Laser ablation for pharmaceutical nanoformulations: Multi-drug nanoencapsulation and theranostics for HIV.

We introduce the use of laser ablation to develop a multi-drug encapsulating theranostic nanoformulation for HIV-1 antiretroviral therapy. Laser ablated nanoformulations of ritonavir, atazanavir, and curcumin, a natural product that has both optical imaging and pharmacologic properties, were produced in an aqueous media containing Pluronic® F127. Cellular uptake was confirmed with the curcumin fluorescence signal localized in the cytoplasm. Formulations produced with F127 had improved water dispersibility, are ultrasmall in size (20-25 nm), exhibit enhanced cellular uptake in microglia, improve blood-brain barrier (BBB) crossing in an in vitro BBB model, and reduce viral p24 by 36 fold compared to formulations made without F127. This work demonstrates that these ultrasmall femtosecond laser-ablated nanoparticles are effective in delivering drugs across the BBB for brain therapy and show promise as an effective method to formulate nanoparticles for brain theranostics, reducing the need for organic solvents during preparation.

Mechanism of stimulated Mie scattering: Light-induced redistribution of self-assembled nanospheres of two-photon absorbing chromophore.

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. Based on the experimental fact that the time-delay of the SMS pulse onset depends on both the pump level and the viscosity of the solvent, a physical model of SMS generation is proposed. Our experimental results have shown that the major contribution to the formation of an induced Bragg grating is spatial redistribution of nanoparticles suspended in the liquid. These nanoparticles are driven by a force that is proportional to the intensity gradient of the standing-wave field resulting from interference between the forward pump beam and the backward Mie scattering beam. When the nanoparticle motion is frozen in a gel-like medium, no SMS is observed, which experimentally supports the validity of the proposed physical model.

Alleviating Luminescence Concentration Quenching in Upconversion Nanoparticles through Organic Dye Sensitization.

The phenomenon of luminescence concentration quenching exists widely in lanthanide-based luminescent materials, setting a limit on the content of lanthanide emitter that can be used to hold the brightness. Here, we introduce a concept involving energy harvesting by a strong absorber and subsequent energy transfer to a lanthanide that largely alleviates concentration quenching. We apply this concept to Nd3+ emitters, and we show both experimentally and theoretically that the optimal doping concentration of Nd3+ in colloidal NaYF4:Nd upconverting nanoparticles is increased from 2 to 20 mol% when an energy harvestor organic dye (indocyanine green, ICG) is anchored onto the nanoparticle surface, resulting in ∼10 times upconversion brightness. Theoretical analysis indicated that a combination of efficient photon harvesting due to the large absorption cross section of ICG (∼30 000 times higher than that of Nd3+), non-radiative energy transfer (efficiency ∼57%) from ICG to the surface bound Nd3+ ions, and energy migration among the Nd3+ ions was able to activate Nd3+ ions inside the nanoparticle at a rate comparable with that of the pronounced short-range quenching interaction at elevated Nd3+ concentrations. This resulted in the optimal concentration increase to produce significantly enhanced brightness. Theoretical modeling shows a good agreement with the experimental observation. This strategy can be utilized for a wide range of other lanthanide-doped nanomaterials being utilized for bioimaging and solar cell applications.

Twisted Thiophene-Based Chromophores with Enhanced Intramolecular Charge Transfer for Cooperative Amplification of Third-Order Optical Nonlinearity.

Exploiting synergistic cooperation between multiple sources of optical nonlinearity, we report the design, synthesis, and nonlinear optical properties of a series of electron-rich thiophene-containing donor-acceptor chromophores with condensed π-systems and sterically regulated inter-aryl twist angles. These structures couple two key mechanisms underlying optical nonlinearity, namely, (i) intramolecular charge transfer, greatly enhanced by increased electron density and reduced aromaticity at chromophore thiophene rings and (ii) a twisted chromophore geometry, producing a manifold of close-lying excited states and dipole moment changes between ground and excited states that are nearly twice that of untwisted systems. Spectroscopic, electrochemical, and nonlinear Z-scan measurements, combined with quantum chemical calculations, illuminate relationships between molecular structure and mechanisms of enhancement of the nonlinear refractive index. Experiment and calculations together reveal ground-state structures that are strongly responsive to the solvent polarity, leading to substantial negative solvatochromism (Δλ ≈ 10(2) nm) and prevailing zwitterionic/aromatic structures in the solid state and in polar solvents. Ground-to-excited-state energy gaps below 2.0 eV are obtained in condensed π-systems, with lower energy gaps for twisted versus untwisted systems. The real part of the second hyperpolarizability in the twisted structures is much greater than the imaginary part, with the highest twist angle chromophore giving |Re(γ)/Im(γ)| ≈ 100, making such chromophores very promising for all-optical-switching applications.

