Cheng Kwan H, Aijmo Jacob, Ma Lun, Yao Mingzhen, Zhang Xing, Como John, Hope-Weeks Louisa J, Huang Juyang, Chen Wei
Department of Physics, Texas Tech University, Lubbock, Texas 79409.
J Phys Chem C Nanomater Interfaces. 2008 Oct 22;112(46):17931-17939. doi: 10.1021/jp8065647.
We have studied the luminescence decay and trace biomaterials detection potential of two surface-functionalized nanoparticles, poly(ethylene glycol) bis(carboxymethyl) ether-coated LaF(3):Ce,Tb (20 nm) and thioglycolic acid-coated ZnS/Mn (5 nm). Upon UV excitation, these nanoparticles emitted fluorescence peaking at 540 and 597 nm, respectively, in solution. Fluorescence imaging revealed that these nanoparticles targeted the trace biomaterials from fingerprints that were deposited on various nonporous solid substrates. Highly ordered, microscopic sweat pores within the friction ridges of the fingerprints were labeled with good spatial resolutions by the nanoparticles on aluminum and polymethylpentene substrates, but not on glass or quartz. In solution, these nanoparticles exhibited multicomponent fluorescence decays of resolved lifetimes ranging from nano-to microseconds and of average lifetimes of ~24 and 130 micros for the coated LaF(3):Ce,Tb and ZnS:Mn, respectively. The long microsecond-decay components are associated with the emitters at or near the nanocrystal core surface that are sensitive to the size, surface-functionalization, and solvent exposure of the nanoparticles. When the nanoparticles were bound to the surface of a solid substrate and in the dried state, a decrease in the microsecond decay lifetimes was observed, indicative of a change in the coating environment of the nanocrystal surface upon binding and solvent removal. The average decay lifetimes for the surface-bound ZnS:Mn in the dried state were ~60, 30, and 11 micros on quartz, aluminum, and polymethylpentene, respectively. These values were still 2 orders of magnitude longer than the typical fluorescence decay background of most substrates (e.g., ~0.36 micros for polymethylpentene) in trace forensic evidence detections. We conclude that coated ZnS: Mn nanoparticles hold great promise as a nontoxic labeling agent for ultrasensitive, time-gated, trace evidence detections in nanoforensic applications.
我们研究了两种表面功能化纳米粒子——聚(乙二醇)双(羧甲基)醚包覆的LaF(3):Ce,Tb(约20纳米)和巯基乙酸包覆的ZnS/Mn(约5纳米)的发光衰减及痕量生物材料检测潜力。在紫外激发下,这些纳米粒子在溶液中分别发射出峰值位于540和597纳米的荧光。荧光成像显示,这些纳米粒子靶向沉积在各种无孔固体基质上的指纹中的痕量生物材料。指纹摩擦嵴内高度有序的微观汗孔在铝和聚甲基戊烯基质上被纳米粒子以良好的空间分辨率标记,但在玻璃或石英上则不然。在溶液中,这些纳米粒子表现出多组分荧光衰减,包覆的LaF(3):Ce,Tb和ZnS:Mn的分辨寿命范围从纳秒到微秒,平均寿命分别约为24和130微秒。微秒级的长衰减组分与纳米晶核表面或其附近的发射体相关,这些发射体对纳米粒子的尺寸、表面功能化和溶剂暴露敏感。当纳米粒子结合到固体基质表面并处于干燥状态时,观察到微秒衰减寿命降低,这表明在结合和去除溶剂后纳米晶表面的包覆环境发生了变化。干燥状态下表面结合的ZnS:Mn在石英、铝和聚甲基戊烯上的平均衰减寿命分别约为60、30和11微秒。在痕量法医证据检测中,这些值仍比大多数基质的典型荧光衰减背景(例如聚甲基戊烯约为0.36微秒)长2个数量级。我们得出结论,包覆的ZnS:Mn纳米粒子作为一种无毒标记剂,在纳米法医应用中的超灵敏、时间分辨、痕量证据检测方面具有巨大潜力。