2012 ©
             Publication
Journal Publication
Title of Article Development and characterisation of highly specificmonoclonal antibody-based immunoassays for the detectionand quantification of genistein-7-O-[α-rhamnopyranosyl-(1!6)]-β-glucopyranoside inDerris scandens(Roxb.) Benth. 
Date of Acceptance 30 October 2023 
Journal
     Title of Journal Phytochemical Analysis 
     Standard SCOPUS 
     Institute of Journal John Wiley & Sons, Ltd. 
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     Volume  
     Issue  
     Month
     Year of Publication 2023 
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     Abstract Introduction:The stem of the plant speciesDerris scandens(Roxb.) Benth.(DS) contains genistein-7-O-[α-rhamnopyranosyl-(1!6)]-β-glucopyranoside (GTG),which is a unique marker. Previous analyses of GTG using antibody-based immunoas-says were compromised because of their high cross-reactivity with structurallyrelated compounds of DS, thereby limiting their applicability in DS quality control.Objective:Conjugation of GTG with carrier proteins was achieved using the Mannichreaction to produce a highly specific monoclonal antibody (mAb) targeting GTG (anti-GTG mAb).Methods:The anti-GTG mAb was generated using hybridoma technology and char-acterised using an indirect competitive enzyme-linked immunosorbent assay (icE-LISA). Both lateral-flow immunoassay (LFIA) and icELISA were developed to detectand quantify GTG in DS raw materials and associated products.Results:icELISA using the anti-GTG mAb showed 100% specificity for GTG, withonly 1.77% cross-reactivity with genistin and less than 0.01% cross-reactivity withother compounds. icELISA demonstrated a linear range for GTG determinationbetween 62.5 and 2000 ng/mL. The limits of detection (LOD) and quantificationwere 49.68 and 62.50 ng/mL for GTG, respectively. The precision of the analysis ran-ged from 1.28% to 4.20% for repeatability and from 1.03% to 7.05% for reproducibil-ity. The accuracy of the analysis ranged from 101.97% to 104.01% for GTG recovery.GTG levels determined via icELISA were consistent with those confirmed via high-performance liquid chromatography (HPLC) (R2=0.9903). Moreover, the LOD ofLFIA for GTG was 500 ng/mL.Conclusion:Immunoassays utilising specific anti-GTG mAbs were successfully devel-oped, including LFIA for rapid GTG detection and icELISA for GTG quantification. 
     Keyword Derris scandens, ELISA, lateral-flow immunoassay, Mannich reaction, monoclonal antibody 
Author
647150006-9 Mr. WORAPOL SAE FOO [Main Author]
Pharmaceutical Sciences Doctoral Degree

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