image of the sensor placed on an artificial eye, (<b>f</b>) schematic representation of optical transmittance testing, (<b>g</b>) optical images (upper) and fluorescent images (lower) of in vitro cytotoxicity evaluation of contact lenses using human umbilical vein endothelial cells at different days (green and red fluorescence shows live and dead cells respectively), (<b>h</b>) average cell viability (percentage of live cells remain similar for 7 days), and (<b>i</b>) number of cells present (increasing number of live cells indicates cell culture reliability) (reprinted with permission from [<a href="#B125-biosensors-14-00483" class="html-bibr">125</a>].</p>
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<p>(<b>a</b>) Photograph of the microfluidic contact lens with colorimetric sensor (scale bar—5 mm), (<b>b</b>) smartphone camera imaging the color variation of sensor (scale bar—1 cm), (<b>c</b>) colorimetric characterization of pH sensor ranging from dark yellow at pH 6 to blue at pH 8 (reprinted with permission from [<a href="#B147-biosensors-14-00483" class="html-bibr">147</a>]), (<b>d</b>–<b>g</b>) mechanically flexible eye patch sensor depicting tensile, torsional, and bending nature, (<b>h</b>) assay process to trigger the chromogenic reaction using the flowing tear stimulated by dacryagogue followed by the removal of eye patch sensor after 30 s for data collection and analysis (reprinted with permission from [<a href="#B151-biosensors-14-00483" class="html-bibr">151</a>]), and (<b>i</b>) multilayered structure of crescent shaped PDMS microfluidic colorimetric sensing patch attached under the right eye of the human face followed by color data acquisition with the aid of a smartphone camera assisted by deep learning artificial intelligence (reprinted with permission from [<a href="#B17-biosensors-14-00483" class="html-bibr">17</a>]).</p>
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<p>(<b>a</b>) Fabrication process of l-lactate sensor on PET substrate molded into a contact-lens shape, (<b>b</b>) flat substrate comprising of sensing unit, interconnects, and electrodes connected to external potentiostat (CE—counter electrode, WE—working electrode, and RE—reference electrode), (<b>c</b>) fabricated contact lens sensor, (<b>d</b>) current response over time for dual sensor setup (S—functionalized sensor, C—control sensor, and D—differential signal), (<b>e</b>) optical image of a lens with the dual sensors configuration, (<b>f</b>) temperature stability of l-lactate sensor where current measurement was performed against l-lactate concentration for a varying temperature of 20–45 °C (reprinted with permission from [<a href="#B100-biosensors-14-00483" class="html-bibr">100</a>]), and (<b>g</b>) tear lactate sensor fabrication and assembly. Tear lactate test strip inserts to a pen-like meter collects tear in contact with conjunctiva using a filter paper. Sensor comprised of carbon working electrode (WE), carbon counter electrode (CE), and silver/silver chloride (Ag/AgCl) reference electrode (RE) (Reprinted with permission from [<a href="#B158-biosensors-14-00483" class="html-bibr">158</a>]).</p>
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28 pages, 2541 KiB  
Review
Intelligent Rapid Asexual Propagation Technology—A Novel Aeroponics Propagation Approach
by Lingdi Tang, Ain-ul-Abad Syed, Ali Raza Otho, Abdul Rahim Junejo, Mazhar Hussain Tunio, Li Hao, Mian Noor Hussain Asghar Ali, Sheeraz Aleem Brohi, Sohail Ahmed Otho and Jamshed Ali Channa
Agronomy 2024, 14(10), 2289; https://doi.org/10.3390/agronomy14102289 - 5 Oct 2024
Viewed by 676
Abstract
Various rapid propagation strategies have been discovered, which has facilitated large-scale plant reproduction and cultivar development. These methods, in many plant species, are used to rapidly generate large quantities (900 mini-tubers/m2) of high-quality propagule (free from contamination) at a relatively low [...] Read more.
