Development of an indirect competitive enzyme-linked immunosorbent assay for formononetin and its application in a cell-based assay using MC3T3-E1 cells

被引:9
|
作者
Fujii, Shunsuke [1 ]
Ohta, Tomoe [2 ]
Ehama, Riho [1 ]
Irikida, Mizuki [1 ]
Nomura, Shuichi [1 ]
Shoyama, Yukihiro [2 ]
Uto, Takuhiro [2 ]
机构
[1] Nagasaki Int Univ, Fac Hlth Management, Dept Hlth & Nutr, 2825 7 Huis Ten Bosch, Sasebo 8593298, Japan
[2] Nagasaki Int Univ, Fac Pharmaceut Sci, Dept Pharmacognosy, 2825 7 Huis Ten Bosch, Sasebo 8593298, Japan
关键词
Formononetin; Monoclonal antibody; Enzyme -linked immunosorbent assay; Cell -based assay; MONOCLONAL-ANTIBODY; LIQUID-CHROMATOGRAPHY; QUALITY-CONTROL; RAT PLASMA; GLYCYRRHIZIN; ISOFLAVONES; LIQUIRITIN; GENISTEIN; DAIDZEIN; MEDICINE;
D O I
10.1016/j.foodchem.2022.134339
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
Formononetin (FMN) is a methoxy isoflavone found abundantly in leguminous plants and associated foods. Several analytical methods have been developed to detect FMN. However, they are costly, complicated, and timeconsuming. This study describes an indirect competitive enzyme-linked immunosorbent assay (icELISA) to determine FMN content in food samples using a monoclonal antibody (mAb) against FMN produced by a newly established hybridoma cell line. Validation studies were conducted, and this assay was found to be sufficiently reliable, with an analytical measurement range of 19.53-1250 ng/mL and a detection limit of 17.42 ng/mL. Furthermore, icELISA was successfully applied for a cell-based assay in which the amount of FMN and ononin uptake was quantified in MC3T3-E1 cells. Hence, icELISA is a simple and reliable method for the detection and quantification of FMN, as well as elucidation of its functions and underlying mechanisms of action.
引用
收藏
页数:8
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