PulseExploreJournal ClubDebatesTrendingResearchersJournals
Instagram
HomeExploreJournal ClubTrending
Synapse
⌘+K
Synapse
May 6, 2026Biosensors0 citationsOpen Access

Longitudinal Monitoring of Metabolic Gradients in Microreactor Culture Platforms by Raman Spectroscopy

View Full Paper
MMMaitane MárquezCIC nanoGUNEJPJavier PlouCIC nanoGUNESMStefan MerkensCIC nanoGUNE

Key Points

  • To develop a platform that monitors metabolic gradients in microreactor cultures to understand cancer progression.
  • Integrated platform using a 3D-printed microreactor and Raman spectroscopy
  • Non-invasive monitoring of living cell cultures
  • Controlled generation of oxygen and nutrient cues
  • Acquisition of label-free Raman spectra
  • Revealed spatial and temporal metabolic variance linked to cancer cell adaptation
  • Identified localized acidification and stress biomarkers in diffusion-limited regions
  • Showed shifts in glucose and lactate as markers of catabolism

Abstract

Metabolic heterogeneity within the cell microenvironment is a key driver of cancer progression and resistance to therapy. However, current approaches lack the spatial and temporal resolution required to capture its dynamics in living systems. While recent advances in 3D cell culture models and metabolomic profiling have improved our understanding of the tumor niche, their integration with real-time optical sensing remains underdeveloped. Here, we present an integrated platform combining a 3D-printed microreactor culture chamber with Raman spectroscopy to enable non-invasive, spatially resolved metabolic monitoring of living cell cultures. Our microreactor platform generates controlled oxygen and nutrient cues while simultaneously acquiring label-free Raman spectra, revealing extracellular metabolic fingerprints linked to cell catabolism (e.g., glucose and lactate shifts) and acidification. Analysis across four cell lines uncovered temporal evolution as the dominant source of metabolic variance, while spatial heterogeneity along oxygen gradients is a secondary factor. In particular, diffusion-limited regions exhibited localized acidification and accumulation of stress biomarkers—such as the release of nucleotides—features that cannot be detected using conventional bulk assays. By providing a versatile platform for real-time mapping, this work enables the mechanistic dissection of cell adaptation to microenvironmental stress and supports the prediction of metabolic signatures underlying drug response and treatment outcomes.

Ask AI
Helpful
Bookmark
Share
View Full Paper

Cite This Study

Márquez et al. (2026) studied this question.

synapsesocial.com/papers/69fa983604f884e66b531f1fhttps://doi.org/10.3390/bios16050266
Ask AI
Helpful
Bookmark
Share
View Full Paper

Also Consider

Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context:

  1. 1Acidity suppresses CD8 + T-cell function by perturbing IL-2, mTORC1, and c-Myc signaling2024 · 41 citations
  2. 2Real time monitoring of multiple parameters in mammalian cell culture bioreactors using an in‐line Raman spectroscopy probe2010 · 319 citations
  3. 3A microfluidic gradient generator to simulate the oxygen microenvironment in cancer cell culture2018 · 32 citations
  4. 4Machine Learning-Assisted Raman Spectroscopy for pH and Lactate Sensing in Body Fluids2020 · 49 citations
  5. 5Gradient-induced instability in tumour spheroids unveils the impact of microenvironmental nutrient changes2024 · 23 citations