Various rapid propagation strategies have been discovered, which has facilitated large-scale plant reproduction and cultivar development. These methods, in many plant species, are used to rapidly generate large quantities (900 mini-tubers/m2) of high-quality propagule (free from contamination) at a relatively low cost in a small space. They are also used for plant preservation. This review article aims to provide potential applications for regeneration and clonal propagation. Plant propagation using advanced agrotechnology, such as aeroponics, is becoming increasingly popular among academics and industrialists. The advancement of asexual aeroponic propagation has been achieved through advancements in monitoring and control systems using IoT and smart sensor technology. New sensor technology systems have gained substantial interest in agriculture in recent years. It is used in agriculture to precisely arrange various operations and objectives while harnessing limited resources with minimal human intervention. Modern intelligent technologies and control systems simplify sensor data collection, making it more efficient than manual data collection, which can be slow and prone to errors. Specific ambient variables like temperature, humidity, light intensity, stock solution concentrations (nutrient water), EC (electrical conductivity), pH values, CO2 content, and atomization parameters (frequency and interval) are collected more effectively through these systems. The use of intelligent technologies provides complete control over the system. When combined with IoT, it aids in boosting crop quality and yield while also lowering production costs and providing data directly to tablets and smartphones in aeroponic propagation systems. It can potentially increase the system’s productivity and usefulness compared to the older manual monitoring and operating methods. Full article
(This article belongs to the Special Issue Smart Farming Technologies for Sustainable Agriculture—2nd Edition)
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<p>Plant tissue culture cycle: 1. Bud; 2. Leaf; 3. Root system; 4. Stem; 5. Plant tissue sample; 6. Tissue sample in culture; 7. Forming of callus; 8. Separation and multiplication; 9. Regenerated plantlet; 10. Plantlet hardening.</p>
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<p>Schematic view of aeroponic system: 1. Plant; 2. Plant supporting raft; 3. Nutrient mist; 4. Misting nozzle; 5. Growth chamber; 6. Nutrient solution; 7. Plant holder; 8. Timer; 9. Nutrient dropdown; 10. Pump.</p>
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<p>Rapid aeroponic propagation machine control system process.</p>
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<p>Smart control and monitoring asexual aeroponic propagation system components and purpose of application.</p>
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<p>Temperature and humidity sensors used in rapid asexual aeroponics propagation technique.</p>
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<p>Working mechanism of NDIR sensor (<b>a</b>), NDIR CO<sub>2</sub> sensor (<b>b</b>), CDS carbon dioxide sensor (<b>c</b>).</p>
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<p>Types of sensors for water level used in rapid aeroponic propagation technique.</p>
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9 pages, 3864 KiB  
Communication
Photoelectric H2S Sensing Based on Electrospun Hollow CuO-SnO2 Nanotubes at Room Temperature
by Cheng Zou, Cheng Peng, Xiaopeng She, Mengqing Wang, Bo Peng and Yong Zhou
Sensors 2024, 24(19), 6420; https://doi.org/10.3390/s24196420 - 3 Oct 2024
Viewed by 522
Abstract
Pure tin oxide (SnO2) as a typical conductometric hydrogen sulfide (H2S) gas-sensing material always suffers from limited sensitivity, elevated operation temperature, and poor selectivity. To overcome these hindrances, in this work, hollow CuO-SnO2 nanotubes were successfully electrospun for [...] Read more.
Pure tin oxide (SnO2) as a typical conductometric hydrogen sulfide (H2S) gas-sensing material always suffers from limited sensitivity, elevated operation temperature, and poor selectivity. To overcome these hindrances, in this work, hollow CuO-SnO2 nanotubes were successfully electrospun for room-temperature (25 °C) trace H2S detection under blue light activation. Among all SnO2-based candidates, a pure SnO2 sensor showed no signal, even toward 10 ppm, while the 1% CuO-SnO2 sensor achieved a limit of detection (LoD) value of 2.5 ppm, a large response of 4.7, and a short response/recovery time of 21/61 s toward 10 ppm H2S, as well as nice repeatability, long-term stability, and selectivity. This excellent performance could be ascribed to the one-dimensional (1D) hollow nanostructure, abundant p-n heterojunctions, and the photoelectric effect of the CuO-SnO2 nanotubes. The proposed design strategies cater to the demanding requirements of high sensitivity and low power consumption in future application scenarios such as Internet of Things and smart optoelectronic systems. Full article
(This article belongs to the Special Issue Electrospun Composite Nanofibers: Sensing and Biosensing Applications)
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<p>Schematic illustration of (<b>a</b>) material preparation, (<b>b</b>) test apparatus, and (<b>c</b>) IDE device.</p>
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<p>XRD patterns for pure SnO<sub>2</sub> and 1% CuO-SnO<sub>2</sub> samples.</p>
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<p>(<b>a</b>,<b>d</b>) SEM images, (<b>b</b>,<b>e</b>) element mapping, and (<b>c</b>,<b>f</b>) TEM images of pure SnO<sub>2</sub> and CuO-SnO<sub>2</sub> samples.</p>
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<p><b>HRTEM images</b> of (<b>a</b>) pure SnO<sub>2</sub> and (<b>b</b>) 1% CuO-SnO<sub>2</sub> samples.</p>
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<p>The performance of the 1% CuO-SnO<sub>2</sub> sensor toward H<sub>2</sub>S gas at room temperature: (<b>a</b>) real-time response, (<b>b</b>) mean response, and (<b>c</b>) response and recovery times for 10 ppm H<sub>2</sub>S under different visible light activations, as well as (<b>d</b>) dynamic response as function of H<sub>2</sub>S concentration and (<b>e</b>) long-term stability with 10 ppm H<sub>2</sub>S under blue light illumination.</p>
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<p>(<b>a</b>) The cross-sensitivity of the 1% CuO−SnO<sub>2</sub> sensor toward different gasses under blue light activation, the energy level relationship (<b>b</b>) before and (<b>c</b>) after intimate contact between both components, and (<b>d</b>) the band diagram of CuO−SnO<sub>2</sub> heterojunctions after H<sub>2</sub>S adsorption under blue light activation.</p>
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15 pages, 6864 KiB  
Article
Advanced Electrochemical Monitoring of Carbendazim Fungicide in Foods Using Interfacial Superassembly of NRPC/NiMn Frameworks
by Shakila Parveen Asrafali, Thirukumaran Periyasamy, Seong Cheol Kim and Jaewoong Lee
Biosensors 2024, 14(10), 474; https://doi.org/10.3390/bios14100474 - 2 Oct 2024
Viewed by 593
Abstract
A simple, sensitive and reliable sensing system based on nitrogen-rich porous carbon (NRPC) and transition metals, NRPC/Ni, NRPC/Mn and NRPC/NiMn was developed and successfully applied as electrode materials for the quantitative determination of carbendazim (CBZ). The synergistic effect of NRPC and bimetals with [...] Read more.
