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生物分析方法与战略视角:应对新型生物缀合物和生物治疗药物传递途径日益增加的复杂性。

Bioanalytical Methods and Strategic Perspectives Addressing the Rising Complexity of Novel Bioconjugates and Delivery Routes for Biotherapeutics.

机构信息

Integrated Bioanalysis, Clinical Pharmacology and Quantitative Pharmacology, Clinical Pharmacology and Safety Sciences, R&D, AstraZeneca, South San Francisco, CA, USA.

出版信息

BioDrugs. 2022 Mar;36(2):181-196. doi: 10.1007/s40259-022-00518-w. Epub 2022 Apr 1.

Abstract

In recent years, an increase in the discovery and development of biotherapeutics employing new modalities, such as bioconjugates or novel routes of delivery, has created bioanalytical challenges. The inherent complexity of conjugated molecular structures means that quantification of the bioconjugate and its multiple components is critical for preclinical/clinical studies to inform drug discovery and development. Moreover, bioconjugates involve additional multifactorial complexity because of the potential for in vivo catabolism and biotransformation, which may require thorough investigations in multiple biological matrices. Furthermore, excipients that enhance absorption are frequently evaluated and employed for the development of oral and inhaled biotherapeutics. Risk-benefit assessments are required for novel or existing excipients that utilize dosages above previously approved levels. Bioanalytical methods that can measure both excipients and potential drug metabolites in biological matrices are highly relevant to these emerging bioanalysis challenges. We discuss the bioanalytical strategies for analyzing bioconjugates such as antibody-drug conjugates and antibody-oligonucleotide conjugates and review recent advances in bioanalytical methods for the quantification and characterization of novel bioconjugates. We also discuss bioanalytical considerations for both biotherapeutics and excipients through novel administration routes and review analyses in various biological matrices, from the extensively studied serum or plasma to tissue biopsy in the context of preclinical and clinical studies from both technical and regulatory perspectives.

摘要

近年来,采用新型给药途径或新型模式(如生物缀合物)的生物治疗药物的发现和开发有所增加,这给生物分析带来了挑战。缀合分子结构的固有复杂性意味着定量分析生物缀合物及其多种成分对于临床前/临床研究至关重要,这可为药物发现和开发提供信息。此外,由于体内代谢和生物转化的可能性,生物缀合物还涉及其他多因素的复杂性,这可能需要在多个生物基质中进行彻底的调查。此外,经常评估和使用可增强吸收的赋形剂来开发口服和吸入用生物治疗药物。对于利用以前批准水平以上剂量的新型或现有赋形剂,需要进行风险-效益评估。能够测量生物基质中赋形剂和潜在药物代谢物的生物分析方法与这些新兴的生物分析挑战密切相关。我们讨论了分析抗体-药物偶联物和抗体-寡核苷酸偶联物等生物缀合物的生物分析策略,并回顾了用于定量和表征新型生物缀合物的生物分析方法的最新进展。我们还从技术和监管角度讨论了通过新型给药途径的生物治疗药物和赋形剂的生物分析注意事项,并回顾了各种生物基质中的分析,从广泛研究的血清或血浆到临床前和临床研究中的组织活检。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0466/8986699/dd61a18ba9e5/40259_2022_518_Fig1_HTML.jpg

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