Abstract:Frequency-doubled femtosecond Er-doped fiber laser is a low-cost and portable excitation source suitable for multiphoton endoscopy. The frequency-doubled wavelength at 780 nm is used to excite the intrinsic fluorescence signal. The frequency-doubling with a periodically poled MgO∶LiNbO 3 (PPLN) is integrated in the distal end of the imaging head to achieve fiber connection. The imaging speed is further improved by optimizing the excitation laser source. A 0.3-mm length of PPLN crystal is selected and the Er-do… Show more
“…2(b), the measured SHG and THG peak wavelength is slightly off their theoretical value of 790/2 nm and 1580/3 nm, respectively. This is considered due to that the excitation beams are broadband sources with a -10 dB bandwidth of >100 nm and >25 nm for the ~1580-and ~790-nm laser beams, respectively [15]. In addition, rather than an ideal Gaussian distribution, the spectrum distributions of both wavelengths are complicated with detailed structures (this is common and typical for fiber-based mode-locked lasers) [15].…”
Section: Resultsmentioning
confidence: 99%
“…This is considered due to that the excitation beams are broadband sources with a -10 dB bandwidth of >100 nm and >25 nm for the ~1580-and ~790-nm laser beams, respectively [15]. In addition, rather than an ideal Gaussian distribution, the spectrum distributions of both wavelengths are complicated with detailed structures (this is common and typical for fiber-based mode-locked lasers) [15]. Based on these factors, an optimal reflective band for the notch dichroic beam splitter DBS3 is considered to be ~520±16 nm.…”
We report on a simultaneous 2-photon and 3-photon signal acquisition method for label-free multiphoton microscopy. With dual excitation wavelengths of 1580 nm and 790 nm and a set of filter designs, multiple contrasts including second harmonic generation, third harmonic generation, and two-photon-excitation-fluorescence images are detected and separated. The spectrum of the nonlinear signals is measured and verified by a spectrometer. Depth-resolved multimodal images are demonstrated on a silicon photonic chip and leaf samples. The simultaneous 2-and 3-photon microscopy is shown to have great potential for label-free in-vivo imaging.
“…2(b), the measured SHG and THG peak wavelength is slightly off their theoretical value of 790/2 nm and 1580/3 nm, respectively. This is considered due to that the excitation beams are broadband sources with a -10 dB bandwidth of >100 nm and >25 nm for the ~1580-and ~790-nm laser beams, respectively [15]. In addition, rather than an ideal Gaussian distribution, the spectrum distributions of both wavelengths are complicated with detailed structures (this is common and typical for fiber-based mode-locked lasers) [15].…”
Section: Resultsmentioning
confidence: 99%
“…This is considered due to that the excitation beams are broadband sources with a -10 dB bandwidth of >100 nm and >25 nm for the ~1580-and ~790-nm laser beams, respectively [15]. In addition, rather than an ideal Gaussian distribution, the spectrum distributions of both wavelengths are complicated with detailed structures (this is common and typical for fiber-based mode-locked lasers) [15]. Based on these factors, an optimal reflective band for the notch dichroic beam splitter DBS3 is considered to be ~520±16 nm.…”
We report on a simultaneous 2-photon and 3-photon signal acquisition method for label-free multiphoton microscopy. With dual excitation wavelengths of 1580 nm and 790 nm and a set of filter designs, multiple contrasts including second harmonic generation, third harmonic generation, and two-photon-excitation-fluorescence images are detected and separated. The spectrum of the nonlinear signals is measured and verified by a spectrometer. Depth-resolved multimodal images are demonstrated on a silicon photonic chip and leaf samples. The simultaneous 2-and 3-photon microscopy is shown to have great potential for label-free in-vivo imaging.
“…This surge in clinical trials has led to the formation of regulations and guidelines for the use of stem cells in treating various neurological disorders [ 20 , 21 ]. Stem cell therapies provide benefit through various mechanisms in the CNS such as replacement of cells, modulating the inflammatory response, and providing neuroprotection [ 22 , 23 , 24 ]. These mechanisms vary depending on the source of stem cells.…”
Section: Stem Cell Therapy: Terminology and Cell Linesmentioning
Stem cell therapy is a rapidly evolving field of regenerative medicine being employed for the management of various central nervous system disorders. The ability to self-renew, differentiate into specialized cells, and integrate into neuronal networks has positioned stem cells as an ideal mechanism for the treatment of epilepsy. Epilepsy is characterized by repetitive seizures caused by imbalance in the GABA and glutamate neurotransmission following neuronal damage. Stem cells provide benefit by reducing the glutamate excitotoxicity and strengthening the GABAergic inter-neuron connections. Similar to the abnormal neuroanatomic location in epilepsy, post-traumatic stress disorder (PTSD) is caused by hyperarousal in the amygdala and decreased activity of the hippocampus and medial prefrontal cortex. Thus, stem cells could be used to modulate neuronal interconnectivity. In this review, we provide a rationale for the use of stem cell therapy in the treatment of PTSD.
“…The pulsewidth is 80 fs for both the 790-nm and 1580-nm pulses. The short pulsewidth is achieved by using a piece of SMF to compensate the dispersion in the EDF laser system [23]. A −10 dB bandwidth is characterized due to the multiple-peak structure in the spectrum.…”
Section: Design Considerationsmentioning
confidence: 99%
“…In this paper, we will address those challenges. In our previous publications [22,23], we have reported a miniature 2PM system using a frequency-doubled EDF laser. In those papers, only the 790 nm beam was utilized while the residual 1580 nm beam was discarded.…”
A multimodal multiphoton microscopy (MPM) is developed to acquire both twophoton microscopy (2PM) and three-photon microscopy (3PM) signals. A dual-wavelength Er-doped fiber laser is used as the light source, which provides the fundamental pulse at 1580 nm to excite third harmonic generation (THG) and the frequency-doubled pulse at 790 nm to excite intrinsic two-photon excitation fluorescence (TPEF) and second harmonic generation (SHG). Due to their different contrast mechanisms, the TPEF, SHG, and THG images can acquire complementary information about tissues, including cells, collagen fibers, lipids, and interfaces, all label-free. The compact MPM imaging probe is developed using miniature objective lens and a micro-electro-mechanical scanner. Furthermore, the femtosecond laser pulses are delivered by a single mode fiber and the signals are collected by a multimode fiber, which makes the miniaturized MPM directly fiber-coupled, compact, and portable. Design considerations on using the dual excitation wavelengths are discussed. Multimodal and label-free imaging by TPEF, SHG, and THG are demonstrated on biological samples. The miniaturized multimodal MPM is shown to have great potential for label-free imaging of thick and live tissues.
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