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Label-free Autofluorescence-detected Mid-ir Photothermal Microscopy
Razumtcev, Aleksandr
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https://hdl.handle.net/2142/116605
Description
- Title
- Label-free Autofluorescence-detected Mid-ir Photothermal Microscopy
- Author(s)
- Razumtcev, Aleksandr
- Contributor(s)
- Simpson, Garth
- Issue Date
- 2022-06-22
- Keyword(s)
- Coblentz Special Session
- Abstract
- The instrumentation and methods to perform autofluorescence-detected photothermal mid-IR (AF-PTIR) microscopy are demonstrated experimentally and applied for chemically-selective label-free imaging of an active pharmaceutical ingredient (API) within a mixture with common pharmaceutical excipients. In AF-PTIR, the heat released from mid-IR absorption induces changes in two-photon excited UV-fluorescence (TPE-UVF) intensity. The spectral dependence of the fluorescence modulation locally informs on chemical composition with a spatial resolution dictated by the diffraction limit of visible light. AF-PTIR is shown to provide an additional level of selectivity in nonlinear optical imaging by mid-IR spectroscopy enabling mapping of the API distribution in the presence of TPE-UVF and second harmonic generation active excipients (\textbf{Fig. 1}). AF-PTIR provides high selectivity and sensitivity in image contrast for aromatic APIs, complementing broadly applicable commercial methods such as optical photothermal mid-IR (O-PTIR) microscopy. \begin{wrapfigure}{l}{0pt} \includegraphics[scale=0.2]{figure_abstract.eps} \end{wrapfigure} \textbf{Figure 1}. (a), (c – f) – Bright field, second harmonic generation (SHG), TPE-UVF, AF-PTIR and O-PTIR images of the field of view respectively. (b) – Segmentation results showing the spatial distribution of individual components (lactose particles are shown in blue, indomethacin in green, TiO$_{2}$ in yellow and Mg stearate is shown in red).
- Publisher
- International Symposium on Molecular Spectroscopy
- Type of Resource
- text
- Language
- eng
- Handle URL
- https://hdl.handle.net/2142/116605
- DOI
- https://doi.org/10.15278/isms.2022.WE04
- Copyright and License Information
- Copyright 2022 held by the authors
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