Laser tissue welding by using collagen excitation at a 1,720 nm near-infrared optical window III.

Laser tissue welding (LTW) is a method of fusing incised tissues together. LTW has the potential to revolutionize plastic surgery and wound healing techniques by its ability to produce watertight, scarless seals with minimal foreign body reaction. While using thermal mechanisms to achieve LTW, energy from the incident laser is absorbed by water in the tissue. As the water temperature increases, partial denaturing of the collagen triple helix briefly occurs, which is quickly followed by renaturation of collagen as the tissue cools, thus providing a watertight seal. This research study investigates the efficacy of direct collagen excitation at 1,720 nm to accomplish LTW. This wavelength falls within the near-infrared (NIR) optical window III. The tensile strengths of pig skin that have been welded with NIR continuous-wave (CW) diode lasers at 1,455 nm, which promote thermal mechanisms of tissue welding, and 1,720 nm wavelengths, are compared. Near-infrared lasers tuned to 1,455 and 1,720 nm were used to weld incised pieces of porcine skin together without extrinsic solders or dyes. The tensile force of the welded tissues was measured using a digital force gauge. The average tensile force of the welded pig skin using the 1,720 nm laser was approximately four times greater than that using the CW 1,455 nm laser, suggesting that LTW accomplished through direct collagen excitation in the NIR optical window III provides greater tensile strengths.

Stokes shift spectroscopy and machine learning for label-free human prostate cancer detection.

The Stokes shift spectra (S3) of human cancerous and normal prostate tissues were collected label free at a selected wavelength interval of 40 nm to investigate the efficacy of the approach based on three key molecules-tryptophan, collagen, and reduced nicotinamide adenine dinucleotide (NADH)-as cancer biomarkers. S3 combines both fluorescence and absorption spectra in one scan. The S3 spectra were analyzed using machine learning (ML) algorithms, including principal component analysis (PCA), nonnegative matrix factorization (NMF), and support vector machines (SVMs). The components retrieved from the S3 spectra were considered principal biomarkers. The differences in the weights of the components between the two types of tissues were found to be significant. Sensitivity, specificity, and accuracy were calculated to evaluate the performance of SVM classification. This research demonstrates that S3 spectroscopy is effective for detecting the changes in the relative concentrations of the endogenous fluorophores in tissues due to the development of cancer label free.

Intraoperative detection of human meningioma using a handheld visible resonance Raman analyzer.

To report for the first time the preliminary results for the evaluation of a VRR-LRR™ analyzer based on visible resonance Raman technique to identify human meningioma grades and margins intraoperatively. Unprocessed primary and recurrent solid human meningeal tissues were collected from 33 patients and underwent Raman analysis during surgeries. A total of 1180 VRR spectra were acquired from fresh solid tissues using a VRR-LRR™ analyzer. A confocal HR Evolution (HORIBA, France SAS) Raman system with 532-nm excitation wavelength was also used to collect data for part of the ex vivo samples after they were thawed from - 80 °C for comparison. The preliminary analysis led to the following observations. (1) The intensity ratio of VRR peaks of protein to fatty acid (I2934/I2888) decreased with the increase of meningioma grade. (2) The ratio of VRR peaks of phosphorylated protein to amid I (I1588/I1639) decreased for the higher grade of meningioma. (3) Three RR vibration modes at 1378, 3174, and 3224 cm-1 which were related to the molecular vibrational bands of oxy-hemeprotein, amide B, and amide A protein significantly changed in peak intensities in the two types of meningioma tissues compared to normal tissue. (4) The changes in the intensities of VRR modes of carotenoids at 1156 and 1524 cm-1 were also found in the meningioma boundary. The VRR-LRR™ analyzer demonstrates a new approach for label-free, rapid, and objective identification of primary human meningioma in quasi-clinical settings. The accuracy for detecting meningioma tissues using support vector machines (SVMs) was over 70% based on Raman peaks of key biomolecules and up to 100% using principal component analysis (PCA).

Femtosecond anti-Stokes conical emission in BK-7 glass and O and E-wave calcite.

The angle of anti-Stokes conical emission (CE) is experimentally measured in the frequency shift span of 2000cm-1 to 9000cm-1. The experiment was performed using a 800 nm 50 fs laser pump in samples of BK-7 glass and calcite in both the O and E-wave configurations. The experimental results of angular emission are then compared to three competing models: the Alfano-Shapiro four wave mixing (FWM) model from 1970, the Luther FWM model from 1994, and the Faccio X-wave model from 2004. Results indicate that in all samples and configurations tested, the original FWM has the best agreement with experimental results in the anti-Stokes span.

