[Establishment of the first national standards for nucleic acid amplification technology assay for HBV DNA]

Zhonghua Gan Zang Bing Za Zhi. 2007 Feb;15(2):107-10.
[Article in Chinese]

Abstract

Objectives: To establish a Chinese national standard for a nucleic acid test (NAT) for HBV DNA.

Methods: The candidate sample of HBV DNA positive plasma was diluted with HBV-negative human plasma. The sample was lyophilised with a concentration of approximately 300,000 copies/ml. The measurement methods used included Roche Amplicor assay (version 2.0) and real-time PCR. The lyophilised preparation was calibrated by the international standard (NIBSC code: 97/746) from NIBSC.

Results: The quantity of this lyophilised preparation was (1.29+/-0.24) x 10(5)IU/ml in comparison with the international standard for HBV DNA 97/746. The stability test indicated that the sample was stable at room temperature (20 to 25 degrees C) for 2 weeks and at 37 degrees C for at least 1 week. Long-term stability was observed at 2 to 8 degrees C for 6 months and at -20 degrees C for more than 2 years with no significant changes. The vial-to-vial imprecision rate was 3.53%.

Conclusion: Based on the results of this study, our lyophilized sample can be used as a standard in China for the nucleic acid test (NAT) for HBV DNA.

Publication types

  • English Abstract
  • Research Support, Non-U.S. Gov't

MeSH terms

  • DNA, Viral / blood*
  • Hepatitis B virus / genetics*
  • Humans
  • Nucleic Acid Amplification Techniques / standards*
  • Plasma / chemistry

Substances

  • DNA, Viral