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16 pages, 1696 KB  
Article
Rapid Finger-Pump Microfluidic Paper-Based Assay Platform for Monitoring Calcium Ions in Human Biofluids
by Kuan-Hsun Huang, Chin-Chung Tseng, Chia-Chun Lee, Cheng-Xue Yu and Lung-Ming Fu
Biosensors 2026, 16(4), 183; https://doi.org/10.3390/bios16040183 - 24 Mar 2026
Abstract
Chronic kidney disease (CKD) is a progressively worsening condition that erodes renal function over time, reduces quality of life, and can ultimately culminate in kidney failure with far-reaching systemic complications. In addition to reduced filtration, worsening kidney function disrupts mineral homeostasis and leads [...] Read more.
Chronic kidney disease (CKD) is a progressively worsening condition that erodes renal function over time, reduces quality of life, and can ultimately culminate in kidney failure with far-reaching systemic complications. In addition to reduced filtration, worsening kidney function disrupts mineral homeostasis and leads to CKD–mineral and bone disorder (CKD-MBD). Dysregulated calcium handling and maladaptive endocrine responses contribute to bone pathology and increase cardiovascular calcification risk; therefore, serial calcium monitoring remains clinically relevant for longitudinal CKD management. Conventional calcium measurements are typically obtained with centralized analyzers or laboratory assays (e.g., colorimetry and electrode/optical readouts). Despite high accuracy, the required instrumentation, controlled operating conditions, and pretreatment steps complicate rapid point-of-care deployment, especially when only microliter-scale biofluids are available. Accordingly, this study develops a finger-actuated microfluidic colorimetric platform capable of determining calcium ion concentrations in human biofluids, such as whole blood, serum, and urine. The platform integrates a three-dimensional PMMA/paper microchip with a compact reader that maintains stable temperature control while enabling CMOS-based optical detection. With just 6 μL of sample, a brief finger press propels the biofluid across an internal filtration layer, generating serum or cleaned urine that subsequently reacts with a pre-deposited murexide reagent. Under optimized conditions (1.6% reagent, 50 °C, 3 min), the signal follows a strong logarithmic relationship with calcium concentration (Y = 47.273 ln X + 28.890; R2 = 0.9905), supporting quantification over 1–40 mg/dL and a detection limit of 0.2 mg/dL. Across 80 clinical CKD specimens spanning serum, whole blood, and urine, results aligned closely with the NM-BAPTA reference assay, with R2 values exceeding 0.97. Full article
(This article belongs to the Special Issue Integrated Microfluidic Biosensing Systems: Designs and Applications)
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31 pages, 3578 KB  
Review
Measurement of Percentage Depth–Dose Distributions in Clinical Dosimetry: Conventional Techniques and Emerging Sensor Technologies
by Giada Petringa, Luigi Raffaele, Giacomo Cuttone, Mariacristina Guarrera, Alma Kurmanova, Roberto Catalano and Giuseppe Antonio Pablo Cirrone
Sensors 2026, 26(6), 1908; https://doi.org/10.3390/s26061908 - 18 Mar 2026
Viewed by 172
Abstract
Percentage depth–dose (PDD) distributions are fundamental to characterizing radiation beams in radiotherapy. This review provides an overview of both methods and sensor technologies for measuring PDD in photon, electron, proton, and carbon-ion beams. We summarize conventional dosimetry techniques, including water-phantom scanning with ionization [...] Read more.
Percentage depth–dose (PDD) distributions are fundamental to characterizing radiation beams in radiotherapy. This review provides an overview of both methods and sensor technologies for measuring PDD in photon, electron, proton, and carbon-ion beams. We summarize conventional dosimetry techniques, including water-phantom scanning with ionization chambers (cylindrical and parallel-plate) and radiochromic film, and discuss their strengths (established accuracy, calibration traceability) and limitations (volume averaging, delayed readout). We then examine emerging sensor technologies designed to improve spatial resolution, speed, and radiation hardness: multi-layer ionization chambers and Faraday cups for one-shot PDD acquisition; scintillator-based detectors (liquid, plastic, and fiber-optic) enabling real-time and high-resolution depth–dose measurements; advanced semiconductor detectors including silicon carbide diodes; as well as novel approaches such as ionoacoustic range sensing for proton beams. For each modality and detector type, we emphasize clinical relevance, measurement accuracy, spatial resolution, radiation durability, and suitability for high dose-per-pulse environments (e.g., FLASH radiotherapy). Current challenges, such as detector response in regions of steep dose gradient, saturation or recombination at ultra-high dose rates, and energy-dependent sensitivity in mixed radiation fields, are analyzed in detail. We also highlight the limitations of each technique and discuss ongoing improvements and prospects for clinical implementation. In summary, no single detector technology fully satisfies all requirements for fast, high-accuracy, high-resolution, radiation-hard PDD measurement, but the integration of emerging sensor innovations into clinical dosimetry promises to enhance the precision and efficiency of radiotherapy quality assurance. Full article
(This article belongs to the Special Issue Advanced Sensors for Human Health Management)
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25 pages, 1735 KB  
Review
Advances in Immunological Methods for the Detection of Escherichia coli O157:H7: A Review
by Linqing Zou, Chang Xue, Mingyu Tao, Qin Ouyang and Cunzheng Zhang
Sensors 2026, 26(6), 1894; https://doi.org/10.3390/s26061894 - 17 Mar 2026
Viewed by 159
Abstract
Escherichia coli O157:H7 (E. coli O157:H7) is a highly virulent foodborne pathogen with an extremely low infectious dose, making its rapid and accurate detection in food and environmental samples critically important. In recent years, significant progress has been made in immunological techniques [...] Read more.