A simple, sensitive and reliable sensing system based on nitrogen-rich porous carbon (NRPC) and transition metals, NRPC/Ni, NRPC/Mn and NRPC/NiMn was developed and successfully applied as electrode materials for the quantitative determination of carbendazim (CBZ). The synergistic effect of NRPC and bimetals with acceptable pore structure together with flower-like morphology resulted in producing a highly conductive and interconnected network in NRPC/NiMn@GCE, which significantly enhanced the detection performance of CBZ. The electrochemical behavior investigated by cyclic voltammetry (CV) showed improved CBZ detection for NRPC/NiMn, due to the controlled adsorption/diffusion process of CBZ by the NRPC/NiMn@GCE electrode. The influences of various factors such as pH, NRPC/NiMn concentration, CBZ concentration and scan rate were studied. Under optimal conditions, 0.1 M phosphate-buffered saline (PBS) with a pH of 7.0 containing 30 µg/mL NRPC/NiMn, a favourable linear range detection of CBZ from 5 to 50 µM was obtained. Moreover, a chronoamperometric analysis showed excellent repeatability, reproducibility and anti-interfering ability of the fabricated NRPC/NiMn@GCE sensor. Furthermore, the sensor showed satisfactory results for CBZ detection in real samples with acceptable recoveries of 96.40–104.98% and low RSD values of 0.25–3.45%. Full article
(This article belongs to the Special Issue Electrochemical Biosensing Platforms for Food, Drug and Health Safety)
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<p>Synthesis of NRPC, NRPC/Mn, NRPC/Ni and NRPC/NiMn.</p>
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<p>XPS spectrum of NRPC/NiMn showing the (<b>a</b>) survey spectrum and (<b>b</b>–<b>f</b>) deconvoluted spectrum for each element.</p>
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<p>SEM images of NRPC, NRPC/Mn, NRPC/Ni and NRPC/NiMn at different magnifications.</p>
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<p>(<b>a</b>–<b>c</b>) TEM images of NRPC/NiMn, (<b>d</b>) SAED pattern, (<b>e</b>–<b>j</b>) elemental mapping and (<b>k</b>) EDX spectrum.</p>
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<p>Electrochemical studies showing (<b>a</b>,<b>b</b>) CV, (<b>c</b>) EIS, (<b>d</b>,<b>e</b>) effect of pH, (<b>f</b>,<b>g</b>) effect of material concentration and (<b>h</b>,<b>i</b>) effect of analyte concentration of the prepared materials.</p>
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<p>Electrochemical studies showing (<b>a</b>,<b>b</b>) effect of scan rate, (<b>c</b>) mechanism of carbendazim detection, (<b>d</b>,<b>e</b>) repeatability, (<b>f</b>) reproducibility, (<b>g</b>) stability and (<b>h</b>,<b>i</b>) anti-interfering ability of NRPC/NiMn.</p>
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<p>Real-time analysis of NRPC/NiMn sensor: (<b>a</b>) Apple, (<b>b</b>) Carrot, (<b>c</b>) Grapes, (<b>d</b>) Blueberry, (<b>e</b>) Broccoli and (<b>f</b>) Tap water.</p>
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14 pages, 28439 KiB  
Article
A Multi-Channel Urine Sensing Detection System Based on Creatinine, Uric Acid, and pH
by Qiya Gao, Jie Fu, Fangying Xiong, Jiawang Wang, Ziyue Qin and Shuang Li
Biosensors 2024, 14(10), 473; https://doi.org/10.3390/bios14100473 - 2 Oct 2024
Viewed by 507
Abstract
Urine analysis represents a crucial diagnostic technique employed in clinical laboratories. Creatinine and uric acid in urine are essential biomarkers in the human body and are widely utilized in clinical analysis. Research has demonstrated a correlation between the normal physiological concentrations of creatinine [...] Read more.
