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1.
Materials (Basel) ; 15(18)2022 Sep 07.
Article in English | MEDLINE | ID: mdl-36143532

ABSTRACT

The optimum femtosecond laser direct writing of Bragg gratings on silica optical waveguides has been investigated. The silica waveguide has a 6.5 × 6.5 µm2 cross-sectional profile with a 20-µm-thick silicon dioxide cladding layer. Compared with conventional grating inscribed on fiber platforms, the silica planar waveguide circuit can realize a stable performance as well as a high-efficiency coupling with the fiber. A thin waveguide cladding layer also facilitates laser focusing with an improved spherical aberration. Different from the circular fiber core matching with the Gaussian beam profile, a 1030-nm, 400-fs, and 190-nJ laser is optimized to focus on the top surface of the square silica waveguide, and the 3rd-order Bragg gratings are inscribed successfully. A 1.5-mm long uniform Bragg gratings structure with a reflectivity of 90% at a 1548.36-nm wavelength can be obtained. Cascaded Bragg gratings with different periods are also inscribed in the planar waveguide. Different reflection wavelengths can be realized, which shows great potential for wavelength multiplexing-related applications such as optical communications or sensing.

4.
Int J Mol Sci ; 21(3)2020 Jan 29.
Article in English | MEDLINE | ID: mdl-32013250

ABSTRACT

Lung squamous cell carcinoma (LUSC) has a poor prognosis, in part due to poor therapeutic response and limited therapeutic alternatives. Lichens are symbiotic organisms, producing a variety of substances with multiple biological activities. (+)-Usnic acid, an important biologically active metabolite of lichens, has been shown to have high anti-cancer activity at low doses. However, there have been no reports regarding the effect of (+)-usnic acid on LUSC cells. This study found that (+)-usnic acid reduced viability and induced apoptosis in LUSC cells by reactive oxygen species (ROS) accumulation. (+)-Usnic acid induced mitochondria-derived ROS production via inhibition of complex I and complex III of the mitochondrial respiratory chain (MRC). Interestingly, the elimination of mitochondrial ROS by Mito-TEMPOL only partially reversed the effect of (+)-usnic acid on cellular ROS production. Further study showed that (+)-usnic acid also induced ROS production via reducing Nrf2 stability through disruption of the PI3K/Akt pathway. The in vitro and in vivo xenograft studies showed that combined treatment of (+)-usnic acid and paclitaxel synergistically suppressed LUSC cells. In conclusion, this study indicates that (+)-usnic acid induces apoptosis of LUSC cells through ROS accumulation, probably via disrupting the mitochondrial respiratory chain (MRC) and the PI3K/Akt/Nrf2 pathway. Therefore, although clinical use of (+)-usnic acid will be limited due to toxicity issues, derivatives thereof may turn out as promising anticancer candidates for adjuvant treatment of LUSC.


Subject(s)
Apoptosis/drug effects , Benzofurans/pharmacology , Electron Transport Chain Complex Proteins/metabolism , Mitochondria/drug effects , NF-E2-Related Factor 2/metabolism , Reactive Oxygen Species/metabolism , Animals , Antineoplastic Agents, Phytogenic/pharmacology , Benzofurans/chemistry , Benzofurans/therapeutic use , Carcinoma, Squamous Cell/drug therapy , Carcinoma, Squamous Cell/metabolism , Carcinoma, Squamous Cell/pathology , Cell Line, Tumor , Electron Transport Chain Complex Proteins/antagonists & inhibitors , Humans , Lung Neoplasms/drug therapy , Lung Neoplasms/metabolism , Lung Neoplasms/pathology , Mice , Mitochondria/metabolism , NF-E2-Related Factor 2/antagonists & inhibitors , Paclitaxel/pharmacology , Phosphatidylinositol 3-Kinases/metabolism , Proto-Oncogene Proteins c-akt/metabolism , Signal Transduction/drug effects , Transplantation, Heterologous
5.
Toxicol Appl Pharmacol ; 387: 114848, 2020 01 15.
Article in English | MEDLINE | ID: mdl-31809756