Escherichia coli O157:H7 (E. coli O157:H7) is a highly virulent foodborne pathogen with an extremely low infectious dose, making its rapid and accurate detection in food and environmental samples critically important. In recent years, significant progress has been made in immunological techniques for the rapid identification of E. coli O157:H7. This review systematically summarizes advances in immunological methods for the detection of E. coli O157:H7 over the past decade, focusing on lateral flow immunoassays (LFIA), enzyme-linked immunosorbent assays (ELISA), immunosensors (optical and electrochemical), and nanobody-based technologies. Key aspects such as detection principles, specificity, antibody types (monoclonal, polyclonal, nanobodies), signal readout mechanisms, and applicability to different sample matrices are compared. Performance parameters, including limit of detection (LOD), specificity, detection time, and matrix compatibility, are summarized to evaluate the advantages and limitations of each method. Furthermore, international food safety standards and regulations (ISO 16654, FDA BAM, USDA) are reviewed to highlight the practical and regulatory requirements of these techniques. On this basis, the role of immunological detection technologies in on-site rapid testing is discussed, with a focus on improvements in sensitivity, specificity, and practicality. Finally, future directions are outlined, including multiplexed assays, integration with molecular biology techniques, and engineering applications of nanobody and recombinant technology. Full article
(This article belongs to the Section Nanosensors)
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33 pages, 35113 KB  
Article
Operation of a Modular 3D-Pixelated Liquid Argon Time-Projection Chamber in a Neutrino Beam
by S. Abbaslu, A. Abed Abud, R. Acciarri, L. P. Accorsi, M. A. Acero, M. R. Adames, G. Adamov, M. Adamowski, C. Adriano, F. Akbar, F. Alemanno, N. S. Alex, K. Allison, M. Alrashed, A. Alton, R. Alvarez, T. Alves, A. Aman, H. Amar, P. Amedo, J. Anderson, D. A. Andrade, C. Andreopoulos, M. Andreotti, M. P. Andrews, F. Andrianala, S. Andringa, F. Anjarazafy, S. Ansarifard, D. Antic, M. Antoniassi, A. Aranda-Fernandez, L. Arellano, E. Arrieta Diaz, M. A. Arroyave, M. Arteropons, J. Asaadi, M. Ascencio, A. Ashkenazi, D. Asner, L. Asquith, E. Atkin, D. Auguste, A. Aurisano, V. Aushev, D. Autiero, D. Ávila Gómez, M. B. Azam, F. Azfar, A. Back, J. J. Back, Y. Bae, I. Bagaturia, L. Bagby, D. Baigarashev, S. Balasubramanian, A. Balboni, P. Baldi, W. Baldini, J. Baldonedo, B. Baller, B. Bambah, F. Barao, D. Barbu, G. Barenboim, P. B̃arham Alzás, G. J. Barker, W. Barkhouse, G. Barr, A. Barros, N. Barros, D. Barrow, J. L. Barrow, A. Basharina-Freshville, A. Bashyal, V. Basque, M. Bassani, D. Basu, C. Batchelor, L. Bathe-Peters, J. B. R. Battat, F. Battisti, J. Bautista, F. Bay, J. L. L. Bazo Alba, J. F. Beacom, E. Bechetoille, B. Behera, E. Belchior, B. Bell, G. Bell, L. Bellantoni, G. Bellettini, V. Bellini, O. Beltramello, A. Belyaev, C. Benitez Montiel, D. Benjamin, F. Bento Neves, J. Berger, S. Berkman, J. Bermudez, J. Bernal, P. Bernardini, A. Bersani, E. Bertholet, E. Bertolini, S. Bertolucci, M. Betancourt, A. Betancur Rodríguez, Y. Bezawada, A. T. Bezerra, A. Bhat, V. Bhatnagar, M. Bhattacharjee, S. Bhattacharjee, M. Bhattacharya, S. Bhuller, B. Bhuyan, S. Biagi, J. Bian, K. Biery, B. Bilki, M. Bishai, A. Blake, F. D. Blaszczyk, G. C. Blazey, E. Blucher, B. Bogart, J. Boissevain, S. Bolognesi, T. Bolton, L. Bomben, M. Bonesini, C. Bonilla-Diaz, A. Booth, F. Boran, R. Borges Merlo, N. Bostan, G. Botogoske, B. Bottino, R. Bouet, J. Boza, J. Bracinik, B. Brahma, D. Brailsford, F. Bramati, A. Branca, A. Brandt, J. Bremer, S. J. Brice, V. Brio, C. Brizzolari, C. Bromberg, J. Brooke, A. Bross, G. Brunetti, M. B. Brunetti, N. Buchanan, H. Budd, J. Buergi, A. Bundock, D. Burgardt, S. Butchart, G. Caceres V., R. Calabrese, R. Calabrese, J. Calcutt, L. Calivers, E. Calvo, A. Caminata, A. F. Camino, W. Campanelli, A. Campani, A. Campos Benitez, N. Canci, J. Capó, I. Caracas, D. Caratelli, D. Carber, J. M. Carceller, G. Carini, B. Carlus, M. F. Carneiro, P. Carniti, I. Caro Terrazas, H. Carranza, N. Carrara, L. Carroll, T. Carroll, A. Carter, E. Casarejos, D. Casazza, J. F. Castaño Forero, F. A. Castaño, C. Castromonte, E. Catano-Mur, C. Cattadori, F. Cavalier, F. Cavanna, S. Centro, G. Cerati, C. Cerna, A. Cervelli, A. Cervera Villanueva, J. Chakrani, M. Chalifour, A. Chappell, A. Chatterjee, B. Chauhan, C. Chavez Barajas, H. Chen, M. Chen, W. C. Chen, Y. Chen, Z. Chen, D. Cherdack, S. S. Chhibra, C. Chi, F. Chiapponi, R. Chirco, N. Chitirasreemadam, K. Cho, S. Choate, G. Choi, D. Chokheli, P. S. Chong, B. Chowdhury, D. Christian, M. Chung, E. Church, M. F. Cicala, M. Cicerchia, V. Cicero, R. Ciolini, P. Clarke, G. Cline, A. G. Cocco, J. A. B. Coelho, A. Cohen, J. Collazo, J. Collot, H. Combs, J. M. Conrad, L. Conti, T. Contreras, M. Convery, K. Conway, S. Copello, P. Cova, C. Cox, L. Cremonesi, J. I. Crespo-Anadón, M. Crisler, E. Cristaldo, J. Crnkovic, G. Crone, R. Cross, A. Cudd, C. Cuesta, Y. Cui, F. Curciarello, D. Cussans, J. Dai, O. Dalager, W. Dallaway, R. D’Amico, H. da Motta, Z. A. Dar, R. Darby, L. Da Silva Peres, Q. David, G. S. Davies, S. Davini, J. Dawson, R. De