Multi-Quantum Dots-Embedded Silica-Encapsulated Nanoparticle-Based Lateral Flow Assay for Highly Sensitive Exosome Detection

被引:32
作者
Kim, Hyung-Mo [1 ]
Oh, Chiwoo [2 ]
An, Jaehyun [1 ]
Baek, Seungki [2 ]
Bock, Sungje [1 ]
Kim, Jaehi [1 ]
Jung, Heung-Su [3 ]
Song, Hobeom [4 ]
Kim, Jung-Won [4 ]
Jo, Ahla [1 ]
Kim, Dong-Eun [1 ]
Rho, Won-Yeop [5 ]
Jang, Jin-Young [6 ]
Cheon, Gi Jeong [7 ,8 ,9 ]
Im, Hyung-Jun [2 ,9 ]
Jun, Bong-Hyun [1 ]
机构
[1] Konkuk Univ, Dept Biosci & Biotechnol, Seoul 05029, South Korea
[2] Seoul Natl Univ, Grad Sch Convergence Sci & Technol, Dept Appl Bioengn, Seoul 16229, South Korea
[3] ZEUS Co Ltd, Hwaseong 18636, South Korea
[4] BioSquare Inc, Seongnam 13209, South Korea
[5] Jeonbuk Natl Univ, Sch Int Engn & Sci, Jeonju 54896, South Korea
[6] Seoul Natl Univ, Dept Surg & Canc, Coll Med, Res Inst, Seoul 03080, South Korea
[7] Seoul Natl Univ, Dept Nucl Med, Coll Med, Seoul 03080, South Korea
[8] Seoul Natl Univ, Canc Res Inst, Seoul 03080, South Korea
[9] Seoul Natl Univ, Grad Sch Convergence Sci & Technol, Dept Mol Med & Biopharmaceut Sci, Seoul 16229, South Korea
基金
新加坡国家研究基金会;
关键词
exosomes; quantitative detection; lateral flow assay; multi-quantum dots-embedded silica-encapsulated silica nanoparticle; test strip;
D O I
10.3390/nano11030768
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Exosomes are attracting attention as new biomarkers for monitoring the diagnosis and prognosis of certain diseases. Colorimetric-based lateral-flow assays have been previously used to detect exosomes, but these have the disadvantage of a high limit of detection. Here, we introduce a new technique to improve exosome detection. In our approach, highly bright multi-quantum dots embedded in silica-encapsulated nanoparticles (M-QD-SNs), which have uniform size and are brighter than single quantum dots, were applied to the lateral flow immunoassay method to sensitively detect exosomes. Anti-CD63 antibodies were introduced on the surface of the M-QD-SNs, and a lateral flow immunoassay with the M-QD-SNs was conducted to detect human foreskin fibroblast (HFF) exosomes. Exosome samples included a wide range of concentrations from 100 to 1000 exosomes/mu L, and the detection limit of our newly designed system was 117.94 exosome/mu L, which was 11 times lower than the previously reported limits. Additionally, exosomes were selectively detected relative to the negative controls, liposomes, and newborn calf serum, confirming that this method prevented non-specific binding. Thus, our study demonstrates that highly sensitive and quantitative exosome detection can be conducted quickly and accurately by using lateral immunochromatographic analysis with M-QD-SNs.
引用
收藏
页码:1 / 10
页数:10
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