Modulation instability induced by cross-phase modulation of transient stimulated Raman scattering and self-phase modulation in calcite.

Pairs of sidebands about the transient stimulated Raman scattering (SRS) 1086cm-1 vibration mode peak are observed for calcite under 517 nm 390 fs pulse excitation. These pairs of side frequency lobes arise from modulation instability (MI) from the interaction of cross-phase modulation (XPM) from self-phase modulation (SPM) and SRS. The pairs of secondary frequencies are attributed to the daughter 1086cm-1 decay product modes from the multiphonon of 3, 4, and 5 decays. The main sideband peak from 1086cm-1 phonon at 546cm-1 suggests the operation of the Orbach effect.

Comparison of continuous wave versus picosecond SRS and the resonance SRS effect.

Stimulated Raman scattering (SRS) is a powerful optical technique for probing the vibrational states of molecules in biological tissues and provides greater signal intensities than when using spontaneous Raman scattering. In this study, we examined the use of continuous wave (cw) and picosecond (ps) laser excitations to generate SRS signals in pure methanol, a carotene-methanol solution, acetone, and brain tissue samples. The cw-SRS system, which utilized two cw lasers, produced better signal-to-noise (S/N) than the conventional ps-SRS system, suggesting that the cw-SRS system is an efficient and cost-effective approach for studying SRS in complex systems like the brain. The cw-SRS approach will reduce the size of the SRS system, allowing for stimulated Raman gain/loss microscopy. In addition, we showed that there exists a resonance SRS (RSRS) effect from the carotene-methanol solution and brain tissue samples using cw laser excitations. The RSRS effect will further improve the signal-to-noise and may be utilized as an enhanced, label-free SRS microscopic tool for the study of biological tissues.

Steady-state stimulated Raman generation and filamentation using complex vector vortex beams.

Stimulated Raman scattering and laser filamentation produced using nanosecond pulsed complex vector vortex beams (CVVB) are investigated in a 20 cm long methanol cell. The CVVB is generated using q-plates and is tested at orbital angular momentum (L) values of 1, 2, 3, and 4 and circular, radial, and azimuthal polarizations. The results illustrate that the stability and intensity of the generated stimulated Raman has dependence on input polarization and L value. During filamentation, the beam is also shown to break up into multiple primary filaments and that there is a reduction in small-scale filamentation when using CVVBs.

Explanation of the competition between O- and E-wave induced stimulated Raman and supercontinuum in calcite under ultrafast laser excitation.

Key optical properties of calcite were measured to unravel the difference between stimulated Raman scattering (SRS) and self-phase modulation (SPM) for the supercontinuum (SC) for ordinary (O) wave and extraordinary (E) wave. These properties are group velocity dispersion, walk-off, spontaneous Raman spectra and cross section, optical 1086cm-1 phonon linewidth, nonlinear susceptibility (χ3), steady-state and transient SRS, and SC caused from SPM. These are investigated for O-waves and E-waves from a 2.7 cm thick calcite crystal. Using 390 fs pulses (∼0.8µJ pulse energy) at 517 nm, the O-wave produced a stronger sharp SRS peak at 1086cm-1 and a weaker SC spectrum in the visible range than the E-wave. The salient difference found between the O- and E-waves for SRS and SPM in calcite is attributed to the larger Raman cross section and the size of nonlinear susceptibility (χ3) for O-waves as compared to E-waves.

Hybrid generation and analysis of vector vortex beams.

A method is described for generating optical vector vortex beams carrying superpositions of orbital angular momentum states by using a tandem application of a spatial light modulator with a vortex retarder. The vortex component has a spatially inhomogeneous phase front that can carry orbital angular momentum, and the vector nature is a spatially inhomogeneous state of polarization in the laser beam profile. The vector vortex beams are characterized experimentally by imaging the beams at points across the focal plane in an astigmatic system using a tilted lens. Mathematical analysis of the Gouy phase shows good agreement with the phase structure obtained in the experimental images. The polarization structure of the vector beam and the orbital angular momentum of the vortex beam are shown to be preserved.

Using the nonseparability of vector beams to encode information for optical communication.

In this work, it is experimentally demonstrated that the nonseparability of vector beams (e.g., radial and azimuthal polarization) can be used to encode information for optical communication. By exploiting the nonseparability of a vector beam's space and polarization degrees of freedom using conventional wave plates, it is shown that 2 bits of information can be encoded when applying the identity and three Pauli operators to its polarization degree of freedom. It is also shown that vector beams can be efficiently decoded with as low as 2.7% cross talk using a Mach-Zehnder interferometer that exploits a higher-order Pancharatnam-Berry phase and liquid crystal q-plates.

