38 results match your criteria: "The Institute for Lasers[Affiliation]"

Multiphoton upconversion lasing in scattering gain media has attracted considerable attention in recent years. LAPONITE® is a scattering medium consisting of 2-D nano-discs that can be dispersed as a transparent solution in aqueous media and forms a gel at high concentration. In this paper, we demonstrate two-photon pumped upconversion regular lasing along forward and backward directions as well as random lasing along all other directions.

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Both lanthanide-containing and fluorine-containing nanomaterials present challenging targets for microbial biosynthesis because these elements are toxic to most bacteria. Here, we overcome these challenges by using an Antarctic Shewanella baltica strain that tolerates these elements and report the first biosynthesis of lanthanide-doped fluoride nanoparticles (NPs) from them. NaYF NPs doped with Er/Yb are prototypical lanthanide-based upconverting nanoparticles (UCNPs) with upconverted luminescence at visible wavelengths under infrared excitation.

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Background: Rare-earth sulfide nanoparticles (NPs) could harness the optical and magnetic features of rare-earth ions for applications in nanotechnology. However, reports of their synthesis are scarce and typically require high temperatures and long synthesis times.

Results: Here we present a biosynthesis of terbium sulfide (TbS) NPs using microorganisms, identifying conditions that allow Escherichia coli to extracellularly produce TbS NPs in aqueous media at 37 °C by controlling cellular sulfur metabolism to produce a high concentration of sulfide ions.

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4-Chlorophenol (4CP) is a well-known environmental contaminant often detected in wastewater, generally arising from industrial processes such as chemical manufacture, pharmaceutical production, and pesticide formulation. 4CP is a matter of great concern since it is persistent and has the potential to have harmful impacts on both aquatic ecosystems and human health, owing to its hazardous and mutagenic properties. Hence, degradation of 4CP is of utmost significance.

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Capsaicin, a chemical compound present in chili peppers, is widely acknowledged as the main contributor to the spicy and hot sensations encountered during consumption. Elevated levels of capsaicin can result in meals being excessively spicy, potentially leading to health issues, such as skin burning, irritation, increased heart rate and circulation, and discomfort in the gastrointestinal system and even inducing nausea or diarrhea. The level of spiciness that individuals can tolerate may vary, so what may be considered incredibly hot for one person could be mild for another.

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Plasticizer-Induced Enhancement of Mesoscale Dissymmetry in Thin Films of Chiral Polymers with Variable Chain Length.

Adv Mater

January 2024

Department of Chemistry and The Institute for Lasers, Photonics, and Biophotonics, University at Buffalo, SUNY, Buffalo, NY, 14260, USA.

Conjugated polymers with chiral side chains are of interest in areas including chiral photonics, optoelectronics, and chemical and biological sensing. However, the low dissymmetry factors of most neat polymer thin films have limited their practical application. Here, a robust method to increase the absorption dissymmetry factor in a poly-fluorene-thiophene (PF8TS series) system is demonstrated by varying molecular weight and introducing an achiral plasticizer, polyethylene mono alcohol (PEM-OH).

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Designing polymeric systems with ultra-high optical activity is instrumental in the pursuit of smart artificial chiroptical materials, including the fundamental understanding of structure/property relations. Herein, we report a diacetylene (DA) moiety flanked by chiral D- and L-FF dipeptide methyl esters that exhibits efficient topochemical photopolymerization in the solid phase to furnish polydiacetylene (PDA) with desired control over the chiroptical properties. The doping of the achiral gold nanoparticles provides plasmonic interaction with the PDAs to render asymmetric shape to the circular dichroism bands.

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Exploring magneto-optic properties of colloidal two-dimensional copper-doped CdSe nanoplatelets.

Nanophotonics

December 2022

Department of Chemistry and The Institute for Lasers, Photonics and Biophotonics, University at Buffalo, Suny, Buffalo, NY 14260, USA.

Transition-metal-doped semiconductor nanocrystals have received significant attention because of their attractive features deeming them invaluable in various technological fields including optoelectronics, bio-photonics, and energy conversion, to name a few. Of particular, these interests are two-dimensional materials with useful optical and magnetic properties combined with their large surface areas opening up new applications in biotechnology. These applications range from multimodal optical and magnetic bioimaging and sensing to measuring the weak magnetic field due to brain waves using their magneto-optic properties stemming from the exchange interaction between the transition metal dopants and the carrier spins.

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Modulating the Chiroptical Response of Chiral Polymers with Extended Conjugation within the Structural Building Blocks.

