Table 1 Comparison of Resolution, acquisition Time, and key findings across applications.

From: Demonstrating soft X-ray tomography in the lab for correlative cryogenic biological imaging using X-rays and light microscopy

Application

Features resolved

Acquisition time

Key findings

Euglena gracilis

~ 54 nm (full-pitch) resolution

~ 1.5 h tomogram

Clear distinction between organelles (chloroplasts, paramylon granules, nucleus, flagella); correlation with chlorophyll fluorescence for targeted cryo-ET/EM.

Saccharomyces cerevisiae (yeast)

~ 54 nm (FRC); 51 nm FWHM

~ 1 h tomogram (29 nm voxel size)

Identification of lipid droplets and vacuoles in 3D; revealed vacuolar lipophagy and multivesicular organisation; quantitative volumetric segmentation feasible.

HeLa cells with 100 nm polymeric nanoparticles (FluoSpheres)

Resolves ~ 100 nm NPs within cytoplasm

~ 1–1.5 h tomogram

Nanoparticles localised to lysosomes; SXT resolved lysosomes, mitochondria, and lipid droplets; correlated FM confirmed NP localisation.

H8N8 breast cancer cells with 50–60 nm zirconyl IOH-NPs

Single NPs (~ 60 nm) resolved

~ 1.5 h tomogram; throughput ~ 20–30 cells in 2 weeks

NP uptake and trafficking to lysosomes; enabled statistical analysis of organelle changes across many cells; demonstrated compatibility with quantitative workflows.

General performance (Siemens star + yeast vs. synchrotron)

25 nm Siemens star; yeast FWHM 51 nm (lab) vs. 39 nm (synchrotron)

30 min (thin cells) – 2 h (thick cells)

High resolution with larger fields of view (up to 45 × 60 μm²) and routine correlative FM-SXT workflows.