4 × 20 Gbit/s mode division multiplexing over free space using vector modes and a q-plate mode (de)multiplexer.

Vector modes are spatial modes that have spatially inhomogeneous states of polarization, such as, radial and azimuthal polarization. In this work, the spatially inhomogeneous states of polarization of vector modes are used to increase the transmission data rate of free-space optical communication via mode division multiplexing. A mode (de)multiplexer for vector modes based on a liquid crystal q-plate is introduced. As a proof of principle, four vector modes each carrying a 20-Gbit/s quadrature phase shift keying signal (aggregate 80 Gbit/s) on a single wavelength channel (λ∼1550 nm) were transmitted ∼1 m over the lab table with <-16.4 dB mode crosstalk. Bit error rates for all vector modes were measured at the 7% forward error correction threshold with power penalties <3.41 dB.

All-digital wavefront sensing for structured light beams.

We present a new all-digital technique to extract the wavefront of a structured light beam. Our method employs non-homogeneous polarization optics together with dynamic, digital holograms written to a spatial light modulator to measure the phase relationship between orthogonal polarization states in real-time, thereby accessing the wavefront information. Importantly, we show how this can be applied to measuring the wavefront of propagating light fields, over extended distances, without any moving components. We illustrate the versatility of the tool by measuring propagating optical vortices, Bessel, Airy and speckle fields. The comparison of the extracted and programmed wavefronts yields excellent agreement.

Femtosecond optical Kerr effect in normal and grades of cancerous breast tissues as a new optical biopsy method.

This study reports on the first use of the optical Kerr effect (OKE) in breast cancer tissue. This proposed optical biopsy method utilizes a Femtosecond Optical Kerr Gate to detect changes in dielectric relaxation and conductivity created by a cancerous infection. Here, the temporal behavior of the OKE is tracked in normal and cancerous samples of human and mouse breast. These tissues display a double peaked temporal structure and its decay rate changes depending on the tissue's infection status. The decay of the secondary peak, attributed to ultrafast plasma response, indicates that the tissue's conductivity has doubled once infected. A slower molecular contribution to the Kerr effect can also be observed in healthy tissues. These findings suggest two possible biomarkers for the use of OKE in optical biopsy. Both markers arise from alterations in the infected tissue's cellular structure, which changes the rate at which electronic and molecular processes occur.

Tunable supercontinuum light vector vortex beam generator using a q-plate.

Spatially coherent multicolored optical vector vortex beams were created using a tunable liquid crystal q-plate and a supercontinuum light source. The feasibility of the q-plate as a tunable spectral filter (switch) was demonstrated, and the polarization topology of the resulting vector vortex beam was mapped. Potential applications include multiplexing for broadband high-speed optical communication, ultradense data networking, and super-resolution microscopy.

Native fluorescence spectra of human cancerous and normal breast tissues analyzed with non-negative constraint methods.

The native fluorescence spectra of human cancerous and normal breast tissues were investigated using the selected excitation wavelength of 340 nm to excite key building block molecules, such as reduced nicotinamide adenine dinucleotide (NADH), collagen, and flavin. The measured emission spectra were analyzed using a non-negative constraint method, namely multivariate curve resolution with alternating least-squares (MCR-ALS). The results indicate that the biochemical changes of tissue can be exposed by native fluorescence spectra analysis. The MCR-ALS-extracted components corresponding to the key fluorophores in breast tissue, such as collagen, NADH, and flavin, show differences of relative contents of fluorophores in cancerous and normal breast tissues. This research demonstrates that the native fluorescence spectroscopy measurements are effective for detecting changes of fluorophores composition in tissues due to the development of cancer. Native fluorescence spectroscopy analyzed by MCR-ALS may have the potential to be a new armamentarium.

Mini review of ultrafast fluorescence polarization spectroscopy [invited].

A mini review is presented on the theory, experiment, and application of the ultrafast fluorescence polarization dynamics and anisotropy with examples of two important medical dyes, namely Indocyanine Green and fluorescein. The time-resolved fluorescence polarization spectra of fluorescent dyes were measured with the excitation of a linearly polarized femtosecond laser pulse, and detected using a streak camera. The fluorescence emitted from the dyes is found to be partially oriented (polarized), and the degree of polarization of emission decreases with time. The decay of the fluorescence component polarized parallel to the excitation beam was found to be faster than that of the perpendicular one. Based on the physical model on the time-resolved polarized emission spectra in nanosecond range first described by Weber [J. Chem. Phys.52, 1654 (1970)], a set of first-order linear differential equations was used to model fluorescence polarization dynamics and anistropy of dye in picoseconds range. Using this model, two important decay parameters were identified separately: the decay rate of total emission intensity and the decay rate of the emission polarization affected by the rotation of fluorescent molecules causing the transfer of emission polarization from one orthogonal component to another. These two decay rates were separated and extracted from the measured time-resolved fluorescence polarization spectra. The emission polarization difference among dyes arising from different molecular volumes was used to enhance the image contrast.

