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Obesity is a global chronic disease linked to various diseases. Increased consumption of added sugars, especially in beverages, is a key contributor to the obesity epidemic. It is essential to reduce or replace sugar intake with low-calorie sweeteners. Here, a natural sweet protein, 3M-brazzein, was investigated as a possible sugar substitute. Mice were exposed to 3M-brazzein or 10% sucrose of equivalent sweetness, in drinking water to mimic human obesity development over 15 weeks. Consumption of 3M-brazzein in liquid form did not cause adiposity hypertrophy, resulting in 33.1 ± 0.4 g body weight and 0.90 ± 0.2 mm fat accumulation, which were 35.9 ± 0.7 g (p = 0.0094) and 1.53 ± 0.067 mm (p = 0.0031), respectively, for sucrose supplement. Additionally, 3M-brazzein did not disrupt glucose homeostasis or affect insulin resistance and inflammation. Due to its naturally low-calorie content, 3M-brazzein could also be a potential sugar substitute that reduces adiposity.

The present study proposes an innovative opto-chemical treatment using a basket-integrated optical device (BIOD) to disinfect mature bacterial biofilm on endoscope channels. A BIOD was designed to position an optical diffuser on the central axis of an endoscope channel and to distribute laser light concentrically to the bacterial biofilm on the channel surface. To apply thermal damage and oxidative stress to the bacterial biofilm, a low concentration of a crosslinking agent (glutaraldehyde ~0.5%) was combined with 808 nm infrared (IR) and 405 nm blue (BL) laser lights. The applied irradiances of IR and BL were 10 W/cm2 and 1.6 W/cm2 for Teflon channel model and 20 W/cm2 and 3.2 W/cm2 for a clinical model, respectively. Individual irradiation of either IR or BL for 180 s induced the maximum temperatures of 62 ± 2 °C and 53 ± 3 °C on the biofilm, respectively. The simultaneous opto-chemical treatment reduced a significant population of the bacterial biofilms (7.5-log10 for Staphylococcus aureus and 7.1-log10 for Pseudomonas aeruginosa), which were 2.9-fold and 3.9-fold higher than that of the standard treatment with 2% glutaraldehyde (GA) solution, respectively. The proposed opto-chemical disinfection method can help reduce multi-drug resistant bacteria and prevent cross-infection during the clinical usage of a flexible endoscope.

Guided surgery often encounters signal saturation and noise, due to strong illumination from the surgical light. The current study developed a customized optical probe filtering incident wavelengths of ≥800 nm to selectively detect near-infrared (NIR) fluorescence signals under strong illumination. The feasibility of the fabricated filter for fluorescence imaging was evaluated with tubes containing indocyanine green (ICG) and lymph nodes in vivo mouse models. The fluorescent images were acquired under three different conditions for comparison: dark room (DR), conventional surgical light (CSL), and filter-assisted surgical light (FSL). ICG at the concentration of 0.7 μg/ml yielded the highest signal intensity Both DR and FSL yielded higher image contrasts (87.3% and 82.6%) compared to CSL (67.0%). The in vivo results confirmed that the proposed optical probe enhanced the image contrast of the lymph nodes in mice by three-fold (i.e., 16.7±4.4% for CSL vs. 55.6±5.0% for FSL; p < 0.05). However, the condition involving DR (68.5±2.4%) continued to generate a slightly higher image contrast compared to that involving FSL. Thus, we can effectively use the NIR fluorescence imaging system simultaneously in the improved surgical light source by the proposed method.

Medical societies and public health agencies rigorously emphasize the importance of adequate disinfection of flexible endoscopes. The aim of this work was to propose a novel opto-chemical disinfection treatment against Staphylococcus aureus grown in mature biofilm on Teflon-based endoscope channel models. Laser irradiation using near-infrared and blue wavelengths combined with a low concentration of chemical disinfectant induced both irreversible thermal denaturation and intercellular oxidative stress as a combined mechanism for an augmented antimicrobial effect. The opto-chemical method yielded a 6.7–log10 reduction of the mature Staphylococcus aureus biofilms (i.e., approximately 1.0-log10 higher than current requirement of standard treatment). The proposed technique may be a feasible disinfection method for mitigating the risk associated with infection transmission.

