| Literature DB >> 33867712 |
Ajaikumar Sukumaran1, Thushara Thomas1, Riji Thomas1, Rhema Elizabeth Thomas1, Jofy K Paul1, D M Vasudevan1.
Abstract
The development of Lateral Flow Immunochromatography Assay can be divided into two levels; standardizing membrane characteristics and optimizing molecular level immunoassay reaction between analyte and detector molecules. In the preliminary phase the reaction specificity of capture and detector antibodies with the analyte has to be checked with other techniques like ELISA. Molarity and pH of conjugation buffer have prime importance in the immunoreaction among analyte and antibodies. Epitope mapping of the capture and detector antibodies is also recommended to confirm the specificity of the assay. Standardization of membrane characteristics directly relates to the sensitivity of the assay through its porosity, hydrophobicity, protein holding/releasing capacity and wicking rate. Under optimised condition a perfect Lateral Flow Immunochromatography Assay should have high on-rate (target binding efficiency), low off-rate (target releasing efficiency) and low Cross-reactivity. In this manuscript, we share our experience, especially on developmental strategies and troubleshooting, that we have experienced during Lateral Flow Immunochromatography Assay kit development. © Association of Clinical Biochemists of India 2020.Entities:
Keywords: Colloidal gold; Lateral flow immunochromatography; Sensitivity; Trisodium citrate
Year: 2020 PMID: 33867712 PMCID: PMC7994469 DOI: 10.1007/s12291-020-00887-5
Source DB: PubMed Journal: Indian J Clin Biochem ISSN: 0970-1915