首页> 外文会议>Society for Biomaterials annual meeting and exposition >Multiplexed biotnarker detection using phase change nanoparticles
【24h】

Multiplexed biotnarker detection using phase change nanoparticles

机译:使用相变纳米粒子的多重生物诱捕器检测

获取原文
获取外文期刊封面目录资料

摘要

Many biomarkers are specific for early stage cancer detection, but no individual biomarker is ideal to distinguish lethal cancer from indolent ones due to lack of tumor specificity. Parallel to efforts of finding specific biomarkers, a feasible way of providing better predictive value is to detect multiple biomarkers from a sample and collectively assess response pattern of more biomarkers. But, existing techniques such as microarrays and nanoparticles are not suitable to detect multiple low concentration biomarkers in a tiny amount of sample due to low sensitivity, low multiplicity and extensive sample preparation. We have detected multiple DNA and protein biomarkers with a panel of phase change nanoparticles of metals and alloys. Nanoparticles attached on a substrate through ligand-biomarker interactions are readout using differential scanning calorimetry, where the peak position and area reflect presence and concentration of biomarkers. This research is innovative for several reasons. (1) It uses an unexplored phenomenon of solid materials, i.e., the temperature of a solid will not rise above its melting point until the entire solid is molten. (2) Sharp melting peak, large thermal scan range and wide choices of materials enhance multiplicity this detection without adding system complexity. (3) The surface grafting density of ligands on nanoparticles is controlled to detect multiple biomarkers with concentrations differing several orders of magnitude.
机译:许多生物标志物对早期癌症检测具有特异性,但是由于缺乏肿瘤特异性,没有任何一种生物标志物能够理想地区分致死性癌症和惰性癌症。与寻找特定生物标志物的努力并行,提供更好的预测价值的可行方法是从样品中检测多种生物标志物,并共同评估更多生物标志物的反应模式。但是,由于低灵敏度,低重复性和广泛的样品制备,诸如微阵列和纳米颗粒之类的现有技术不适用于检测少量样品中的多种低浓度生物标志物。我们已经用一组金属和合金的相变纳米颗粒检测了多种DNA和蛋白质生物标志物。通过差示扫描量热法读取通过配体-生物标记物相互作用附着在底物上的纳米粒子,其中峰的位置和面积反映了生物标记物的存在和浓度。这项研究具有创新性,原因有几个。 (1)它使用了固体材料的一种未曾探索过的现象,即,固体的温度直到整个固体融化后才会升高到其熔点以上。 (2)尖锐的熔解峰,较大的热扫描范围和多种材料选择可增加这种检测的多样性,而不会增加系统的复杂性。 (3)控制配体在纳米颗粒上的表面接枝密度,以检测浓度相差几个数量级的多种生物标志物。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号