J Phys Chem Lett

October 2022

Department of Chemistry and The Institute for Lasers, Photonics and Biophotonics, University at Buffalo (SUNY), Buffalo, New York 14260, United States.

Advancing the emerging area of chiral photonics requires modeling-guided concepts of chiral material design to enhance optical activity and associated optical rotatory dispersion. Herein, we introduce conformational engineering achieved by tuning polymer backbone conjugation through introduction of thiophene structural units in a chiral fluorene polymer backbone. Our theoretical calculations reveal a relationship between the structural conformation and the resultant rotational strength.

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Boron-based nano-formulations look very promising for biomedical applications, including photo- and boron neutron capture therapies, but the fabrication of non-toxic water-dispersible boron nanoparticles (NPs), which contain the highest boron atom concentration, is difficult using currently available chemical and plasma synthesis methods. Here, we demonstrate purely aqueous synthesis of clean boron NPs by methods of femtosecond laser ablation from a solid boron target in water, thus free of any toxic organic solvents, and characterize their properties. We show that despite highly oxidizing water ambience, the laser-ablative synthesis process follows an unusual scenario leading to the formation of boron NPs together with boric acid (HBO) as an oxidation by-product coating the nanoparticles, which acts to stabilize the elemental boron NPs dispersion.

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Lifetime of the H Electronic State in Tm-Doped Upconverting Nanoparticles for NIR Nanothermometry.

J Phys Chem B

December 2021

Department of Chemistry, University at Buffalo, The State University of New York, Buffalo, New York 14260-3000, United States.

Emission bands from thermally coupled states in lanthanide-doped nanoparticles have been studied for ratiometric nanothermometry in biological applications. Unfortunately certain factors such as water absorption distort the intensity, limiting the accuracy of ratiometric nanothermometry. However, the decay time of such states does not suffer from such distortions.

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There is widespread interest in developing agents to modify tumor hypoxia in head and neck squamous cell carcinomas (HNSCC). Here, we report on the synthesis, characterization, and potential utility of ultra-small NaYF:Nd/NaGdF nanocrystals coated with manganese dioxide (usNP-MnO) for spatiotemporal modulation of hypoxia in HNSCC. Using a dual modality imaging approach, we first visualized the release of Mn using T1-weighted magnetic resonance imaging (MRI) and modulation of oxygen saturation (%sO) using photoacoustic imaging (PAI) in vascular channel phantoms.

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In this paper, we report an approach to polymerization of a nanocomposite containing UV-polymerizable organic material and inorganic, NaYbF:Tm core-based nanoparticles (NPs), which are optimized for upconversion of near infrared (NIR) to ultraviolet (UV) and blue light. Our approach is compatible with numerous existing UV-polymerizable compositions and the NaYF: Yb, Tm core-based NPs are much more stable against harsh conditions than NIR organic photo-initiators proposed earlier. The use of a core-shell design for the NPs can provide a suitable method for binding with organic constituents of the nanocomposite, while maintaining efficient NIR-to-UV/blue conversion in the NaYbF core.

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We report the observation of backward stimulated Mie scattering (SMS) due to light-field induced spatial redistribution of self-assembled nanospheres of a two-photon resonant organic chromophore in water, pumped by ∼10-ns laser pulses of ∼816-nm wavelength. The pump-energy threshold for generating backward stimulated scattering in such a system is remarkably lower than that in pure water. The gain of backscattering originates from an induced Bragg grating that reflects partial energy from the pump beam into the backward Mie scattering beam.

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Doubly resonant infrared-visible sum-frequency generation (DR-IVSFG) spectroscopy, encompassing coupled vibrational and electronic transitions, provides a powerful method to gain a deep understanding of nuclear motion in photoresponsive surface adsorbates and interfaces. Here, we use DR-IVSFG to elucidate the role of vibronic coupling in a surface-confined donor-acceptor substituted azobenzene. Our study reveals some unique features of DR-IVSFG that have not been previously reported.

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Core-shell nanostructures associated with photonics techniques have found innumerous applications in diagnostics and therapy. In this work, we introduce a novel core-shell nanostructure design that serves as a multimodal optical imaging contrast agent for dental adhesion evaluation. This nanostructure consists of a rare-earth-doped (NaYF :Yb 60%, Tm 0.

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Emerging Nanomedicine Approaches to Targeting HIV-1 and Antiretroviral Therapy.

Future Virol

February 2016

Center for Integrated Global Health Sciences; Translational Pharmacology Research Core, New York State Center of Excellence in Bioinformatics and Life Sciences; School of Pharmacy and Pharmaceutical Sciences; University at Buffalo, Buffalo, NY, USA; Department of Medicine, School of Medicine and Biomedical Sciences, University at Buffalo, Buffalo NY, USA.