Aguiar, P. Debbins, M. P. Decowski, A. de Gouvêa, P. C. De Holanda, P. De Jong, P. Del Amo Sanchez, G. De Lauretis, A. Delbart, M. Delgado, A. Dell’Acqua, G. Delle Monache, N. Delmonte, P. De Lurgio, R. Demario, G. De Matteis, J. R. T. de Mello Neto, A. P. A. De Mendonca, D. M. DeMuth, S. Dennis, C. Densham, P. Denton, G. W. Deptuch, A. De Roeck, V. De Romeri, J. P. Detje, J. Devine, K. Dhanmeher, R. Dharmapalan, M. Dias, A. Diaz, J. S. Díaz, F. Díaz, F. Di Capua, A. Di Domenico, S. Di Domizio, S. Di Falco, L. Di Giulio, P. Ding, L. Di Noto, E. Diociaiuti, G. Di Sciascio, V. Di Silvestre, C. Distefano, R. Di Stefano, R. Diurba, M. Diwan, Z. Djurcic, S. Dolan, M. Dolce, M. J. Dolinski, D. Domenici, S. Dominguez, S. Donati, S. Doran, D. Douglas, T. A. Doyle, F. Drielsma, D. Duchesneau, K. Duffy, K. Dugas, P. Dunne, B. Dutta, D. A. Dwyer, A. S. Dyshkant, S. Dytman, M. Eads, A. Earle, S. Edayath, D. Edmunds, J. Eisch, W. Emark, P. Englezos, A. Ereditato, T. Erjavec, C. O. Escobar, J. J. Evans, E. Ewart, A. C. Ezeribe, K. Fahey, A. Falcone, M. Fani’, D. Faragher, C. Farnese, Y. Farzan, J. Felix, Y. Feng, M. Ferreira da Silva, G. Ferry, E. Fialova, L. Fields, P. Filip, A. Filkins, F. Filthaut, G. Fiorillo, M. Fiorini, S. Fogarty, W. Foreman, J. Fowler, J. Franc, K. Francis, D. Franco, J. Franklin, J. Freeman, J. Fried, A. Friedland, M. Fucci, S. Fuess, I. K. Furic, K. Furman, A. P. Furmanski, R. Gaba, A. Gabrielli, A. M Gago, F. Galizzi, H. Gallagher, M. Galli, N. Gallice, V. Galymov, E. Gamberini, T. Gamble, R. Gandhi, S. Ganguly, F. Gao, S. Gao, D. Garcia-Gamez, M. Á. García-Peris, S. Gardiner, A. Gartman, A. Gauch, P. Gauzzi, S. Gazzana, G. Ge, N. Geffroy, B. Gelli, S. Gent, L. Gerlach, A. Ghosh, T. Giammaria, D. Gibin, I. Gil-Botella, A. Gioiosa, S. Giovannella, A. K. Giri, V. Giusti, D. Gnani, O. Gogota, S. Gollapinni, K. Gollwitzer, R. A. Gomes, L. S. Gomez Fajardo, D. Gonzalez-Diaz, J. Gonzalez-Santome, M. C. Goodman, S. Goswami, C. Gotti, J. Goudeau, C. Grace, E. Gramellini, R. Gran, P. Granger, C. Grant, D. R. Gratieri, G. Grauso, P. Green, S. Greenberg, W. C. Griffith, K. Grzelak, L. Gu, W. Gu, V. Guarino, M. Guarise, R. Guenette, M. Guerzoni, D. Guffanti, A. Guglielmi, F. Y. Guo, A. Gupta, V. Gupta, G. Gurung, D. Gutierrez, P. Guzowski, M. M. Guzzo, S. Gwon, A. Habig, L. Haegel, R. Hafeji, L. Hagaman, A. Hahn, J. Hakenmüller, T. Hamernik, P. Hamilton, J. Hancock, M. Handley, F. Happacher, B. Harris, D. A. Harris, L. Harris, A. L. Hart, J. Hartnell, T. Hartnett, J. Harton, T. Hasegawa, C. M. Hasnip, R. Hatcher, S. Hawkins, J. Hays, M. He, A. Heavey, K. M. Heeger, A. Heindel, J. Heise, P. Hellmuth, L. Henderson, K. Herner, V. Hewes, A. Higuera, A. Himmel, E. Hinkle, L. R. Hirsch, J. Ho, J. Hoefken Zink, J. Hoff, A. Holin, T. Holvey, C. Hong, S. Horiuchi, G. A. Horton-Smith, R. Hosokawa, T. Houdy, B. Howard, R. Howell, I. Hristova, M. S. Hronek, H. Hua, J. Huang, R. G. Huang, X. Huang, Z. Hulcher, A. Hussain, G. Iles, N. Ilic, A. M. Iliescu, R. Illingworth, G. Ingratta, A. Ioannisian, M. Ismerio Oliveira, C. M. Jackson, V. Jain, E. James, W. Jang, B. Jargowsky, D. Jena, I. Jentz, C. Jiang, J. Jiang, A. Jipa, J. H. Jo, F. R. Joaquim, W. Johnson, C. Jollet, R. Jones, N. Jovancevic, M. Judah, C. K. Jung, K. Y. Jung, T. Junk, Y. Jwa, M. Kabirnezhad, A. C. Kaboth, I. Kadenko, O. Kalikulov, D. Kalra, M. Kandemir, S. Kar, G. Karagiorgi, G. Karaman, A. Karcher, Y. Karyotakis, S. P. Kasetti, L. Kashur, A. Kauther, N. Kazaryan, L. Ke, E. Kearns, P. T. Keener, K. J. Kelly, R. Keloth, E. Kemp, O. Kemularia, Y. Kermaidic, W. Ketchum, S. H. Kettell, N. Khan, A. Khvedelidze, D. Kim, J. Kim, M. J. Kim, S. Kim, B. King, M. King, M. Kirby, A. Kish, J. Klein, J. Kleykamp, A. Klustova, T. Kobilarcik, L. Koch, K. Koehler, L. W. Koerner, D. H. Koh, M. Kordosky, T. Kosc, V. A. Kostelecký, I. Kotler, W. Krah, R. Kralik, M. Kramer, F. Krennrich, T. Kroupova, S. Kubota, M. Kubu, V. A. Kudryavtsev, G. Kufatty, S. Kuhlmann, A. Kumar, J. Kumar, M. Kumar, P. Kumar, P. Kumar, S. Kumaran, J. Kunzmann, V. Kus, T. Kutter, J. Kvasnicka, T. Labree, M. Lachat, T. Lackey, I. Lalău, A. Lambert, B. J. Land, C. E. Lane, N. Lane, K. Lang, T. Langford, M. Langstaff, F. Lanni, J. Larkin, P. Lasorak, D. Last, A. Laundrie, G. Laurenti, E. Lavaut, H. Lay, I. Lazanu, R. LaZur, M. Lazzaroni, S. Leardini, J. Learned, T. LeCompte, G. Lehmann Miotto, R. Lehnert, M. Leitner, H. Lemoine, D. Leon Silverio, L. M. Lepin, J.-Y. Li, S. W. Li, Y. Li, R. Lima, C. S. Lin, D. Lindebaum, S. Linden, R. A. Lineros, A. Lister, B. R. Littlejohn, J. Liu, Y. Liu, S. Lockwitz, I. Lomidze, K. Long, J. Lopez, I. López de Rego, N. López-March, J. M. LoSecco, A. Lozano Sanchez, X.