Hepatic fibrogenesis is characterized by activation of hepatic stellate cells (HSCs) and accumulation of extracellular matrix (ECM). The impact of ECM on TGF-β-mediated fibrogenic signaling pathway in HSCs has remained obscure. We studied the role of non-receptor tyrosine kinase focal adhesion kinase (FAK) family members in TGF-β-signaling in HSCs. We used a CCl4-induced liver fibrosis mice model to evaluate the effect of FAK family kinase inhibitors on liver fibrosis. RT-PCR and Western blot were used to measure the expression of its target genes; α-SMA, collagen, Nox4, TGF-β1, Smad7, and CTGF. Pharmacological inhibitors, siRNA-mediated knock-down, and plasmid-based overexpression were adopted to modulate the function and the expression level of proteins. Association of PYK2 activation with liver fibrosis was confirmed in liver samples from CCl4-treated mice and patients with significant fibrosis or cirrhosis. TGF-β treatment up-regulated expression of α-SMA, type I collagen, NOX4, CTGF, TGF-β1, and Smad7 in LX-2 cells. Inhibition of FAK family members suppressed TGF-β-mediated fibrogenic signaling. SiRNA experiments demonstrated that TGF-β1 and Smad7 were upregulated via Smad-dependent pathway through FAK activation. In addition, CTGF induction was Smad-independent and PYK2-dependent. Furthermore, RhoA activation was essential for TGF-β-mediated CTGF induction, evidenced by using ROCK inhibitor and dominant negative RhoA expression. We identified that TGF-β1-induced activation of PYK2-Src-RhoA triad leads to YAP/TAZ activation for CTGF induction in liver fibrosis. These findings provide new insights into the role of focal adhesion molecules in liver fibrogenesis, and targeting PYK2 may be an attractive target for developing novel therapeutic strategies for the treatment of liver fibrosis.

Benzalkonium chloride (BKC) is a commonly used preservative in personal care products and pharmaceutical preparations. However, its ecological risks are not well understood because of lack of monitoring data and ecotoxicological information. In the present study, occurrence of BKC was investigated in the waters near a pharmaceutical manufacturing complex of South Korea and its acute and chronic ecotoxicities were evaluated using Daphnia magna and Japanese medaka (Oryzias latipes). Associated ecological risks were estimated by calculating hazard quotients (HQs). In addition, endocrine disruption potency of BKC was compared with those of other frequently used preservatives using human adrenal (H295R) and rat pituitary (GH3) cells. High concentration of BKC was detected at locations near the pharmaceutical manufacturing plants, i.e., 35.8 μg/L for dodecyl benzyl dimethyl ammonium chloride (BKC–C12), and 21.6 μg/L tetradecyl benzyl dimethyl ammonium chloride (BKC–C14). In Daphnia, 48 h immobilization EC50 and 21 d reproduction NOEC were determined at 41.1 μg/L and ≥10.8 μg/L, respectively. For O. latipes, 96 h LC50 was determined at 246 μg/L while the growth inhibition NOEC was ≥113.4 μg/L following early life stage exposure. BKC significantly up-regulated vitellogenin gene of juvenile fish, indicating its endocrine disrupting potential in fish. Exposure to BKC increased steroid hormone level in H295R cells, and induced cytotoxicity in GH3 cells. HQ values of BKC were determined at greater than one in the ambient water near pharmaceutical manufacturing facilities. Considering high ecological risk and endocrine disrupting potential, long-term consequences of BKC contamination in aquatic ecosystem need to be examined.

