Pennucci Jason, Hays Amanda, Adamowicz Wendy, Azadeh Mitra, Benhammadi Mohamed, Portabella Enric Bertran, Cheng MingLai, Colletti Kelly, Dholakiya Sanjay L, Doddareddy Rajitha, Duchstein Lara, Durham Jennifer, Guelman Sebastian, Gullick Bryan, Herr Kate, Jani Darshana, Jani Niketa, Johansson Oskar, John Kaarthik, Kubista Mikael, Lavelle Amy, Li Geng, Li Yanchun, Liu Hsing-Yin, Lochmann Timothy, Ma Haiyan, Moritz Benjamin, Murphy Jacqueline, Park Alice, Peddigari Suresh, Piche Marie-Soleil, Ramaswamy Swarna Suba, Reddy Asha, Smet Muriel, Stanta Johannes, Valentine Jenny, Veirs Katherine, Vepachedu Venkata, Wissel Mark, Wu Meizhen, Xu Bin, Zondlo Susan
Moderna, Inc, Cambridge, Massachusetts, USA.
BioAgilytix Laboratories, Durham, North Carolina, USA.
AAPS J. 2025 Sep 18;27(6):144. doi: 10.1208/s12248-025-01122-w.
Lipid nanoparticle-messenger RNA (LNP-mRNA) drug products are a growing class of drug modalities. The unique composition of these drug products requires multiple measurements to account for the different components of these drug modalities. Pharmacokinetic (PK) measurements include measurement of the encapsulated mRNA and components of the LNP in circulation to understand the effectiveness of the therapeutic mRNA. The PK measurements can utilize many different platforms including PCR. Current regulatory guidance documents for bioanalytical method validation are specific to ligand binding and chromatographic assay methods and difficult to interpret for use with molecular workflows. The purpose of this paper is to provide information on considerations for validation of regulated reverse transcription quantitative PCR (RT-qPCR) assays that are used to support the pharmacokinetic analysis of LNP-mRNA drug products.
脂质纳米颗粒-信使核糖核酸(LNP-mRNA)药物产品是一类不断发展的药物形式。这些药物产品的独特组成需要进行多次测量,以考量这些药物形式的不同成分。药代动力学(PK)测量包括测量循环中封装的mRNA和LNP的成分,以了解治疗性mRNA的有效性。PK测量可利用包括PCR在内的许多不同平台。当前生物分析方法验证的监管指导文件特定于配体结合和色谱分析方法,难以解读以用于分子工作流程。本文的目的是提供有关用于支持LNP-mRNA药物产品药代动力学分析的法定逆转录定量PCR(RT-qPCR)测定法验证考量因素的信息。