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We experimentally observed an accumulative type of nonlinear attenuation and distortion of slow light, i.e., Rydberg polaritons, with the Rydberg state $|32D_{5/2}\rangle$ in the weak-interaction regime. The present effect of attenuation and distortion cannot be explained by considering only the dipole-dipole interaction (DDI) between Rydberg atoms in $|32D_{5/2}\rangle$. Our observation can be attributed to the atoms in the dark Rydberg states other than those in the bright Rydberg state, i.e., $|32D_{5/2}\rangle$, driven by the coupling field. The dark Rydberg states are all the possible states, in which the population decaying from $|32D_{5/2}\rangle$ accumulated over time, and they were not driven by the coupling field. Consequently, the DDI between the dark and bright Rydberg atoms increased the decoherence rate of the Rydberg polaritons. We performed three different experiments to verify the above hypothesis, to confirm the existence of the dark Rydberg states, and to measure the decay rate from the bright to dark Rydberg states. In the theoretical model, we included the decay process from the bright to dark Rydberg states and the DDI effect induced by both the bright and dark Rydberg atoms. All the experimental data of slow light taken at various probe Rabi frequencies were in good agreement with the theoretical predictions based on the model. This study pointed out an additional decoherence rate in the Rydberg-EIT effect, and provides a better understanding of the Rydberg-polariton system.

We proposed utilizing a medium with a high optical depth (OD) and a Rydberg state of low principal quantum number, $n$, to create a weakly-interacting many-body system of Rydberg polaritons, based on the effect of electromagnetically induced transparency (EIT). We experimentally verified the mean field approach to weakly-interacting Rydberg polaritons, and observed the phase shift and attenuation induced by the dipole-dipole interaction (DDI). The DDI-induced phase shift or attenuation can be viewed as a consequence of the elastic or inelastic collisions among the Rydberg polaritons. Using a weakly-interacting system, we further observed that a larger DDI strength caused a width of the momentum distribution of Rydberg polaritons at the exit of the system to become notably smaller as compared with that at the entrance. In this study, we took $n =32$ and the atomic (or polariton) density of 5$\times10^{10}$ (or 2$\times10^{9}$) cm$^{-3}$. The observations demonstrate that the elastic collisions are sufficient to drive the thermalization process in this weakly-interacting many-body system. The combination of the $\mu$s-long interaction time due to the high-OD EIT medium and the $\mu$m$^2$-size collision cross section due to the DDI suggests a new and feasible platform for the Bose-Einstein condensation of the Rydberg polaritons.

The effect of electromagnetically induced transparency (EIT) combined with Rydberg-state atoms provides high optical nonlinearity to efficiently mediate the photon-photon interaction. However, the decay rate of Rydberg coherence, i.e., the decoherence rate, plays an important role in optical nonlinear efficiency and can be largely influenced by laser frequency fluctuation. In this work, we carried out a systematic study of the effect of laser frequency fluctuation on the decoherence rate. We derive an analytical formula that quantitatively describes the relationship between the decoherence rate and laser frequency fluctuation. The formula is experimentally verified by using the $\mathrm{\ensuremath{\Lambda}}$-type EIT system of laser-cooled $^{87}\mathrm{Rb}$ atoms, in which one can either completely eliminate or controllably introduce the effect of laser frequency fluctuation. We also include the effect of Doppler shift caused by the atomic thermal motion in the formula, which can be negligible in the $\mathrm{\ensuremath{\Lambda}}$-type EIT experiment but significant in the Rydberg-EIT experiment. Utilizing the atoms of 350 $\ensuremath{\mu}\mathrm{K}$, we study the decoherence rate in the Rydberg-EIT system involving the state of $|32{D}_{5/2}\ensuremath{\rangle}$. The experimental data are consistent with the predictions from the formula. We are able to achieve a rather low decoherence rate of $2\ensuremath{\pi}\ifmmode\times\else\texttimes\fi{}48$ kHz at a moderate coupling Rabi frequency of $2\ensuremath{\pi}\ifmmode\times\else\texttimes\fi{}4.3$ MHz.

