Biosensors and Bioelectronics: X最新文献

{"title":"Purpald-functionalized biosensor for simultaneous electrochemical detection of ascorbic acid, uric acid, L-cysteine and lipoic acid","authors":"Pandiaraja Varatharajan ,&nbsp;Muniyandi Maruthupandi ,&nbsp;Vinoth Kumar Ponnusamy ,&nbsp;Nagamalai Vasimalai","doi":"10.1016/j.biosx.2024.100458","DOIUrl":"10.1016/j.biosx.2024.100458","url":null,"abstract":"<div><p>The polymer purpald (4-amino-3-hydrazino-5-mercapto-1,2,4-triazole) film on glassy carbon electrode (p-Purpald@GCE) was fabricated using purpald monomer by electropolymerization method, and the modified electrode was applied as a probe for the simultaneous sensing of ascorbic acid (AA), uric acid (UA), L-cysteine (L-Cys) and lipoic acid (LA). The modified p-Purpald@GCE was well characterized by Scanning electrode microscopy (SEM), X-ray photoelectron spectroscopy (XPS), Cyclic Voltammetry (CV), Electrochemical impedance spectroscopy (EIS) and Differential Pulse Voltammetry (DPV) techniques. CV, EIS results were confirmed the good electrocatayst nature of p-Purpald@GCE. Independent and simultaneous detection of AA, UA, L-Cys, and LA ware performed by DPV method. For Independent detection, based on the oxidation current changes, we have calculated the limit of detection (LOD) of 392, 137, 341 and 200 nM (LOD) = 3S/m) for AA, UA, L-Cys and LA, respectively. The simultaneous detection of AA, UA, L-Cys, and LA executed and LOD found to be 364, 132, 275 and 192 nM, respectively. The modified electrode shows the high selectivity towards AA, UA, L-Cys and LA even in the presence of high concentration of other interferences. The developed sensor technique will be useful for the sensitive and simultaneous detection of AA, UA, L-Cys, and LA in food and clinical samples.</p></div>","PeriodicalId":260,"journal":{"name":"Biosensors and Bioelectronics: X","volume":"17 ","pages":"Article 100458"},"PeriodicalIF":10.61,"publicationDate":"2024-03-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2590137024000220/pdfft?md5=66f27f51a9ee52632ea406e3046188cb&pid=1-s2.0-S2590137024000220-main.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140084143","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Green sources for carbon dots synthesis in sensing for food application – A review","authors":"Amru Daulay ,&nbsp;Lukman Hakim Nasution ,&nbsp;Miftahul Huda ,&nbsp;Muhammad Amin ,&nbsp;Muhamad Nikmatullah ,&nbsp;Supiyani ,&nbsp;Yusmiati","doi":"10.1016/j.biosx.2024.100460","DOIUrl":"https://doi.org/10.1016/j.biosx.2024.100460","url":null,"abstract":"<div><p>Carbon dots (CDs) are the most promising nanomaterials of zero-dimensional nanoparticle materials because they have strong fluorescence properties, good photoluminescence conversion, stability, and inter-charge transfer performance. CDs also have the advantages of good biocompatibility, low toxicity, and hydrophilic properties. CDs are generally synthesized through two approaches: top-down and bottom-up. Green synthesis of environmentally friendly CDs with easy and simple procedures has become an exciting concern lately and in the future. In addition to green synthesis, green carbon sources such as biomass waste have promising potential. The advantages of fluorescence CDs make them applicable in food sensing. Fluorescent resonance energy transfer, photoinduced electron transfer, and internal screening effect mechanisms enable precise detection of heavy metal ions, food additives, foodborne pathogens, nutrient composition, pesticide residues, and veterinary drug residues. This review provides a brief overview and future perspectives on green synthesis CDs and their applications for more advanced food sensing in food safety analysis.</p></div>","PeriodicalId":260,"journal":{"name":"Biosensors and Bioelectronics: X","volume":"17 ","pages":"Article 100460"},"PeriodicalIF":10.61,"publicationDate":"2024-03-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2590137024000244/pdfft?md5=49a621ca800c79a4fed1c122976543e3&pid=1-s2.0-S2590137024000244-main.