In this study, we developed a UV-LED/H2O2/Cu2+ system to remove cyanide, which is typically present in metal electroplating wastewater. The results showed the synergistic effects of UV-LED, H2O2, and Cu2+ ions on cyanide removal in comparison with UV-LED photolysis, H2O2 oxidation, UV-LED/H2O2, and H2O2/Cu2+ systems. Cyanide was removed completely in 30 min in the UV-LED/H2O2/Cu2+ system, and its loss followed pseudo-first order kinetics. Statistically, both H2O2 and Cu2+ ions showed positive effects on cyanide removal, but Cu2+ ions exhibited a greater effect. The highest cyanide removal rate constant (k = 0.179 min−1) was achieved at pH 11, but the lowest was achieved at pH 12.5 (k = 0.064 min−1) due to the hydrolysis of H2O2 (pKa of H2O2 = 11.75). The presence of dissolved organic matter (DOM) inhibited cyanide removal, and the removal rate constant exhibited a negative linear correlation with DOM (R2 = 0.987). The removal rate of cyanide was enhanced by the addition of Zn2+ ions (from 0.179 to 0.457 min−1), while the co-existence of Ni2+ or Cr+6 ion with Cu2+ ion reduced cyanide removal. The formation of OH radicals in the UV-LED/H2O2/Cu2+ system was verified using an aminophenyl fluorescence (APF) probe. Cyanate ions and ammonia were detected as the byproducts of cyanide decomposition. Finally, an acute toxicity reduction of 64.6% was achieved in the system within 1 h, despite a high initial cyanide concentration (100 mg/L). In terms of removal efficiency and toxicity reduction, the UV-LED/H2O2/Cu2+ system may be an alternative method of cyanide removal from wastewaters.

A coherency of photoacoustic and ultrasound waves is dependent on the accuracy of the speedof- sound. This study evaluates the feasibility of a speed-of-sound estimation method for dual photoacoustic and ultrasound waves using laser-activated phase-change perfluorohexane nanodroplets (PFHnDs). The proposed method demonstrates that the estimated speed-of-sound (ESS) is close to the expected speed-of-sound for the medium (deviation = 0.3%), so it is useful for phase aberration correction in dual ultrasound and photoacoustic imaging.

Palladium(II) complexes, LnPdCl2 (Ln = LA–LI), with N,N′-bidentate imine ligands derived from picolinaldehyde and substituted anilines have been synthesized and structurally characterized. Molecular structures revealed a distorted square plane geometry around Pd(II) centre in LnPdCl2 (Ln = LA–LC) obtained via coordination with pyridine and imine nitrogens and two chloro ligands. Pd(II) complexes LnPdCl2 (Ln = LA–LI) initiate polymerisation of methylmethacrylate (MMA) in the presence of modified methylaluminoxane (MMAO). The complex LIPdCl2 (of which the ligand was N-furfuryl substituted) showed the highest catalytic activity for the polymerisation of MMA with an activity of 7.08 × 104 g PMMA/mol·Pd·h at 60 °C. All the complexes yielded syndio-rich poly(methyl methacrylate) (PMMA) ([rr] = 0.70). Notably, the substituents on the imine moiety of the iminopyridine fragments affects the activities towards MMA polymerization, whereas the stereoselectivities remained unchanged.

Bisphenol A (BPA) is one of the most widely used chemicals in various consumer products. In thermal papers such as receipts and tickets, BPA is used as a heat-activated developer. Cashiers are therefore suspected to be a vulnerable group of exposure to BPA, but neither contribution of receipt handling to the total body burden of BPA among cashiers, nor related health effects are well characterized. Female cashiers (n = 54) were recruited from seven retail shops of a major supermarket chain in Korea, and urinary levels of BPA and metabolic syndrome (MetS) related biomarkers were measured. In order to estimate the contribution of receipt handling to the body burden of BPA, an intervention was designed on the use of gloves: the subjects were asked not to wear gloves during the work for one week, and in the following week, to wear gloves. Urine samples were collected at pre-shift and post-shift for the first two consecutive days in each week, and urinary BPA concentrations were measured. In cashiers without gloves, about a two-fold increase in urinary BPA concentrations was observed after work-shift. When the cashiers wore gloves, however, urinary BPA levels showed no changes. Higher urinary BPA concentrations were associated with greater levels of fasting insulin and insulin resistance. Our observation shows that receipt handling among the cashiers could double the BPA exposure levels at post-shift compared to those at pre-shift, and use of simple protective equipment such as gloves could effectively reduce the BPA exposure levels. Keywords: Bisphenol A, Receipt, Cashier, Dermal exposure, Metabolic syndrome

