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Optimum Combined Lenses for Confocal Biochip Scanning System
作者姓名:黄国亮  程京  周玉祥  冯继宏  刘诚迅  金国藩  邬敏贤  严瑛白  张腾飞  李林
作者单位:HUANG Guoliang,CHENG Jing,ZHOU Yuxiang 1,FENG Jihong,LIU Chengxun,JIN Guofan WU Minxian,YAN Yingbai ZHANG Tengfei,LI Lin 1.Department of Biological Sciences and Technology,Tsinghua University,Beijing 100084,China; Beijing National B
基金项目:Supported by the National High-Tech DevelopmentProgram of China(No.863 -10 3 -13 0 -5 0 2 ),the“973”National Science Foundation of China (No.G19990 1160 3 ),the National Natural ScienceFoundation of China (No. 3 0 0 0 0 0 40 ),the NaturalScie
摘    要:IntroductionLaboratory-on-a-chip technology1 5] has gainedinterest in recent years,and consists of threeclassic steps:sample preparation,biochemicalreaction,and detection analysis.Many researchgroups have used small biochips to studypolymerase chain reaction (PCR) amplification1 ] ,DNA sequencing2 ] ,ligase chain reaction(LCR) 3] ,dielectrophoresis of cell separation,andcapillary electrophoresis4 ,5] .Some importantbiochip detection systems6 8] have been developed,such as the dual-la…


Optimum Combined Lenses for Confocal Biochip Scanning System
HUANG Guoliang,CHENG Jing,ZHOU Yuxiang ,FENG Jihong,LIU Chengxun,JIN Guofan WU Minxian,YAN Yingbai ZHANG Tengfei,LI Lin.Optimum Combined Lenses for Confocal Biochip Scanning System[J].Tsinghua Science and Technology,2002,7(4).
Authors:HUANG Guoliang  CHENG Jing  ZHOU Yuxiang  FENG Jihong  LIU Chengxun  JIN Guofan WU Minxian  YAN Yingbai ZHANG Tengfei  LI Lin
Institution:HUANG Guoliang,CHENG Jing,ZHOU Yuxiang 1,FENG Jihong,LIU Chengxun,JIN Guofan WU Minxian,YAN Yingbai ZHANG Tengfei,LI Lin 1.Department of Biological Sciences and Technology,Tsinghua University,Beijing 100084,China, Beijing National B
Abstract:Laboratory-on-a-chip technology has attracted wide interest in recent years, where the sample preparation, bio-chemical reaction, separation, detection and analysis are performed in a small biochip of the size of a fingernail. To obtain a high detection sensitivity of 1 fluors/μm2 (one fluorescence molecule per square micrometer) in biochip scanning systems, the scanning objective lens is required to have a high numerical aperture (>0.5), very small focal spot (<5 μm), and long back focal length (>3 mm). This study presents the design of optimum combined lenses including scanning objective and fluorescence focal lenses. The scanning objective had a high numerical aperture (NA) of 0.72, a very small focal spot of 1.67 μm, a long back focal length of 3.2 mm, and a high resolving power of 760 lines/mm. The fluorescence focal lenses had an NA of 0.3, a fluorescence focal spot of 16 μm, a long back focal length of 16.7 mm and a resolving power of 590 lines/mm. The phase aberrations of the combined lenses, including the aspherical aberration and the chromatic aberration corresponding to wavelengths of 532, 570, 635, and 670 nm, were well-corrected. The encircled energy diagram of the lenses was within the diffraction limit. The study also included the focal spot diagram, the optical path difference diagram, the transverse ray fan plot, and the modulation transfer function. A confocal biochip scanning system with designed combined lenses was developed and some experiments were conducted on a multi-channel biochip.
Keywords:lens  confocal  fluorescence  gene  DNA  biochip
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