目的 建立一种灵敏度高、特异性好且快速的酶联免疫吸附测定(ELISA)方法,用以检测食蟹猴体内的国产重组抗CD20单克隆抗体(YKY-101).方法 采用双抗夹心的ELISA方法对YKY-101进行定量,以大鼠抗Rituximab为一抗,加入YKY-101后,再加入辣根过氧化物酶(HRP)标记的羊抗人IgG,加入底物显色,采用酶标仪读取450 nm(参比波长630 nm)处吸光度值.结果 建立并验证了灵敏度高、稳定性良好的检测猴血清中YKY-101的ELISA方法.结论 该ELISA方法能够满足YKY-101临床前毒代动力学的要求,可应用于猴血清中YKY-101的浓度检测.%Objective To establish a high sentitive, specific and rapid ELISA method for the determination of rh-anti-CD20 monoclonal antibody (YK-101)in cynomolgus monkey. Methods A quantitative sandwich ELISA for assay of YKY-101 was developed usingrat anti-Rituximab antibody for capturing and goat anti-human IgG-HRP for detecting. Following that,color was developed by the substrate solution and the rection was stopped by stop solution.Then the plate was analyzed with a microplate reader at a wavelength of 450nm/630nm. Results A high sentitive and stable method was established for the determination of YK-101 in cynomolgus monkey.Conclusion Itproved that the ELISA method was feasible for the dectetion of YK-101 in serum of cynomolgus monkey,which meet the requirements of the pre-clinical guidance fortoxicokinetics.
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