Cooperative coupling of cyanine and tictoid twisted π-systems to amplify organic chromophore cubic nonlinearities.

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.

Nonlinear optical absorption and stimulated Mie scattering in metallic nanoparticle suspensions.

The nonlinear optical properties of four metallic (Au-, Au/Ag-, Ag-, and Pt-) nanoparticle suspensions in toluene have been studied in both femtosecond and nanosecond regimes. Nonlinear transmission measurements in the femtosecond laser regime revealed two-photon absorption (2PA) induced nonlinear attenuation, while in the nanosecond laser regime a stronger nonlinear attenuation is due to both 2PA and 2PA-induced excited-state absorption. In the nanosecond regime, at input pump laser intensities above a certain threshold value, a new type of stimulated (Mie) scattering has been observed. Being essentially different from all other well known molecular (Raman, Brillouin) stimulated scattering effects, the newly observed stimulated Mie scattering from the metallic nanoparticles exhibits the features of no frequency shift and low pump threshold requirement. A physical model of induced Bragg grating initiated by the backward Mie scattering from metallic nanoparticles is proposed to explain the gain mechanism of the observed stimulated scattering effect.

Twisted π-system chromophores for all-optical switching.

Molecular chromophores with twisted π-electron systems have been shown to possess unprecedented values of the quadratic hyperpolarizability, ß, 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 (1.87 × 10(-13) cm(2)/W), leading to self-focusing. Furthermore, the third-order response includes a remarkably low two-photon absorption coefficient, which means minimal nonlinear optical losses: the T factor, α(2)λ/n(2), is 0.308. These characteristics are attributed to closely spaced singlet biradical and zwitterionic states and offer promise for applications in all-optical switching.

Superior optical limiting, stabilization, and spatio-temporal reshaping of ultrashort laser pulses in an opto-stable intrinsic polymer film.

A chemically modified poly(fluorene-alt-benzothiadiazole) (PFBT) polymer film is reported to exhibit high two-photon absorbing capability and chemical/physical stability upon the action of high-power laser pulses of ~780 nm wavelength and ~160 fs duration. A nonlinear transmission measurement is conducted by varying the input intensity from ~20 to ~600 GW/cm2, the corresponding nonlinear transmission of a ~70 µm thick film is reduced from ~0.8 to 0.18, indicating a superior optical limiting behavior. In the meantime, intensity fluctuation of laser pulses can be significantly reduced after passing through the same film sample. Based on the intensity-dependent nonlinear attenuation mechanism, a straightforward optical reshaping effect on spatio-temporal profiles of the laser pulses has also been demonstrated.

Additive controlled synthesis of gold nanorods (GNRs) for two-photon luminescence imaging of cancer cells.

Gold nanorods (GNRs) with a longitudinal surface plasmon resonance peak that is tunable from 600 to 1100 nm have been fabricated in a cetyl trimethylammoniumbromide (CTAB) micellar medium using hydrochloric acid and silver nitrate as additives to control their shape and size. By manipulating the concentrations of silver nitrate and hydrochloric acid, the aspect ratio of the GNRs was reliably and reproducibly tuned from 2.5 to 8. The GNRs were first coated with polyelectrolyte multilayers and then bioconjugated to transferrin (Tf) to target pancreatic cancer cells. Two-photon imaging excited from the bioconjugated GNRs demonstrated receptor-mediated uptake of the bioconjugates into Panc-1 cells, overexpressing the transferrin receptor (TfR). The bioconjugated GNR formulation exhibited very low toxicity, suggesting that it is biocompatible and potentially suitable for targeted two-photon bioimaging.

Degenerate multi-photon properties of spirofluorene derivatives.

Two- and three-photon absorption properties of the fluorene-based chromophores have been investigated. The two- and three-photon absorption cross-section are found to be increased with the strength of the electron donor groups in the order of N-ethylcarbazoyl (1), triphenylamino (2), and N,N-dibutylanilino (3) groups. This nonlinear absorption enhancement can be interpreted by the increase of intramolecular charge transfer facilitated by strong electron donors and the decreased detuning energy (deltaE). Furthermore, direct laser microfabrication by two-photon photopolymerization with compound 2 as a two-photon sensitizer was carried out. Laser exposure time-dependent lateral voxel size has also been studied.