-G. Lu, K. B. Luk, X. Luo, E. Luppi, A. A. Machado, P. Machado, C. T. Macias, J. R. Macier, M. MacMahon, S. Magill, C. Magueur, K. Mahn, A. Maio, N. Majeed, A. Major, K. Majumdar, A. Malige, S. Mameli, M. Man, R. C. Mandujano, J. Maneira, S. Manly, K. Manolopoulos, M. Manrique Plata, S. Manthey Corchado, L. Manzanillas-Velez, E. Mao, M. Marchan, A. Marchionni, D. Marfatia, C. Mariani, J. Maricic, F. Marinho, A. D. Marino, T. Markiewicz, F. Das Chagas Marques, M. Marshak, C. M. Marshall, J. Marshall, L. Martina, J. Martín-Albo, D. A. Martinez Caicedo, M. Martinez-Casales, F. Martínez López, S. Martynenko, V. Mascagna, A. Mastbaum, M. Masud, F. Matichard, G. Matteucci, J. Matthews, C. Mauger, N. Mauri, K. Mavrokoridis, I. Mawby, F. Mayhew, T. McAskill, N. McConkey, B. McConnell, K. S. McFarland, C. McGivern, C. McGrew, A. McNab, C. McNulty, J. Mead, L. Meazza, V. C. N. Meddage, A. Medhi, M. Mehmood, B. Mehta, P. Mehta, F. Mei, P. Melas, L. Mellet, T. C. D. Melo, O. Mena, H. Mendez, D. P. Méndez, A. Menegolli, G. Meng, A. C. E. A. Mercuri, A. Meregaglia, M. D. Messier, S. Metallo, W. Metcalf, M. Mewes, H. Meyer, T. Miao, J. Micallef, A. Miccoli, G. Michna, R. Milincic, F. Miller, G. Miller, W. Miller, A. Minotti, L. Miralles Verge, C. Mironov, S. Miscetti, C. S. Mishra, P. Mishra, S. R. Mishra, D. Mladenov, I. Mocioiu, A. Mogan, R. Mohanta, T. A. Mohayai, N. Mokhov, J. Molina, L. Molina Bueno, E. Montagna, A. Montanari, C. Montanari, D. Montanari, D. Montanino, L. M. Montaño Zetina, M. Mooney, A. F. Moor, M. Moore, Z. Moore, D. Moreno, G. Moreno-Granados, O. Moreno-Palacios, L. Morescalchi, C. Morris, E. Motuk, C. A. Moura, G. Mouster, W. Mu, L. Mualem, J. Mueller, M. Muether, A. Muir, Y. Mukhamejanov, A. Mukhamejanova, M. Mulhearn, D. Munford, L. J. Munteanu, H. Muramatsu, J. Muraz, M. Murphy, T. Murphy, A. Mytilinaki, J. Nachtman, Y. Nagai, S. Nagu, D. Naples, S. Narita, J. Nava, A. Navrer-Agasson, N. Nayak, M. Nebot-Guinot, A. Nehm, J. K. Nelson, O. Neogi, J. Nesbit, M. Nessi, D. Newbold, M. Newcomer, D. Newmark, R. Nichol, F. Nicolas-Arnaldos, A. Nielsen, A. Nikolica, J. Nikolov, E. Niner, X. Ning, K. Nishimura, A. Norman, A. Norrick, P. Novella, A. Nowak, J. A. Nowak, M. Oberling, J. P. Ochoa-Ricoux, S. Oh, S. B. Oh, A. Olivier, T. Olson, Y. Onel, Y. Onishchuk, A. Oranday, M. Osbiston, J. A. Osorio Vélez, L. O’Sullivan, L. Otiniano Ormachea, L. Pagani, G. Palacio, O. Palamara, S. Palestini, J. M. Paley, M. Pallavicini, C. Palomares, S. Pan, M. Panareo, P. Panda, V. Pandey, W. Panduro Vazquez, E. Pantic, V. Paolone, A. Papadopoulou, R. Papaleo, D. Papoulias, S. Paramesvaran, J. Park, S. Parke, S. Parsa, S. Parveen, M. Parvu, D. Pasciuto, S. Pascoli, L. Pasqualini, J. Pasternak, G. Patel, J. L. Paton, C. Patrick, L. Patrizii, R. B. Patterson, T. Patzak, A. Paudel, J. Paul, L. Paulucci, Z. Pavlovic, G. Pawloski, D. Payne, A. Peake, V. Pec, E. Pedreschi, S. J. M. Peeters, W. Pellico, E. Pennacchio, A. Penzo, O. L. G. Peres, Y. F. Perez Gonzalez, L. Pérez-Molina, C. Pernas, J. Perry, D. Pershey, G. Pessina, G. Petrillo, C. Petta, R. Petti, M. Pfaff, V. Pia, G. M. Piacentino, L. Pickering, L. Pierini, F. Pietropaolo, V. L. Pimentel, G. Pinaroli, S. Pincha, J. Pinchault, K. Pitts, P. Plesniak, K. Pletcher, K. Plows, C. Pollack, T. Pollmann, F. Pompa, X. Pons, N. Poonthottathil, V. Popov, F. Poppi, J. Porter, L. G. Porto Paixão, M. Potekhin, M. Pozzato, R. Pradhan, T. Prakash, M. Prest, F. Psihas, D. Pugnere, D. Pullia, X. Qian, J. Queen, J. L. Raaf, M. Rabelhofer, V. Radeka, J. Rademacker, F. Raffaelli, A. Rafique, A. Rahe, S. Rajagopalan, M. Rajaoalisoa, I. Rakhno, L. Rakotondravohitra, M. A. Ralaikoto, L. Ralte, M. A. Ramirez Delgado, B. Ramson, S. S. Randriamanampisoa, A. Rappoldi, G. Raselli, T. Rath, P. Ratoff, R. Ray, H. Razafinime, R. F. Razakamiandra, E. M. Rea, J. S. Real, B. Rebel, R. Rechenmacher, J. Reichenbacher, S. D. Reitzner, E. Renner, S. Repetto, S. Rescia, F. Resnati, C. Reynolds, M. Ribas, S. Riboldi, C. Riccio, G. Riccobene, J. S. Ricol, M. Rigan, A. Rikalo, E. V. Rincón, A. Ritchie-Yates, D. Rivera, A. Robert, A. Roberts, E. Robles, M. Roda, D. Rodas Rodríguez, M. J. O. Rodrigues, J. Rodriguez Rondon, S. Rosauro-Alcaraz, P. Rosier, D. Ross, M. Rossella, M. Ross-Lonergan, T. Rotsy, N. Roy, P. Roy, P. Roy, C. Rubbia, D. Rudik, A. Ruggeri, G. Ruiz Ferreira, K. Rushiya, B. Russell, S. Sacerdoti, N. Saduyev, S. K. Sahoo, N. Sahu, S. Sakhiyev, P. Sala, G. Salmoria, S. Samanta, M. C. Sanchez, A. Sánchez-Castillo, P. Sanchez-Lucas, D. A. Sanders, S. Sanfilippo, D. Santoro, N. Saoulidou, P. Sapienza, I. Sarcevic, I. Sarra, G. Savage, V. Savinov, G. Scanavini, A. Scanu, A. Scaramelli, T. Schefke, H. Schellman, S. Schifano, P. Schlabach, D. Schmitz, A. W. Schneider, K. Scholberg, A. Schroeder, A. Schukraft, B. Schuld, S. Schwartz, A. Segade, E. Segreto, A. Selyunin, C. R. Senise, J. Sensenig, S. H. Seo, D. Seppela, M. H. Shaevitz, P. Shanahan, P. Sharma, R. Kumar, S. Sharma Poudel, K. Shaw, T. Shaw, K. Shchablo, J. Shen, C. Shepherd-Themistocleous, J. Shi, W. Shi, S. Shin, S. Shivakoti, A. Shmakov, I. Shoemaker, D. Shooltz, R. Shrock, M. Siden, J. Silber, L. Simard, J. Sinclair, G. Sinev, Jaydip Singh, J. Singh, L. Singh, P. Singh, V. Singh, S. Singh Chauhan, R. Sipos, C. Sironneau, G. Sirri, K. Siyeon, K. Skarpaas, J. Smedley, J. Smith, P. Smith, J. Smolik, M. Smy, M. Snape, E. L. Snider, P. Snopok, M. Soares Nunes, H. Sobel, M. Soderberg, H. Sogarwal, C. J. Solano Salinas, S. Söldner-Rembold, N. Solomey, V. Solovov, W. E. Sondheim, M. Sorbara, M. Sorel, J. Soto-Oton, A. Sousa, K. Soustruznik, D. Souza Correia, F. Spinella, J. Spitz, N. J. C. Spooner, D. Stalder, M. Stancari, L. Stanco, J. Steenis, R. Stein, H. M. Steiner, A. F. Steklain Lisbôa, J. Stewart, B. Stillwell, J. Stock, T. Stokes, T. Strauss, L. Strigari, A. Stuart, J. G. Suarez, J. Subash, A. Surdo, L. Suter, A. Sutton, K. Sutton, Y. Suvorov, R. Svoboda, S. K. Swain, C. Sweeney, B. Szczerbinska, A. M. Szelc, A. Sztuc, A. Taffara, N. Talukdar, J. Tamara, H. A. Tanaka, S. Tang, N. Taniuchi, A. M. Tapia Casanova, A. Tapper, S. Tariq, E. Tatar, R. Tayloe, A. M. Teklu, K. Tellez Giron Flores, J. Tena Vidal, P. Tennessen, M. Tenti, K. Terao, F. Terranova, G. Testera, T. Thakore, A. Thea, S. Thomas, A. Thompson, C. Thorpe, S. C. Timm, E. Tiras, V. Tishchenko, S. Tiwari, N. Todorović, L. Tomassetti, A. Tonazzo, D. Torbunov, D. Torres Muñoz, M. Torti, M. Tortola, Y. Torun, N. Tosi, D. Totani, M. Toups, C. Touramanis, V. Trabattoni, D. Tran, J. Trevor, E. Triller, S. Trilov, D. Trotta, J. Truchon, D. Truncali, W. H. Trzaska, Y. Tsai, Y.