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Upconverting Nanoparticle-based Enhanced Luminescence Lateral-Flow Assay for Urinary Biomarker Monitoring.
Arai, Marylyn Setsuko; Kim, Hyunho; Pascavis, Madeleine; Cha, Baekdong; Brambilla, Gabriel; Cho, Young Kwan; Park, Jinho; Vilela, Raquel R C; de Camargo, Andrea S S; Castro, Cesar M; Lee, Hakho.
Afiliação
  • Arai MS; São Carlos Institute of Physics, University of São Paulo, São Carlos, SP 13566-590, Brazil.
  • Kim H; Center for Systems Biology, Massachusetts General Hospital, Harvard Medical School, Boston, Massachusetts 02114, United States.
  • Pascavis M; Center for Systems Biology, Massachusetts General Hospital, Harvard Medical School, Boston, Massachusetts 02114, United States.
  • Cha B; Center for Systems Biology, Massachusetts General Hospital, Harvard Medical School, Boston, Massachusetts 02114, United States.
  • Brambilla G; Korea Institute of Machinery & Material, Daejeon 34103, South Korea.
  • Cho YK; São Carlos Institute of Physics, University of São Paulo, São Carlos, SP 13566-590, Brazil.
  • Park J; Center for Systems Biology, Massachusetts General Hospital, Harvard Medical School, Boston, Massachusetts 02114, United States.
  • Vilela RRC; Center for Systems Biology, Massachusetts General Hospital, Harvard Medical School, Boston, Massachusetts 02114, United States.
  • de Camargo ASS; São Carlos Institute of Physics, University of São Paulo, São Carlos, SP 13566-590, Brazil.
  • Castro CM; Glass Division, Federal Institute of Materials Research and Testing (BAM), 12489 Berlin ,Germany.
  • Lee H; Friedrich-Schiller University (FSU), 07743 Jena, Germany.
ACS Appl Mater Interfaces ; 16(29): 38243-38251, 2024 Jul 24.
Article em En | MEDLINE | ID: mdl-38980927
ABSTRACT
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@mSiO2@Au). These coatings synergistically enhance emission by over 40-fold and facilitate biomolecule conjugation, rendering UCNP@mSiO2@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─kidney injury molecule-1 (KIM-1) and neutrophil gelatinase-associated lipocalin (NGAL)─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.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Biomarcadores / Nanopartículas / Lipocalina-2 / Receptor Celular 1 do Vírus da Hepatite A / Ouro Limite: Humans Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Biomarcadores / Nanopartículas / Lipocalina-2 / Receptor Celular 1 do Vírus da Hepatite A / Ouro Limite: Humans Idioma: En Ano de publicação: 2024 Tipo de documento: Article