Urine analysis represents a crucial diagnostic technique employed in clinical laboratories. Creatinine and uric acid in urine are essential biomarkers in the human body and are widely utilized in clinical analysis. Research has demonstrated a correlation between the normal physiological concentrations of creatinine and uric acid in urine and an increased risk of hypertension, cardiovascular diseases, and kidney disease. Furthermore, the pH of urine indicates the body’s metabolic processes and homeostatic balance. In this study, an integrated multi-channel electrochemical sensing system was developed, combining electrochemical analysis techniques, microelectronic design, and nanomaterials. The architecture of an intelligent medical detection system and the production of an interactive interface for smartphones were accomplished. Initially, multi-channel selective electrodes were designed for creatinine, uric acid, and pH detection. The detection range was 10 nM to 100 μM for creatinine, 100 μM to 500 μM for uric acid, and 4 to 9 for pH. Furthermore, interference experiments were also conducted to verify the specificity of the sensors. Subsequently, multi-channel double-sided sensing electrodes and function-integrated hardware were designed, with the standard equations of target analytes stored in the system’s read-only memory. Moreover, a WeChat mini-program platform was developed for smartphone interaction, enabling off-body detection and real-time display of target analytes through smartphones. Finally, the aforementioned electrochemical detection electrodes were integrated with the smart sensing system and wirelessly interfaced with smartphones, allowing for intelligent real-time detection in primary healthcare and individual household settings. Full article
(This article belongs to the Special Issue State-of-the-Art Biosensors in China (2nd Edition))
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<p>Multi-channel urine sensing system. (<b>a</b>) Schematic diagram of the modification process of dual-sided sensing electrodes for a multi-channel urine sensing system. (<b>b</b>) Schematic diagram of the multi-channel urine sensing system structure. (<b>c</b>) Multi-channel urine sensing printed circuit board and its various parts’ functions.</p>
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<p>Characterization of multi-channel sensing electrodes. (<b>a</b>) SEM characterization of the bare electrode; (<b>b</b>) TEM characterization of N-Gr; (<b>c</b>) SEM characterization of the AuNPs/N-Gr electrode; electrochemical characterization of (<b>d</b>) the creatinine sensing electrode, (<b>e</b>) the uric acid sensing electrode, and (<b>f</b>) the pH sensing electrode.</p>
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<p>Detection results of multi-channel sensors. (<b>a</b>) Sensing detection results for creatinine, with a detection range of 10 nM to 100 μM. (<b>b</b>) Sensing detection results for uric acid, with a detection range of 100 μM to 500 μM. (<b>c</b>) Sensing detection results for pH, with forward and reverse detection in solutions ranging from pH 4 to 9. The standard fitting curves for sensing detection are shown in (<b>d</b>) for creatinine, (<b>e</b>) for uric acid, and (<b>f</b>) for pH.</p>
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<p>Interference test of multi-channel sensors. (<b>a</b>) DPV curve of the creatinine sensor for detecting different interferents. (<b>b</b>) DPV curve of the uric acid sensor for detecting different interferents. (<b>c</b>) OCP curve of the pH sensor detecting different interferents. Bar graph of the interference test signal for the creatinine sensor (<b>d</b>) and uric acid sensor (<b>e</b>).</p>
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<p>(<b>a</b>) WeChat mini-program interface. (<b>b</b>) Displayed results of multi-channel sensing detection on the WeChat mini-program. Sensing detection results of creatinine (<b>c</b>), uric acid (<b>d</b>), and pH (<b>e</b>) in artificial urine.</p>
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13 pages, 8819 KiB  
Article
Optimized Drop-Casted Polyaniline Thin Films for High-Sensitivity Electrochemical and Optical pH Sensors
by Bruna Eduarda Darolt Mücke, Beatriz Cotting Rossignatti, Luis Miguel Gomes Abegão, Martin Schwellberger Barbosa and Hugo José Nogueira Pedroza Dias Mello
Polymers 2024, 16(19), 2789; https://doi.org/10.3390/polym16192789 - 1 Oct 2024
Viewed by 567
Abstract
Conducting polymers used in chemical sensors are attractive because of their ability to confer reversible properties controlled by the doping/de-doping process. Polyaniline (PANI) is one of the most prominent materials used due to its ease of synthesis, tailored properties, and higher stability. Here, [...] Read more.