Backward stimulated Bragg scattering in multiphoton active CdTe(x)Se(1-x) quantum dots system.

The backward stimulated Bragg scattering (SBgS) of CdTe(x)Se(1-x) quantum dots in chloroform is investigated at three pump laser wavelengths (532, 816, and 1064 nm) in nanosecond regime. The spectral and temporal structures of the backward stimulated scattering and pump threshold dependence on the concentration are presented in this paper. The energy conversion efficiency from input pump pulse to SBgS pulse was measured to be >or=14%. In addition, the samples exhibit multi- (two-, three-)photon absorption capability over the spectral range we investigated. More importantly, both mechanisms of SBgS and multiphoton absorption provided an enhanced optical limiting performance. The measured nonlinear transmissivity was changed from approximately 0.73 to approximately 0.17 for 532 nm laser pulses and from approximately 0.9 to approximately 0.35 for 816 nm laser pulses when the input pulse energy was changed from 10 to approximately 1500 microJ.

Novel fluorophore based on a multi-substituted olefin skeleton with enhanced three-photon absorption in the femtosecond regime.

A new multipolar fluorophore based on a multi-substituted olefin skeleton that possesses strong three-photon absorption and optical-limiting properties in the femtosecond regime has been designed and synthesized; this archetype suggests a new strategy to further optimize molecular structures toward enhanced nonlinear absorptivities based on known materials.

Multi-photon excitation properties of CdSe quantum dots solutions and optical limiting behavior in infrared range.

Multi-photon absorption and excitation properties of CdSe quantum dots in hexane with different dot-sizes have been investigated. The two- and three-photon absorption (2PA and 3PA) coefficients were measured by using ~160-fs laser pulses at wavelengths of ~775-nm and ~1300-nm, respectively. The dependence of one-, two- and three-photon induced fluorescence spectra as well as their double-exponential decay on the dot-sizes was studied. Based on the fluorescence emission spectra and temporal decay constants for a given sample solution excited by one-, two-and three-photon absorption, it can be concluded that the transition pathways for fluorescence emission and decay under one-, two- and three-photon excitation are nearly identical. The optical power limiting capabilities based on 2PA and 3PA mechanisms are demonstrated separately. In addition, a saturation behavior of 3PA at ~1300 nm was observed.

Nonlinear Photoacoustic Imaging by in situ Multiphoton Upconversion and Energy Transfer.

In recent years, photoacoustic tomography (PAT) is increasingly used in biomedical research, as it allows for direct visualization of optical absorption in deep tissue. In addition to vascular and hemodynamic imaging using endogenous contrasts, PAT is also capable of imaging neural and molecular dynamics with extrinsic contrasts. While near-infrared (NIR)-absorbing contrasts are preferred for deep tissue imaging, compared to visible-light-absorbing contrasts, they are much harder to design and synthesize with good environmental stability. We introduce here a new PAT mode which utilizes nonlinear multiphoton upconversion of NIR light in situ to visible light, thus exciting locally a dye that can generate strong photoacoustic signal. This approach allows to take advantage of a large library of visible-light-absorbing dyes that can enable functional imaging, such as imaging of voltage, oxygen, pH, and ion channel activities. Two types of upconversion materials are utilized in this work: 1) a two-photon absorbing and emitting dye that is efficiently excited by NIR nanosecond laser pulses to enable pulsed laser-based PAT (pulsed-PAT); and 2) rare-earth containing inorganic nanocrystals that absorb continuous-wave (CW) NIR light by sequential multiphoton absorption through real intermediate states to enable intensity-modulated CW laser-based PAT (CW-PAT). Since both cases produce highly localized nonlinear photoacoustic signal, which has very weak scattering in tissue, we can achieve high contrast 3-D volume imaging of deep tissues. In this study, we validated the principle of our approach in different PAT modes and successfully detected enhanced photoacoustic signals from a visible-light-absorbing dye embedded deep in tissue. With vast variety of functionalized organic dyes operating in the visible range, our mode of nonlinear photoacoustic imaging will find great applications in preclinical and clinical researches.

Experimental and quantum chemical studies of cooperative enhancement of three-photon absorption, optical limiting, and stabilization behaviors in multibranched and dendritic structures.

