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Polysaccharide based cancer cell specific nano-carrier for photodynamic therapy

첫 페이지 보기
  • 발행기관
    한국당과학회 바로가기
  • 간행물
    한국당과학회 학술대회 바로가기
  • 통권
    2013 한국당과학회 동계학술대회 (2013.02)바로가기
  • 페이지
    pp.36-37
  • 저자
    Byoung-chan Bae, Kun Na
  • 언어
    영어(ENG)
  • URL
    https://www.earticle.net/Article/A212700

※ 원문제공기관과의 협약기간이 종료되어 열람이 제한될 수 있습니다.

원문정보

초록

영어
Photodynamic therapy (PDT), which employs photosensitizers (PSs), a light source with appropriate wavelength, and oxygen molecules, has potential for the treatment of various tumors and non-oncological diseases due to its high efficiency in directly producing cellular death, vascular shutdown, and immune activation. For the past decade, many PSs were developed with improved optical and chemical properties. However, some weak points still remain such as low solubility and low tumor specificity by hydrophobic PSs. So, many PDT studies based on soluble polysaccharide carriers such as PSs conjugated polysaccharide nanocarrier and PSs loaded nanocarrier have been carried out in order to improve the water solubility and target specificity of PSs. In case of our group, we prepared the polysaccharide based nanocarrier system composed of cancer cell target-moiety-labeled polysaccharide-graft PS by a dialysis method to improve their targeting efficiency and water solubility. The synthesis was confirmed by 1H NMR spectroscopy, and degree of substitution was determined by UV-spectrophotometery. The size of spherical nanogels was approximately 170 nm, and its photocytotoxicity was studied by an XTT assay. While the PS grafted nanocarrier circulated in the blood, the nanocarrier’s photoactivity may be suppressed by a self-quenching effect between PS molecules in the PS grafted nanocarrier system, similar to the fluorescence resonance energy transfer (FRET) effect. Because the PS grafted nanocarrier system is thought to be internalized into cancer cells following tissue penetration, its photoactivity may be restored without the FRET effect by cleavage of its ester bonds through enzymatic attack in the extracellular matrix and cellular compartments such as lysosomes. The PS grafted nanocarrier system showed a self-quenching activity in the aqueous environment, and has the capacity of tumor tissue targeting by nano-size induced EPR. After accumulation of the PS grafted nanocarrier system in tumors, the fluorescence signals will be gradually enhanced by the release of the PS from broken PS grafted nanocarrier caused by cleavable ester linkage. The phototoxicity effects in the cells by the irradiation of external light resulted in generation of singlet oxygen, at the same time when the near-infrared fluorescence molecular imaging can be detected.

저자

  • Byoung-chan Bae [ Department of Biotechnology, The Catholic University of Korea, 43-1 Yokkok2-dong, Wonmi-gu, Bucheon City 420-743, Republic of Korea ]
  • Kun Na [ Department of Biotechnology, The Catholic University of Korea, 43-1 Yokkok2-dong, Wonmi-gu, Bucheon City 420-743, Republic of Korea ]

참고문헌

자료제공 : 네이버학술정보

간행물 정보

발행기관

  • 발행기관명
    한국당과학회 [Korean Society for Glycoscience]
  • 설립연도
    2006
  • 분야
    의약학>약학
  • 소개
    본 학회는 화학, 생화학, 분자생물학, 미생물학, 식품공학, 의학, 약학, 유전공학 및 생물공학, 환경 및 기타 공업 등 전 분야의 탄수화물관련 이론과 기술을 연구 발전시키고 산학협동을 통해 이를 보급하여 국내 관련 산업의 발전 및 국민생활의 과학화에 기여하고자 하며, 이러한 목표와 비젼의 실현을 위해 회원들이 적극적인 참여와 활동을 전개하고자 한다.

간행물

  • 간행물명
    한국당과학회 학술대회
  • 간기
    연간
  • 수록기간
    2006~2022
  • 십진분류
    KDC 517 DDC 614

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