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Manipulating Magneto-Optic Properties of a Chiral Polymer by Doping with Stable Organic Biradicals.

Nano Lett

September 2016

The Institute for Lasers, Photonics and Biophotonics, State University of New York at Buffalo, Buffalo, New York 14260, United States.

We report the first example of tuning the large magneto-optic activity of a chiral polymer by addition of stable organic biradicals. The spectral dispersion of Verdet constant, which quantifies magneto-optic response, differs substantially between the base polymer and the nanocomposite. We employed a microscopic model, supported by atomistic calculations, to rationalize the behavior of this nanocomposite system.

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Macrophage Targeted Nanoparticles for Antiretroviral (ARV) Delivery.

J Pers Nanomed

November 2015

Department of Medicine, School of Medicine and Biomedical Sciences, University at Buffalo, Buffalo NY, USA.

Objective: To reduce the amount of the antiretroviral (ARV) nevirapine necessary to achieve therapeutic concentrations using macrophage targeted nanoparticles.

Methods: Core-shell nanoparticles were prepared from FDA approved, biodegradable and biocompatible polymers, with poly(lactic-co-glycolic) acid (PLGA) as the core and chitosan (CS) as the shell using a water/oil/water method. Nevirapine was encapsulated in the core of the nanoparticles.

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We report a new class of hybrid π-electron chromophores with a large, sign-tunable third-order nonlinear optical (NLO) response, achieved via cooperative coupling of cyanine dye bond-length alternation effects with the rich density of states in zwitterionic twisted π-system chromophores. A combined synthetic, linear/nonlinear spectroscopic, and quantum chemical study reveals exceptional third-order response exceeding the sum of the individual chromophore contributions.

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Photonic activation of plasminogen induced by low dose UVB.

PLoS One

October 2015

BioPhotonics Group, Department of Nanomedicine, International Iberian Nanotechnology Laboratory (INL), Braga, Portugal.

Activation of plasminogen to its active form plasmin is essential for several key mechanisms, including the dissolution of blood clots. Activation occurs naturally via enzymatic proteolysis. We report that activation can be achieved with 280 nm light.

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Modulating the structure of EGFR with UV light: new possibilities in cancer therapy.

PLoS One

December 2015

BioPhotonics Group, Department of Nanomedicine, International Iberian Nanotechnology Laboratory (INL), Braga, Portugal. 2. BioPhotonics Group, Department of Nanomedicine, International Iberian Nanotechnology Laboratory (INL), Braga, Portugal and 6 Department of Clinical Medicine, Aalborg University, Søndre Skovvej 15, 9000 Aalborg, Denmark.

The epidermal growth factor receptor (EGFR) is a member of the ErbB family of receptor tyrosine kinases. EGFR is activated upon binding to e.g.

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Unlabelled: Infectious diseases are a worldwide health concern. For some infections, a common feature is the intracellular residence of the pathogen and evasion of the host immune response. In the case of tuberculosis (TB), Mycobacterium tuberculosis evades clearance within macrophages through suppression of intracellular reactive oxygen and nitrogen species (ROS/RNS) and pro-inflammatory cytokines.

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Exploring the amphiphilicity of PEGylated gold nanorods: mechanical phase transfer and self-assembly.

Chem Commun (Camb)

October 2013

The Institute for Lasers, Photonics and Biophotonics, University at Buffalo-SUNY, Buffalo, New York 14260-3000, USA.

We introduce a mechanical approach to phase transfer of PEGylated gold nanorods. Amphiphilic PEG ligands can be switched between hydrophilic and hydrophobic states by applying mechanical force. PEG-GNRs in their hydrophobic state self-assemble into rings, a phenomenon previously observed only for GNRs capped with hydrophobic ligands.

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Twisted π-system chromophores for all-optical switching.

J Am Chem Soc

May 2011

The Institute for Lasers, Photonics and Biophotonics, State University of New York at Buffalo, Buffalo, New York 14260, USA.

Molecular chromophores with twisted π-electron systems have been shown to possess unprecedented values of the quadratic hyperpolarizability, β, with very large real parts and much smaller imaginary parts. We report here an experimental and theoretical study which shows that these twisted chromophores also possess very large values of the real part of the cubic hyperpolarizability, γ, which is responsible for nonlinear refraction. Thus, for the two-ring twisted chromophore TMC-2 at 775 nm, relatively close to one-photon resonance, n(2) extrapolated to neat substance is large and positive (1.

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