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140134486","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Gold nanoparticle–based lateral-flow immunochromatographic biosensing assays for the diagnosis of infections","authors":"Olga I. Guliy,&nbsp;Lev A. Dykman","doi":"10.1016/j.biosx.2024.100457","DOIUrl":"10.1016/j.biosx.2024.100457","url":null,"abstract":"<div><p>Infections cause concern for mankind, and sometimes their diagnosis may take much time. Owing to its high sensitivity, rapidity, and specificity, the immunochromatographic assay (ICA) is used widely to diagnose infections. The use of the ICA for this purpose makes it possible to detect dangerous diseases early, prevent their progress, strongly reduce the treatment cost and mortality, and increase life expectancy. One promising ICA format involves the use of gold nanoparticles. Here we present the principles and history of ICA use for the diagnosis of infections and discuss the prospects for using gold nanoparticles in the ICA. We present data on the methods used to make and conjugate gold nanoparticles and on the effect of particle size and shape on ICA sensitivity. We discuss the prospects for using the ICA to diagnose bacterial and viral infections, and we review instrumental methods for quantifying ICA results. Finally, we discuss the prospects for using the gold nanoparticle–based ICA in the diagnosis of infections.</p></div>","PeriodicalId":260,"journal":{"name":"Biosensors and Bioelectronics: X","volume":"17 ","pages":"Article 100457"},"PeriodicalIF":10.61,"publicationDate":"2024-03-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2590137024000219/pdfft?md5=8654bd97075b580b24f5f83aa803d582&pid=1-s2.0-S2590137024000219-main.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140054659","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Non-enzymatic electrochemical sensing platform based on metal oxide-loaded biopolymer for voltammetric measurement of hepatoprotective metadoxine drug in pharmaceutical formulation and human blood serum","authors":"Manish S. Sengar ,&nbsp;Priya Kumari ,&nbsp;Neha Sengar ,&nbsp;Soami P. Satsangee ,&nbsp;Rajeev Jain","doi":"10.1016/j.biosx.2024.100453","DOIUrl":"10.1016/j.biosx.2024.100453","url":null,"abstract":"<div><p>This study focuses on the first-ever high-sensitivity, low-cost, and quick response electrochemical estimation of metadoxine (MTD) in pharmaceuticals and human blood serum using a non-enzymatic nanocomposite modified glassy carbon electrode (CuO/CH/GCE) loaded with chitosan. The electroactive surface of GCE was produced by drop-casting a suspension of CuO/CH nanocomposite in N,N-dimethylformamide (DMF) onto the non-enzymatic electrode surface. Synthesized nanocomposite was characterised by using XRD, XPS, EDX, TEM, Raman and FESEM techniques. EIS technique was utilized to study the enhanced charge-transfer phenomenon occurring at the surface of modified sensor. The electrooxidation of MTD at CuO/CH/GCE surface is depending at pH of supporting electrolyte, scan rate and concentration of analyte. CV and SWV technique were used to carry out electrochemical study, optimised voltammetric response is observed in the BR buffer at pH 2.5, with irreversible diffusion-controlled process. Within the linear concentration range of MTD from 1.99 μg/L to 29.56 μg/L, this sensor exhibited lowest LOD (0.64 μg/L) and LOQ (2.14 μg/L). The MTD in pharmaceutical formulation and human blood serum can be determined with this highly selective peak potential (Ep ∼ 1.2 V), repeatable (%RSD 0.91), and reproducible (%RSD 2.31) method. The average percentage recovery in human blood serum and pharmaceutical formulation is 99.89% and 99.90%. This paper reports a lowest LOD value for MTD detection in the comparison with other reported methods (Table S1). None of the selected excipients were found to interfere more than 5% with redox potential of MTD without affecting the performance of sensor.</p></div>","PeriodicalId":260,"journal":{"name":"Biosensors and Bioelectronics: X","volume":"17 ","pages":"Article 100453"},"PeriodicalIF":10.61,"publicationDate":"2024-02-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2590137024000177/pdfft?md5=109df676fa512a6da046be990582ac28&pid=1-s2.0-S2590137024000177-main.