Higher harmonics and supercontinuum generated from the Kerr response time in different states of matter from a universal electromagnetic model.

There is a need for a universal model to describe higher harmonic generation (HHG) in different states of matter. Based on an electromagnetic model (EM), the generation of odd higher harmonic (HHG) and supercontinuum (SC) from intense fs and ps pulses for visible, NIR, and MIR lasers is simulated based on the parameters from experimental observation. HHG and SC depend critically on the different Kerr material response times τ from the ultrafast on the order of 100 as for electronic cloud distortion to fast ~ 10 fs from plasma and molecular redistribution and to the slower picoseconds rotational and vibrational molecular processes. The number of odd HHG generated is shown to depend critically on the fastest Kerr response time on the order of ~ 1 fs from electronic self-phase modulation (ESPM). In this study, different states of matter from noble gas Argon to condensed matter ZnO and LBG are simulated showing the dependence on the Kerr response time to produce HHG for various applications in Physics, Chemistry, Biology, and Engineering. The EM model is universal to produce HHG and SC in different states of matter.

Femtosecond Optical Kerr Gate in tissues.

The Optical Kerr Effect is investigated for the first time in biological tissues. This nonlinear effect was explored in both human brain and avian breast tissues using a time-resolved femtosecond pump-probe Optical Kerr Gate that looks for phase changes that arise in the probe from the pump induced Kerr refractive index change. The tissue samples produced a unique ultrafast (700-800 fs) doubled peaked temporal signal, which is indicative of interplay between the different ultrafast mechanisms (electronic plasma and molecular) that make up the Kerr index. The unique profile was replicated in theoretical simulations. The properties of the temporal profile varied between samples suggesting that it could be used as a new diagnostic. Understanding this behavior can help improve the scientific understanding of nonlinear spectral diagnostic techniques and potentially create a new Kerr-based optical biopsy method.

A Handheld Visible Resonance Raman Analyzer Used in Intraoperative Detection of Human Glioma.

There is still a lack of reliable intraoperative tools for glioma diagnosis and to guide the maximal safe resection of glioma. We report continuing work on the optical biopsy method to detect glioma grades and assess glioma boundaries intraoperatively using the VRR-LRRTM Raman analyzer, which is based on the visible resonance Raman spectroscopy (VRR) technique. A total of 2220 VRR spectra were collected during surgeries from 63 unprocessed fresh glioma tissues using the VRR-LRRTM Raman analyzer. After the VRR spectral analysis, we found differences in the native molecules in the fingerprint region and in the high-wavenumber region, and differences between normal (control) and different grades of glioma tissues. A principal component analysis-support vector machine (PCA-SVM) machine learning method was used to distinguish glioma tissues from normal tissues and different glioma grades. The accuracy in identifying glioma from normal tissue was over 80%, compared with the gold standard of histopathology reports of glioma. The VRR-LRRTM Raman analyzer may be a new label-free, real-time optical molecular pathology tool aiding in the intraoperative detection of glioma and identification of tumor boundaries, thus helping to guide maximal safe glioma removal and adjacent healthy tissue preservation.

Fano resonance line shapes in the Raman spectra of tubulin and microtubules reveal quantum effects.

Microtubules are self-assembling biological nanotubes made of the protein tubulin that are essential for cell motility, cell architecture, cell division, and intracellular trafficking. They demonstrate unique mechanical properties of high resilience and stiffness due to their quasi-crystalline helical structure. It has been theorized that this hollow molecular nanostructure may function like a quantum wire where optical transitions can take place, and photoinduced changes in microtubule architecture may be mediated via changes in disulfide or peptide bonds or stimulated by photoexcitation of tryptophan, tyrosine, or phenylalanine groups, resulting in subtle protein structural changes owing to alterations in aromatic flexibility. Here, we measured the Raman spectra of a microtubule and its constituent protein tubulin both in dry powdered form and in aqueous solution to determine if molecular bond vibrations show potential Fano resonances, which are indicative of quantum coupling between discrete phonon vibrational states and continuous excitonic many-body spectra. The key findings of this work are that we observed the Raman spectra of tubulin and microtubules and found line shapes characteristic of Fano resonances attributed to aromatic amino acids and disulfide bonds.