ABSTRACT

Non-small cell lung cancer (NSCLC) is the most common type of lung cancer with a disappointing prognosis. The aim of this study was to investigate the anticancer effect of sesamin and the underlying mechanism. The MTT assay was used to detect the proliferation of NSCLC cells. The cell cycle and apoptosis were analyzed by flow cytometry. The protein levels of Akt, p-Akt (Ser473), p53, cyclin D1, CDK2, MDM2, p-MDM2 (Ser166) were detected by western blotting. The expression of p-Akt (Ser473), p53 and Ki67 in vivo was analyzed by IHC. Histopathologic analyses of major organs (heart, liver, spleen, lung and kidney) were performed by H&E staining. The results show that sesamin suppressed cell proliferation and induced apoptosis of NSCLC cells (A549 and H1792) in a dose-dependent manner. Treatment with sesamin caused cell cycle arrest at G1 phase and inhibited cyclin D1 and CDK2 expression. In addition, sesamin inhibited Akt activity and upregulated p53 expression both in vivo and in vitro. When Akt and p53 were suppressed by LY294002 and PFTα, respectively, sesamin exerted no additional effects. The in vivo results mostly matched the in vitro findings. Specifically, sesamin exerted little damage to major organs. Taken together, this study demonstrates that sesamin suppresses NSCLC cell proliferation by induction of G1 phase cell cycle arrest and apoptosis via Akt/p53 pathway. Therefore, sesamin may be a promising adjuvant treatment for NSCLC therapy.


Subject(s)
Apoptosis/drug effects , Carcinoma, Non-Small-Cell Lung/drug therapy , Dioxoles/pharmacology , Lignans/pharmacology , Lung Neoplasms/drug therapy , Signal Transduction/drug effects , Animals , Benzothiazoles/pharmacology , Carcinoma, Non-Small-Cell Lung/pathology , Cell Line, Tumor , Cell Proliferation/drug effects , Chromones/pharmacology , Dioxoles/therapeutic use , Female , G1 Phase Cell Cycle Checkpoints/drug effects , Humans , Lignans/therapeutic use , Lung Neoplasms/pathology , Mice , Morpholines/pharmacology , Proto-Oncogene Proteins c-akt/antagonists & inhibitors , Proto-Oncogene Proteins c-akt/metabolism , Toluene/analogs & derivatives , Toluene/pharmacology , Tumor Suppressor Protein p53/antagonists & inhibitors , Tumor Suppressor Protein p53/metabolism , Xenograft Model Antitumor Assays
6.
J Hazard Mater ; 153(1-2): 685-94, 2008 May 01.
Article in English | MEDLINE | ID: mdl-17936503

ABSTRACT

Municipal solid waste (MSW) source-classified collection represents a change in MSW management in China and other developing countries. Comparative experiments were performed to evaluate the effect of a newly established MSW source-classified collection system on the emission of PCDDs/Fs (polychlorinated dibenzo-p-dioxins and dibenzofurans) and heavy metals (HMs) from a full-scale incinerator in China. As a result of presorting and dewatering, the chlorine level, heavy metal and water content were lower, but heat value was higher in the source-classified MSW (classified MSW) as compared with the conventionally mixed collected MSW (mixed MSW). The generation of PCDDs/Fs in flue gas from the classified MSW incineration was 9.28 ng I-TEQ/Nm(3), only 69.4% of that from the mixed MSW incineration, and the final emission of PCDDs/Fs was only 0.12 ng I-TEQ/Nm(3), although activated carbon injection was reduced by 20%. The level of PCDDs/Fs in fly ash from the bag filter was 0.27 ng I-TEQ/g. These results indicated that the source-classified collection with pretreatment could improve the characteristics of MSW for incineration, and significantly decrease formation of PCDDs/Fs in MSW incineration. Furthermore, distributions of HMs such as Cd, Pb, Cu, Zn, Cr, As, Ni, Hg in bottom ash and fly ash were investigated to assess the need for treatment of residual ash.


Subject(s)
Air Pollutants/analysis , Benzofurans/analysis , Incineration/methods , Metals, Heavy/analysis , Polychlorinated Dibenzodioxins/analogs & derivatives , Waste Products/classification , Carbon/analysis , China , Coal Ash , Dibenzofurans, Polychlorinated , Industrial Waste/analysis , Particulate Matter/analysis , Polychlorinated Dibenzodioxins/analysis
7.
Talanta ; 58(1): 153-64, 2002 Aug 16.
Article in English | MEDLINE | ID: mdl-18968742

ABSTRACT

A simple, fast and sensitive light-emitting diode (LED)-based photometric method for the differential determination of ppb-ppm levels of As(III) and As(V) in potable water in the presence of ppm levels of phosphate was developed. The detection chemistry is based on the well-known formation of arsenomolybdate, followed by reduction to heteropoly blue. The front-end of the measurement system is configured to selectively retain P(V) and As(V), based on the considerable difference of the pK(a) of the corresponding acids relative to As(III). Thus, it is As(III) that is injected into the medium, oxidized in-line with KBrO(3) to As(V) and forms Mo-blue that is detected by an LED-based detector. Only As(III) is measured if the sample is injected as such; if all As in the sample is prereduced to As(III) (by the addition of cysteine, in a provided in-line arrangement), the system measures As(V)+As(III). In the present form, limit of detection (LOD) (S/N=3) is less than 8 mug l(-1) As, and the linear range extends to 2.4 mg l(-1). Potential interference from dissolved silica and Fe(III) is eliminated by the addition of NaF to the sample.

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