Conducting polymers used in chemical sensors are attractive because of their ability to confer reversible properties controlled by the doping/de-doping process. Polyaniline (PANI) is one of the most prominent materials used due to its ease of synthesis, tailored properties, and higher stability. Here, PANI thin films deposited by the drop-casting method on fluorine-doped tin oxide (FTO) substrates were used in electrochemical and optical sensors for pH measurement. The response of the devices was correlated with the deposition parameters; namely, the volume of deposition solution dropped on the substrate and the concentration of the solution, which was determined by the weight ratio of polymer to solvent. The characterisation of the samples aimed to determine the structure–property relationship of the films and showed that the chemical properties, oxidation states, and protonation level are similar for all samples, as concluded from the cyclic voltammetry and UV–VIS spectroscopic analysis. The sensing performance of the PANI film is correlated with its relative physical properties, thickness, and surface roughness. The highest electrochemical sensitivity obtained was 127.3 ± 6.2 mV/pH, twice the Nernst limit—the highest pH sensitivity reported to our knowledge—from the thicker and rougher sample. The highest optical sensitivity, 0.45 ± 0.05 1/pH, was obtained from a less rough sample, which is desirable as it reduces light scattering and sample oxidation. The results presented demonstrate the importance of understanding the structure–property relationship of materials for optimised sensors and their potential applications where high-sensitivity pH measurement is required. Full article
(This article belongs to the Special Issue Polymer Materials for Sensors and Actuators)
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<p>The electrochemical (<b>a</b>) and spectroscopic (<b>b</b>) characterisations of the set of PANI thin films deposited with a volume of deposition solution dropped on the substrate equal to 20 μL. The weight ratio of polymer–solvent for the samples is 1:100, 1:200, 1:300, 1:400 and 1:500.</p>
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<p>The electrochemical pH sensor for drop-casted PANI thin films. The CVs for different pH buffer electrolytes for sample PANI20500 are shown in (<b>a</b>). Calibration curves plotted as <span class="html-italic">E</span><sub>1/2</sub> vs. pH of the set of PANI thin films deposited with volume of deposition solution equal to 20 μL (<b>b</b>). The sensitivities of the samples are shown in (<b>c</b>). The sensitivities were calculated from the redox potential calibration curve, and the highest value obtained was 127.3 ± 6.2 mV/pH for sample PANI20100. The linearities of the samples are shown in (<b>d</b>). The lowest linearity obtained was 98.3% in PANI15100.</p>
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<p>The optical pH sensor for drop-casted PANI thin films. The normalized absorbance spectra for different pH buffer electrolytes for sample PANI20500 are shown in (<b>a</b>). The sensitivities of the samples are shown in (<b>b</b>). The sensitivities were calculated from the calibration curve of integrated normalized absorbance, and the highest value obtained was 0.45 ± 0.05 1/pH in PANI20500. The linearities of the samples are shown in (<b>c</b>). The lowest linearity obtained was 81% in PANI05100.</p>
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<p>The thickness (<b>a</b>) and surface roughness, (<b>b</b>) R<sub>Q</sub> (root mean square deviation) of the drop-casted PANI thin films. PANI20100 is the thicker and rougher sample.</p>
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<p>SEM characterization of the drop-casted PANI thin films deposited with 20 μL of solution. Samples deposited from solution with weight ratio: 1:100, 1:200, 1:300, 1:400 and 1:500 in (<b>a</b>–<b>e</b>), respectively.</p>
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<p>Optical (left <span class="html-italic">y</span>-axis) and electrochemical (right <span class="html-italic">y</span>-axis) sensitivity are shown according to the roughness of the PANI thin films deposited with 20 μL of solution.</p>
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13 pages, 7015 KiB  
Article
Theoretical Study of the Adsorption and Sensing Properties of Cr-Doped SnP3 Monolayer for Dissolved Characteristic Gases in Oil
by Chengjiang Wang, Xiangjia Liu, Feiyang Xie, Xuze Wang and Pengdi Zhang
Materials 2024, 17(19), 4812; https://doi.org/10.3390/ma17194812 - 30 Sep 2024
Viewed by 329
Abstract
Dissolved gas analysis (DGA) is a vital method for the online detection of transformer operation state. The adsorption performance of a SnP3 monolayer modified by transition metal Cr regarding six characteristic gases (CO, C2H4, C2H2 [...] Read more.
