Table 1 Methods typically used to characterise particles (viruses, extracellular vesicles, and protein aggregates) and their ability for phage counting, size distribution characterisation, and detection of aggregates in suspension.

From: Real-time monitoring by interferometric light microscopy of phage suspensions for personalised phage therapy

Methods

Measurements

Analysis time

Counting

Size distribution

Aggregation

Spectroscopy29,30,31

 Turbidimetry

No

No

Yes

 < 10 min

 UV/Vis-spectroscopy

No

No

Yes

 < 10 min

Scattering17,29,31

 SAXS, MALLS, SLS

No

Yes

Yes

Min to hour

Combined light scattering and Brownian motion17,18,19,20,21,22,28,29,31

 DLS

Yes

Yes

Yes

15–20 min

 NTA

Yes

Yes

Yes

15–20 min

 ILM

Yes

Yes

Yes

 < 10 min

Microscopy17,18,19,23,24,25,26,29,33

 Optical

No

No

Yes

15–20 min

 Epifluorescence

Yes

No

Yes

Hours

 Electronic

No

Yes

Yes

Hours

 AFM

No

Yes

Yes

Hours

Miscellaneous17,18,19,27,29

 FCM

Yes

Yes

Yes

Min to hour

 qPCR

Yes

No

No

Hours

 Plaque assay

Yes

No

No

Hours

  1. Small-angle X-ray, SAXS; Multi-angle laser light scattering, MALLS; Static light scattering, SLS; Dynamic light scattering, DLS; Nanoparticle tracking analysis, NTA; Interferometric light microscopy, ILM; Atomic force microscopy, AFM; Flow cytometry, FCM; Quantitative real-time polymerase chain reaction, qPCR.