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

Abstract Understanding the biophysical and biochemical properties of molecular nanocarriers under physiological conditions with minimal interference is critical for advancing photopharmacology, drug delivery, nanotheranostics and synthetic biology. However, analytical methods often struggle to combi...

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Main Authors: T. Gölz, E. Baù, J. Zhang, K. Kaltenecker, D. Trauner, S. A. Maier, F. Keilmann, T. Lohmüller, A. Tittl
Format: Article
Language:English
Published: Nature Portfolio 2025-07-01
Series:Nature Communications
Online Access:https://doi.org/10.1038/s41467-025-61341-9
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author T. Gölz
E. Baù
J. Zhang
K. Kaltenecker
D. Trauner
S. A. Maier
F. Keilmann
T. Lohmüller
A. Tittl
author_facet T. Gölz
E. Baù
J. Zhang
K. Kaltenecker
D. Trauner
S. A. Maier
F. Keilmann
T. Lohmüller
A. Tittl
author_sort T. Gölz
collection DOAJ
description Abstract Understanding the biophysical and biochemical properties of molecular nanocarriers under physiological conditions with minimal interference is critical for advancing photopharmacology, drug delivery, nanotheranostics and synthetic biology. However, analytical methods often struggle to combine precise chemical imaging and dynamic measurements without perturbative labeling. This challenge is exemplified by azobenzene-based photoswitchable lipids, which are intriguing reagents for controlling nanocarrier properties on fast timescales, enabling precise light-induced drug release. Here, we leverage the chemical recognition and high spatio-temporal resolution of scattering-type scanning near-field optical microscopy (s-SNOM) to demonstrate a non-destructive, label-free technique for mid-infrared imaging and spectroscopy of individual photoswitchable liposomes. Our transient nanoscopy approach enables imaging below the diffraction limit and tracks dynamics with sampling times as fast as 30 ms. We resolve photoinduced changes in shape and MIR spectral signature of individual vesicles and discover abrupt and delayed photoisomerization dynamics. Our findings highlight the method’s potential for studying complex dynamics of unlabeled nanoscale soft matter.
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institution Kabale University
issn 2041-1723
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publisher Nature Portfolio
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series Nature Communications
spelling doaj-art-49fb976d065449bdbd7fb1556ab7b9322025-08-20T04:01:41ZengNature PortfolioNature Communications2041-17232025-07-0116111110.1038/s41467-025-61341-9Transient infrared nanoscopy resolves the millisecond photoswitching dynamics of single lipid vesicles in waterT. Gölz0E. Baù1J. Zhang2K. Kaltenecker3D. Trauner4S. A. Maier5F. Keilmann6T. Lohmüller7A. Tittl8Department of Physics, Chair in Hybrid Nanosystems, Nano-Institute Munich, Ludwig-Maximilians-Universität MünchenDepartment of Physics, Chair in Hybrid Nanosystems, Nano-Institute Munich, Ludwig-Maximilians-Universität MünchenDepartment of Physics, Chair for Photonics and Optoelectronics, Nano-Institute Munich, Ludwig-Maximilians-Universität MünchenDepartment of Physics, Chair in Hybrid Nanosystems, Nano-Institute Munich, Ludwig-Maximilians-Universität MünchenDepartment of Chemistry, University of PennsylvaniaSchool of Physics and Astronomy, Monash UniversityDepartment of Physics, Chair in Hybrid Nanosystems, Nano-Institute Munich, Ludwig-Maximilians-Universität MünchenDepartment of Physics, Chair for Photonics and Optoelectronics, Nano-Institute Munich, Ludwig-Maximilians-Universität MünchenDepartment of Physics, Chair in Hybrid Nanosystems, Nano-Institute Munich, Ludwig-Maximilians-Universität MünchenAbstract Understanding the biophysical and biochemical properties of molecular nanocarriers under physiological conditions with minimal interference is critical for advancing photopharmacology, drug delivery, nanotheranostics and synthetic biology. However, analytical methods often struggle to combine precise chemical imaging and dynamic measurements without perturbative labeling. This challenge is exemplified by azobenzene-based photoswitchable lipids, which are intriguing reagents for controlling nanocarrier properties on fast timescales, enabling precise light-induced drug release. Here, we leverage the chemical recognition and high spatio-temporal resolution of scattering-type scanning near-field optical microscopy (s-SNOM) to demonstrate a non-destructive, label-free technique for mid-infrared imaging and spectroscopy of individual photoswitchable liposomes. Our transient nanoscopy approach enables imaging below the diffraction limit and tracks dynamics with sampling times as fast as 30 ms. We resolve photoinduced changes in shape and MIR spectral signature of individual vesicles and discover abrupt and delayed photoisomerization dynamics. Our findings highlight the method’s potential for studying complex dynamics of unlabeled nanoscale soft matter.https://doi.org/10.1038/s41467-025-61341-9
spellingShingle T. Gölz
E. Baù
J. Zhang
K. Kaltenecker
D. Trauner
S. A. Maier
F. Keilmann
T. Lohmüller
A. Tittl
Transient infrared nanoscopy resolves the millisecond photoswitching dynamics of single lipid vesicles in water
Nature Communications
title Transient infrared nanoscopy resolves the millisecond photoswitching dynamics of single lipid vesicles in water
title_full Transient infrared nanoscopy resolves the millisecond photoswitching dynamics of single lipid vesicles in water
title_fullStr Transient infrared nanoscopy resolves the millisecond photoswitching dynamics of single lipid vesicles in water
title_full_unstemmed Transient infrared nanoscopy resolves the millisecond photoswitching dynamics of single lipid vesicles in water
title_short Transient infrared nanoscopy resolves the millisecond photoswitching dynamics of single lipid vesicles in water
title_sort transient infrared nanoscopy resolves the millisecond photoswitching dynamics of single lipid vesicles in water
url https://doi.org/10.1038/s41467-025-61341-9
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