Dissolved gas analysis (DGA) is a vital method for the online detection of transformer operation state. The adsorption performance of a SnP3 monolayer modified by transition metal Cr regarding six characteristic gases (CO, C2H4, C2H2, CH4, H2, C2H6) dissolved in oil was studied. The study reveals the relevant adsorption and gas-sensing response mechanisms through calculations of the adsorption energy, density of states, differential charge density, energy gap, and recovery time. The results display a considerable increase in the adsorption effect of the Cr-SnP3 monolayer on six gases. The CO, C2H2, and C2H4 gases lead to chemical adsorption, and the CH4, H2, and C2H6 gases lead to physical adsorption. Combined with the recovery time, the Cr-SnP3 monolayer has a strong adsorption effect on CO and C2H2 gases at normal temperatures and even high temperatures, and the adsorption is stable. C2H4 gas can be rapidly desorbed from the Cr-SnP3 monolayer at 398 K. Therefore, the Cr-SnP3 monolayer can be expected to serve as a CO and C2H2 gas adsorbent and a resistive gas sensor for C2H4 gas. This research offers a theoretical foundation for the development of the Cr-SnP3 monolayer in gas-sensitive materials. Full article
(This article belongs to the Section Materials Simulation and Design)
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<p>Intrinsic SnP<sub>3</sub> monolayer and four different doping sites.</p>
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<p>Structures of (<b>a</b>) CO, (<b>b</b>) C<sub>2</sub>H<sub>4</sub>, (<b>c</b>) C<sub>2</sub>H<sub>2</sub>, (<b>d</b>) CH<sub>4</sub>, (<b>e</b>) H<sub>2</sub>, and (<b>f</b>) C<sub>2</sub>H<sub>6</sub> molecules.</p>
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<p>(<b>a</b>) Top view and (<b>b</b>) side view of the optimal doping structure of Cr-SnP<sub>3</sub>.</p>
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<p>(<b>a</b>) TDOS of intrinsic SnP<sub>3</sub> and Cr-SnP<sub>3</sub> monolayer; (<b>b</b>) PDOS of Cr-SnP<sub>3</sub> monolayer.</p>
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<p>The optimal adsorption model of (<b>a</b>) CO, (<b>b</b>) C<sub>2</sub>H<sub>4</sub>, (<b>c</b>) C<sub>2</sub>H<sub>2</sub>, (<b>d</b>) CH<sub>4</sub>, (<b>e</b>) H<sub>2</sub>, and (<b>f</b>) C<sub>2</sub>H<sub>6</sub> molecules on an intrinsic SnP<sub>3</sub> monolayer.</p>
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<p>The optimal adsorption model of (<b>a</b>) CO, (<b>b</b>) C<sub>2</sub>H<sub>4</sub>, (<b>c</b>) C<sub>2</sub>H<sub>2</sub>, (<b>d</b>) CH<sub>4</sub>, (<b>e</b>) H<sub>2</sub>, and (<b>f</b>) C<sub>2</sub>H<sub>6</sub> molecules on the Cr-SnP<sub>3</sub> monolayer.</p>
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<p>TDOS and PDOS of (<b>a1</b>,<b>a2</b>) CO, (<b>b1</b>,<b>b2</b>) C<sub>2</sub>H<sub>4</sub>, (<b>c1</b>,<b>c2</b>) C<sub>2</sub>H<sub>2</sub>, (<b>d1</b>,<b>d2</b>) CH<sub>4</sub>, (<b>e1</b>,<b>e2</b>) H<sub>2</sub>, and (<b>f1</b>,<b>f2</b>) C<sub>2</sub>H<sub>6</sub> adsorption systems.</p>
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<p>Differential charge density distributions of (<b>a</b>) CO, (<b>b</b>) C<sub>2</sub>H<sub>4</sub>, (<b>c</b>) C<sub>2</sub>H<sub>2</sub>, (<b>d</b>) CH<sub>4</sub>, (<b>e</b>) H<sub>2</sub>, and (<b>f</b>) C<sub>2</sub>H<sub>6</sub> molecules on the Cr-SnP<sub>3</sub> monolayer.</p>
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<p>HOMO and LUMO distributions of Cr-SnP<sub>3</sub> monolayer and six gas-molecule-adsorption systems.</p>
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<p>Recovery time of C<sub>2</sub>H<sub>2</sub>, CO, and C<sub>2</sub>H<sub>4</sub>.</p>
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<p>Comparison of the adsorption energy of SnP<sub>3</sub>, Pd-SnP<sub>3</sub>, and Cr-SnP<sub>3</sub> monolayers on dissolved gas in oil.</p>
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21 pages, 4361 KiB  
Article
Curcumin-Based Molecularly Imprinted Polymer Electropolymerized on Single-Use Graphite Electrode for Dipyridamole Analysis
by Daniel Preda, Gabriel Lucian Radu, Emilia-Elena Iorgulescu, Mihaela-Carmen Cheregi and Iulia Gabriela David
Molecules 2024, 29(19), 4630; https://doi.org/10.3390/molecules29194630 - 29 Sep 2024
Viewed by 396
Abstract
A new molecularly imprinted polymer (MIP)-based disposable electrochemical sensor for dipyridamole (DIP) determination was obtained. The sensor was rapidly prepared by potentiodynamic electrochemical polymerization on a pencil graphite electrode (PGE) using curcumin (CUR) as a functional monomer and DIP as a template molecule. [...] Read more.
