热带病与寄生虫学
熱帶病與寄生蟲學
열대병여기생충학
TROPICAL DISEASES AND PARASITOLOGY
2014年
3期
140-142
,共3页
呼明闯%汪天平%王恩木%章乐生%司武敏%杨荣笙%罗俊平%郝晓君%翟杜娟
呼明闖%汪天平%王恩木%章樂生%司武敏%楊榮笙%囉俊平%郝曉君%翟杜娟
호명틈%왕천평%왕은목%장악생%사무민%양영생%라준평%학효군%적두연
日本血吸虫抗体检测试剂盒(IHA法)%阴%阳性冻干参考品%稳定性
日本血吸蟲抗體檢測試劑盒(IHA法)%陰%暘性凍榦參攷品%穩定性
일본혈흡충항체검측시제합(IHA법)%음%양성동간삼고품%은정성
Schistosoma japonicum%Negative and positive freeze-dried reference substance%Stability
目的:建立日本血吸虫抗体检测试剂盒(IHA法)参考品的制备方法。方法采用33.3%的饱和硫酸铵提取日本血吸虫抗体IgGγ球蛋白,经过离子交换剂DEAE层析过滤后,用Lowry法测定蛋白浓度。标定和验证合格后制成冻干阳性标准参考品。采取健康试验兔血清经处理、标定后冻干作为阴性标准参考品。用阴、阳性同批号冻干参考品各100份,分别在1、3、5、7、9、11、13、15、17、19、21、24月后,用ELISA和IHA测定冻干参考品实验室保存条件下的稳定性。结果冻干参考品经过ELISA和IHA两种免疫学方法检测其效价符合要求,其阳性符合率和阴性符合率均为100%,各时间点测定均符合要求。结论本方法制备的阴性和阳性血清冻干品可以作为日本血吸虫抗体检测试剂盒(IHA法)的参考品,其冻干品稳定性满足试剂盒保存两年的要求。
目的:建立日本血吸蟲抗體檢測試劑盒(IHA法)參攷品的製備方法。方法採用33.3%的飽和硫痠銨提取日本血吸蟲抗體IgGγ毬蛋白,經過離子交換劑DEAE層析過濾後,用Lowry法測定蛋白濃度。標定和驗證閤格後製成凍榦暘性標準參攷品。採取健康試驗兔血清經處理、標定後凍榦作為陰性標準參攷品。用陰、暘性同批號凍榦參攷品各100份,分彆在1、3、5、7、9、11、13、15、17、19、21、24月後,用ELISA和IHA測定凍榦參攷品實驗室保存條件下的穩定性。結果凍榦參攷品經過ELISA和IHA兩種免疫學方法檢測其效價符閤要求,其暘性符閤率和陰性符閤率均為100%,各時間點測定均符閤要求。結論本方法製備的陰性和暘性血清凍榦品可以作為日本血吸蟲抗體檢測試劑盒(IHA法)的參攷品,其凍榦品穩定性滿足試劑盒保存兩年的要求。
목적:건립일본혈흡충항체검측시제합(IHA법)삼고품적제비방법。방법채용33.3%적포화류산안제취일본혈흡충항체IgGγ구단백,경과리자교환제DEAE층석과려후,용Lowry법측정단백농도。표정화험증합격후제성동간양성표준삼고품。채취건강시험토혈청경처리、표정후동간작위음성표준삼고품。용음、양성동비호동간삼고품각100빈,분별재1、3、5、7、9、11、13、15、17、19、21、24월후,용ELISA화IHA측정동간삼고품실험실보존조건하적은정성。결과동간삼고품경과ELISA화IHA량충면역학방법검측기효개부합요구,기양성부합솔화음성부합솔균위100%,각시간점측정균부합요구。결론본방법제비적음성화양성혈청동간품가이작위일본혈흡충항체검측시제합(IHA법)적삼고품,기동간품은정성만족시제합보존량년적요구。
Obiective To establish the method of preparing the freeze-dried reference substance of indirect hemagglutination assay kit for the diagnosis of schistosomiasis japonica. Methods Schistosoma japonicum antibodies, IgG γ-globulins were purified by 33.3%saturated ammonium sulfate, then filtered through DEAE exchange chromatography, and finally the protein concentration was tested by Lowry method. It was prepared as positive standard reference substance after calibration and validation. The sera from healthy rabbits after processing and calibration were freeze-dried as negative standard reference substance. The stability in laboratory storage conditions of 100 copies of negative and positive of freeze-dried reference substance were detected respectively after 1, 3, 5, 7, 9, 11, 13, 15, 17, 19, 21, and 24 months by ELISA and IHA. Results The titers of freeze-dried reference substance met the requirements after the test by two kinds of method, and its positive coincidence rate and negative coincidence rate were all 100%. Conclusion The negative and positive freeze-dried sera prepared by this method can be utilized as the reference substance of indirect hemagglutination assay kit, and their stabilities meet the requirements of storing for two years.