In this study, T2- and T*2-weighted imaging potential of polysorbate-coated magnetic nanocrystals (P-MNCs) was investigated as a blood-pool contrast agent using a 9L-rat glioma model after intravenous injection via 3.0T MRI. Magnetic nanocrystals (MNCs, Fe3O4) synthesized by the thermal decomposition method were coated with polysorbate 80 using a nanoemulsion method to generate a water-stable MRI contrast agent. The physical properties and MR imaging capability of P-MNCs were verified. The orthotopic tumor models were established by implanting 9L-rat glioma cells into the rat brain. After tail-vein injection of P-MNCs, T2- and T*2-weighted imaging of tumor sites was performed. Blood clearance and biodistribution studies were also performed. The hydrodynamic diameter of P-MNCs was 10.5 ± 0.8 nm and a spherical magnetic core was confirmed. The r2 value of P-MNCs was calculated to be 114.1 mM−1 s−1. Heterogeneous contrast T2-weighted MRI images of the 9L-rat glioma model were visualized at the tumor site before injecting the MRI contrast agent. In particular, T*2-weighted images demonstrated more obvious signal intensity changes than did T2-weighted images. Neovasculature in the tumor tissue was clearly observed in T*2 images compared with T2-weighted images. The blood half-life of P-MNCs was 2 h and the Fe ion concentration of blood had returned to the baseline after 16 h. Well-tailored P-MNCs can be effectively used as a novel MRI contrast agent for visualizing of vasculatures for solid tumors via T2- and T*2-weighted imaging.

A synthetic process for constructing an organo-metal nanohybrid is described. This process uses polyaniline as a ligand in order to fabricate magnetic nanoparticles. This nanohybrid shows imaging potential uses as a magnetic resonance imaging contrast agent and a redox-sensing probe simultaneously both in vitro and in vivo.

Oleyl dextran-coated magnetic nanoclusters (ODMCs) are fabricated for the accurate detection of macrophage-rich atherosclerotic plaques using magnetic resonance (MR) imaging. Dextran is introduced to the cluster surface of magnetic nanocrystals (MNCs) through self-assembly using amphiphilic oleic acid-conjugated dextran (ODex) to provide not only hydrophilicity but also a high affinity to macrophages. Enhanced magnetism of the ODMCs is engineered by optimizing the degree of substitution (DS) of the oleyl group in ODex and the concentration of ODex used for the synthesis of ODMC. Consequently, ODMCs exhibit significantly increased T2 relaxivity and excellent macrophage-targeting ability without cytotoxicity, in vitro. Moreover, in vivo T2-weighted MR imaging after intravenous injection of ODMCs into a rat artery balloon injury model demonstrates considerable MR contrast strength efficacy in the plaques of the injured carotid artery. These novel ODMCs may offer a highly efficient MR imaging nanoprobes for the selective diagnosis of atherosclerosis.

An electrohydrodynamic atomization (EHDA) system that generates an electrospray can achieve particle formation and encapsulation by accumulating an electric charge on liquid flowing out from the nozzle. A novel coaxial EHDA system for continuous fabrication of water-stable magnetic nanoparticles (MNPs) is established, based on a cone-jet mode of electrospraying. Systemic variables, such as flow rates from dual nozzles and inducing voltages, are controlled to enable the preparation of water-soluble MNPs coated by polysorbate 80. The PEGylated MNPs exhibit water stability. The magnetic resonance imaging potential of these MNPs is confirmed by in vivo imaging using a gastric cancer xenograft mouse model. Thus, this advanced coaxial EHDA system demonstrates remarkable capabilities for the continuous encapsulation of MNPs to render them water-stable while preserving their properties as imaging agents.

We experimentally demonstrate switching can be occurred between D1 |F'=1>, |F'=2> and D2 |F'=2> pulses. Each of pulses is probe field of triple-A system composed of 87Rb D1 and D2 transition line.

Oleyl dextran-coated magnetic nanoclusters (ODMCs) are fabricated for the accurate detection of macrophage-rich atherosclerotic plaques using magnetic resonance (MR) imaging. Dextran is introduced to the cluster surface of magnetic nanocrystals (MNCs) through self-assembly using amphiphilic oleic acid-conjugated dextran (ODex) to provide not only hydrophilicity but also a high affinity to macrophages. Enhanced magnetism of the ODMCs is engineered by optimizing the degree of substitution (DS) of the oleyl group in ODex and the concentration of ODex used for the synthesis of ODMC. Consequently, ODMCs exhibit significantly increased T2 relaxivity and excellent macrophage-targeting ability without cytotoxicity, in vitro. Moreover, in vivo T2-weighted MR imaging after intravenous injection of ODMCs into a rat artery balloon injury model demonstrates considerable MR contrast strength efficacy in the plaques of the injured carotid artery. These novel ODMCs may offer a highly efficient MR imaging nanoprobes for the selective diagnosis of atherosclerosis.