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139927573","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Robust and flexible electrochemical lactate sensors for sweat analysis based on nanozyme-enhanced electrode","authors":"Pei Li ,&nbsp;Pramod K. Kalambate ,&nbsp;Kenneth D. Harris ,&nbsp;Abebaw B. Jemere ,&nbsp;Xiaowu (Shirley) Tang","doi":"10.1016/j.biosx.2024.100455","DOIUrl":"10.1016/j.biosx.2024.100455","url":null,"abstract":"<div><p>In this work, nickel oxide (NiO) nanostructures deposited by glancing angle deposition (GLAD) are fabricated to achieve highly specific catalytic electrooxidation of lactate, replacing the natural enzyme lactate oxidase for electrochemical detection of lactate in sweat. GLAD NiO electrodes exhibit high sensitivity (412 μA mM⁻¹ cm⁻²), wide linear detection range (1–45 mM), low detection limit (3 μM), and excellent specificity in artificial sweat samples. The unique microporous structure of the GLAD NiO electrodes, combined with their high surface area, high catalytic activity, and excellent conductivity, enhance the performance of the sensor and demonstrate their exceptional effectiveness in the sensitive detection of lactate. In-house fabricated gold counter, and stable solid-state Ag/AgCl reference electrodes, all fabricated on a flexible PET substrate along with the GLAD NiO working electrode, demonstrate performance comparable to commercial Pt auxiliary and Ag/AgCl (1M KCl) reference electrodes in lactate detection, along with outstanding flexibility, tested at various radii of curvature (15 mm, 7.5 mm, and 5 mm). The durable and long-lasting GLAD NiO electrode chips overcome numerous challenges in transport, storage, and operation, paving the way for the development of wearable lactate sensors that can detect lactate levels in sweat.</p></div>","PeriodicalId":260,"journal":{"name":"Biosensors and Bioelectronics: X","volume":"17 ","pages":"Article 100455"},"PeriodicalIF":10.61,"publicationDate":"2024-02-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2590137024000190/pdfft?md5=f9c66c171415d33813f315f86d28def3&pid=1-s2.0-S2590137024000190-main.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139811977","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Reduced amplification by phi29 DNA polymerase in the presence of unbound oligos during reaction in RCA","authors":"Darío Sánchez Martín ,&nbsp;Tingting Li ,&nbsp;Marie Wrande ,&nbsp;Linus Sandegren ,&nbsp;Bo Tian ,&nbsp;Maria Strømme ,&nbsp;Teresa Zardán Gómez de la Torre","doi":"10.1016/j.biosx.2024.100456","DOIUrl":"10.1016/j.biosx.2024.100456","url":null,"abstract":"<div><p>Synthetic single-stranded oligonucleotides play crucial roles in DNA amplification reactions for various applications, such as serving as primers, enabling magnetic separation, and generating dsDNA for subsequent digestion. Typically, these oligos are added in excess to ensure rapid binding to their intended targets. However, while performing rolling circle amplification (RCA) using phi29 DNA polymerase, we observed a decrease in amplification efficiency when oligos were present in the reaction. This phenomenon was consistently observed in two separate laboratories, prompting this study to delve into the root causes responsible for the decline in RCA efficiency. The lowered efficiency was consistent regardless of the manufacturer or any mutations in the phi29 polymerase. We identified several variables that influenced RCA efficiency, mainly the length of the oligos used and the presence of modifications, particularly those obstructing 3’ end digestion. This strongly suggests that the exonuclease domain of phi29 DNA polymerase is responsible for the competition-based inhibition. Our investigation shows that even picomole quantities of oligos can significantly reduce total DNA production during the phi29 DNA polymerase-mediated amplification process. Conversely, the addition of oligos to the reaction did not impede the efficiency of Bst 3.0 polymerase, likely due to the lack of an exonuclease domain of said polymerase. While increasing the quantity of phi29 DNA polymerase in the reaction partially alleviated the adverse effects of excess oligos, we believe it is crucial to carefully optimize the oligo quantities to achieve maximum amplification of the desired targets.</p></div>","PeriodicalId":260,"journal":{"name":"Biosensors and Bioelectronics: X","volume":"17 ","pages":"Article 100456"},"PeriodicalIF":10.61,"publicationDate":"2024-02-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2590137024000207/pdfft?md5=d287c9aee31a57315a7717b990891ab8&pid=1-s2.0-S2590137024000207-main.