-T. Tsai, Z. Tsamalaidze, K. V. Tsang, N. Tsverava, S. Z. Tu, S. Tufanli, C. Tunnell, J. Turner, M. Tuzi, M. Tzanov, M. A. Uchida, J. Ureña González, J. Urheim, T. Usher, H. Utaegbulam, S. Uzunyan, M. R. Vagins, P. Vahle, G. A. Valdiviesso, E. Valencia, R. Valentim, Z. Vallari, E. Vallazza, J. W. F. Valle, R. Van Berg, D. V. Forero, A. Vannozzi, M. Van Nuland-Troost, F. Varanini, D. Vargas Oliva, N. Vaughan, K. Vaziri, A. Vázquez-Ramos, J. Vega, J. Vences, S. Ventura, A. Verdugo, M. Verzocchi, K. Vetter, M. Vicenzi, H. Vieira de Souza, C. Vignoli, C. Vilela, E. Villa, S. Viola, B. Viren, G. V. Stenico, R. Vizarreta, A. P. Vizcaya Hernandez, S. Vlachos, G. Vorobyev, Q. Vuong, A. V. Waldron, L. Walker, H. Wallace, M. Wallach, J. Walsh, T. Walton, L. Wan, B. Wang, H. Wang, J. Wang, M. H. L. S. Wang, X. Wang, Y. Wang, D. Warner, L. Warsame, M. O. Wascko, D. Waters, A. Watson, K. Wawrowska, A. Weber, C. M. Weber, M. Weber, H. Wei, A. Weinstein, S. Westerdale, M. Wetstein, K. Whalen, A. J. White, L. H. Whitehead, D. Whittington, F. Wieler, J. Wilhlemi, M. J. Wilking, A. Wilkinson, C. Wilkinson, F. Wilson, R. J. Wilson, P. Winter, J. Wolcott, J. Wolfs, T. Wongjirad, A. Wood, K. Wood, E. Worcester, M. Worcester, K. Wresilo, M. Wright, M. Wrobel, S. Wu, W. Wu, Z. Wu, M. Wurm, J. Wyenberg, B. M. Wynne, Y. Xiao, I. Xiotidis, B. Yaeggy, N. Yahlali, E. Yandel, G. Yang, J. Yang, T. Yang, A. Yankelevich, L. Yates, U. Yevarouskaya, K. Yonehara, T. Young, B. Yu, H. Yu, J. Yu, W. Yuan, M. Zabloudil, R. Zaki, J. Zalesak, L. Zambelli, B. Zamorano, A. Zani, O. Zapata, L. Zazueta, G. P. Zeller, J. Zennamo, J. Zettlemoyer, K. Zeug, C. Zhang, S. Zhang, Y. Zhang, L. Zhao, M. Zhao, E. D. Zimmerman, S. Zucchelli, V. Zutshi, R. Zwaska and On behalf of the DUNE Collaborationadd Show full author list remove Hide full author list
Instruments 2026, 10(1), 18; https://doi.org/10.3390/instruments10010018 - 17 Mar 2026
Viewed by 356
Abstract
The 2x2 Demonstrator, a prototype for the Deep Underground Neutrino Experiment (DUNE) liquid argon (LAr) Near Detector, was exposed to the Neutrinos from the Main Injector (NuMI) neutrino beam at Fermi National Accelerator Laboratory (Fermilab). This detector is a prototype of a new [...] Read more.
The 2x2 Demonstrator, a prototype for the Deep Underground Neutrino Experiment (DUNE) liquid argon (LAr) Near Detector, was exposed to the Neutrinos from the Main Injector (NuMI) neutrino beam at Fermi National Accelerator Laboratory (Fermilab). This detector is a prototype of a new modular design for a liquid argon time-projection chamber (LArTPC), comprising a two-by-two array of four modules, each further segmented into two optically isolated LArTPCs. The 2x2 Demonstrator features a number of pioneering technologies, including a low-profile resistive field shell to establish drift fields, native 3D ionization pixelated imaging, and a high-coverage dielectric light readout system. The 2.4-tonne active mass detector is flanked upstream and downstream by supplemental solid-scintillator tracking planes, repurposed from the MINERvA experiment, which track ionizing particles exiting the argon volume. The antineutrino beam data collected by the detector over a 4.5 day period in 2024 include over 30,000 neutrino interactions in the LAr active volume—the first neutrino interactions reported by a DUNE detector prototype. During its physics-quality run, the 2x2 Demonstrator operated at a nominal drift field of 500 V/cm and maintained good LAr purity, with a stable electron lifetime of approximately 1.25 ms. This paper describes the detector and supporting systems, summarizes the installation and commissioning, and presents the initial validation of collected NuMI beam and off-beam self-triggers. In addition, it highlights observed interactions in the detector volume, including candidate muon antineutrino events. Full article
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37 pages, 2901 KB  
Review
Organs-on-Chips in Drug Development: Engineering Foundations, Artificial Intelligence, and Clinical Translation
by Nilanjan Roy and Luca Cucullo
Biosensors 2026, 16(3), 155; https://doi.org/10.3390/bios16030155 - 11 Mar 2026
Viewed by 654
Abstract
Organ-on-a-chip (OoC) technologies, also termed microphysiological systems (MPSs), integrate microfluidics, engineered biomaterials, human-derived cells, and on-chip biosensing to model human physiology in microscale devices that deliver quantitative, time-resolved readouts. This review surveys the 2010–2025 literature, emphasizing how sensing, standardized sampling, and analytics enable [...] Read more.