Pt-based alloy nanoframes have shown great potential as electrocatalysts toward the oxygen reduction reaction (ORR) in fuel cells. However, the intrinsically infirm nanoframes could be severely deformed during extended electro-cyclings, which eventually leads to the loss of the initial catalytic activity. Therefore, the structurally robust nanoframe is a worthy synthetic target. Furthermore, ternary alloy phase electrocatalysts offer more opportunities in optimizing the stability and activity than binary alloy ones. Herein, we report a robust PtCuNi ternary nanoframe, structurally fortified with an inner-lying PtCu dendrite, which shows a highly active and stable catalytic performance toward ORR. Remarkably, the PtCu@PtCuNi catalyst exhibited 11 and 16 times higher mass and specific activities than those of commercial Pt/C.

Porcine protegrin-1 (PG-1) is a broad-spectrum antimicrobial peptide (AMP) with potent antimicrobial activities. We produced recombinant PG-1 and evaluated its cytotoxicity toward various types of mammalian cell lines, including embryonic fibroblasts, retinal cells, embryonic kidney cells, neuroblastoma cells, alveolar macrophage cells, and neutrophils. The sensitivity of the different mammalian cells to cytotoxic damage induced by PG-1 differed significantly among the cell types, with retinal neuron cells and neutrophils being the most significantly affected. A circular dichroism analysis showed there was a precise correlation between conformational changes in PG-1 and the magnitude of cytotoxicity among the various cell type. Subsequently, a green fluorescent protein (GFP) penetration assay using positively charged GFPs indicated there was a close correlation between the degree of penetration of charged GFP into cells and the magnitude of PG-1 cytotoxicity. Furthermore, we also showed that inhibition of the synthesis of anionic sulphated proteoglycans on the cell surface decreases the cytotoxic damage induced by PG-1 treatment. Taken together, the observed cytotoxicity of PG-1 towards different membrane surfaces is highly driven by the membrane’s anionic properties. Our results reveal a possible mechanism underlying cell-type dependent differences in cytotoxicity of AMPs, such as PG-1, toward mammalian cells.

Bisphenol S (BPS) and 4-hydroxyphenyl 4-isoprooxyphenylsulfone (BPSIP) have been used as substitutes for bisphenol A (BPA) owing to increased regulation of BPA in plastics. In this study, long-term toxicity tests of BPS and BPSIP were performed using Daphnia magna and Moina macrocopa. The predicted no-effect concentration (PNEC) of BPA, BPS, and BPSIP were derived by the assessment factor (AF) method and the species sensitivity distribution (SSD) method. An ecological risk assessment was performed based on the measured environmental concentrations of BPA in surface water worldwide and the derived PNECs. The chronic NOEC of D. magna was 2.5 mg/L for BPS and 0.5 mg/L for BPSIP, and that of M. macrocopa was 0.03 mg/L for BPS and 0.1 mg/L for BPSIP. The PNECAF was generally one order of magnitude less than the PNECSSD, and the PNEC of BPS was 10 times lower than that of BPA. The hazard quotients of BPA and BPS exceeded 1, indicating that concentrations in ambient water conditions could pose a potential risk to aquatic organisms. Since the use of alternative compounds is increasing, further monitoring data of the water environment and chronic toxicity in various aquatic organisms appears to be necessary.

