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Plenary Lecture, Chair : Jeong-Woo Choi (Sogang Univ., Korea)

Extended-Nano Fluidics and Optical Absorption Detection by TLM Detection for Bio-analysis

첫 페이지 보기
  • 발행기관
    한국생물공학회 바로가기
  • 간행물
    한국생물공학회 학술대회 바로가기
  • 통권
    2012 춘계학술대회 및 국제심포지움 (2012.04)바로가기
  • 페이지
    pp.70-70
  • 저자
    Takehiko KITAMORI
  • 언어
    영어(ENG)
  • URL
    https://www.earticle.net/Article/A174023

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원문정보

초록

영어
Micro and extended-nano (EN) fluidic device technology has brought evolutional progress in chemistry and medical biology although it is still on the way of development for practical use. In terms of the sample volume, analytical instrumentation technology is getting new tools to reduce the volume evolutionally, that is the micro and EN fluidic device providing nano, pico, femt and atto litter orders. Micro fluidic devices are almost in practical use. We proposed the micro unit operation (MUO) and continuous flow chemical processing (CFCP) concept for realizing chemical circuit on a microchip, and it became a chemical CPU for an analytical instrument in which the sample volume is nano to pico litter which is almost the same as single cell volume. The size region of 101-102 nm, that is EN space, is still unexplored area. In our group, we fabricated extended-nano channels into glass microchips, and succeeded in fluidic control and chemical processing such as chromatographic separation. In those EN fluidics, the MUO and CFCP concepts are kept. Actually, we applied the extended-nano channels and spaces to pico-litter immunoassay and atto-litter chromatography. Pico-litter is smaller than the volume of a living cell, and therefore, single cell single molecule analysis will be available. The atto-litter chromatography is really challenging, and some examples will be introduced in this talk. One of the critical issues of micro/EN fluidic technology is detection and determination. Especially, optical detection of non-fluorescent analytes is quite difficult, because optical pass length of channels is extremely short. Therefore, we developed the thermal lens micro-detection (TLM) method, and it was proved to be a very powerful detector even at zmol regions. However, optical pass length is a couple of orders shorter in EN, and it was still very difficult. Therefore, we got an idea of introducing differential interference contrast (DIC) optical configuration into TLM. DIC-TLM enabled us to detect optical absorption in EN optical pass length, and we could obtain chromatogram of non-fluorescent molecules. Principle of DIC is based on wave optics, and EN optical pass length was still sufficiently long comparing to wavelength for detection of phase shift induced by TL effect in EN channels. The combination of EN fluidics and DIC-TLM will be a powerful tool for single cell analysis and other various kinds of nano technologies.

저자

  • Takehiko KITAMORI [ Department of Applied Chemistry, School of Engineering, The University of Tokyo, 7-3-1 Hongo, Bunkyo-ku, Tokyo 113-8656, Japan. ]

참고문헌

자료제공 : 네이버학술정보

간행물 정보

발행기관

  • 발행기관명
    한국생물공학회 [The Korean Society for Biotechnology and Bioengineering]
  • 설립연도
    1984
  • 분야
    공학>생물공학
  • 소개
    이 법인은 생물 공학의 발전과 보급에 이바지하고, 회원 상호 간의 연구 협력과 친목을 도모함을 목적으로 한다 1. 생물공학 분야의 발전을 위한 연구 협력 2. 생물공학의 실용화를 촉진시키기 위한 산학 협동 3. 학술연구 발표회, 강연회, 연수회 등 학술활동의 개최 4. 국,영문 학술지,소식지,학술회의 Proceedings 및 학술도서의 발간 5. 생물공학 발전을 위한 정책 건의 6. 기타 국제 교류 등 본 학회의 목적 달성을 위한 제반 활동

간행물

  • 간행물명
    한국생물공학회 학술대회
  • 간기
    반년간
  • 수록기간
    1985~2013
  • 십진분류
    KDC 476 DDC 576

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