Niedbala R S, Feindt H, Kardos K, Vail T, Burton J, Bielska B, Li S, Milunic D, Bourdelle P, Vallejo R
OraSure Technologies, Inc., 150 Webster Street, Bethlehem, Pennsylvania 18015-1389, USA.
Anal Biochem. 2001 Jun 1;293(1):22-30. doi: 10.1006/abio.2001.5105.
Up-Converting Phosphor Technology (UPT) is based on lanthanide-containing, submicrometer-sized, ceramic particles that can absorb infrared light and emit visible light. Biological matrices do not up-convert; hence, there is no contribution to test background from sample autofluorescence. Up-converting phosphors do not photobleach and are inert to common assay interferants such as hemoglobin. A reader called UPlink has been developed to interrogate lateral flow test strips that utilize UPT labels. The reader contains a miniaturized, 1-W, infrared laser with peak emission at 980 nm. Preliminary assays that use up-converting phosphor labels, including tests for a drugs of abuse panel and Escherichia coli O157:H7, have been developed. In a "sandwich" assay format, 10(3) org/mL E. coli O157:H7 organisms were detectable in a negative control background of 10(9) other organisms per milliliter of culture medium. Coefficients of variation in concentrations tested from 0 to 10(7) org/mL were all < or =10%. In a competitive inhibition assay format, a multiplexed test simultaneously detected amphetamine, methamphetamine, phencyclidine, and opiates in saliva. For all assays, the percent displacement at 10 ng/mL was > or =40% demonstrating performance comparable with lab-based, commercially available EIAs. All assays were complete in 10 min. The development of rapid tests using UPT creates new applications for on-site testing with sensitivity not available using other label technologies.
上转换磷光技术(UPT)基于含镧系元素的亚微米级陶瓷颗粒,这些颗粒能够吸收红外光并发射可见光。生物基质不会发生上转换;因此,样品自身荧光不会对检测背景产生影响。上转换磷光体不会发生光漂白,并且对血红蛋白等常见检测干扰物呈惰性。已开发出一种名为UPlink的读取器,用于检测使用UPT标记的侧向流动测试条。该读取器包含一个小型化的1瓦红外激光器,其峰值发射波长为980纳米。已经开发出了使用上转换磷光体标记的初步检测方法,包括对滥用药物检测组和大肠杆菌O157:H7的检测。在“夹心”检测形式中,在每毫升培养基中含有10⁹个其他生物体的阴性对照背景下,能够检测到10³个/毫升的大肠杆菌O157:H7生物体。在0至10⁷个/毫升的测试浓度范围内,变异系数均≤10%。在竞争性抑制检测形式中,一种多重检测方法可同时检测唾液中的苯丙胺、甲基苯丙胺、苯环己哌啶和阿片类物质。对于所有检测,在10纳克/毫升时的置换百分比≥40%,表明其性能与基于实验室的市售酶免疫分析方法相当。所有检测在10分钟内完成。使用UPT开发快速检测方法为现场检测创造了新的应用,其灵敏度是其他标记技术所无法达到的。