4.8 Article

Hierarchical Plasmonic-Fluorescent Labels for Highly Sensitive Lateral Flow Immunoassay with Flexible Dual-Modal Switching

Journal

ACS APPLIED MATERIALS & INTERFACES
Volume 12, Issue 52, Pages 58149-58160

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acsami.0c18667

Keywords

optical label; hierarchical structure; assembly; mesoporous silica; in vitro diagnosis

Funding

  1. National Natural Science Foundation of China [21875218, U1909214, 51672248, 51872261]
  2. Zhejiang Provincial Natural Science Foundation of China [LGF20B010001, LR19E020002]
  3. Fund Program for the Scientific Activities of Selected Returned Overseas Professionals in Shanxi province [2016-14]
  4. Science and Technology Achievements Transformation Guide project of Shanxi province [201804D131041]

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Lateral flow immunoassay (LFIA), as a prominent point-of-care (POC) test platform, has been extensively adopted for rapid, on-site, and facile diagnosis of pathogen infections and disease biomarkers. Exploring novel structured optical labels of LFIA with amplified signal and complementary detection modes favors the sensitive and flexible POC diagnosis. Here, bimodal labels with both colorimetric and fluorescent readout were fabricated via a layered sequential assembly strategy based on affinity templates and hydrophobic metal-containing nanounits. High-quality colorimetric and fluorescent nanoparticles were densely incorporated into the colloidal supports and confined in separated regions, without interfering with each other. The hierarchical integration of gold nanoparticles and quantum dots with high loading density and good optical preservation realized dual readout and amplified signals from the assemblies of individual single nanoparticles. The all-in-one optical labels allowed both colorimetric and fluorescent detection of cystatin C (Cys C) after surface conjugation with antibodies. The LFIA strips revealed noninterfering dual signals for both visual inspection and quantitative detection of Cys C via the naked eye and portable devices, respectively. The limits of detection by colorimetric and fluorescent modes were 0.61 and 0.24 ng mL(-1), respectively. The novel LFIA platform demonstrated sensitive, specific, and reproducible POC testing of biomarkers with flexible detection modes and was reliable for clinical diagnosis.

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