Optical Design of an LED Lighting Source for Fluorescence Microscopes

In this study, we reveal an LED light source model applied in fluorescence microscopes. This optical model is composed of a confocal total internal reflection lens array system (CTLAS) with a nine-LED array. The CTLAS optical system that we designed consists of a total internal reflection (TIR) lens...

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Main Authors: Tai-Chih Kuo, Ting-Jou Ding, Jui-Hui Lin, Shih-Hsin Ma
Format: Article
Language:English
Published: MDPI AG 2019-10-01
Series:Applied Sciences
Subjects:
Online Access:https://www.mdpi.com/2076-3417/9/21/4574
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spelling doaj-233dc07918494d0f8d6889105e3213442020-11-25T01:23:33ZengMDPI AGApplied Sciences2076-34172019-10-01921457410.3390/app9214574app9214574Optical Design of an LED Lighting Source for Fluorescence MicroscopesTai-Chih Kuo0Ting-Jou Ding1Jui-Hui Lin2Shih-Hsin Ma3Department of Biochemistry and Molecular Cell Biology, Taipei Medical University, Taipei City 11031, TaiwanDepartment of Materials and Energy Engineering, Ming Dao University, No.369, Wen-Hua Rd., Pitou, Chang Hua 52345, TaiwanDepartment of Photonics, Feng Chia University, No. 100, Wenhwa Rd., Seatwen, Taichung City 40724, TaiwanDepartment of Photonics, Feng Chia University, No. 100, Wenhwa Rd., Seatwen, Taichung City 40724, TaiwanIn this study, we reveal an LED light source model applied in fluorescence microscopes. This optical model is composed of a confocal total internal reflection lens array system (CTLAS) with a nine-LED array. The CTLAS optical system that we designed consists of a total internal reflection (TIR) lens array and a confocal system. The electrical power of the nine-LED array is 7.9 watts, which is lower than traditional light sources, such as the original 120-watt halogen lamps used in fluorescence microscopes (Zeiss, Axio Imager 2). We have successfully applied the CTLAS system to an Axio Imager 2 fluorescence microscope to observe the vascular bundle organization, modified with Cy3 fluorescence molecules, and have found that in the process of system assembly, the fabrication errors of optical lenses could have a critical effect on the CTLAS system. The results of our experiment show that, in order to achieve the same illuminance as that of the halogen lamp, the displacement error tolerances of the lateral x-axis and the longitudinal z-axis must be controlled within 1.3 mm and 1.7 mm, respectively.https://www.mdpi.com/2076-3417/9/21/4574led light sourceoptical modeluniformityoptical design
collection DOAJ
language English
format Article
sources DOAJ
author Tai-Chih Kuo
Ting-Jou Ding
Jui-Hui Lin
Shih-Hsin Ma
spellingShingle Tai-Chih Kuo
Ting-Jou Ding
Jui-Hui Lin
Shih-Hsin Ma
Optical Design of an LED Lighting Source for Fluorescence Microscopes
Applied Sciences
led light source
optical model
uniformity
optical design
author_facet Tai-Chih Kuo
Ting-Jou Ding
Jui-Hui Lin
Shih-Hsin Ma
author_sort Tai-Chih Kuo
title Optical Design of an LED Lighting Source for Fluorescence Microscopes
title_short Optical Design of an LED Lighting Source for Fluorescence Microscopes
title_full Optical Design of an LED Lighting Source for Fluorescence Microscopes
title_fullStr Optical Design of an LED Lighting Source for Fluorescence Microscopes
title_full_unstemmed Optical Design of an LED Lighting Source for Fluorescence Microscopes
title_sort optical design of an led lighting source for fluorescence microscopes
publisher MDPI AG
series Applied Sciences
issn 2076-3417
publishDate 2019-10-01
description In this study, we reveal an LED light source model applied in fluorescence microscopes. This optical model is composed of a confocal total internal reflection lens array system (CTLAS) with a nine-LED array. The CTLAS optical system that we designed consists of a total internal reflection (TIR) lens array and a confocal system. The electrical power of the nine-LED array is 7.9 watts, which is lower than traditional light sources, such as the original 120-watt halogen lamps used in fluorescence microscopes (Zeiss, Axio Imager 2). We have successfully applied the CTLAS system to an Axio Imager 2 fluorescence microscope to observe the vascular bundle organization, modified with Cy3 fluorescence molecules, and have found that in the process of system assembly, the fabrication errors of optical lenses could have a critical effect on the CTLAS system. The results of our experiment show that, in order to achieve the same illuminance as that of the halogen lamp, the displacement error tolerances of the lateral x-axis and the longitudinal z-axis must be controlled within 1.3 mm and 1.7 mm, respectively.
topic led light source
optical model
uniformity
optical design
url https://www.mdpi.com/2076-3417/9/21/4574
work_keys_str_mv AT taichihkuo opticaldesignofanledlightingsourceforfluorescencemicroscopes
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AT juihuilin opticaldesignofanledlightingsourceforfluorescencemicroscopes
AT shihhsinma opticaldesignofanledlightingsourceforfluorescencemicroscopes
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