Department of Chemistry, Wayne State University, 5101 Cass Avenue, Detroit, Michigan 48202, United States.
Anal Chem. 2022 May 24;94(20):7433-7441. doi: 10.1021/acs.analchem.2c01232. Epub 2022 May 10.
Lipid nanoparticles serve as drug delivery vehicles for biopharmaceutical products. The lipid membrane shields internal nucleic-acid drug cargo from enzymatic degradation and facilitates cellular uptake of the drug. However, existing methods to assess drug loading within liposomes are limited to averaged bulk measurements, which obscures heterogeneity of the biopharmaceutical formulation. This report describes the development of a single-liposome analysis method to measure copy numbers of DNA within liposomes and assess population heterogeneity. This novel measurement was achieved by integrating two orthogonal polymerase chain reaction (PCR) techniques─digital PCR (dPCR) and quantitative PCR (qPCR)─within a single microfluidic assay. The dPCR dimension quantified liposomes to validate their capture in the single-liposome analysis regime. The qPCR dimension quantified DNA copy numbers packaged within each liposome. The ability of digital quantitative PCR (dqPCR) to analyze large numbers of individual liposomes in parallel revealed significant population heterogeneity, which could not be obtained from standard bulk analysis methods. Our innovative measurement of internal DNA cargo from single liposomes has the potential to inform liposome synthesis procedures and create more uniform liposomal biopharmaceutical formulations to enhance drug safety and efficacy.
脂质纳米颗粒可作为生物制药产品的药物递送载体。脂质膜可保护内部核酸药物货物免受酶的降解,并促进药物进入细胞。然而,现有的评估脂质体中药物载量的方法仅限于平均批量测量,这掩盖了生物制药制剂的异质性。本报告描述了一种单脂质体分析方法的开发,用于测量脂质体内部 DNA 的拷贝数并评估群体异质性。通过在单个微流控测定中整合两种正交聚合酶链反应 (PCR) 技术——数字 PCR (dPCR) 和定量 PCR (qPCR),实现了这一新颖的测量。dPCR 维度量化了脂质体以验证它们在单脂质体分析方案中的捕获。qPCR 维度定量了每个脂质体中包装的 DNA 拷贝数。数字定量 PCR (dqPCR) 分析大量单个脂质体的能力揭示了显著的群体异质性,而这无法从标准批量分析方法中获得。我们对单个脂质体内部 DNA 货物的创新性测量有可能为脂质体合成程序提供信息,并创建更均匀的脂质体生物制药制剂,以提高药物安全性和疗效。