Industrial wastewater discharge is one of major threats to the sustainability of aquatic environment. Rapid and sensitive detection of toxic wastewater discharge and appropriate control if necessary are therefore crucial. In the present study, a 1 h Daphnia magna exposure with heartbeat as an observation endpoint was developed and assessed for its utility as a rapid toxicity screening measure. Two types of metal-rich industrial wastewater, i.e., metal plating and the semiconductor industry were chosen as target samples, and the 1 h heartbeat assay was applied. Based on a literature search, four metals, i.e., Cu, Cr, Ni and Zn were identified as major chemicals of ecotoxicological concerns in these wastewaters. The effective concentrations determined for each metal from the D. magna 1 h heartbeat test were comparable to those derived from the conventional D. magna 48 h immobilization test. Copper sulfate (CuSO4) was determined as the most toxic, followed by potassium dichromate (K2Cr2O7), nickel sulfate (NiSO4) and zinc sulfate (ZnSO4). For ternary mixtures, the 1 h heartbeat test showed also comparable responses to those of the 48 h immobilization test, suggesting its utility for screening the toxicity of simple metal mixtures. For the site-sampled metal plating water, the rapid heartbeat assay showed similar responses to those of the 48 h immobilization assay. However, for the semiconductor industry wastewater, clearly different responses were observed in both the heartbeat and immobilization assays, probably due to the influence of other contaminants with different modes of action that are present in the wastewater. Our observations showed that the D. magna 1 h heartbeat test can be considered as a rapid ecotoxicity screening measure for certain wastewaters with simple metal mixtures.

The G protein-coupled receptor (GPCR) family of proteins comprises signaling proteins that mediate cellular responses to various hormones and neurotransmitters, and serves as a prime target for drug discovery. Towards our goal of discovering secondary metabolites from natural sources that can function as neuronal drugs, we evaluated the modulatory effect of eckol on various GPCRs via cell-based functional assays. In addition, we conducted in silico predictions to obtain molecular insights into the functional effects of eckol. Functional assays revealed that eckol had a concentration-dependent agonist effect on dopamine D3 and D4 receptors. The half maximal effective concentration (EC50) of eckol for the dopamine D3 and D4 receptors was 48.62 &plusmn, 3.21 and 42.55 &plusmn, 2.54 &micro, M, respectively, while the EC50 values of dopamine as a reference agonist for these two receptors were 2.9 and 3.3 nM, respectively. In silico studies revealed that a low binding energy in addition to hydrophilic, hydrophobic, &pi, &ndash, alkyl, and &pi, &pi, T-shaped interactions are potential mechanisms by which eckol binds to the dopamine receptors to exert its agonist effects. Molecular dynamics (MD) simulation revealed that Phe346 of the dopamine receptors is important for binding of eckol, similar to eticlopride and dopamine. Our results collectively suggest that eckol is a potential D3/D4 agonist for the management of neurodegenerative diseases, such as Parkinson&rsquo, s disease.

Photoacoustic imaging (PAI) is a hybrid imaging modality with high resolution and sensitivity that can be beneficial for cancer staging. Due to insufficient endogenous photoacoustic (PA) contrast, the development of exogenous agents is critical in targeting cancerous tumors. The current study demonstrates the feasibility of marine-oriented material, astaxanthin, as a biocompatible PA contrast agent. Both silicon tubing phantoms and ex vivo bladder tissues are tested at various concentrations (up to 5 mg/ml) of astaxanthin to quantitatively explore variations in PA responses. A Q-switched Nd : YAG laser (λ = 532 nm) in conjunction with a 5 MHz ultrasound transducer is employed to generate and acquire PA signals from the samples. The phantom results presented that the PA signal amplitudes increase linearly with the astaxanthin concentrations (threshold detection = 0.31 mg/ml). The tissue injected with astaxanthin yields up to 16-fold higher PA signals, compared with that with saline. Due to distribution of the injected astaxanthin, PAI can image the margin of astaxanthin boles as well as quantify their volume in 3D reconstruction. Further investigations on selective tumor targeting are required to validate astaxanthin as a potential biocompatible contrast agent for PAI-assisted bladder cancer detection.