Organ-on-a-chip (OoC) technologies, also termed microphysiological systems (MPSs), integrate microfluidics, engineered biomaterials, human-derived cells, and on-chip biosensing to model human physiology in microscale devices that deliver quantitative, time-resolved readouts. This review surveys the 2010–2025 literature, emphasizing how sensing, standardized sampling, and analytics enable clinical concordance and fit-for-purpose regulatory use. We synthesize advances in (i) materials, fabrication, and microfluidic design; (ii) organ- and disease-focused case studies; and (iii) translational benchmarks that align chip outputs with clinical pharmacokinetics, toxicology, and biomarker datasets. Across organ systems, platforms increasingly incorporate vascularization, immune components, and organoid hybrids, paired with real-time measurements of barrier integrity, metabolism, electrophysiology, and secreted biomarkers using impedance (TEER), electrochemical, and optical modalities. Representative benchmarking studies report cardiac OoCs achieving AUROC ≥ 0.85 for torsadogenic risk classification, and renal chips improving prediction of transporter-mediated clearance relative to conventional in vitro assays. We summarize validation approaches and regulatory developments relevant to new approach methodologies, including the FDA Modernization Act 2.0, and discuss how AI and multi-omics can automate signal and image analysis, harmonize cross-platform datasets, and support digital-twin workflows that couple OoC measurements to in silico models. Overall, biosensor-enabled OoCs are progressing toward quantitatively benchmarked platforms for safety pharmacology, ADME/PK–PD, and precision medicine. Full article
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22 pages, 2624 KB  
Review
From Population Averaging to Single Event Resolution: Evolution of Sensing Platforms for Membrane Fusion
by Yazhuo Feng, Xuanzhu Zhao, Zhangbao Sun, Zhangrong Lou and Sheng Zhang
Sensors 2026, 26(5), 1669; https://doi.org/10.3390/s26051669 - 6 Mar 2026
Viewed by 269
Abstract
Membrane fusion is fundamental to intracellular transport and signal transduction, with its dysregulation implicated in various diseases. Deciphering its transient, microscale dynamics requires advanced sensing technologies. This review systematically evaluates optical and electrochemical sensing platforms for in vitro studies of membrane fusion. Optical [...] Read more.
Membrane fusion is fundamental to intracellular transport and signal transduction, with its dysregulation implicated in various diseases. Deciphering its transient, microscale dynamics requires advanced sensing technologies. This review systematically evaluates optical and electrochemical sensing platforms for in vitro studies of membrane fusion. Optical sensing platforms provide greater intuitive readout of membrane fusion events, whereas electrochemical sensing platforms enable label-free, single-event resolution. We revisit classical fluorescence resonance energy transfer (FRET) strategies for lipid and content mixing, tracing their evolution from ensemble measurements to real-time, multiparameter, single-vesicle analysis. We further examine electrochemical platforms based on nanodisc-black lipid membranes (ND-BLMs) and solid-supported lipid bilayers (SLBs), highlighting their unique capabilities in characterizing fusion pore kinetics and virus–host membrane fusion. ND-BLM-based systems are irreplaceable for probing fusion pore kinetics, owing to their sub-millisecond temporal resolution and being essentially free from ion saturation and depletion effects. Meanwhile, SLB-based electrochemical sensing platforms excel at high-throughput detection of viral membrane fusion events by virtue of their excellent compatibility and facile integration. These sensors provide powerful tools for elucidating the molecular mechanisms underlying SNARE-mediated membrane fusion and viral fusion processes. Finally, this review outlines future directions centered on the integration of multimodal sensing and the construction of physiomimetic membranes, emphasizing the critical role of cross-scale, multiparameter sensing in bridging molecular mechanisms with biological functions and advancing the diagnosis and treatment of membrane fusion-related diseases. Full article
(This article belongs to the Section Optical Sensors)
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20 pages, 13517 KB  
Article
Dual-Readout Self-Resetting CMOS Image Sensor for Resolving Sub-Percent Optical Contrast in Biomedical Imaging
by Kiyotaka Sasagawa, Subaru Iwaki, Kenji Morimoto, Ryoma Okada, Hironari Takehara, Makito Haruta, Hiroyuki Tashiro and Jun Ohta
Sensors 2026, 26(4), 1396; https://doi.org/10.3390/s26041396 - 23 Feb 2026
Viewed by 556
Abstract
We report a dual-readout self-resetting CMOS image sensor that achieves a signal-to-noise ratio (SNR) exceeding 70 dB and resolves sub-percent optical contrast variations by effectivly suppressing reset artifacts. The proposed sensor employs a Dual-Readout architecture with two independent scanners operating with a temporal [...] Read more.
We report a dual-readout self-resetting CMOS image sensor that achieves a signal-to-noise ratio (SNR) exceeding 70 dB and resolves sub-percent optical contrast variations by effectivly suppressing reset artifacts. The proposed sensor employs a Dual-Readout architecture with two independent scanners operating with a temporal offset; while one readout system is in the self-reset “dead time”, the other remains active, thereby physically ensuring continuous data acquisition. To minimize pixel area while achieving high reconstruction accuracy, a minimum frame-to-frame difference algorithm is utilized for signal restoration without requiring in-pixel counters. A prototype chip fabricated in a 0.35-μm process demonstrated SNR characteristics near the shot-noise limit, with a peak SNR exceeding 70 dB. Vascular phantom experiments using a carbon black suspension successfully visualized ±0.25% contrast fluctuations—dynamic signals previously undetectable by conventional sensors. This device provides a powerful platform for high-precision bio-imaging applications, including brain surface blood flow monitoring, where both wide dynamic range and high SNR are essential. Full article
(This article belongs to the Section Optical Sensors)
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15 pages, 1601 KB  
Article
Detection of Shielded Nuclear Materials Using Superheated Liquid Detectors
by Leonardo Rodrigues and Miguel Felizardo
Particles 2026, 9(1), 20; https://doi.org/10.3390/particles9010020 - 18 Feb 2026
Viewed by 392
Abstract
Superheated liquid detectors (SLDs) exhibit strong sensitivity to fast neutrons and intrinsic insensitivity to gamma radiation, making them promising candidates for detecting shielded nuclear materials in security and non-proliferation applications. This work evaluates the feasibility of octafluoropropane-based superheated droplet detectors (SDDs) for identifying [...] Read more.
