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Development of a Lateral Flow Immunochromatographic Strip for Rapid and Quantitative Detection of Small Molecule Compounds
Published on: November 13, 2021
Development of a sensitive immunochromatographic kit using fluorescent silica nanoparticles for rapid serodiagnosis
Hiroshi Tachibana1, Azumi Kakino1, Makoto Kazama1
1Department of Infectious Diseases,Tokai University School of Medicine,Isehara, Kanagawa 259-1193,Japan.
Insights
A new immunochromatographic kit for amebiasis diagnosis uses a specific Entamoeba histolytica antigen. This rapid test shows high accuracy, offering a valuable tool for detecting parasitic infections.
Area of Science:
- Parasitology
- Immunology
- Medical Diagnostics
Background:
- Amebiasis diagnosis relies on accurate serological methods.
- The C-terminal region of Entamoeba histolytica galactose- and N-acetyl-D-galactosamine-inhibitable lectin (C-Igl) has shown potential as a diagnostic antigen.
Purpose of the Study:
- To develop and evaluate a novel immunochromatographic kit for the rapid serodiagnosis of amebiasis.
Main Methods:
- An immunochromatographic kit was created using fluorescent silica nanoparticles coated with C-Igl.
- The kit utilizes a hand-held reader to measure fluorescent intensity.
- Evaluation involved testing with a monoclonal antibody and human serum samples.
Main Results:
- The kit detected as little as 100 pg of specific antibody.
- Positive results were obtained with 20 µL of serum within 30 minutes.
- The kit correctly identified samples from symptomatic patients, asymptomatic carriers, and showed 100% sensitivity and 97.6% specificity against controls.
Conclusions:
- The developed immunochromatographic kit is effective for rapid and accurate serodiagnosis of amebiasis.
- This diagnostic tool holds promise for clinical application in identifying Entamoeba histolytica infections.
Abstract:
We have previously shown that the C-terminal region of the intermediate subunit of Entamoeba histolytica galactose- and N-acetyl-D-galactosamine-inhibitable lectin (C-Igl) is a useful antigen for serodiagnosis of amebiasis. An immunochromatographic kit was developed using fluorescent silica nanoparticles coated with C-Igl prepared in Escherichia coli. Samples for examination were added to the freeze-dried particles and then applied to the immunochromatographic device, in which a test line on the membrane was also coated with C-Igl. Fluorescent intensity was measured using a hand-held reader. In an evaluation of the kit using a human monoclonal antibody, the minimum amount of C-Igl specific antibody showing positive results was 100 pg. In the evaluation of serum samples with different antibody titers in indirect immunofluorescent antibody tests in the kit, 20 µL of serum was sufficient to obtain positive results at 30 min. Serum samples from symptomatic patients with amebic colitis and amebic liver abscess and those from asymptomatic E. histolytica-cyst carriers showed positive results in the kit. Based on evaluation using sera from healthy controls and patients with other infectious diseases, the sensitivity and specificity of the kit were 100 and 97.6%, respectively. Therefore, we conclude that the newly developed kit is useful for rapid serodiagnosis of amebiasis.
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