31 research outputs found

    Relationship between Plasma Concentrations of Afatinib and the Onset of Diarrhea in Patients with Non-Small Cell Lung Cancer

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    We evaluated the area under the plasma concentration–time curve (AUC) of afatinib required to avoid the onset of grade 2 or higher diarrhea. The C0 and AUC0–24 of afatinib were significant higher in patients with grade 2 diarrhea than in those with grade 0–1 diarrhea. The areas under the receiver operator curves were 0.795 with the highest sensitivity (89%) and specificity (74%) at an AUC0–24 threshold of 823.5 ng h/mL, and 0.754 with the highest sensitivity (89%) and specificity (74%) at a C0 threshold of 28.5 ng/mL. In Kaplan–Meier analysis based on these cut-off AUC0–24 and C0 values, the median time to the incidence of grade 2 diarrhea was 16 days. The predicted AUC0–24 of afatinib from the single point of C6 showed the highest correlation with the measured AUC0–24 (r2 = 0.840); however, a significant correlation between the AUC0–24 and C0 was also observed (r2 = 0.761). C0 could be used as a marker of therapeutic drug monitoring because afatinib C0 was related to AUC0–24. Therefore, afatinib C0 should be monitored on day 8 after beginning therapy, and the daily dose of afatinib should be adjusted as an index with a cut-off value of 28.5 ng/mL

    子宮内膜症性腸閉塞に対する経肛門的イレウスチューブの有用性

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    One of the causative diseases of intestinal obstruction in young women is bowel endometriosis. During the course of ectopic endometriosis, it is estimated that about 10% of patients develop bowel endometriosis. The first step in treatment is drug therapy. In cases of bowel endometriosis of the colon or rectum leading to intestinal obstruction, laparotomy is often required. A 47-year-old woman with a history of endometriosis was undergoing drug therapy. She developed abdominal pain and nausea, and was diagnosed with septic shock and fecal ileus. A transanal drainage tube was inserted for decompression. The patient’s general condition improved, and a laparoscopic low anterior resection was performed on the 23rd day. The patient was discharged on the 10th postoperative day without any postoperative problems. This case suggests that even in the case of septic shock caused by rectal stricture due to intestinal endometriosis, initial treatment with transanal decompression may stabilize the general condition, and may be superior in cosmetic change

    The cardiomyocyte disrupts pyrimidine biosynthesis in non-myocytes to regulate heart repair

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    Various populations of cells are recruited to the heart after cardiac injury, but little is known about whether cardiomyocytes directly regulate heart repair. Using a murine model of ischemic cardiac injury, we demonstrate that cardiomyocytes play a pivotal role in heart repair by regulating nucleotide metabolism and fates of nonmyocytes. Cardiac injury induced the expression of the ectonucleotidase ectonucleotide pyrophosphatase/phosphodiesterase 1 (ENPP1), which hydrolyzes extracellular ATP to form AMP. In response to AMP, cardiomyocytes released adenine and specific ribonucleosides that disrupted pyrimidine biosynthesis at the orotidine monophosphate (OMP) synthesis step and induced genotoxic stress and p53-mediated cell death of cycling nonmyocytes. As nonmyocytes are critical for heart repair, we showed that rescue of pyrimidine biosynthesis by administration of uridine or by genetic targeting of the ENPP1/AMP pathway enhanced repair after cardiac injury. We identified ENPP1 inhibitors using small molecule screening and showed that systemic administration of an ENPP1 inhibitor after heart injury rescued pyrimidine biosynthesis in nonmyocyte cells and augmented cardiac repair and postinfarct heart function. These observations demonstrate that the cardiac muscle cell regulates pyrimidine metabolism in nonmuscle cells by releasing adenine and specific nucleosides after heart injury and provide insight into how intercellular regulation of pyrimidine biosynthesis can be targeted and monitored for augmenting tissue repair

    One Step Preparation of Fe–FeO–Graphene Nanocomposite through Pulsed Wire Discharge

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    The Fe–FeO–graphene nanocomposite material was produced successfully by pulsed wire discharge in graphene oxide (GO) suspension. Pure iron wires with a diameter of 0.25 mm and a length of 100 mm were used in the experiments. The discharge current and voltage were recorded to analyze the process of the pulsed wire discharge. The as-prepared samples—under different charging voltages—were recovered and characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), Raman spectroscopy, and transmission electron microscopy (TEM). Curved and loose graphene films that were anchored with spherical Fe and FeO nanoparticles were obtained at the charging voltage of 8–10 kV. The present study discusses the mechanism by which the Fe–FeO–graphene nanocomposite material was formed during the pulsed wire discharge process

    Quantitative granitic weathering assessment for rock mass classification optimization of tunnel face using image analysis technique

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    Weathering degree is one of the key criteria used to determine tunnel support with the main difficulty is in assessing the weathering grade of the tunnel face. This study applied CIEL*a*b colour space and image analysis to a rock mass tunnel face. The authors used the Japanese Highway (JH) Rock Mass Classification System to classify the rock mass tunnel face. JudGeo converted the RGB photographs to L*a*b values. This study compared the quantitative evaluation system's performance to manual tunnel face mapping by geologists using six JH Rock Mass Classification samples (Class B, CI, CII, DI, DII, and E). The analysis showed good correlations between four (B; CI; CII; DI) of six rock mass classes. The tunnel face mapping showed two rock mass classes above grade (DII and E). This technique can effectively identify the degree of weathering grades of the tunnel face, especially for fresh to moderately weathered tunnel faces

    Preparation of Few-Layer Graphene by Pulsed Discharge in Graphite Micro-Flake Suspension

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    Few-layer graphene nanosheets were produced by pulsed discharge in graphite micro-flake suspension at room temperature. In this study, the discharging current and voltage data were recorded for the analysis of the pulsed discharge processes. The as-prepared samples were recovered and characterized by various techniques, such as TEM, SEM, Raman, XRD, XPS, FT-IR, etc. The presence of few-layer graphene (3–9 L) in micrometer scale was confirmed. In addition, it is investigated that the size of recovered graphene nanosheets are influenced by the initial size of utilized graphite micro-flake powder. Based on the process of pulsed discharge and our experimental results, the formation mechanism of few-layer graphene was discussed. The influence of charging voltage on as-prepared samples is also investigated

    Relationship between Plasma Concentrations of Afatinib and the Onset of Diarrhea in Patients with Non-Small Cell Lung Cancer

    No full text
    We evaluated the area under the plasma concentration–time curve (AUC) of afatinib required to avoid the onset of grade 2 or higher diarrhea. The C0 and AUC0–24 of afatinib were significant higher in patients with grade 2 diarrhea than in those with grade 0–1 diarrhea. The areas under the receiver operator curves were 0.795 with the highest sensitivity (89%) and specificity (74%) at an AUC0–24 threshold of 823.5 ng·h/mL, and 0.754 with the highest sensitivity (89%) and specificity (74%) at a C0 threshold of 28.5 ng/mL. In Kaplan–Meier analysis based on these cut-off AUC0–24 and C0 values, the median time to the incidence of grade 2 diarrhea was 16 days. The predicted AUC0–24 of afatinib from the single point of C6 showed the highest correlation with the measured AUC0–24 (r2 = 0.840); however, a significant correlation between the AUC0–24 and C0 was also observed (r2 = 0.761). C0 could be used as a marker of therapeutic drug monitoring because afatinib C0 was related to AUC0–24. Therefore, afatinib C0 should be monitored on day 8 after beginning therapy, and the daily dose of afatinib should be adjusted as an index with a cut-off value of 28.5 ng/mL
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