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Collaborative Study for Establishment of a Ph. Eur. BRP for B19 Virus DNA Testing of Plasma Pools by NAT. K.H. Buchheit, A. Daas, C.M. Nübling, J.M. Spieser 3 July 2003. SoGAT XVI. Candidate BRP. B19 positive plasma (ca 10 9 IU/ml), from window phase Liquid bulk material (10 6 IU/ml)
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Collaborative Study for Establishment of a Ph. Eur. BRP for B19 Virus DNA Testing of Plasma Pools by NAT K.H. Buchheit, A. Daas, C.M. Nübling, J.M. Spieser 3 July 2003 SoGAT XVI
Candidate BRP B19 positive plasma (ca 109 IU/ml), from window phase Liquid bulk material (106 IU/ml) • Diluent: Human plasma negative for HCV, HBV, HIV1 (NAT & serology) Lyophilisation: • ca 5400 vials, 0.5 ml • residual water: 0.98 ± 0.65% K.H. Buchheit SoGAT 3/7/03
Collaborative study • 16 labs (OMCLs, manuf., NAT test labs, kit manuf.) • Calibration vs 1st IS (500 000 IU/vial) • B19 negative plasma as dilution matrix • Qualitative assay (13 labs) • 4 independent tests • dilution series proposed • ≥ 3 half-log dil. around dilutional end point • Quantitative assay (5 labs) • Measure in parallel, diff. conc., linear range K.H. Buchheit SoGAT 3/7/03
Results (1)(Values as log10 IU/ml) • Qualitative assay (n = 12) 5.64 ± 0.17 (C.L.: 67 - 150%) • Quantitative assay (n = 5) 5.83 ± 0.05 (C.L.: 88 - 113%) • Combined 5.80 ± 0.05 (C.L.: 86 - 117%) 630 957 IU/ml K.H. Buchheit SoGAT 3/7/03
Results (2) Grey cells: qualitative assays Black cells: quantitative assays K.H. Buchheit SoGAT 3/7/03
cBRP suitable for intended purpose • Assigned potency: 105.8 IU/ml • Dilution for threshold control: 1/101.8 = 1/63 No. positive results/ no. assays for each dilution K.H. Buchheit SoGAT 3/7/03
Next Steps • OMCL guideline for B19 NAT validation (M. Nübling) • Validation panel • PTS studies for OMCLs & manufactures (if requested) K.H. Buchheit SoGAT 3/7/03