Microfluidics enabled multi-omics triple-shot mass spectrometry for cell-based therapies.

IF 2.6 4区 工程技术 Q2 BIOCHEMICAL RESEARCH METHODS Biomicrofluidics Pub Date : 2024-01-23 eCollection Date: 2024-01-01 DOI:10.1063/5.0175178
Gianna A Slusher, Peter A Kottke, Austin L Culberson, Mason A Chilmonczyk, Andrei G Fedorov
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Abstract

In recent years, cell-based therapies have transformed medical treatment. These therapies present a multitude of challenges associated with identifying the mechanism of action, developing accurate safety and potency assays, and achieving low-cost product manufacturing at scale. The complexity of the problem can be attributed to the intricate composition of the therapeutic products: living cells with complex biochemical compositions. Identifying and measuring critical quality attributes (CQAs) that impact therapy success is crucial for both the therapy development and its manufacturing. Unfortunately, current analytical methods and tools for identifying and measuring CQAs are limited in both scope and speed. This Perspective explores the potential for microfluidic-enabled mass spectrometry (MS) systems to comprehensively characterize CQAs for cell-based therapies, focusing on secretome, intracellular metabolome, and surfaceome biomarkers. Powerful microfluidic sampling and processing platforms have been recently presented for the secretome and intracellular metabolome, which could be implemented with MS for fast, locally sampled screening of the cell culture. However, surfaceome analysis remains limited by the lack of rapid isolation and enrichment methods. Developing innovative microfluidic approaches for surface marker analysis and integrating them with secretome and metabolome measurements using a common analytical platform hold the promise of enhancing our understanding of CQAs across all "omes," potentially revolutionizing cell-based therapy development and manufacturing for improved efficacy and patient accessibility.

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用于细胞疗法的微流体多组学三重质谱分析。
近年来,细胞疗法改变了医疗方式。这些疗法在确定作用机理、开发精确的安全性和有效性检测方法以及实现低成本规模化产品生产方面面临着诸多挑战。问题的复杂性可归因于治疗产品错综复杂的成分:具有复杂生化成分的活细胞。识别和测量影响疗法成功与否的关键质量属性 (CQAs) 对于疗法的开发和生产都至关重要。遗憾的是,目前用于识别和测量 CQA 的分析方法和工具在范围和速度上都很有限。本视角探讨了微流控质谱(MS)系统全面表征细胞疗法CQAs的潜力,重点关注分泌组、细胞内代谢组和表面组生物标记物。最近针对分泌物组和细胞内代谢组推出了功能强大的微流控采样和处理平台,该平台可与 MS 结合使用,对细胞培养物进行快速、局部采样筛选。然而,表面组分析仍然受到缺乏快速分离和富集方法的限制。开发用于表面标记分析的创新微流控方法,并使用通用分析平台将其与分泌组和代谢组测量相结合,有望增强我们对所有 "omes "的CQAs的了解,从而有可能彻底改变细胞疗法的开发和生产,提高疗效和患者的可及性。
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来源期刊
Biomicrofluidics
Biomicrofluidics 生物-纳米科技
CiteScore
5.80
自引率
3.10%
发文量
68
审稿时长
1.3 months
期刊介绍: Biomicrofluidics (BMF) is an online-only journal published by AIP Publishing to rapidly disseminate research in fundamental physicochemical mechanisms associated with microfluidic and nanofluidic phenomena. BMF also publishes research in unique microfluidic and nanofluidic techniques for diagnostic, medical, biological, pharmaceutical, environmental, and chemical applications. BMF offers quick publication, multimedia capability, and worldwide circulation among academic, national, and industrial laboratories. With a primary focus on high-quality original research articles, BMF also organizes special sections that help explain and define specific challenges unique to the interdisciplinary field of biomicrofluidics. Microfluidic and nanofluidic actuation (electrokinetics, acoustofluidics, optofluidics, capillary) Liquid Biopsy (microRNA profiling, circulating tumor cell isolation, exosome isolation, circulating tumor DNA quantification) Cell sorting, manipulation, and transfection (di/electrophoresis, magnetic beads, optical traps, electroporation) Molecular Separation and Concentration (isotachophoresis, concentration polarization, di/electrophoresis, magnetic beads, nanoparticles) Cell culture and analysis(single cell assays, stimuli response, stem cell transfection) Genomic and proteomic analysis (rapid gene sequencing, DNA/protein/carbohydrate arrays) Biosensors (immuno-assay, nucleic acid fluorescent assay, colorimetric assay, enzyme amplification, plasmonic and Raman nano-reporter, molecular beacon, FRET, aptamer, nanopore, optical fibers) Biophysical transport and characterization (DNA, single protein, ion channel and membrane dynamics, cell motility and communication mechanisms, electrophysiology, patch clamping). Etc...
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