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利用抗柴胡皂苷a单克隆抗体开发柴胡皂苷a检测系统。

Development of an assay system for saikosaponin a using anti-saikosaponin a monoclonal antibodies.

作者信息

Zhu Shu-Hang, Shimokawa Shin-ichi, Tanaka Hiroyuki, Shoyama Yukihiro

机构信息

Department of Pharmacognosy, Graduate School of Pharmaceutical Sciences, Kyushu University, 3-1-1 Maidashi, Higashi-ku, Fukuoka 812-8582, Japan.

出版信息

Biol Pharm Bull. 2004 Jan;27(1):66-71. doi: 10.1248/bpb.27.66.

Abstract

For immunization, saikosaponin a (SSa) was conjugated with bovine serum albumin (BSA). The hapten number in an antigen conjugate was determined to be eleven by matrix-assisted laser adsorption/ionization time-of-flight mass spectrometry (MALDI-TOF Mass). Hybridomas secreting monoclonal antibodies (MAb) against SSa were produced by fusing splenocytes immunized with SSa-BSA conjugate and a hypoxanthine-aminopterin-thymidine-sensitive (HAT) mouse myeloma cell line, P3-X63-Ag8-653. A high specific MAb against SSa was selected from hybridomas using enzyme-linked immunosorbent assay (ELISA) analysis. Weak cross-reactivities occurred with saikosaponin c, b(2) and d, which are stereochemical and/or functional isomers of SSa, but no cross-reactivities were observed with other related steroidal glycosides. The full range of the assay extends 26 ng/ml to 1.5 microg/ml of SSa. Good correlation of SSa concentrations in a crude extract of Bupleuri radix between ELISA and HPLC methods was obtained after hydrolysis of acyl saikosaponins by treatment with a mild alkaline solution. The newly established ELISA has been applied for the quantitative assay of SSa in the Bupleuri radix and the Kampo medicines (TCM) prescribed with Bupleuri radix.

摘要

为了进行免疫,将柴胡皂苷a(SSa)与牛血清白蛋白(BSA)偶联。通过基质辅助激光吸附/电离飞行时间质谱(MALDI-TOF Mass)测定抗原偶联物中的半抗原数量为11。通过将用SSa-BSA偶联物免疫的脾细胞与次黄嘌呤-氨基蝶呤-胸腺嘧啶核苷敏感(HAT)小鼠骨髓瘤细胞系P3-X63-Ag8-653融合,制备分泌抗SSa单克隆抗体(MAb)的杂交瘤。使用酶联免疫吸附测定(ELISA)分析从杂交瘤中筛选出高特异性的抗SSa单克隆抗体。该单克隆抗体与柴胡皂苷c、b(2)和d(它们是SSa的立体化学和/或功能异构体)存在较弱的交叉反应,但与其他相关甾体糖苷未观察到交叉反应。该检测方法的线性范围为26 ng/ml至1.5 μg/ml的SSa。在用温和碱性溶液处理使酰基柴胡皂苷水解后,ELISA法与HPLC法测定的柴胡粗提物中SSa浓度具有良好的相关性。新建立的ELISA法已应用于柴胡及含柴胡的汉方药物(中药)中SSa的定量测定。

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