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139872072","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Vibrio vulnificus marine pathogen detection with thin-film impedance biosensors","authors":"Arnau Pérez Roig ,&nbsp;Bergoi Ibarlucea ,&nbsp;Carmen Amaro ,&nbsp;Gianaurelio Cuniberti","doi":"10.1016/j.biosx.2024.100454","DOIUrl":"https://doi.org/10.1016/j.biosx.2024.100454","url":null,"abstract":"<div><p><em>Vibrio vulnificus</em> (Vv) is a marine pathogen that can cause rapid death by septicemia (vibriosis) in humans and several fish species. This pathogen is considered a biomarker of climate change, as both its presence and vibriosis incidence in coastal environments are increasing because of global warming. Currently, gold-standard methods for Vv detection are all PCR-based, requiring expensive equipment and skilled personnel, which hinders their use on a global scale. The aim of this work was to design and test a more affordable method that could be used worldwide for both vibriosis diagnosis and pathogen monitoring in water. To this end, we functionalized thin film microelectrodes with thiolated single-stranded DNA sequences complementary to the species-specific genetic marker, the gene <em>vvha</em>, and monitored the impedance changes upon hybridization. We tested the biosensor specificity with synthetic and natural DNA samples (from cultures of Vv and <em>V. cholerae</em>, a closely related species) and determined the detectable concentration range. The results obtained showed that this biosensor was specific for Vv, achieving detection down to 1 pM synthetic DNA and DNA extracted from 10² bacteria mL⁻¹, which is equivalent to that obtained by PCR. Consequently, this biosensor could be used on a global scale for vibriosis diagnostics, health risk studies and climate change monitoring, with potential application for <em>in situ</em> detection.</p></div>","PeriodicalId":260,"journal":{"name":"Biosensors and Bioelectronics: X","volume":"17 ","pages":"Article 100454"},"PeriodicalIF":10.61,"publicationDate":"2024-02-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2590137024000189/pdfft?md5=af3b0aefae9767e5f3c6747487932fd8&pid=1-s2.0-S2590137024000189-main.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139737797","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Portable optical biosensor for point-of-care monitoring of salivary glucose using a paper-based microfluidic strip","authors":"Shweta Panwar ,&nbsp;Paulami Sarkar ,&nbsp;D. Syed Kasim ,&nbsp;Raksha Anand ,&nbsp;Akanksha Priya ,&nbsp;Shyam Prakash ,&nbsp;Sandeep Kumar Jha","doi":"10.1016/j.biosx.2024.100452","DOIUrl":"10.1016/j.biosx.2024.100452","url":null,"abstract":"<div><p>The manuscript describes a technique for fabrication and validation of a standalone handheld optical biosensor designed for non-invasive monitoring of glucose through saliva. In this cost-effective process, a 3D-printed glucose test strip was filled with sieving paste comprising of cellulose, polyethylene glycol (PEG), polyvinyl alcohol (PVA) and glycerol, onto which, glucose oxidase-peroxidase (GOD-POD) enzymes and 2,2′-azino-bis(3-ethylbenzothiazoline-6-sulfonic acid) (ABTS) chromogenic dye were co-immobilized. The enzymatic reaction produced H₂O₂ as by-product with which the ABTS reacted, leading to colour change on the detection zone of the strip which was detected by the developed glucometer. The in-house developed meter included an optically isolated section in its structure for inserting the strip to prevent interference from the ambient light conditions. The biosensor exhibited a broad detection range of 28–204 mg/dL of glucose concentration, with a sensitivity of 26.89 count/mg/dL and a limit of detection (LOD) at 28 mg/dL, within a response time of 120 s. The device along with strips was validated with clinical samples, comparing salivary glucose levels (SGL) to blood glucose levels (BGL) using a commercial glucometer i.e., Accu-Chek Active. Student's t-test on clinical data yielded p-values of 0.018, 0.01, 0.008, and 0.003 in fasting and post-prandial samples of non-diabetic and diabetic patients respectively, which represents a significant correlation. The device also passed Clarke's error grid analysis and is hence considered medically acceptable. The low-cost and simple-to-use saliva-based glucometer should be ideally suited for mass screening of diabetes as well as day-to-day health check-ups in a non-invasive and painless manner.