A new molecularly imprinted polymer (MIP)-based disposable electrochemical sensor for dipyridamole (DIP) determination was obtained. The sensor was rapidly prepared by potentiodynamic electrochemical polymerization on a pencil graphite electrode (PGE) using curcumin (CUR) as a functional monomer and DIP as a template molecule. After the optimization of the conditions (pH, monomer–template ratio, scan rate, number of cyclic voltammetric cycles applied in the electro-polymerization process and extraction time of the template molecule) for MIP formation, DIP voltammetric behavior at the modified electrode (MIP_PGE) was investigated. DIP oxidation took place in a pH-dependent, irreversible mixed diffusion-adsorption controlled process. Differential pulse voltammetry (DPV) and adsorptive stripping differential pulse voltammetry (AdSDPV) were used to quantify DIP from pharmaceutical and tap water samples. Under optimized conditions (Britton–Robinson buffer at pH = 3.29), the obtained linear ranges were 5.00 × 10−8–1.00 × 10−5 mol/L and 5.00 × 10−9–1.00 × 10−7 mol/L DIP for DPV and AdSDPV, respectively. The limits of detection of the methods were 1.47 × 10−8 mol/L for DPV and 3.96 × 10−9 mol/L DIP for AdSDPV. Full article
(This article belongs to the Section Analytical Chemistry)
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Figure 1

Figure 1
<p>Structural formula of dipyridamole (DIP).</p>
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<p>CV curves recorded at PGE for (<b>a</b>) 5.00 × 10<sup>−4</sup> mol/L CUR and (<b>b</b>) mixture of 5.00 × 10<sup>−4</sup> mol/L CUR and 2.50 × 10<sup>−5</sup> mol/L DIP in 0.2 mol/L NaOH solution, scan rate 0.100 V/s. Inset: expanded section of the potential window containing the CUR and DIP signals.</p>
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<p>Impedance spectra recorded and fitted for all the tested working electrodes. To obtain the Nyquist plot, 1.00 × 10<sup>−3</sup> mol/L [Fe(CN)<sub>6</sub>]<sup>4−</sup>/[Fe(CN<sub>6</sub>)]<sup>3−</sup> in acetate buffer solution with pH = 4.50 was used (DC potential of 0.230 V and frequency in the range 0.1 Hz–10.0 kHz). The equivalent circuit employed for the fitting curve is presented schematically above.</p>
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<p>(<b>a</b>) DP voltammograms recorded at MIP_PGE for 5.00 × 10<sup>−5</sup> mol/L DIP in BRB solutions with different pH values and (<b>b</b>) the dependencies of DIP oxidation peak potential (E<sub>p</sub>)/current (I<sub>p</sub>) recorded by DPV at MIP_PGE on the pH of the supporting electrolyte.</p>
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<p>(<b>a</b>) CV curves recorded at different scan rates at MIP_PGE for 1.50 × 10<sup>−4</sup> mol/L DIP in BRB solution with pH = 3.29; and the dependencies (<b>b</b>) I<sub>p</sub> = f(v), (<b>c</b>) I<sub>p</sub> = f (v<sup>1/2</sup>) and (<b>d</b>) log I<sub>p</sub> = f (log v).</p>
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<p>(<b>a</b>) CV curves recorded at different scan rates at MIP_PGE for 1.50 × 10<sup>−4</sup> mol/L DIP in BRB solution with pH = 3.29; and the dependencies (<b>b</b>) I<sub>p</sub> = f(v), (<b>c</b>) I<sub>p</sub> = f (v<sup>1/2</sup>) and (<b>d</b>) log I<sub>p</sub> = f (log v).</p>
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<p>DP voltammograms recorded at MIP_PGE for BRB pH 3.29 solutions containing different DIP concentrations between (<b>a</b>) 5.00 × 10<sup>−8</sup>–5.00 × 10<sup>−6</sup> and (<b>b</b>) 1.00 × 10<sup>−5</sup>–1.00 × 10<sup>−4</sup> mol/L.</p>
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<p>AdSDP voltammograms recorded at MIP_PGE for different DIP concentrations in BRB solution with pH = 3.29; t<sub>acc</sub> 30 s; E<sub>acc</sub> −0.400 V.</p>
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<p>The variation of the anodic peak current recorded at MIP_PGE for 1.00 × 10<sup>−5</sup> mol/L DIP in BRB solution with pH = 3.29 at different periods of time, including 0, 24, 48 and 72 h after the sensor preparation.</p>
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<p>DPV peak currents recorded at MIP_PGE for 2.00 × 10<sup>−6</sup> mol/L DIP in BRB solution with pH = 3.29, without and with a 50-fold excess of different possible interfering species.</p>
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<p>(<b>a</b>) DP voltammograms for 10 mL DIPIRIDAMOL tablets working solution in BRB pH = 3.29, recorded at MIP_PGE. The initial sample and the 3 × 0.025 mL addition of 1.00 × 10<sup>−3</sup> mol/L DIP is also presented; (<b>b</b>) the dependence of the DIP oxidation signal on the C<sub>add</sub> DIP.</p>
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<p>Possible mechanism for DIP electrooxidation at MIP_PGE in BRB solution with pH = 3.29.</p>
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<p>Schematic representation of the steps involved in the preparation of the MIP_PGE.</p>
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19 pages, 5553 KiB  
Article
Developing 1,4-Diethyl-1,2,3,4-tetrahydroquinoxalin-substituted Fluorogens Based on GFP Chromophore for Endoplasmic Reticulum and Lysosome Staining
by Daniil I. Rudik, Maxim M. Perfilov, Anatolii I. Sokolov, Cheng Chen, Nadezhda S. Baleeva, Ivan N. Myasnyanko, Alexander S. Mishin, Chong Fang, Yulia A. Bogdanova and Mikhail S. Baranov
Int. J. Mol. Sci. 2024, 25(19), 10448; https://doi.org/10.3390/ijms251910448 - 27 Sep 2024
Viewed by 516
Abstract
In the present study, we demonstrated that the introduction of a 1,4-diethyl-1,2,3,4-tetrahydroquinoxalin moiety into the arylidene part of GFP chromophore-derived compounds results in the formation of environment-sensitive fluorogens. The rationally designed and synthesized compounds exhibit remarkable solvent- and pH-dependence in fluorescence intensity. The [...] Read more.
