Qi Xiao-Hua, Zhang Li-Wei, Zhang Xin-Xiang
Beijing National Laboratory for Molecular Sciences, Key Laboratory of Bioorganic Chemistry and Molecular Engineering of MOE, Institute of Analytical Chemistry, College of Chemistry, Peking University, Beijing, P. R. China.
Electrophoresis. 2008 Aug;29(16):3398-405. doi: 10.1002/elps.200700673.
A multitarget antibody immunoaffinity column was proposed for the purification and enrichment of nandrolone, testosterone, and methyltestosterone from urine. Nandrolone-3-site substituted antigen was designed and synthesized and the polyclonal antibody was prepared with immunizing rabbits. The stationary phase of the immunoaffinity column was synthesized by covalently bonding the antibodies specific to nandrolone, testosterone, and methyltestosterone onto CNBr-actived Sepharose 4B. The analytes of interest were extracted with a methanol/water mixture in one step. The immunoaffinity column showed high affinity and high selectivity to a class of structurally related compounds. The elution was then transferred to a micellar electrokinetic CE system with a running buffer of sodium borate and sodium cholate for separation and determination. Recoveries of the three steroids from complex matrix were 88-94% with RSD values less than 5.2%. Optimization of the immunoaffinity column purification was achieved and the feasibility of the technique for the analysis of steroid hormone was discussed. The results indicated that the combination of multi-immunoaffinity column and CE was an effective technique, which was rapid, simple, and sensitive for the assay of steroids.
提出了一种多靶点抗体免疫亲和柱,用于从尿液中纯化和富集诺龙、睾酮和甲基睾酮。设计并合成了诺龙三位点取代抗原,通过免疫家兔制备了多克隆抗体。免疫亲和柱的固定相是通过将诺龙、睾酮和甲基睾酮特异性抗体共价结合到溴化氰活化的琼脂糖凝胶4B上合成的。目标分析物用甲醇/水混合物一步提取。该免疫亲和柱对一类结构相关化合物表现出高亲和力和高选择性。然后将洗脱液转移到以硼酸钠和胆酸钠为运行缓冲液的胶束电动毛细管电泳系统中进行分离和测定。从复杂基质中回收这三种甾体的回收率为88 - 94%,相对标准偏差值小于5.2%。实现了免疫亲和柱纯化的优化,并讨论了该技术用于甾体激素分析的可行性。结果表明,多免疫亲和柱和毛细管电泳的结合是一种有效的技术,对甾体测定快速、简单且灵敏。