Developing highly active and structurally robust electrocatalysts for hydrogen evolution reaction (HER) is of paramount importance for sustainable and clean production of hydrogen. Metal sulphides exposing catalytically active sites, in particular, have been actively pursued as advanced HER catalysts. Herein we report high-performance Rh2S3-based HER catalysts with excellent activity and durability. Hollow Rh2S3 hexagonal nanoprisms with controlled size and thickness could be conveniently prepared by one-step formation of core–shell nanoprisms followed by the etching of the core, and they show high surface areas and highly exposed edge sites. The hollow Rh2S3 nanoprisms exhibit very high HER activity and excellent stability under harsh acidic conditions.

This study was to determine the effect of oleogel on lipid metabolism in rats fed high-fat diet. Male SD rats (n = 32; 4-wk-old) and obese Zucker rats (n = 6) fed either beef tallow containing high fat diet (HFD) or beeswax oleogel containing canola oil (BOG) for 2 months. Substitution of 50% BT by BOG significantly reduced body weight. Increased serum triglyceride by HFD was reduced (P

A facile synthetic strategy has been developed for size-controlled PtCu@Ru nanorattles via co-decomposition of Ru and Cu precursors in the presence of Pt nanoparticles. The presence of Pt nanoparticles induces a fast decomposition of Cu precursors, leading to the growth of the Cu phase on the Pt seeds. The Pt nanoparticle surface is partially alloyed with the Cu phase to form a PtCu alloy phase. Subsequent decomposition of Ru precursors leads to the formation of the Ru shell. The Cu layer between the core and shell of the intermediate PtCu@Cu@Ru nanoparticle, generated as a kinetic product, is then in situ removed by a CTAB (cetyltrimethylammonium bromide)-induced destabilization process to yield a novel nanorattle structure with a Pt-based core and a porous Ru shell. The diameter of the Ru shell could be conveniently controlled by varying the ratio of employed Cu and Ru precursors.

Copper sulphide materials have received great attention due to their low bandgap semiconducting properties. As compared to other chalcogenides, few synthetic examples have been reported, and a simple and scalable synthetic method for preparing size- and shape-controlled copper sulphide nanoparticles is required for potential wide application of these materials. Herein, a facile one pot scalable synthetic route has been developed for preparing highly monodisperse djurleite Cu1.94S hexagonal nanoplates. The thermal decomposition of a single precursor CuSCN was found suitable for preparing a large quantity of highly monodisperse Cu1.94S hexagonal nanoplates; a multi-gram scale product could be obtained in a single step. Under the synthetic scheme developed, the width of Cu1.94S nanoplates with a thickness of ~ 10 nm could be easily tuned from 70 nm to 130 nm. Their optical properties were investigated and their photothermal effect was also studied by photothermal optical coherence reflectometry (PT OCR). Cu1.94S hexagonal nanoplates showed a considerable photothermal effect, which was found to depend on the nanoparticle concentration.

Currently, much work has focused on the engineering of bone using adipose-derived stem cells (ADSCs), which differentiate into osteogenic cells. This study was conducted to assess the bone-regenerating capacity of ADSCs with genetic modification.ADSCs were cultured and transduced with recombinant adenovirus-expressing bone morphogenetic protein-2 (rAd/BMP-2). Two 5-mm full-thickness bone defects were created on the parietal bones of 24 rats. The defects were left empty (n = 12), restored with a scaffold alone (n = 12), transplanted with ADSCs in osteogenic media (n = 12), or transplanted with rAd/BMP-2-transduced ADSCs (n = 12). Six defects from each group were assessed by histologic observation, histomorphometric analysis, and microcomputed tomography (micro-CT) imaging at 4 and 8 weeks after transplantation.Increased new bone formation was observed in the rAd/BMP-2-transduced ADSC groups, compared with the other groups. On micro-CT, significant differences were noted in bone volume-to-tissue volume ratios between rAd/BMP-2-transduced ADSCs group and the other groups at both time points (P0.05).The result demonstrates that transferring BMP-2 promotes the osteogenic differentiation of ADSCs and enhances bone regeneration. Under limitation of this study, genetic modification of ADSCs with BMP-2 could be adopted in clinical application.

