Mert Aktürk, Gökhan Gümüş, B. Sarıoǧlu, Y. D. Gökdel
{"title":"多扫描模式激光扫描共聚焦显微系统","authors":"Mert Aktürk, Gökhan Gümüş, B. Sarıoǧlu, Y. D. Gökdel","doi":"10.3906/ELK-1807-268","DOIUrl":null,"url":null,"abstract":"In this paper, a table-top, reflective mode, laser scanning confocal microscopy system that is capable of scanning the target specimen alternately through various scanning devices and methods is proposed. We have developed a laser scanning confocal microscopy system to utilize combinations of various scanning devices and methods and to be able to characterize the optical performance of different scanners and micromirrors that are frequently used in scanning microscopy systems such as multiphoton microscopy, optical coherence tomography, or confocal microscopy. By integrating the scanner to be characterized on the same optical path with a galvanometric scan mirror, which is the conventional benchmarking scanning unit in a typical scanning microscope, we obtain two major advantages: (1) microscopy images are automatically acquired from the same location on the target specimen without having any time- consuming alignment problem and accordingly provide a high-quality optical comparison opportunity, and (2) it totally eliminates the utilization of a second scanning microscopy to benchmark the performance of the scanner-based system and considerably reduces the time spent for imaging, which is a crucial factor for a freshly excised tissue, especially under a fluorescence microscope. The system is composed of a 658 nm laser source, collimation optics, a 2D galvanometer, a 2D polymer micro-scanner, an objective lens with a numerical aperture of 0.40, a 100 μm pinhole, a PMT, a DAQ card and peripheral electronics as well as a Matlab software that simultaneously controls the system through a personal computer. Prototype of the proposed flexible LSCM system is first optically characterized using a USAF resolution target. Subsequently, we provided images of red blood and bacteria cells to demonstrate the systems’ capability for clinical diagnostics. It is reported that maximum FOV and lateral resolution of the proposed LSCM are measured to be 420 μm x 360 μm and 1 μm with galvanometer and, and 117 μm x 117 μm and 3.2 μm with the polymer scanner unit, respectively.","PeriodicalId":49410,"journal":{"name":"Turkish Journal of Electrical Engineering and Computer Sciences","volume":"148 1","pages":""},"PeriodicalIF":1.2000,"publicationDate":"2019-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"2","resultStr":"{\"title\":\"Multiscanning mode laser scanning confocal microscopy system\",\"authors\":\"Mert Aktürk, Gökhan Gümüş, B. Sarıoǧlu, Y. D. Gökdel\",\"doi\":\"10.3906/ELK-1807-268\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"In this paper, a table-top, reflective mode, laser scanning confocal microscopy system that is capable of scanning the target specimen alternately through various scanning devices and methods is proposed. We have developed a laser scanning confocal microscopy system to utilize combinations of various scanning devices and methods and to be able to characterize the optical performance of different scanners and micromirrors that are frequently used in scanning microscopy systems such as multiphoton microscopy, optical coherence tomography, or confocal microscopy. By integrating the scanner to be characterized on the same optical path with a galvanometric scan mirror, which is the conventional benchmarking scanning unit in a typical scanning microscope, we obtain two major advantages: (1) microscopy images are automatically acquired from the same location on the target specimen without having any time- consuming alignment problem and accordingly provide a high-quality optical comparison opportunity, and (2) it totally eliminates the utilization of a second scanning microscopy to benchmark the performance of the scanner-based system and considerably reduces the time spent for imaging, which is a crucial factor for a freshly excised tissue, especially under a fluorescence microscope. The system is composed of a 658 nm laser source, collimation optics, a 2D galvanometer, a 2D polymer micro-scanner, an objective lens with a numerical aperture of 0.40, a 100 μm pinhole, a PMT, a DAQ card and peripheral electronics as well as a Matlab software that simultaneously controls the system through a personal computer. Prototype of the proposed flexible LSCM system is first optically characterized using a USAF resolution target. Subsequently, we provided images of red blood and bacteria cells to demonstrate the systems’ capability for clinical diagnostics. 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Multiscanning mode laser scanning confocal microscopy system
In this paper, a table-top, reflective mode, laser scanning confocal microscopy system that is capable of scanning the target specimen alternately through various scanning devices and methods is proposed. We have developed a laser scanning confocal microscopy system to utilize combinations of various scanning devices and methods and to be able to characterize the optical performance of different scanners and micromirrors that are frequently used in scanning microscopy systems such as multiphoton microscopy, optical coherence tomography, or confocal microscopy. By integrating the scanner to be characterized on the same optical path with a galvanometric scan mirror, which is the conventional benchmarking scanning unit in a typical scanning microscope, we obtain two major advantages: (1) microscopy images are automatically acquired from the same location on the target specimen without having any time- consuming alignment problem and accordingly provide a high-quality optical comparison opportunity, and (2) it totally eliminates the utilization of a second scanning microscopy to benchmark the performance of the scanner-based system and considerably reduces the time spent for imaging, which is a crucial factor for a freshly excised tissue, especially under a fluorescence microscope. The system is composed of a 658 nm laser source, collimation optics, a 2D galvanometer, a 2D polymer micro-scanner, an objective lens with a numerical aperture of 0.40, a 100 μm pinhole, a PMT, a DAQ card and peripheral electronics as well as a Matlab software that simultaneously controls the system through a personal computer. Prototype of the proposed flexible LSCM system is first optically characterized using a USAF resolution target. Subsequently, we provided images of red blood and bacteria cells to demonstrate the systems’ capability for clinical diagnostics. It is reported that maximum FOV and lateral resolution of the proposed LSCM are measured to be 420 μm x 360 μm and 1 μm with galvanometer and, and 117 μm x 117 μm and 3.2 μm with the polymer scanner unit, respectively.
期刊介绍:
The Turkish Journal of Electrical Engineering & Computer Sciences is published electronically 6 times a year by the Scientific and Technological Research Council of Turkey (TÜBİTAK)
Accepts English-language manuscripts in the areas of power and energy, environmental sustainability and energy efficiency, electronics, industry applications, control systems, information and systems, applied electromagnetics, communications, signal and image processing, tomographic image reconstruction, face recognition, biometrics, speech processing, video processing and analysis, object recognition, classification, feature extraction, parallel and distributed computing, cognitive systems, interaction, robotics, digital libraries and content, personalized healthcare, ICT for mobility, sensors, and artificial intelligence.
Contribution is open to researchers of all nationalities.