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Updated: Mar 13, 2026

Development of a Lateral Flow Immunochromatographic Strip for Rapid and Quantitative Detection of Small Molecule Compounds
Published on: November 13, 2021
Lectin-based lateral flow assay: proof-of-concept
Pavel Damborský1, Katarzyna M Koczula2, Andrea Gallotta2
1Department of Glycobiotechnology, Center for Glycomics, Institute of Chemistry, Slovak Academy of Sciences, Dubravska cesta 9, Bratislava 84105, Slovakia. pavel.damborsky@gmail.com jaroslav.katrlik@savba.sk.
This study introduces a novel lectin-based lateral flow assay (LFA) for detecting prostate cancer biomarkers. The assay rapidly and accurately determines prostate specific antigen (PSA) glycosylation, offering improved prostate cancer diagnosis.
Area of Science:
- Biochemistry
- Analytical Chemistry
- Biotechnology
Background:
- Lateral flow assays (LFAs) are widely used for rapid analyte detection, typically employing antibody or nucleic acid recognition.
- Prostate specific antigen (PSA) is a biomarker for prostate cancer (PCa), but its glycosylation status offers greater specificity for disease progression.
- Current lectin-based assays can be complex; a simpler, rapid alternative is needed for clinical applications.
Purpose of the Study:
- To develop and validate a novel lectin-based lateral flow assay (LFA) for determining the glycosylation of free prostate specific antigen (fPSA).
- To utilize lectins as biorecognition elements in an LFA for enhanced specificity in prostate cancer biomarker detection.
Main Methods:
- Developed a lectin-based LFA using Sambucus nigra (SNA) lectin to detect α-2,6 sialic acid on fPSA.
- Employed Maackia amurensis lectin II (MAA II) as a negative control, which binds α-2,3 sialic acid.
- The assay involves applying a sample to a strip, with results available within 10 minutes using commercial components.
Main Results:
- Successfully detected α-2,6 sialic acid on fPSA using the SNA lectin-based LFA.
- Demonstrated the specificity of the assay by using MAA II as a negative control.
- The developed LFA provides rapid (within 10 minutes) and simple detection of fPSA glycosylation.
Conclusions:
- A novel lectin-based LFA has been successfully developed for the specific detection of fPSA glycosylation.
- This approach offers a rapid, simple, and effective alternative to existing lectin-based assays for clinical diagnosis.
- The methodology holds potential for application to a wide range of other clinically significant biomarkers.

