Program in Biotechnology, Faculty of Science, Chulalongkorn University, Patumwan, Bangkok 10330, Thailand.
Electrochemistry and Optical Spectroscopy Center of Excellence (EOSCE), Department of Chemistry, Faculty of Science, Chulalongkorn University, Patumwan, Bangkok 10330, Thailand.
J Zhejiang Univ Sci B. 2019;20(2):193-204. doi: 10.1631/jzus.B1800112.
In this work, a novel conjugate of ractopamine and bovine serum albumin (RAC-BSA) has been developed via the Mannich reaction, with a mole coupling ratio for RAC-BSA of 9:1. The proposed conjugation method provides a simple and one-step method with the use of fewer reagents compared with other conjugation methods for competitive immunoassays. RAC-BSA conjugation was used to fabricate a competitive lateral flow strip test for RAC detection in animal feed. For sample preparation, RAC was spiked in swine feed purchased from the local markets in Thailand, and methanol and running buffer at a volume ratio of 10:90 was used as extraction buffer. The procedures for sample preparation were completed within 25 min. Under optimal conditions, the limit of detection (LOD), assessed by the naked eye within 5 min, was found to be 1 ng/g. A semi-quantitative analysis was also conducted using a smart phone and computer software, with a linearity of 0.075-0.750 ng/g, calculated LOD of 0.10 ng/g, calculated limit of quantitation of 0.33 ng/g, and good correlation of 0.992. The recoveries were found in the range of 96.4%-103.7% with a relative standard deviation of 2.5%-3.6% for intra- and inter-assays. Comparison of the results obtained by the strip test with those obtained by enzyme-linked immunosorbent assay had a good agreement in terms of accuracy. Furthermore, this strip test exhibited highly specific RAC detection without cross reactivity with related compounds. Therefore, the RAC-BSA conjugation via the Mannich reaction can be accepted as a one-step and easy conjugation method and applied to the competitive lateral flow strip test.
在这项工作中,通过曼尼希反应开发了一种新型的莱克多巴胺与牛血清白蛋白(RAC-BSA)缀合物,其 RAC-BSA 的摩尔偶联比为 9:1。与其他用于竞争性免疫分析的缀合方法相比,所提出的缀合方法提供了一种简单的一步法,使用的试剂更少。RAC-BSA 缀合物用于制备用于检测动物饲料中 RAC 的竞争性横向流动条带测试。对于样品制备,将 RAC 添加到从泰国当地市场购买的猪饲料中,甲醇和运行缓冲液以 10:90 的体积比用作提取缓冲液。样品制备程序在 25 分钟内完成。在最佳条件下,通过肉眼在 5 分钟内评估的检测限(LOD)发现为 1ng/g。还使用智能手机和计算机软件进行了半定量分析,线性度为 0.075-0.750ng/g,计算的 LOD 为 0.10ng/g,计算的定量限为 0.33ng/g,相关性良好,为 0.992。回收率在 96.4%-103.7%范围内,内和间分析的相对标准偏差为 2.5%-3.6%。条带测试获得的结果与酶联免疫吸附测定法获得的结果在准确性方面具有良好的一致性。此外,该条带测试显示出对 RAC 的高度特异性检测,与相关化合物无交叉反应。因此,通过曼尼希反应的 RAC-BSA 缀合可以被接受为一种一步法和简单的缀合方法,并应用于竞争性横向流动条带测试。