The coherent control of optical images has garnered attention because all information embedded in optical images is expected to be controlled in a parallel way. One of the most important control processes is switch for information delivery. We experimentally demonstrated phase-controlled optical image switching in a double-Lambda system where the transmission of the image through a medium was switched. Two independent laser sources were adopted for a double-Lambda system such that images inscribed in two weak probe light beams were incoherent with each other. Arbitrary phase was added to the optical images to show that switching could be accomplished just with the relative phase difference between the probe pixels. (C) 2013 Optical Society of America

Here we introduce a new class of smart imaging probes hybridizing polysorbate 80 coated-magnetic nanoparticles with vascular endothelial growth factor receptor 2 (VEGFR2)-targetable aptamer for specific magnetic resonance (MR) imaging of angiogenesis from glioblastoma.

An understanding of neovascularization and/or angiogenesis in cancer is acutely required for effective cancer therapy due to concerns about tumor growth and metastasis. In particular, integrin αvβ3 is closely associated with cell migration and invasion during angiogenesis. Hence, we developed aptamer(αvβ3)-conjugated magnetic nanoparticles (Apt(αvβ3)-MNPs) to enable precise detection of integrin-expressing cancer cells using magnetic resonance imaging. Apt(αvβ3)-MNPs exhibited not only cytocompatibility, but also an efficient targeting ability with high magnetic sensitivity through in vitro/in vivo studies. The results of this study demonstrate that Apt(αvβ3)-MNPs have the potential to be used for accurate tumor diagnosis and therapy.

Multimodal imaging systems may eliminate the disadvantages of individual imaging modality by providing complementary information about cellular and molecular activites. In this sutdy, we developed a reverse complementary multimodal imaging system to image microRNAs (miRNA, miR) during neurognesis using transferrin receptor (TfR) and a magnetic fluorescence (MF) nanoparticle-conjugated peptide targeting TfR (MF targeting TfR). Both in vitro and in vivo imaging demonstrated that, in the absence of miR9 during pre-differentiation of P19 cells, the MF targeting TfR nanoparticles greatly targeted TfR and were successfully internalized into P19 cells, resulting in high fluorescence and low MR signals. When the miR9 was highly expressed during neurogenesis of P19 cells, the MF targeting TfR nanoparticles were hardly targeted due to the miR9 function, which represses the expression and functional activity of TfR from the miRNA TfR reproter gene, resulting in low fluorescence and high MR signals. The reverse complementary multimodal miRNA imaging system may serve as a new imaging probe to montior miRNA-involved cellular developments and diseases.

Phase-controlled optical image switching with low light intensity was demonstrated in a double-Λ system. Switching by interference in a double-Λ system was observed as having a 90 % switching depth between incoherent image pixels.

We theoretically studied a triple-Λ system comprising three pairs of coupling-probe fields. Three probe fields were phase-dependently switched with a switching depth above 80%, at which the group-velocity matching of all probe pulses was available under slow light-propagation conditions. We considered the probe susceptibility as the superposition of three-photon transitions to systematically understand the multi-photon interference in a triple-Λ system, which can be applied to systems with N−Λ (N≥1). This helped us to tailor the probe susceptibility by adjusting the detuning and phases of the coupling and probe fields. This work can be applied to all-optical switching gates for triple-photons and can enhance the speed of processing optical information.

Multi-photon interference effects of the optical loop in a double-Λ/V system aid coherent photon control, especially all-optical switching between single photons. In the multi-photon interference, phase fluctuations induced by the mechanical vibration of the optical components should be removed to observe the high fidelity of photon controls. We solved this problem by overlapping coupling and probe beams that have opposite phase shifts in the optical loop system to cancel out phase fluctuation induced by mechanical vibration. We used two independent laser sources to generate two pairs of coupling-probe fields that are resonant on a double-Λ system. The removal of vibrational phase fluctuation was confirmed by comparison with a normal phase-dependent light-switching experiment.