A facile one step route has been developed for the synthesis of trimetallic Cu@RhRu core-shell concave nanooctahedra by co-decomposition of Ru, Rh and Cu precursors. A mechanistic study reveals that nanoparticles with a CuRh alloy core and a Ru shell are initially formed and a subsequent migration of Rh to the shell results in the Cu@RhRu core-shell concave nanooctahedron. The shell exhibits atomically mixed Ru and Rh phases with an fcc atomic structure, although the hcp atomic structure is commonly found for the bulk Ru. We also report an unusually high catalytic activity of the Cu@RhRu octahedral nanocrystals toward the oxygen evolution reaction in alkaline solution.

Gate oxide and interface trap charges are critical parameters for device reliability and their generation and recovery are investigated under AC and DC oxide field stress on n-channel MOSFETs by C-V, I–V, and CP measurements. The interface traps generation is the same under both DC and AC stress but oxide charge trap generation is higher at AC stress than DC stress. The oxide charge and interface trap generation rate is independent of frequency from low to 10MHz but increase with stress time. The generated interface traps are positioned in the middle of the band gap and oxide traps are negatively charged and located in the upper half of the energy band gap due to the electron injection from the inversion layer. Both interface and oxide trap charges are characterized by high frequency and quasi-static C-V measurement.

A new and accurate approach to gate oxide reliability measurements for the determination of the gate oxide quality and lifetime estimation on MOSFET is presented. An accurate gate oxide thickness calculation by gate current provides oxide thickness variations better than conventional CV measurement. A gate oxide quality by gate current analysis is well correlated to the time dependent dielectric breakdown (TDDB) method. The results present that oxide lifetime is better at lower gate current in same oxide thickness where device process is same but different fabrication facilities (FAB).

Due to its excellent spatial resolution, fast and reliable performance, cost and wide availability, ultrasound should be considered the imaging modality of choice for many applications including molecular imaging. However, ultrasound imaging cannot image molecular content of tissue due to trade-off between spatial resolution and penetration depth. Consequently, contrast agents have been developed both to enhance the contrast of ultrasound images and to make the images molecularly specific. Most ultrasound contrast agents, however, are micrometer sized and may not be applicable to wide range of pathology-specific cellular and molecular imaging. We have developed an imaging technique - magneto-motive ultrasound (MMUS) imaging, capable of imaging magnetic nanoparticles subjected to time-varying magnetic field. The result of our studies indicate that magnetically excited nanoparticles can be used as contrast agents in magneto-motive ultrasound imaging thus expanding the role of ultrasound imaging to cellular scales and molecular sensitivity.

We report the extraction of silicon via a carbothermal reduction process using a CO2 laser beam as a heat source. The surface of a mixture of silica and carbon black powder became brown after laser beam irradiation for a few tens of seconds, and clear peaks of crystalline silicon were observed by Raman shift measurements, confirming the successful carbothermal reduction of silica. The influence of process parameters, including the laser beam intensity, radiation time, nitrogen gas flow in a reaction chamber, and the molar ratios of silica/carbon black of the mixture, on the carbothermal reduction process is explained in detail.

C-phycocyanin, a natural blue-colored pigment-protein complex was explored as a novel photosensitizer for use in low-level laser therapy under 625-nm laser illumination. C-phycocyanin produced singlet oxygen radicals and the level of reactive oxygen species (ROS) were raised in extended time of treatment. It did not exhibit any visible toxic effect in the absence of light. Under 625-nm laser irradiation, c-phycocyanin generated cytotoxic stress through ROS induction, which killed MDA-MB-231 breast cancer cells depending on concentrations. Different fluorescent staining of laser-treated cells explored apoptotic cell death characteristics like the shrinking of cells, cytoplasmic condensation, nuclei cleavage, and the formation of apoptotic bodies. In conclusion, phycocyanin is a non-toxic fluorescent pigment that can be used in low-level light therapy.