Publications by authors named "Xing-Yu Guo"

Rationale: This article summarized the nursing experience of phlebitis caused by intravenous infusion of amphotericin B cholesterol sulfate complex in a patient with myelodysplastic syndrome.

Patient Concerns: A 59-year-old man with myelodysplastic syndrome complicated with fungal infection was treated with antifungal therapy.

Diagnoses: Patient with myelodysplastic syndrome was diagnosed with secondary phlebitis caused by liposomal amphotericin B.

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This study aims to explore the consistency between macroscopic identification and DNA barcoding identification of Amomi Fructus. With the DNA barcoding identification results, we evaluated the reliability of identifying Amomi Fructus quality by combining macroscopic traits with main volatile chemical components. Thirteen batches of Amomi Fructus samples were collected for identification.

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Article Synopsis
  • Nutmeg is a popular spice and Chinese herbal medicine, but it is susceptible to mildew during storage due to its volatile components and fatty oils.
  • This study used an electronic nose (E-nose) to quickly and reliably detect different levels of mildew in nutmeg samples.
  • The findings showed that the E-nose results were consistent with chemical analyses (HPLC and GC-MS), leading to the creation of a model that categorizes nutmeg samples into mildew-free, slight mildew, and mildew, demonstrating E-nose's potential for quality evaluation in herbal medicines.
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This study adopted headspace-gas chromatography-mass spectrometry(HS-GC-MS) and electronic nose to detect volatile components from Myristicae Semen samples with varying degrees of mildew, aiming at rapidly identifying odor changes and substance basis of Myristicae Semen mildew. The experimental data were analyzed by electronic nose and principal component analysis(PCA). The results showed that Myristicae Semen samples were divided into the following three categories by electronic nose and PCA: mildew-free samples, slightly mildewy samples, and mildewy samples.

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This study was to identify anti-metastatic active fractions and compounds of (). The results indicated that 50 µg/mL ethyl acetate fraction () can dramatically inhibit mouse melanoma B16 cells migration and invasion . In B16 cells pulmonary and hepatic metastasis assays, 50 µg/mL alleviated mouse lung and liver weights, the number of metastatic nodules and the levels of TNF-α and IL-6 in mouse serum and organs.

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In recent years, haze pollution in China is becoming increasingly serious, especially in the Beijing-Tianjin-Hebei region. In order to identify the temporal and spatial distributional characteristics of PM aerosol mass concentration in the region, this study selected the inland plain of the Beijing-Tianjin-Hebei region as the research area, and used MODIS AOD as the main predictor in a mixed effects model to establish the daily relationship of AOD-PM in the study area, from 2013 to 2014. The model was validated by a ten-fold cross validation method.

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Background: Cancer related inflammation plays a fatal role in the metastatic process, which can foster tumor growth, angiogenesis and dissemination. Sparstolonin B (SsnB), derived from Chinese medicine of the tubers of Scirpus yagara, is a TLR2 and TLR4 antagonists. It has exhibited multiple activities of anti-inflammatory, anti-cancer, anti-obesity and anti-hepatitis.

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As discovered by Warburg 80 years ago most malignant cells rely more on glycolysis than normal cells. The high rate of glycolysis provides faster ATP production and greater lactic acid for tumor proliferation and invasion, thus indicating a potential target in anticancer therapy. Our previous studies demonstrated that 3-bromopyruvate (3-BrPA) and sodium citrate (SCT) inhibited tumor cell proliferation in vitro.

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Glycolysis is the primary method utilized by cancer cells to produce the energy (adenosine triphosphate, ATP) required for cell proliferation. Therefore, inhibition of glycolysis may inhibit tumor growth. We previously found that both 3-bromopyruvate (3-BrPA) and sodium citrate (SCT) can inhibit glycolysis in vitro; however, the underlying inhibitory mechanisms remain unclear.

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