{"title":"检测模块增加了显微镜的空间带宽乘积。","authors":"Charlie Kersuzan, Aymerick Bazin, Amaury Badon","doi":"10.1364/OL.563495","DOIUrl":null,"url":null,"abstract":"<p><p>Capturing biological specimens at large scales with sub-micron resolution is crucial for biomedical research, but conventional cameras often cannot handle the pixel requirements. While most microscopes use motorized stages to move samples and capture images tile by tile, we propose a method that eliminates the need for sample movement. Our approach integrates a scanning mechanism within the microscope's detection unit, enabling sequential capture of sub-areas of the field of view (FOV) without physically moving the sample. This \"remote scanning\" method works with all camera-based microscopes, and we demonstrate its effectiveness in both bright-field and epifluorescence microscopy. This technique is ideal for imaging motion-sensitive samples and large biological specimens, as evidenced in this study with millimeter-scale engineered tissues.</p>","PeriodicalId":19540,"journal":{"name":"Optics letters","volume":"50 11","pages":"3688-3691"},"PeriodicalIF":3.3000,"publicationDate":"2025-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Detection module to increase the spatial bandwidth product of a microscope.\",\"authors\":\"Charlie Kersuzan, Aymerick Bazin, Amaury Badon\",\"doi\":\"10.1364/OL.563495\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Capturing biological specimens at large scales with sub-micron resolution is crucial for biomedical research, but conventional cameras often cannot handle the pixel requirements. While most microscopes use motorized stages to move samples and capture images tile by tile, we propose a method that eliminates the need for sample movement. Our approach integrates a scanning mechanism within the microscope's detection unit, enabling sequential capture of sub-areas of the field of view (FOV) without physically moving the sample. This \\\"remote scanning\\\" method works with all camera-based microscopes, and we demonstrate its effectiveness in both bright-field and epifluorescence microscopy. This technique is ideal for imaging motion-sensitive samples and large biological specimens, as evidenced in this study with millimeter-scale engineered tissues.</p>\",\"PeriodicalId\":19540,\"journal\":{\"name\":\"Optics letters\",\"volume\":\"50 11\",\"pages\":\"3688-3691\"},\"PeriodicalIF\":3.3000,\"publicationDate\":\"2025-06-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Optics letters\",\"FirstCategoryId\":\"101\",\"ListUrlMain\":\"https://doi.org/10.1364/OL.563495\",\"RegionNum\":2,\"RegionCategory\":\"物理与天体物理\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"OPTICS\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Optics letters","FirstCategoryId":"101","ListUrlMain":"https://doi.org/10.1364/OL.563495","RegionNum":2,"RegionCategory":"物理与天体物理","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"OPTICS","Score":null,"Total":0}
Detection module to increase the spatial bandwidth product of a microscope.
Capturing biological specimens at large scales with sub-micron resolution is crucial for biomedical research, but conventional cameras often cannot handle the pixel requirements. While most microscopes use motorized stages to move samples and capture images tile by tile, we propose a method that eliminates the need for sample movement. Our approach integrates a scanning mechanism within the microscope's detection unit, enabling sequential capture of sub-areas of the field of view (FOV) without physically moving the sample. This "remote scanning" method works with all camera-based microscopes, and we demonstrate its effectiveness in both bright-field and epifluorescence microscopy. This technique is ideal for imaging motion-sensitive samples and large biological specimens, as evidenced in this study with millimeter-scale engineered tissues.
期刊介绍:
The Optical Society (OSA) publishes high-quality, peer-reviewed articles in its portfolio of journals, which serve the full breadth of the optics and photonics community.
Optics Letters offers rapid dissemination of new results in all areas of optics with short, original, peer-reviewed communications. Optics Letters covers the latest research in optical science, including optical measurements, optical components and devices, atmospheric optics, biomedical optics, Fourier optics, integrated optics, optical processing, optoelectronics, lasers, nonlinear optics, optical storage and holography, optical coherence, polarization, quantum electronics, ultrafast optical phenomena, photonic crystals, and fiber optics. Criteria used in determining acceptability of contributions include newsworthiness to a substantial part of the optics community and the effect of rapid publication on the research of others. This journal, published twice each month, is where readers look for the latest discoveries in optics.