Transient infrared nanoscopy resolves the millisecond photoswitching dynamics of single lipid vesicles in water

TL;DR

This study introduces a non-invasive, high-resolution infrared nanoscopy technique to observe the rapid photoswitching dynamics of single lipid vesicles in water, providing new insights into nanocarrier behavior without perturbation.

Contribution

The paper demonstrates the first use of transient scattering-type scanning near-field optical microscopy for label-free, millisecond-resolution imaging of photoswitchable liposomes, capturing their shape and spectral changes.

Findings

Resolved photoinduced shape changes of vesicles.

Tracked spectral signature shifts during photoswitching.

Achieved 50 ms temporal resolution for vesicle dynamics.

Abstract

Understanding the biophysical and biochemical properties of molecular nanocarriers under physiological conditions and with minimal interference is crucial for advancing nanomedicine, photopharmacology, drug delivery, nanotheranostics and synthetic biology. Yet, analytical methods struggle to combine precise chemical imaging and measurements without perturbative labeling. This challenge is exemplified for azobenzene-based photoswitchable lipids, which are intriguing reagents for controlling nanocarrier properties on fast timescales, enabling, e.g., precise light-induced drug release processes. Here, we leverage the chemical recognition and high spatio-temporal resolution of scattering-type scanning near-field optical microscopy (s-SNOM) to demonstrate non-destructive, label-free mid-infrared (MIR) imaging and spectroscopy of photoswitchable liposomes below the diffraction limit and the tracking of their dynamics down to 50 ms resolution. The vesicles are adsorbed on an ultrathin 10-nm SiN membrane, which separates the sample space from the tip space for stable and hour-long observations. By implementing a transient nanoscopy approach, we accurately resolve, for the first time, photoinduced changes in both the shape and the MIR spectral signature of individual vesicles and reveal abrupt change dynamics of the underlying photoisomerization process. Our findings highlight the methods potential for future studies on the complex dynamics of unlabeled nanoscale soft matter, as well as, in a broader context, for host-guest systems, energy materials or drugs.