Metabolite identification and quantitation of RBD1016 siRNA: a direct comparison of hybridization-based LC-FD and LC-HRAM assays.

IF 1.8 4区 医学 Q3 BIOCHEMICAL RESEARCH METHODS Bioanalysis Pub Date : 2024-01-01 Epub Date: 2023-11-15 DOI:10.4155/bio-2023-0161
Yuhuan Ji, Zhaoxu Guo, Min Yan, Limin Chu, Min Meng, Yantao Chu, Hong Yu, Laixin Wang
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引用次数: 0

Abstract

Aim: RBD1016 is an N-acetylgalactosamine-conjugated siRNA drug currently in a phase II trial for treatment of chronic hepatitis B virus. To evaluate its absorption, distribution, metabolism and excretion (ADME) and pharmacokinetic/pharmacodynamic (PK/PD) properties, two LC-based bioanalytical methods, LC-high-resolution/accuracy MS and LC-fluorescence detection, were developed and qualified. Materials & methods: The LC-high-resolution/accuracy MS method was used for metabolite identification and simultaneous quantitation of the antisense and sense strands as well as their respective metabolites. The LC-fluorescence detection assay was primarily used for analyzing the antisense strand and its metabolites in low-concentration plasma samples. The two methods were successfully bridged by analyzing the same sets of study samples. Results & conclusion: Both methods were found to have excellent accuracy/precision, specificity and reproducibility to support ADME and PK/PD studies of RBD1016 siRNA.

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RBD1016 siRNA的代谢物鉴定和定量:基于杂交的LC-FD和LC-HRAM测定的直接比较。
目的:RBD1016是一种n -乙酰半乳糖胺偶联siRNA药物,目前正在进行治疗慢性乙型肝炎病毒的II期试验。为评价其吸收、分布、代谢和排泄(ADME)及药代动力学/药效学(PK/PD)特性,建立并验证了两种基于lc的生物分析方法:lc -高分辨率/精确质谱法和lc -荧光法。材料与方法:采用lc -高分辨率/精确质谱法进行代谢物鉴定,同时定量反义链和正链及其各自的代谢物。lc -荧光检测主要用于分析低浓度血浆样品中的反义链及其代谢物。通过分析同一组研究样本,这两种方法成功地架起了桥梁。结果与结论:两种方法均具有良好的准确性/精密度、特异性和重复性,可支持RBD1016 siRNA的ADME和PK/PD研究。
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来源期刊
Bioanalysis
Bioanalysis BIOCHEMICAL RESEARCH METHODS-CHEMISTRY, ANALYTICAL
CiteScore
3.30
自引率
16.70%
发文量
88
审稿时长
2 months
期刊介绍: Reliable data obtained from selective, sensitive and reproducible analysis of xenobiotics and biotics in biological samples is a fundamental and crucial part of every successful drug development program. The same principles can also apply to many other areas of research such as forensic science, toxicology and sports doping testing. The bioanalytical field incorporates sophisticated techniques linking sample preparation and advanced separations with MS and NMR detection systems, automation and robotics. Standards set by regulatory bodies regarding method development and validation increasingly define the boundaries between speed and quality. Bioanalysis is a progressive discipline for which the future holds many exciting opportunities to further reduce sample volumes, analysis cost and environmental impact, as well as to improve sensitivity, specificity, accuracy, efficiency, assay throughput, data quality, data handling and processing. The journal Bioanalysis focuses on the techniques and methods used for the detection or quantitative study of analytes in human or animal biological samples. Bioanalysis encourages the submission of articles describing forward-looking applications, including biosensors, microfluidics, miniaturized analytical devices, and new hyphenated and multi-dimensional techniques. Bioanalysis delivers essential information in concise, at-a-glance article formats. Key advances in the field are reported and analyzed by international experts, providing an authoritative but accessible forum for the modern bioanalyst.
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