This paper reports on cooperative enhancement of three-photon absorption (3PA) cross section, studied by nonlinear transmission method, in going from a one-branched to a three-branched and then to a dendritic structure. Experimentally, we observe a 72% enhanced 3PA cross-section value in going from the one-branched chromophore to the dendritic chromophore, and a 49% enhanced 3PA cross-section value in going from the one-branched chromophore to the three-branched chromophore, when the 3PA cross-section values are normalized per structure unit. Quantum chemical calculation for the one- and three-branched structures, using the cubic response (CR) theory applied to a single determinant self-consistent field (SCF) reference state, also predicts such an enhancement. Two-dimensional pi-delocalization, resulting in extended charge-transfer network in the case of the multibranched structures, is the main cause of the cooperative enhancement. Owing to the increased 3PA cross-section value for the dendritic chromophore, improved optical limiting performance at an optical communication wavelength of 1310 nm was observed, compared with the one-branched (or three-branched) chromophore, using comparable structure-unit-based concentrations. Optical stabilization capability of the dendritic chromophore was also observed at this wavelength.

Synthesis of C60-diphenylaminofluorene dyad with large 2PA cross-sections and efficient intramolecular two-photon energy transfer.

The first, highly two-photon active C60 derivative comprised of a A-sp3-D conjugate structure was synthesized showing effective two-photon absorption cross-sections (sigma 2' = 196 x 10(-48) cm4 sec-1 molecule-1) in the nanosecond regime among the best values for diphenylaminofluorene-based AFX chromophores.

Manipulating nanoscale interactions in a polymer nanocomposite for chiral control of linear and nonlinear optical functions.

The design, synthesis, and supramolecular organization of a nanocomposite in which nanoscale excitonic interactions between quantum dots and the chiral polymer dramatically enhance the optical activity is reported. This material is highly suitable for application in the emerging field of chiral photonics.

Water-soluble two-photon absorbing nitrosyl complex for light-activated therapy through nitric oxide release.

A water-soluble nitrosyl complex with large two-photon absorption was synthesized by incorporating a two-photon absorbing chromophore with tetra(ethylene glycol) units, into the Roussin's red salt. The nitrosyl complex exhibits quenched emission due to energy transfer from the two-photon chromophore to the Roussin's red salt. The nitric oxide (NO) release induced by one- or two-photon irradiation was detected by EPR spectroscopy with a chemical probe, the Fe(II)- N-(dithiocarbamoyl)- N-methyl- d-glucamine (Fe-MGD) complex. Increased one- or two-photon excited fluorescence, with a concomitant photochemical release of NO, was observed upon one- or two-photon light irradiation. With the observed light-dependent cytotoxicity against cancer cells of the water-soluble nitrosyl complex, it was demonstrated that two-photon-functionalized nitrosyl complexes can be effective NO donors for light-activated treatment.

Two- and three-photon absorption and frequency upconverted emission of silicon quantum dots.

In this communication, we present the experimental results of two- and three-photon excitation studies on silicon quantum dots (QDs) in chloroform (as well as in water) by using femtosecond laser pulses with wavelengths of 778 and 1,335 nm and a pulse duration approximately 160 fs. The photoluminescence spectral distributions are nearly the same upon one-, two-, and three-photon excitation. With one- and two-photon excitation, the temporal relaxation measurements of photoluminescence emission manifest the same multiexponential decay behavior in the time range from 0.05 ns to 15 micros, characterized by three successive decay constants: 0.75 ns, 300 ns, and 5 micros, respectively. Finally, the two-photon absorption spectrum in the spectral range of 650-900 nm and the three-photon absorption spectrum in the spectral range of 1,150-1,400 nm have been measured.

Infrared two-photon-excited visible lasing from a DNA-surfactant-chromophore complex.

Infrared two-photon-pumped and cavity-enhanced frequency upconversion lasing has been achieved in a novel DNA-surfactant-chromophore complex (DSCC) gel system, which is a new step toward producing a biological laser. Once the focused intensity of the 150 fs and approximately 775 nm pump laser beam is higher than a certain threshold level, highly directional stimulated emission at approximately 582 nm wavelength can be observed from a 1 cm long DSCC complex gel cell. With cavity feedback provided by the two optical windows, the pump threshold can be further reduced, the highly directional output lasing can be greatly enhanced, and the output spectral linewidth can be reduced to less than 1/5 of the spontaneous fluorescence spectral bandwidth.