Abstract

A fluorescent fullerene nanoparticle (NP)-based lateral flow immunochromatographic assay (LFIA) was developed for the rapid and quantitative detection of C-reactive protein (CRP) in serum. The polyclonal CRP-antibody-conjugated fullerene NPs were simply prepared by 1-ethyl-3-(3-dimethyllaminopropyl)-carbodiimide hydrochloride coupling after carboxylation of fluorescent fullerene NPs. By applying the CRP-antibody-conjugated fullerene NPs to a lateral flow test strip, quantitative analysis of CRP in serum was possible at a concentration range of 0.1–10 ng/ml within 15 min. We anticipate that this novel fluorescent fullerene NP-based LFIA can be useful for the rapid and accurate sensing of biological and chemical species, contributing to the disease diagnosis and prognosis, environmental monitoring, and food safety.

Highlights

  • The lateral flow immunochromatographic assay (LFIA) is a common technique for the detection of such diverse analytes as hormones, disease-related biomarkers, and toxins in the clinical, environmental, and food industry fields, because of its simplicity and rapidity [1,2,3,4,5,6,7,8]

  • To overcome the drawbacks of colloidal gold (CG)-based LFIA, various materials have been developed as reporters, including fluorescent microspheres (FMs), quantum dots (QDs), up-conversion nanoparticles (UCNPs), carbon nanoparticles (CNPs), and platinum nanoparticles (PtNPs) [9,10,11,12,13]

  • C-reactive protein (CRP)-C60-tetraethylene glycol (TEG) preparation process is uncomplicated and easy to perform under ambient conditions, whereas other reporting materials, e.g., semiconducting QDs and

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Summary

Introduction

The lateral flow immunochromatographic assay (LFIA) is a common technique for the detection of such diverse analytes as hormones, disease-related biomarkers, and toxins in the clinical, environmental, and food industry fields, because of its simplicity and rapidity [1,2,3,4,5,6,7,8]. To overcome the drawbacks of CG-based LFIA, various materials have been developed as reporters, including fluorescent microspheres (FMs), quantum dots (QDs), up-conversion nanoparticles (UCNPs), carbon nanoparticles (CNPs), and platinum nanoparticles (PtNPs) [9,10,11,12,13]. Park et al Nano Convergence (2019) 6:35 protein that is a non-specific but sensitive inflammation marker, especially in the case of bacterial infection It is known as a potential indicator of cardiovascular disease, e.g., coronary heart disease, ischemic stroke, and acute myocardial infarction [16,17,18]. Since the developed ­C60-TEG-based LFIA achieves sufficiently high sensitivity and quantitative analysis of a target molecule, the ­C60-TEG-based LFIA can be used as an advanced fluorescent LFIA for disease diagnosis and prognosis, environmental monitoring, and food safety

Results and discussion
Conclusion
Experimental section
Preparation of a lateral flow immunochromatographic test strip
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