We have demonstrated anticorrelated light switching between multiphoton transition channels in a nonresonant double-Λ system. Two-color probe transitions, using rubidium D1 (795 nm) and D2 (780 nm), were included in our double-Λ system. In anticorrelated light switching, one of two probe transitions is selected as transparent while the other is selected as opaque. In this configuration, we observed completely different behavior from that seen in a resonant double-Λ system, in which both probe transmissions are transparent or opaque simultaneously. Furthermore, we observed a noise correlation between two-color probe transmissions when the phase fluctuation of the two probe lasers was converted to the intensity fluctuation. The relative phase fluctuation between the two probe lasers induced an anticorrelation between the intensity noises of two probe lasers in a nonresonant double-Λ system, while a correlation was induced in a resonant double-Λ system. The intensity fluctuation (correlated or anticorrelated) was easily controlled by detuning the double-Λ system. The noise anticorrelation effect is clearly interpreted as arising from the anticorrelated light switching in a nonresonant double-Λ system. This system can be used for noise control as well as optical switching between incoherent two-color laser lights.

In this study, we developed the maleimidyl magnetic nanoplatform, which enables functional targeting of a biomarker-specific moiety for molecular imaging via MRI. The maleimide group of the maleimidyl magnetic nanoplatform is conjugated with a thiol group without additional crosslinkers and side products. A physicochemical analysis was conducted to verify the effectiveness of the maleimidyl magnetic nanoplatform, and the existence of the maleimidyl group was investigated using the platform. To prepare biomarker-specific MRI probes, a thiolated aptamer and peptide were immobilized onto the maleimidyl group of the maleimidyl magnetic nanoplatform. The fabricated MRI probes were applied to four cancer cell lines: HT1080, MCF7, MKN45, and HEK293T. To investigate the potential of the molecular MRI probe, the target-biomarker specificity was confirmed without serious cytotoxicity, and in vivo MRI analysis using a xenograft mouse model was demonstrated. We believe these results will be useful for fabricating molecular MRI probes for the diagnosis of cancer.

Nucleic acid-based aptamers have been developed for the specific delivery of diagnostic nanoprobes. Here, we introduce a new class of smart imaging nanoprobe, which is based on hybridization of a magnetic nanocrystal with a specific aptamer for specific detection of the angiogenic vasculature of glioblastoma via magnetic resonance (MR) imaging. The magnetic nanocrystal imaging core was synthesized using the thermal decomposition method and enveloped by carboxyl polysorbate 80 for water solubilization and conjugation of the targeting moiety. Subsequently, the surface of the carboxylated magnetic nanocrystal was modified with amine-functionalized aptamers that specifically bind to the vascular growth factor receptor 2 (VEGFR2) that is overexpressed on angiogenic vessels. To assess the targeted imaging potential of the aptamer-conjugated magnetic nanocrystal for VEGFR2 markers, the magnetic properties and MR imaging sensitivity were investigated using the orthotopic glioblastoma mouse model. In in vivo tests, the aptamer-conjugated magnetic nanocrystal effectively targeted VEGFR2 and demonstrated excellent MR imaging sensitivity with no cytotoxicity.

Magnetic nanoclusters (MNCs) are agglomerated individual magnetic nanoparticles (MNPs) that show great promise in increasing magnetic resonance imaging (MRI) sensitivity. Here, we report an effective strategy to engineer MNCs based on double-ligand modulation to enhance MRI sensitivity. The oleic acid-coated individual MNPs self-assembled and then were enveloped by polysorbate 80, using a nanoemulsion method to prepare MNCs. By modulating the amounts of the two ligands, and thus the size and magnetic content of the resultant MNCs, we were able to enormously improve MRI sensitivity.

We showed experimentally interference could be occurred between incoherent lights in a double-Λ lambda transition implemented with rubidium atomic vapor. Switching of probe transmission was controlled by the phases of two independent probe lasers with low light intensity. More than 70 % of the probe transmission could be switched by ultra-weak incoherent field. We suggested optically cryptic information could be delivered by the phase-controlled switching with incoherent fields in a double-Λ system.

We fabricated dextran-coated magnetic nanoclusters (Dex-MNCs) for targeted magnetic resonance (MR) imaging of inflammatory macrophages. Dex-MNCs were prepared through encapsulation of hydrophobic magnetic nanocrystals (MNCs) by pyrenyl dextran in order that MNCs could achieve increased colloidal stability in aqueous phase as well as strongly interact with macrophages. Dex-MNCs exhibited biocompatibility and sufficient targeting efficiency against macrophages with strengthened MR contrast effect from in vitro/in vivo studies. Considering these results, we confirmed that Dex-MNCs could accurately detect inflammatory macrophagevia MR imaging.