Improvement and optimization of performance verification on enzyme linked immunosorbent assay for determination of hepatitis B markers
10.3969/j.issn.1673-4130.2015.23.003
- VernacularTitle:酶联免疫吸附试验检测乙型肝炎5项性能评价的改进与优化
- Author:
Jing SHI
;
Ya ZHANG
;
Lin ZOU
;
Pu CHEN
;
Liping ZHANG
- Publication Type:Journal Article
- Keywords:
hepatitis B markers;
enzyme linked immunosorbent assay;
performance verification
- From:
International Journal of Laboratory Medicine
2015;(23):3369-3371
- CountryChina
- Language:Chinese
-
Abstract:
Objective To evaluate the performance of enzyme linked immunosorbent assay (ELISA) kit in detection of Hepatitis B virus(HBV) markers by using improved and optimized method ,so as to provide a practical and feasible method and reagents for clinical laboratory .Methods ELISA test was used for the detection of HBV markers .The gradient dilution method was used to e‐valuate the lower limit .The verifiation of cut off value was carried out based on clinical and laboratory standards institute (CLSI) EP12‐A2 document .Samples with cut off values were collected to evaluate the precision ,including repeatability and intermediate precision .The coincidence rates were counted through comparing the results of ELISA with those of external quality assessment and those detected by using Abbott i4000SR chemiluminescence instrument .Results The lower detection limit of HBsAg ,HBsAb , HBeAg ,HBeAb and HBcAb were 0 .2 IU/mL ,20 mIU/mL ,1 NCU/mL ,0 .75 NCU/mL and 0 .05 NCU/mL respectively .The cut‐off value(C50 )± 20% concentration included the concentration range between C5 and C95 .The within‐run coefficient of variation (CV)≤15% ,in sandwich method the between‐run CV≤25% ,in competition method the between‐run CV≤35% .The positive and negative coincidence rates in accuracy and comparing with i 4000SR all were more than 95% and all κ>0 .75 .Conclusion ELISA tests for HBV markers in our laboratory could meet the requirements of the detection performance and clinical needs .
