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[一种用于快速检测人参皂苷Re的侧向流动免疫层析试纸条检测方法的开发]

[Development of a lateral flow dipstick immunoassay for rapid detection of ginsenoside Re].

作者信息

Nan Tie-Gui, Cao Zhen, He Li-Shan, Yuan Yuan, Huang Lu-Qi, Wang Bao-Min

机构信息

College of Agronomy and Biotechnology, China Agricultural University, Beijing 100193, China.

出版信息

Zhongguo Zhong Yao Za Zhi. 2013 Aug;38(16):2586-9.

Abstract

A sensitive antibody-based lateral flow dipstick was developed for ginsenoside Re (GRe) detection. The stick consisted of a sample pad, a conjugate pad, membrane and an absorbent pad. The membrane was coated with two capture reagents, GRe-BSA conjugate and goat anti-mouse antibodies, forming a test line and a control line, respectively. The conjugate pad was saturated with colloidal gold particles coated with affinity purified monoclonal anti-GRe antibody. The visual detection limit was 200 microg x L(-1) of GRe and the reaction time was 10 min. The Panax ginseng roots were identified after these samples (10 mg) were extracted with 5 mL tap water for 30 min at room temperature, and the extracts were tested by the dipsticks and ELISA kit. The true and false P. ginseng could be distinguished with dipsticks. The dipstick could be used to detect the quality of the P. ginseng samples when the extract was diluted 100-folds. The results were compared with those obtained using an indirect competitive enzyme-linked immunosorbent assay (icELISA). The dipstick assay proved to be a sensitive and rapid tool for quality control of P. ginseng.

摘要

开发了一种基于抗体的灵敏侧向流动试纸条用于人参皂苷Re(GRe)检测。该试纸条由样品垫、结合垫、膜和吸水垫组成。膜上包被有两种捕获试剂,即GRe-BSA偶联物和山羊抗小鼠抗体,分别形成检测线和对照线。结合垫用包被有亲和纯化抗GRe单克隆抗体的胶体金颗粒饱和。GRe的目视检测限为200μg x L(-1),反应时间为10分钟。将这些样品(10mg)用5mL自来水在室温下提取30分钟后对人参根进行鉴定,提取物用试纸条和ELISA试剂盒检测。用试纸条可以区分真假人参。当提取物稀释100倍时,该试纸条可用于检测人参样品的质量。将结果与使用间接竞争酶联免疫吸附测定(icELISA)获得的结果进行比较。试纸条检测被证明是一种用于人参质量控制的灵敏且快速的工具。

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