Abstract

Multiplex lateral flow immunoassay (LFIA) is largely used for point-of-care testing to detect different pathogens or biomarkers in a single device. The increasing demand for multitargeting diagnostics requires multi-informative single tests. In this study, we demonstrated three strategies to upgrade standard multiplex LFIA to multimodal capacity. As a proof-of-concept, we applied the strategies to the differential diagnosis of Human Immunodeficiency Virus (HIV) infection, a widespread pathogen, for which conventional multiplex LFIA testing is well-established. In the new two-parameter LFIA (x2LFIA), we exploited color encoding, in which the binding of multiple targets occurs in one reactive band and the color of the probe reveals which one is present in the sample. By combining the sequential alignment of several reactive zones along the membrane of the LFIA strip and gold nanoparticles and gold nanostars for the differential visualization, in this demonstration, the x2LFIA can furnish information on HIV serotype and stage of infection in a single device. Three immunosensors were designed. The use of bioreagents as the capturing ligand anchored onto the membrane or as the detection ligand labelled with gold nanomaterials affected the performance of the x2LFIA. Higher detectability was achieved by the format involving the HIV-specific antigens as capturing agent and labelled secondary bioligands (anti-human immunoglobulins M and protein G) as the probes.

Highlights

  • The use of point-of-care test (POCT) has been extensively employed in developing countries, where laboratory settings are often unavailable [1]

  • Casein-biotin for conjugation to gold nanoparticles (GNP) was obtained from In3diagnostics (Torino, Italy)

  • Preliminary, we investigated the applicability of the signal resolution obtained through labelling the specific recognition elements with dual color gold nanomaterials

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Summary

Introduction

The use of point-of-care test (POCT) has been extensively employed in developing countries, where laboratory settings are often unavailable [1]. The increasing demand for simultaneous detection of multiple biomarkers in a single assay, has resulted in the development of unnumbered multiplexed LFIAs [5,6,7,8]. Multiplexing approaches exploiting probes with tuneable signals have been reported, based on fluorescence and chemiluminescence encoding [15,16,17].

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