Mr. Rumelo Amor Profile

Rumelo Amor

at Univ of Strathclyde

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Publications (2)

Proceedings Article | 9 March 2015 Paper

Standing-wave excitation of fluorescence in a laser-scanning microscope allows precise contour mapping of the red blood cell membrane

Rumelo Amor, Sumeet Mahajan, William Amos, Gail McConnell

Proceedings Volume 9330, 933010 (2015) https://doi.org/10.1117/12.2075644

KEYWORDS: Blood, Mirrors, Microscopes, Moire patterns, Electroluminescent displays, Modulation, Luminescence, Photography, Glasses, Objectives

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Proceedings Article | 22 February 2013 Open Access

Promising new wavelengths for multi-photon microscopy: thinking outside the Ti:Sapphire box

Greg Norris, Rumelo Amor, John Dempster, William Amos, Gail McConnell

Proceedings Volume 8588, 858802 (2013) https://doi.org/10.1117/12.2008189

KEYWORDS: Optical parametric oscillators, Sapphire lasers, Mirrors, Atomic force microscopy, Luminescence, Crystals, Microscopes, Laser scanners, Imaging systems, Microscopy

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Multi-photon excitation (MPE) imaging is dominated by the Ti:Sapphire laser as the source for excitation. However, it is limited when considering 3PE of common fluorophores and efficient 2PE of UV dyes which require wavelengths beyond the range of the Ti:Sapphire. Two ultra-short pulsed sources are presented as alternatives: a novel optical parametric oscillator (OPO) geometry (1400–1600nm) and the sum-frequency mixing of an OPO and Yb-doped fibre laser, providing a tunable output (626-635nm). For long wavelengths, we report three-photon laser scanning microscopy (3PLSM) using a bi-directional pumped optical parametric oscillator (OPO) with signal wavelength output at 1500 nm. This novel laser was used to overcome the high optical loss in the infrared spectral region observed in laser scanning microscopes and objective lenses that renders them otherwise difficult to use for imaging. To test our system, we performed 3PLSM auto-fluorescence imaging of live plant cells at 1500 nm, specifically Spirogyra, and compared performance with two-photon excitation (2PLSM) imaging using a femtosecond pulsed Ti:Sapphire laser at 780 nm. Analysis of cell viability based on cytoplasmic organelle streaming and structural changes of cells revealed that at similar peak powers, 2PLSM caused gross cell damage after 5 minutes but 3PLSM showed little or no interference with cell function after 15 minutes. The 1500 nm OPO was thus shown to be a practical laser source for live cell imaging. For short wavelengths, we report the use of an all-solid-state ultra-short pulsed source specifically for two-photon microscopy at wavelengths shorter than those of the conventional Ti:Sapphire laser. Our approach involved sumfrequency mixing of the output from the long-wavelength OPO described above with residual pump radiation to generate fs-pulsed output in the red spectral region. We demonstrated the performance of our ultra-short pulsed system using fluorescently labelled and autofluorescent tissue, and compared with conventional Ti:Sapphire excitation. We observed a more than 3-fold increase in fluorescence signal intensity using our visible laser source in comparison with the Ti:Sapphire laser for two-photon excitation at equal illumination powers of 22 mW or less.

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