In the present study, we demonstrated that the introduction of a 1,4-diethyl-1,2,3,4-tetrahydroquinoxalin moiety into the arylidene part of GFP chromophore-derived compounds results in the formation of environment-sensitive fluorogens. The rationally designed and synthesized compounds exhibit remarkable solvent- and pH-dependence in fluorescence intensity. The solvent-dependent variation in fluorescence quantum yield makes it possible to use some of the proposed compounds as polarity sensors suitable for selective endoplasmic reticulum fluorescent labeling in living cells. Moreover, the pH-dependent emission intensity variation of other fluorogens makes them selective fluorescent labels for the lysosomes in living cells. Full article
(This article belongs to the Section Molecular Biology)
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<p>Normalized absorption and emission spectra of compound <b>2</b>.</p>
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<p>Fluorescence of compounds <b>3</b>, <b>4</b>, <b>7a</b>, <b>7b</b>, and <b>7c</b> at various pH. (<b>A</b>) Normalized fluorescence intensity at various pH for compounds <b>3</b> (540 nm), <b>4</b> (530 nm), <b>7a</b> (630 nm), <b>7b</b> (660 nm), and <b>7c</b> (640 nm). (<b>B</b>–<b>F</b>) Emission spectra at various pH for compounds <b>3</b> ((<b>B</b>), excitation 460 nm), <b>4</b> ((<b>C</b>), excitation 460 nm), <b>7a</b> ((<b>D</b>), excitation 480 nm), <b>7b</b> ((<b>E</b>), excitation 490 nm), and <b>7c</b> ((<b>F</b>), excitation 480 nm).</p>
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<p>Live-cell imaging with chromophore <b>2</b> using confocal microscopy. ER-staining of (<b>A</b>) 3T3 NiH and (<b>B</b>) h9c2 cells by 5 μM of <b>2</b> (added from 1 mM DMSO stock solution, incubation 1 min). Images were pseudo-colored using with Fiji Lookup Tables “NanoJ-Orange” grading. (<b>C</b>–<b>E</b>) Co-localization analysis of 5 μM of chromophore <b>2</b> in HeLa Kyoto cells compared to 1 μM ER-tracker Red (Invitrogen, added from 1 mM stock in DMSO, incubation 5 min). Pearson co-localization analysis followed by Costes randomized test resulted in 0.70. (<b>E</b>) 2D intensity histogram of fluorescence from green (<b>2</b>, shown in green pseudo-color) and red (ER-tracker Red, shown in red pseudo-color) channels. Scale bars are 10 μm (<b>A</b>–<b>D</b>).</p>
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<p>Live-cell imaging with chromophores <b>7a</b>, <b>7b</b>, and <b>7c</b> using confocal microscopy. Lysosomes staining of HeLa Kyoto cells by (<b>A</b>) 5 μM of <b>7a</b> (added from 10 mM DMSO stock solution, incubation 1 min), (<b>B</b>) 1 μM of <b>7b</b> (added from 1 mM DMSO stock solution, incubation 1 min), and (<b>C</b>) 5 μM of <b>7c</b> (added from 10 mM DMSO stock solution, incubation 1 min). Images were pseudo-colored using Fiji Lookup Tables “NanoJ-Orange” grading. (<b>D</b>–<b>F</b>) Co-localization analysis of 5 μM of <b>7a</b> chromophore in HeLa Kyoto cells compared to LAMP-1-mTurquoise2. Pearson co-localization analysis followed by Costes randomized test resulted in 0.86. (F) 2D intensity histogram of fluorescence from green (LAMP-1-mTurquoise2, shown in green pseudo-color) and red (<b>7a</b>, shown in red pseudo-color) channels. (<b>G</b>–<b>I</b>) Co-localization analysis of 1 μM of <b>7b</b> chromophore in HeLa Kyoto cells compared to LAMP-1-mTurquoise2. Pearson co-localization analysis followed by Costes randomized test resulted in 0.72. (<b>I</b>) 2D intensity histogram of fluorescence from green (LAMP-1-mTurquoise2, shown in green pseudo-color) and red (<b>7b</b>, shown in red pseudo-color) channels. (<b>J</b>–<b>L</b>) Co-localization analysis of 5 μM of <b>7c</b> chromophore in HeLa Kyoto cells compared to LAMP-1-mTurquoise2. Pearson co-localization analysis followed by Costes randomized test resulted in 0.87. (<b>L</b>) 2D intensity histogram of fluorescence from green (LAMP-1-mTurquoise2, shown in green pseudo-color) and red (<b>7c</b>, shown in red pseudo-color) channels. Scale bars are 10 μm (<b>A</b>–<b>E</b>,<b>G</b>,<b>H</b>,<b>J</b>,<b>K</b>).</p>
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<p>Analogues of GFP chromophore with low or high solvent- and pH-dependent FQY variations.</p>
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<p>Synthesis of all compounds presented in this work.</p>
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<p>The nature of pH-dependent FQY variations in <span class="html-italic">meta</span>-substituted conformationally locked arylidene imidazolones presented in this work and proposed earlier [<a href="#B56-ijms-25-10448" class="html-bibr">56</a>].</p>
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