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Preparation of Near-Infrared Quantum Dots-Herceptin Conjugates for Cancer Imaging
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  • Preparation of Near-Infrared Quantum Dots-Herceptin Conjugates for Cancer Imaging
  • Preparation of Near-Infrared Quantum Dots-Herceptin Conjugates for Cancer Imaging
저자명
Lee. Dong-Kwan,Lee. Yong-Kyu
간행물명
Macromolecular research
권/호정보
2010년|18권 7호|pp.641-647 (7 pages)
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한국고분자학회
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정기간행물|ENG|
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이 논문은 한국과학기술정보연구원과 논문 연계를 통해 무료로 제공되는 원문입니다.
서지반출

기타언어초록

High-quality, near-infrared CdTe/CdSe core/shell quantum dots (QDs) formed in organic solvents can be dissolved completely in water using amphiphilic polymers, such as octylamine-modified poly(acrylic acid). The native hydrophobic ligands of QDs may be retained and used to interact with an amphiphilic polymer. Neutralized, octylamine-modified poly(acrylic acid) complexes hydrophobically capped CdTe/CdSe QDs, making them water-soluble. Fluorescence spectrophotometry showed that the quantum dot-polymer composites have strong photo-luminescence and are very stable in aqueous solutions. The surfaces of the water-soluble QDs can be conjugated to biomolecules, such as antibodies that target the human breast cancer cell line SK-BR-3, which is over expresses the HER-2 receptor (epidermal growth factor receptor-2). QD-Bioconjugates were characterized by UV-Vis spectroscopy, fluorescence photospectroscopy and confocal microscopy. Finally, it was confirmed that QDs-antibody bioconjugates efficiently labeled the cell membranes (targeted to HER-2 receptors) by comparing the water soluble QDs and QDs-antibody bioconjugates.