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[31种乙肝表面抗原酶免疫分析试剂盒的分析灵敏度评估]

[Evaluation on the analytical sensitivity of 31 HBsAg enzyme immunoassay kits].

作者信息

Gu Wen-Jie, Huang Wei-Jin, Zhou Cheng, Wu Xing, Lan Hai-Yun, Yao Xin, Lin Jing-Xiang, Li He-Min, Liang Zheng-Lun, Zhuang Hui

机构信息

National Institute for the Control of Pharmaceutical and Biological Products, Beijing 100050, China.

出版信息

Zhonghua Liu Xing Bing Xue Za Zhi. 2009 Aug;30(8):841-4.

Abstract

OBJECTIVE

To study the analytical sensitivity on 31 HBsAg enzyme immunoassy (EIA) test kits.

METHODS

Thirty one HBsAg EIA kits produced by domestic or overseas manufactories and applied for approval during May 2007 to May 2008, were evaluated using the national reference panels. The hyperbolic curve of the log A value and log concentration for the national sensitivity standards was established. The cut-off value of each kit was substituted into the curvilinear equation to determine the analytical sensitivity which was compared between different HBsAg EIA kits.

RESULTS

Twenty seven (351 lots) domestic and 4 (27 lots) overseas kits were compared. Among 378 lots of the 31 HBsAg EIA kits, only 2 lots of the domestic kits had a lower sensitivity when tested with the national HBsAg reference panels, with an average approvalr ate of 99.43% (349/351). The mean analytical sensitivity of the domestic kits for adr, adw, ay serotypes were 0.307, 0.419, 0.513 ng/ml, respectively. There was a significant difference between serotypes (F = 97.30, P < 0.01). The mean analytical sensitivity of the overseas kits for adr, adw, ay serotypes were 0.054, 0.066, 0.050 ng/ml respectively, with no significant difference between serotypes (F = 0.65, P > 0.05). The analytical sensitivity of the overseas kits for all the three serotypes was higher than that of the domestic kits (P < 0.01). There was no significant difference found between the analytical sensitivities of the kits produced by the same manufactory using 30- or 60-minute incubation of detection (P > 0.05). In contrast, there was significant difference noticed between the analytical sensitivities of the kits produced by the same manufactory when tested for 10 or 15-minute coloration of the results (P < 0.01).

CONCLUSION

Analytical sensitivity of the HBsAg EIA domestic kits should be further improved, especially for detecting adw and ay serotypes.

摘要

目的

研究31种乙肝表面抗原(HBsAg)酶免疫分析(EIA)检测试剂盒的分析灵敏度。

方法

采用国家参考品对2007年5月至2008年5月期间申请注册的31种国内外厂家生产的HBsAg EIA试剂盒进行评估。建立国家灵敏度标准品的对数吸光度(log A)值与对数浓度的双曲线方程。将各试剂盒的临界值代入曲线方程,计算分析灵敏度,并对不同HBsAg EIA试剂盒的分析灵敏度进行比较。

结果

比较了27种(351批)国产试剂盒和4种(27批)进口试剂盒。在31种HBsAg EIA试剂盒的378批产品中,用国家HBsAg参考品检测时,只有2批国产试剂盒灵敏度较低,平均合格率为99.43%(349/351)。国产试剂盒对adr、adw、ay血清型的平均分析灵敏度分别为0.307、0.419、0.513 ng/ml。不同血清型之间差异有统计学意义(F = 97.30,P < 0.01)。进口试剂盒对adr、adw、ay血清型的平均分析灵敏度分别为0.054、0.066、0.050 ng/ml,不同血清型之间差异无统计学意义(F = 0.65,P > 0.05)。进口试剂盒三种血清型的分析灵敏度均高于国产试剂盒(P < 0.01)。同一厂家生产的试剂盒检测孵育时间为30分钟或60分钟时,分析灵敏度差异无统计学意义(P > 0.05)。相反,同一厂家生产的试剂盒结果显色时间为10分钟或15分钟时,分析灵敏度差异有统计学意义(P < 0.01)。

结论

国产HBsAg EIA试剂盒的分析灵敏度有待进一步提高,尤其是在检测adw和ay血清型时。

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