Microflow LC-MS for Clinical Proteomics & Metabolomics


Robust, reproducible workflows for clinical research that overcome immunoassay limitations.

LC-MS as a Core Technology for Clinical Analysis

Liquid chromatography–mass spectrometry (LC-MS) has become an essential analytical technology in clinical research and translational studies. While immunoassays such as ELISA remain widely used in clinical diagnostics, LC-MS provides molecular specificity that is difficult to achieve with antibody-based methods, particularly for small molecules and proteins with post-translational modifications (PTMs).

ELISA vs LC-MS: Complementary Capabilities in Clinical Research

Capability ELISA LC-MS
Small-molecule detection Generally not feasible Direct molecular detection
Protein isoforms Limited specificity Isoform-resolved
Post-translational modifications (PTMs) Often indistinguishable Directly measureable
Multiplexing Single or limited analytes Multiple analytes per run
Assay development Antibody-dependent Method-driven

Microflow LC-MS: Balancing Sensitivity and Robustness for Clinical Workflows

Microflow LC-MS has emerged as a practical compromise between nanoLC and analytical-flow LC, balancing robustness, reproducibility, and sensitivity for clinical workflows that demand consistent performance over long analytical sequences. It is particularly powerful in analyzing limited amounts of biofluid samples such as blood, plasma, CSF, and urine, as well as tissue biopsies and dry blood spots.

Microflow LC-MS is therefore emerging as a preferred approach for clinical proteomics, metabolomics, and translational research applications.

Comparison of LC Flow Regimes and Clinical Suitability

Parameter NanoLC Microflow LC Analyical Flow LC
Typical flow rate < 1 µL/min 1-50 µL/min > 100 µL/min
Sensitivity Very high High Moderate
Robustness Low High Very High
Operator dependence High Moderate-low Low
Clinical workflow suitability Limited by robustness Strong Limited by sensitivity

How Newomics Enables Robust Clinical MS Workflows

As clinical laboratories increasingly adopt microflow LC-MS, the LC-MS front-end becomes a critical determinant of sensitivity, robustness, and reproducibility. The Newomics UniESI platform integrates:

  • Patented multinozzle M3 emitters
  • MEA microfluidic chips
  • Stabilized electrospray performance at microflow rates
  • Nanoflow-like sensitivity with microflow robustness

This combination improves tolerance to sample variability and supports the long analytical sequences typical in clinical proteomics and metabolomics.

UniESI is vendor-agnostic and compatible with mass spectrometers from five major manufacturers, enabling standardized workflows across heterogeneous clinical instrument fleets.

Application Notes and Recent Webinars

Application notes describe validated microflow LC-MS workflows for clinical research, including analysis of proteins with post-translational modifications, targeted proteomics, and quantitative metabolomics.

Recorded webinars and technical discussions provide additional context and practical guidance for implementing microflow LC-MS in clinical MS workflows.

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