# Chemical analysis of extracellular vesicles by synchrotron-based X-ray imaging and scattering techniques: a review and perspective

**Authors:** Li Huang, Yan Chen, Xiutian Guo, Limin Zhou

PMC · DOI: 10.3389/fbioe.2025.1769106 · Frontiers in Bioengineering and Biotechnology · 2026-01-12

## TL;DR

This paper reviews how synchrotron-based X-ray techniques can better analyze the chemical structure of extracellular vesicles, which are important for cell communication and drug delivery.

## Contribution

The paper introduces synchrotron-based X-ray imaging and scattering as novel methods for chemically analyzing extracellular vesicles with high specificity and sensitivity.

## Key findings

- Synchrotron X-ray techniques offer intrinsic chemical specificity for EV analysis.
- These methods can quantify EV morphology and bilayer structures effectively.
- They overcome limitations of conventional methods like labeling artifacts and low sensitivity.

## Abstract

Extracellular vesicles (EVs) are nanoscale lipid bilayer-enclosed particles released by cells, which have been explored as pivotal mediators for intercellular communication, biomarkers for diseases and nano-carriers for drug delivery. Unraveling their structural and chemical heterogeneity is crucial for understanding the biogenesis, cargo sorting, and functional mechanisms of EVs. However, by far it remains challenging to characterize the intrinsic physicochemical properties of EVs due to their varied intracellular origins, poly-disperse size distribution and dynamic membrane organization. Conventional imaging and light scattering methods either lack the chemical sensitivity or suffer from labeling artifacts. Here in this review, we summarize research work using synchrotron-based X-ray imaging and scattering techniques to resolve the chemical structural complexity of EVs with intrinsic chemical specificity and enhanced sensitivity. The feasibility and effectiveness of X-ray imaging and scattering tools on quantifying critical structural parameters of EVs including morphology, core-shell and bilayer structure is discussed. We hope it will inspire future in-depth work to bridge the gap between structural and biological functionality in EVs research.

## Full-text entities

- **Chemicals:** lipid (MESH:D008055)

## Full text

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## Figures

2 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12833409/full.md

## References

48 references — full list in the complete paper: https://tomesphere.com/paper/PMC12833409/full.md

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Source: https://tomesphere.com/paper/PMC12833409