Superheated liquid detectors (SLDs) exhibit strong sensitivity to fast neutrons and intrinsic insensitivity to gamma radiation, making them promising candidates for detecting shielded nuclear materials in security and non-proliferation applications. This work evaluates the feasibility of octafluoropropane-based superheated droplet detectors (SDDs) for identifying neutron-emitting materials concealed behind common attenuators. A combined acoustic and optical readout system was implemented, including a validated pulse-shape analysis method and a machine-learning-based bubble detection algorithm using YOLOv5. The optical system achieved a detection precision of approximately 80% within the defined region of interest. While the acoustic system remains the primary and more mature detection channel, the optical approach demonstrates feasibility but is not yet operationally ready for field deployment. Experiments with an AmBe neutron source and various shielding materials demonstrate that SDDs reliably detect fast neutrons under realistic inspection conditions while remaining insensitive to gamma radiation. These results support the feasibility of SLD-based systems as low-cost, passive tools for detecting shielded nuclear materials in field environments. Full article
(This article belongs to the Section Experimental Physics and Instrumentation)
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10 pages, 1845 KB  
Article
Preliminary Results of the 64-Channel SiPM Readout MIZAR ASIC
by Andrea Di Salvo, Emanuele Trossarello, Micol Maria Bargelli, Federico Reynaud, Matteo Abrate, Richard Wheadon, Marco Mignone, Angelo Rivetti, Sara Garbolino and Mario Edoardo Bertaina
Particles 2026, 9(1), 16; https://doi.org/10.3390/particles9010016 - 13 Feb 2026
Viewed by 313
Abstract
This work describes the development of the Multi-channel Integrated Zone-sampling Analogue-memory based Readout (MIZAR) ASIC. This 64-channel chip was designed as part of NASA’s POEMMA Balloon with RADIO (PBR) mission, which aims to detect Ultra-High-Energy Cosmic Rays (UHECRs) and τ showers produced by [...] Read more.
This work describes the development of the Multi-channel Integrated Zone-sampling Analogue-memory based Readout (MIZAR) ASIC. This 64-channel chip was designed as part of NASA’s POEMMA Balloon with RADIO (PBR) mission, which aims to detect Ultra-High-Energy Cosmic Rays (UHECRs) and τ showers produced by the interaction of Cosmic Neutrinos (CNs) in the crust. The ASIC was implemented to read out a tile of 8 × 8 Silicon Photomultipliers (SiPMs) used to acquire the optical Cherenkov signals generated by Extensive Air Showers (EASs). A channel is partitioned into 256 cells where each one integrates an analogue memory, a Wilkinson Analog-to-Digital Converter (ADC) and a digital memory operating at the nominal sampling rate of 200 MS/s (with a 5 ns integration time). The signal is digitized on-chip, then the converted data is read out by an FPGA. The MIZAR also provides a 64-bit hitmap as a first-level trigger which can be elaborated by an external firmware. This ASIC can also be configured to further segment the channels into units of 32 or 64 cells each and the ADC resolution can be set to a range between 8 and 12 bits. The chip was designed in a commercial 65 nm CMOS technology node and it was submitted for production in December 2024. The ASICs were delivered in March 2025. Full article
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39 pages, 8743 KB  
Review
A Review of Aggregation-Based Colorimetric and SERS Sensing of Metal Ions Utilizing Au/Ag Nanoparticles
by Shu Wang, Lin Yin, Yanlong Meng, Han Gao, Yuhan Fu, Jihui Hu and Chunlian Zhan
Biosensors 2026, 16(2), 110; https://doi.org/10.3390/bios16020110 - 8 Feb 2026
Viewed by 568
Abstract
The accurate monitoring and dynamic analysis of metal ions are of considerable practical significance in environmental toxicology and life sciences. Colorimetric analysis and surface-enhanced Raman scattering (SERS) sensing technologies, utilizing the aggregation effect of gold and silver nanoparticles (Au/Ag NPs), have emerged as [...] Read more.
The accurate monitoring and dynamic analysis of metal ions are of considerable practical significance in environmental toxicology and life sciences. Colorimetric analysis and surface-enhanced Raman scattering (SERS) sensing technologies, utilizing the aggregation effect of gold and silver nanoparticles (Au/Ag NPs), have emerged as prominent methods for rapid metal ion detection. While sharing a common plasmonic basis, these two techniques serve distinct yet complementary analytical roles: colorimetric assays offer rapid, instrument-free visual screening ideal for point-of-care testing (POCT), whereas SERS provides superior sensitivity and structural fingerprinting for precise quantification in complex matrices. Furthermore, the synergistic integration of these modalities facilitates the development of dual-mode sensing platforms, enabling mutual signal verification for enhanced reliability. This article evaluates contemporary optical sensing methodologies utilizing aggregation effects and their advancements in the detection of diverse metal ions. It comprehensively outlines methodological advancements from nanomaterial fabrication to signal transduction, encompassing approaches such as biomass-mediated green synthesis and functionalization, targeted surface ligand engineering, digital readout systems utilizing intelligent algorithms, and multimodal synergistic sensing. Recent studies demonstrate that these techniques have attained trace-level identification of target ions regarding analytical efficacy, with detection limits generally conforming to or beyond applicable environmental and health safety regulations. Moreover, pertinent research has enhanced detection linear ranges, anti-interference properties, and adaptability for POCT, validating the usefulness and developmental prospects of this technology for analysis in complicated matrices. Full article
(This article belongs to the Section Optical and Photonic Biosensors)
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35 pages, 1280 KB  
Review
Luminescence-Based Strategies for Detecting β-Lactamase Activity: A Review of the Last Decade
by Michał Jakub Korytkowski, Anna Baraniak, Alicja Boryło and Paweł Rudnicki-Velasquez
Life 2026, 16(2), 250; https://doi.org/10.3390/life16020250 - 2 Feb 2026
Viewed by 457
Abstract
Rapid detection of β-lactamase activity is becoming increasingly important as β-lactam resistance spreads at an alarming rate and conventional diagnostics often require several hours to deliver actionable results. Over the past decade, methods based on luminescence, bioluminescence, chemiluminescence, and fluorescence have become powerful [...] Read more.
Rapid detection of β-lactamase activity is becoming increasingly important as β-lactam resistance spreads at an alarming rate and conventional diagnostics often require several hours to deliver actionable results. Over the past decade, methods based on luminescence, bioluminescence, chemiluminescence, and fluorescence have become powerful tools for the functional assessment of resistance resulting from β-lactamase activity. These approaches provide highly sensitive, activity-based readouts, often within minutes, and frequently rely on simple optical instrumentation. In this review, we summarize recent developments in luminescent probe design between 2015 and 2025, with emphasis on reaction mechanisms, analytical performance, and the ability of these systems to discriminate between different β-lactamases, including narrow-spectrum enzymes, AmpC, ESBL, and carbapenemases. We also discuss their applications in bacterial cultures, clinical isolates, complex biological matrices and, in some cases, in vivo models. While luminescent assays are not yet positioned to replace standard susceptibility testing, they offer a practical and increasingly robust complement to culture-based and molecular methods. The emerging trends highlighted here, such as self-immobilizing fluorogenic probes, chemiluminescent relay systems, nanomaterial-based sensors and AI-assisted mobile platforms, suggest that luminescent β-lactamase detection could play a meaningful role in future rapid diagnostics and resistance surveillance. Full article
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14 pages, 13741 KB  
Article
Visual Screening of Genetic Polymorphisms in eae Gene of Escherichia coli O157:H7 with Single-Nucleotide Resolution by ARMS-PCR-Mediated Lateral Flow Strip
by Noor Fatima, Liangliang Jiang, Siying Sun, Li Yao, Yubo Peng, Daoli Chen and Wei Chen
Sensors 2026, 26(3), 907; https://doi.org/10.3390/s26030907 - 30 Jan 2026
Viewed by 397
Abstract
Development of rapid, precise and fieldable detection methods for foodborne pathogens is one of the essential requirements in food safety and public health. In this research, the single-nucleotide polymorphisms (SNPs) in the eae gene of Escherichia coli O157:H7 are well visually identified with [...] Read more.
