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Immunochromatographic assay for the detection of pseudojujubogenin glycosides
Author(s) -
Imsungnoen Natnapa,
Phrompittayarat Watoo,
Ingkaninan Kornkanok,
Tanaka Hiroyuki,
Putalun Waraporn
Publication year - 2008
Publication title -
phytochemical analysis
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.574
H-Index - 72
eISSN - 1099-1565
pISSN - 0958-0344
DOI - 10.1002/pca.1098
Subject(s) - chemistry , reagent , chromatography , glycoside , detection limit , conjugate , immunoassay , monoclonal antibody , sample preparation , antibody , organic chemistry , mathematical analysis , mathematics , immunology , biology
Bacopa monnieri contains pseudojujubogenin glycosides as pharmacologically active compounds. In order to screen large numbers of plant samples for the presence of pseudojujubogenin glycosides, a rapid and simple assay system is required for application to small quantities of test materials. Immunoassays using monoclonal antibodies could be useful for the determination of small quantities of pseudojujubogenin glycosides in plant extracts. Objective The objective of this work was to develop a simple method for the detection of pseudojujubogenin glycosides by the immunochromatographic strip test using anti‐bacopaside I monoclonal antibody. Methodology The qualitative assay was based on a competitive immunoassay in which the detector reagent consisted of a colloidal gold particle coated with the respective anti‐bacopaside I MAb. The capture reagent was a bacopaside I‐human serum albumin conjugate immobilised onto a test strip membrane. Results The sample containing pseudojujubogenin glycosides and the detection reagent were incubated with the immobilised capture reagent. The glycosides in the sample competed in binding to the limited amount of antibodies in the detection reagent with the immobilised bacopaside I‐HSA conjugates and, hence, positive samples showed no colour in the capture spot zone. The detection limit for the strip test was 125 ng/mL. Conclusion The assay system was found to be useful as a rapid and simple screening method for the detection of pseudojujubogenin glycosides in plants. Copyright © 2008 John Wiley & Sons, Ltd.

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