Upconverting Nanoparticle-based Enhanced Luminescence Lateral-Flow Assay for Urinary Biomarker Monitoring

被引:1
|
作者
Arai, Marylyn Setsuko [1 ,2 ]
Kim, Hyunho [2 ]
Pascavis, Madeleine [2 ]
Cha, Baekdong [3 ]
Brambilla, Gabriel [1 ]
Cho, Young Kwan [2 ]
Park, Jinho [2 ]
Vilela, Raquel R. C. [1 ]
de Camargo, Andrea S. S. [4 ,5 ]
Castro, Cesar M. [2 ,6 ]
Lee, Hakho [2 ,7 ]
机构
[1] Univ Sa~o Paulo, Sa~o Carlos Inst Phys, BR-13566590 Sa~o Carlos, SP, Brazil
[2] Harvard Med Sch, Massachusetts Gen Hosp, Ctr Syst Biol, Boston, MA 02114 USA
[3] Korea Inst Machinery & Mat, Daejeon 34103, South Korea
[4] BAM Fed Inst Mat Res & Testing, Glass Div, D-12489 Berlin, Germany
[5] Friedrich Schiller Univ FSU, D-07743 Jena, Germany
[6] Harvard Med Sch, Massachusetts Gen Hosp, Canc Ctr, Boston, MA 02114 USA
[7] Harvard Med Sch, Massachusetts Gen Hosp, Dept Radiol, Boston, MA 02114 USA
基金
巴西圣保罗研究基金会;
关键词
biosensor; upconverting nanoparticles; lateralflow; portable sensor; kidney injury; KIDNEY INJURY; SURFACE; SHELL;
D O I
10.1021/acsami.4c06117
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Development of efficient portable sensors for accurately detecting biomarkers is crucial for early disease diagnosis, yet remains a significant challenge. To address this need, we introduce the enhanced luminescence lateral-flow assay, which leverages highly luminescent upconverting nanoparticles (UCNPs) alongside a portable reader and a smartphone app. The sensor's efficiency and versatility were shown for kidney health monitoring as a proof of concept. We engineered Er3+- and Tm3+-doped UCNPs coated with multiple layers, including an undoped inert matrix shell, a mesoporous silica shell, and an outer layer of gold (UCNP@mSiO(2)@Au). These coatings synergistically enhance emission by over 40-fold and facilitate biomolecule conjugation, rendering UCNP@mSiO(2)@Au easy to use and suitable for a broad range of bioapplications. Employing these optimized nanoparticles in lateral-flow assays, we successfully detected two acute kidney injury-related biomarkers & horbar;kidney injury molecule-1 (KIM-1) and neutrophil gelatinase-associated lipocalin (NGAL)& horbar;in urine samples. Using our sensor platform, KIM-1 and NGAL can be accurately detected and quantified within the range of 0.1 to 20 ng/mL, boasting impressively low limits of detection at 0.28 and 0.23 ng/mL, respectively. Validating our approach, we analyzed clinical urine samples, achieving biomarker concentrations that closely correlated with results obtained via ELISA. Importantly, our system enables biomarker quantification in less than 15 min, underscoring the performance of our novel UCNP-based approach and its potential as reliable, rapid, and user-friendly diagnostics.
引用
收藏
页码:38243 / 38251
页数:9
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