Development of rapid, precise and fieldable detection methods for foodborne pathogens is one of the essential requirements in food safety and public health. In this research, the single-nucleotide polymorphisms (SNPs) in the eae gene of Escherichia coli O157:H7 are well visually identified with the designed amplification refractory mutation system–polymerase chain reaction (ARMS-PCR) mediated lateral flow strip (LFS). Allele-specific primers were designed and optimized to discriminate the mutant-type genes from wild-type genes with single-nucleotide resolution in a simple visual format. The single-nucleotide variation in the eae gene could be easily differentiated by the observation of an optical signal on the T line of the LFS without any devices. Assay performance results show that it has a high sensitivity and specificity with the single-nucleotide differentiation ratio as low as 0.1%. This genetic polymorphisms screening performance could enumerate complex genetic variation into a simple and direct yes/no readout, highlighting the ultra-easy SNP screening mode and the simplicity of the result output for practical applications. This ARMS-PCR mediated LFS offers a straightforward, swift, and economical strategy for SNP identification with great potential for use in evolution of bacterial resistance genes and viral evolution under different environmental stresses. Full article
(This article belongs to the Special Issue Nucleic Acid-Based Biosensors for Molecular Diagnostics)
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16 pages, 9974 KB  
Article
Towards Real-Time Aquatic Monitoring of Strontium-90: Performance Evaluation of CaF2(Eu) and ZnSe(Al,O) Scintillators
by Arjana Kolnikaj, Kelum A. A. Gamage, Olaoluwa Popoola, James Graham and Antonio Di Buono
Sensors 2026, 26(3), 900; https://doi.org/10.3390/s26030900 - 29 Jan 2026
Viewed by 444
Abstract
A compact, in situ beta-spectroscopy approach for real-time monitoring of Strontium-90 (Sr-90) in contaminated groundwater has been investigated. Two inorganic scintillators, CaF2(Eu) and ZnSe(Al,O), were coupled to silicon photomultipliers (SiPMs) and evaluated experimentally using custom front-end electronics. This was also modelled [...] Read more.
A compact, in situ beta-spectroscopy approach for real-time monitoring of Strontium-90 (Sr-90) in contaminated groundwater has been investigated. Two inorganic scintillators, CaF2(Eu) and ZnSe(Al,O), were coupled to silicon photomultipliers (SiPMs) and evaluated experimentally using custom front-end electronics. This was also modelled with Monte Carlo simulations using the Geant4 toolkit. Although simulations correctly predicted ZnSe(Al,O) has an advantage due to its higher light yield and optical transport, experimental measurements additionally revealed practical limitations of the readout electronics which were not captured in the simulation model. ZnSe(Al,O) showed excellent agreement with the simulated detector response (R2 ≈ 0.86; χ2/NDF ≈ 27). It also attains a higher relative detection efficiency (∼61.5%), yielding faithful capture of the composite Sr-90/Y-90 spectrum with only minor suppression at the extreme high-energy tail. CaF2(Eu) exhibits a deficit at low-mid energies and an apparent enhancement in the high-energy tail. This is consistent with threshold and photon-statistics losses and leads to poorer agreement with simulation (χ2/NDF ≈ 179) and lower overall efficiency (∼22.7%). These findings identify ZnSe(Al,O) as the stronger candidate for an underwater, in situ Sr-90 beta-spectroscopy system and motivate targeted optimisation of SiPM coupling and crystal-edge reflectivity in future designs. Full article
(This article belongs to the Section Intelligent Sensors)
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23 pages, 13361 KB  
Article
Conceptual Design and Structural Assessment of a Hemispherical Two-Chamber Water Cherenkov Detector for Extensive Air-Shower Arrays
by Jasmina Isaković, Marina Manganaro and Michele Doro
Universe 2026, 12(2), 29; https://doi.org/10.3390/universe12020029 - 24 Jan 2026
Viewed by 351
Abstract
A conceptual design study is presented for a hemispherical, two-chamber water Cherenkov detector instrumented with bladder-embedded light traps. The detector consists of a rigid aluminium vessel enclosing a water volume that is divided into an outer, optically black chamber and a inner, reflective [...] Read more.
A conceptual design study is presented for a hemispherical, two-chamber water Cherenkov detector instrumented with bladder-embedded light traps. The detector consists of a rigid aluminium vessel enclosing a water volume that is divided into an outer, optically black chamber and a inner, reflective chamber lined by a flexible bladder. Arrays of light-trap modules, based on plastic scintillators with wavelength-shifting elements and thin silicon photomultipliers, are integrated into the bladder and selected inner surfaces. This geometry is intended to enhance muon tagging, increase acceptance for inclined air showers, and enable improved discrimination between electromagnetic and hadronic components. The study describes the mechanical and optical layout of the detector, the baseline aluminium housing, and the use of 3D-printed hexagonal prototypes to validate integration of the bladder and readout electronics. A first-order structural assessment based on thin-shell and plate theory is presented, indicating large safety margins for the hemispherical shells and identifying the flat base as the mechanically most loaded component. While GEANT4 simulations for detector response to extensive air showers in the atmosphere and performance measurements are left to future work, the present study establishes a mechanically validated, costed baseline design and outlines the steps needed to assess its impact in air-shower arrays. Full article
(This article belongs to the Section High Energy Nuclear and Particle Physics)
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18 pages, 1868 KB  
Review
Stray Light Analysis and Mitigation Perspectives for Next Generation Gravitational-Wave Detectors
by Eleonora Polini and Antonino Chiummo
Galaxies 2026, 14(1), 5; https://doi.org/10.3390/galaxies14010005 - 21 Jan 2026
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Abstract
The low-frequency sensitivity of gravitational-wave detectors can be degraded by noise arising from the re-coupling of stray light with the main interferometer beam. This review describes the re-coupling mechanism and shows how the experience gained with current detectors can be used to anticipate [...] Read more.
The low-frequency sensitivity of gravitational-wave detectors can be degraded by noise arising from the re-coupling of stray light with the main interferometer beam. This review describes the re-coupling mechanism and shows how the experience gained with current detectors can be used to anticipate and mitigate stray-light issues in third-generation instruments. We summarize the work carried out on numerical simulations and on the extensive characterization of stray light originating from both core and auxiliary optics. We also discuss possible improvements to the interferometric readout system aimed at reducing stray-light-induced noise, as well as diagnostic approaches for identifying potentially harmful scattering elements. Overall, this review summarizes best practices for the effective control of stray light in future gravitational-wave detectors, supporting design approaches aimed at preventing unforeseen noise issues. Full article
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