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A new time-resolved fluorometric microarray detection system using core-shell-type fluorescent nanosphere and its application to allergen microarray

delete2006-05-20
delete8
PRE
AI
T
Takeshi Matsuya *
K
Kazuhiko Otake
S
Shigeru Tashiro
N
Nobuhiro Hoshino
M
Motomi Katada
T
Tsuneo Okuyama
DOI:10.1007/s00216-006-0455-9delete
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摘要

摘要

En 中文
We have developed a new time-resolved fluorometric (TRF) microarray detection system consisting of fluorescent NH2 nanosphere, TRF microarray detector and gamma-irradiated polystyrene chip. Using the TRF microarray detector, we detected 500 particles of the fluorescent nanosphere in one channel. Cross-talk fluorescence from the adjacent channels was little observed in the TRF microarray detector (< 0.0004 %). The TRF microarray detection system was further applied for serum allergen-specific immunoglobulin E (IgE) multi-analyses. As a labeled tag antibody, an anti-human IgE Fab' fragment-conjugated fluorescent nanosphere (Fab' nanosphere) was prepared as described previously. As a chip surface appropriate for allergen immobilization, the polystyrene chip surface was modified by gamma irradiation. The immunoassay reactivity using the gamma-irradiated polystyrene chip was approximately 2.5-times improved compared with that of the non-treated polystyrene chip. Non-specific adsorption of the Fab' nanosphere onto the gamma-irradiated polystyrene chip surface was very low level (< 0.0009 %). In only 20 mu l of serum, six allergen-specific IgEs could be simultaneously determined in one reaction well in fewer than 90 min. Good correlation curves were obtained between the microarray immunoassay and the CAP RAST fluoro-enzyme immunoassay (CAP/RAST FEIA) method (r > 0.961). Reproducibility (CVs) of the microarray immunoassay was 8.6 % to 19.0 % (n=5).
Keyword:
fluorescent nanosphere
microarray
time-resolved fluorescence
allergy-specific IgE

期刊

Analytical and Bioanalytical Chemistry 封面图
Analytical and Bioanalytical Chemistry
IF:
3.8
论文数:
1.8W
被引数:
3.5W

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