PEGylated Gold Nanoparticles Conjugated to Monoclonal F19 Antibodies as Targeted Labeling Agents for Human Pancreatic Carcinoma Tissue

单克隆抗体 胶体金 共轭体系 抗体 西妥昔单抗 胰腺癌 纳米颗粒 癌症研究 纳米技术 胰腺癌 材料科学 化学 医学 癌症 内科学 免疫学 有机化学 聚合物
作者
Wolfgang Eck,Gary A. Craig,Aruna Sigdel,Gerd Ritter,Lloyd J. Old,Laura H. Tang,Murray F. Brennan,Peter J. Allen,Michael D. Mason
出处
期刊:ACS Nano [American Chemical Society]
卷期号:2 (11): 2263-2272 被引量:254
标识
DOI:10.1021/nn800429d
摘要

In this study, we describe optical detection of antibody-conjugated nanoparticles bound to surgically resected human pancreatic cancer tissue. Gold nanoparticles stabilized by heterobifunctional polyethylene glycol (PEG) were prepared using approximately 15 nm spherical gold cores and covalently coupled to F19 monoclonal antibodies. The heterobifunctional PEG ligands contain a dithiol group for stable anchoring onto the gold surface and a terminal carboxy group for coupling of antibodies to the outside of the PEG shell. The nanoparticle-antibody bioconjugates form highly stable dispersions and exhibit long-term resistance to agglomeration. This has been demonstrated by dynamic light scattering, size exclusion chromatography, and transmission electron microscopy. The nanoparticle bioconjugates were used to label tumor stroma in approximately 5 mum thick sections of resected human pancreatic adenocarcinoma. After rinsing away nonbound nanoparticles and fixation, the tissue samples were imaged by darkfield microscopy near the nanoparticle resonance scattering maximum (approximately 560 nm). The images display pronounced tissue features and suggest that this novel labeling method could provide for facile identification of cancer tissue. Tumor samples treated with gold nanoparticles conjugated to nonspecific control antibodies and noncancerous pancreatic tissue treated with mAb-F19-conjugated gold nanoparticles both exhibited correctly negative results and showed no tissue staining.
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