Department of Clinical Pharmacology and Pharmacoepidemiology, Heidelberg University Hospital, Im Neuenheimer Feld 410, 69120, Heidelberg, Germany.
German Center for Infection Research (DZIF), Heidelberg Partner Site, Im Neuenheimer Feld 410, 69120, Heidelberg, Germany.
Anal Bioanal Chem. 2021 Sep;413(22):5645-5654. doi: 10.1007/s00216-021-03384-7. Epub 2021 May 20.
Bulevirtide is a first-in-class entry inhibitor of the hepatitis B and hepatitis delta virus blocking the sodium/bile acid co-transporter NTCP, and was recently approved for the treatment of hepatitis D as a priority medicine (prime) in an accelerated assessment by the European Medicines Agency. It is a very large lipopeptide comprising 47 amino acids in its sequence and a myristoylation at the N-terminus. For support of clinical development, we established highly sensitive plasma quantification assays using 100 μL of plasma, spanning concentrations of 0.1 to 100 ng/mL and 1 to 1000 ng/mL with the option to measure ten-fold diluted samples up to 10,000 ng/mL. Quantification was performed with UPLC-MS/MS measurements after extraction with protein precipitation. Both assays were fully validated according to the pertinent guidelines of the FDA and EMA, including incurred sample reanalyses and cross-validation using clinical study samples. Graphical abstract.
布乐维替德是一种新型的乙型肝炎和丁型肝炎病毒进入抑制剂,可阻断钠离子/胆盐共转运蛋白 NTCP,最近被欧洲药品管理局(EMA)加速评估作为优先药物(prime)批准用于治疗丁型肝炎。它是一种非常大的脂肽,其序列包含 47 个氨基酸,在 N 末端进行豆蔻酰化。为了支持临床开发,我们建立了使用 100 μL 血浆的高灵敏度血浆定量检测方法,检测浓度范围为 0.1 至 100ng/mL 和 1 至 1000ng/mL,具有测量十倍稀释样品至 10,000ng/mL 的选项。定量采用超高效液相色谱-串联质谱(UPLC-MS/MS)测量,在蛋白质沉淀提取后进行。两个检测方法均根据 FDA 和 EMA 的相关指南进行了全面验证,包括使用临床研究样品进行了遗留样品重新分析和交叉验证。