Open Access3,3′-thiodipropanol as a versatile refractive index-matching mounting medium for fluorescence microscopy
Author(s) -
Milvia Alata,
Juan Carlos Martínez Cervantes,
Adrian Saul Jimenez Roldán,
Mario Rodríguez,
Azucena Pérez Vega,
Valeria Piazza
Publication year - 2019
Publication title -
biomedical optics express
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.362
H-Index - 86
ISSN - 2156-7085
DOI - 10.1364/boe.10.001136
Subject(s) - fluorescence , microscopy , refractive index , fluorescence microscope , materials science , optical microscope , optics , dispersion (optics) , microscope , analytical chemistry (journal) , nanotechnology , chemistry , scanning electron microscope , optoelectronics , chromatography , composite material , physics
High resolution fluorescence microscopy requires optimization of the protocols for biological sample preparation. The optical and chemical characteristics of mounting media are among the things that could be modified to achieve optimal image formation. In our search for chemical substances that could perform as mounting media, 3,3'-thiodipropanol (TDP) emerged as a sulfide with potentially interesting characteristics. In this work, several tests of its performance as a mounting medium for fluorescence microscopy of biological samples were performed, including the labeling of filamentous actin with fluorescent phalloidins. The refractive index dispersion curve of pH-adjusted TDP was experimentally obtained in the visible range and compared to the dispersion curves of commercial and lab-made mounting media. The effects on the fluorescence of commonly used dyes were tested by using TDP as a solvent and measuring the relative fluorescence quantum yield of the dyes. By being able to mix TDP in any concentration with water and 2,2'-thiodiethanol (TDE), it was possible not only to fine-tune the refractive index of the resulting solution, but also to preserve the compatibility of TDP with the most popular and efficient fluorescent actin staining used in biological microscopy.