</p></div>","PeriodicalId":260,"journal":{"name":"Biosensors and Bioelectronics: X","volume":"17 ","pages":"Article 100452"},"PeriodicalIF":10.61,"publicationDate":"2024-02-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2590137024000165/pdfft?md5=6079c2eb7aa736c6042d9fe826728f82&pid=1-s2.0-S2590137024000165-main.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139817391","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Non-enzymatic electrochemical detection of methylglyoxal in saliva using a polyaniline/nickel oxide nanohybrid biosensor: A noninvasive approach for diabetes diagnosis","authors":"Subramanian Vasanth,&nbsp;Humayun Amir,&nbsp;Nagomony Ponpandian,&nbsp;Chinnuswamy Viswanathan","doi":"10.1016/j.biosx.2024.100444","DOIUrl":"10.1016/j.biosx.2024.100444","url":null,"abstract":"<div><p>Methylglyoxal (MG) is a prominent biomarker for diabetic syndromes and ageing disorders. In the present study, a non-enzymatic electrochemical detection of MG in human saliva at low levels was achieved via polyaniline/nickel oxide nanohybrid modified graphite sheet (PANI/NiO/GS) electrode. The physical characteristics and structure of the PANI/NiO nanohybrid showed the presence of NiO flakes embedded within the irregular granular like structure of PANI matrices. Chronoamperometric (CA) analysis of the nanohybrid electrode showed excellent electrocatalytic activity towards MG with the linear range from 1 to 10 μM in 0.1 M phosphate buffer (pH 7). The proposed sensor boasts a high sensitivity of 1.136 μA.μM⁻¹ including a lower limit of detection of 2.64 nM. The real-time functionality of the proposed biosensor was also employed to estimate the precise quantification of MG levels in both healthy and diabetic patients' saliva. For the healthy and diabetes samples, the recovery values for MG were 95–103 % and 102–111 %, respectively. This approach is truly noninvasive and circumvents the discomforts associated with the traditional modalities.</p></div>","PeriodicalId":260,"journal":{"name":"Biosensors and Bioelectronics: X","volume":"17 ","pages":"Article 100444"},"PeriodicalIF":10.61,"publicationDate":"2024-01-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2590137024000086/pdfft?md5=674c68aedf012f0c96e8069884f4477f&pid=1-s2.0-S2590137024000086-main.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139586908","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Modern technology advances of Pseudomonas aeruginosa based biosensor approach","authors":"Dhanendiren Narayanasamy ,&nbsp;Safura Taufik ,&nbsp;Ahmad Farid Mohd Azmi ,&nbsp;Siti Aminah Mohd Nor ,&nbsp;Jahwarhar Izuan Abdul Rashid","doi":"10.1016/j.biosx.2024.100441","DOIUrl":"10.1016/j.biosx.2024.100441","url":null,"abstract":"<div><p>The threat posed by microbial infections to human health remains very significant, particularly in considering the increasing mechanisms of antibiotic resistance. <em>Pseudomonas aeruginosa</em> is known for its antibiotic resistance and is linked to serious conditions like ventilator-associated pneumonia and cystic fibrosis. Rapid infection elimination relies on identifying harmful bacteria and preventing colonization. Due to the redox-active nature of <em>P. aeruginosa</em> biomarkers metabolites, several electrochemical sensing approaches are being evaluated as diagnostic platforms for the rapid and precise detection of <em>P. aeruginosa</em> with high sensitivity. These sensors must be developed and modified to achieve optimal selectivity, sensitivity, and biocompatibility, enabling dynamic, real-time metabolite detection. This minireview highlights recent advancements in electrochemical and optical biosensors for detecting <em>P. aeruginosa</em> biomarkers, particularly pyocyanin. It highlighted design, analytical performance, biological recognition elements, and personalized wearable electrochemical sensor devices. It concludes with the future suggestions of sensor concepts for clinical diagnostics, environmental monitoring, and food safety.</p></div>","PeriodicalId":260,"journal":{"name":"Biosensors and Bioelectronics: X","volume":"17 ","pages":"Article 100441"},"PeriodicalIF":10.61,"publicationDate":"2024-01-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2590137024000050/pdfft?md5=099bb01d4140f2dbaab739e43f653384&pid=1-s2.0-S2590137024000050-main.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139552342","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}