Detection of analytes by immunoassay using up-converting phosphor technology

被引:287
作者
Niedbala, RS [1 ]
Feindt, H [1 ]
Kardos, K [1 ]
Vail, T [1 ]
Burton, J [1 ]
Bielska, B [1 ]
Li, S [1 ]
Milunic, D [1 ]
Bourdelle, P [1 ]
Vallejo, R [1 ]
机构
[1] OraSure Technol Inc, Bethlehem, PA 18015 USA
关键词
Testing - Phosphors - Light - Light emission;
D O I
10.1006/abio.2001.5105
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
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 less than or equal to 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 greater than or equal to 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. (C) 2001 Academic Press.
引用
收藏
页码:22 / 30
页数:9
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