158 research outputs found

    Π Π°Π·Ρ€Π°Π±ΠΎΡ‚ΠΊΠ° систСмы управлСния вСнтиляторной установки

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    ΠžΠ±ΡŠΠ΅ΠΊΡ‚ΠΎΠΌ исслСдования являСтся: систСма управлСния вСнтиляторной установки. ЦСль Ρ€Π°Π±ΠΎΡ‚Ρ‹ - исслСдованиС ΠΌΠ΅Ρ‚ΠΎΠ΄ΠΎΠ² Ρ€Π΅Π°Π»ΠΈΠ·Π°Ρ†ΠΈΠΈ Π°Π»Π³ΠΎΡ€ΠΈΡ‚ΠΌΠΎΠ² управлСния вСнтиляционной систСмы Π½Π° ΠΏΡ€ΠΎΠ³Ρ€Π°ΠΌΠΌΠΈΡ€ΡƒΠ΅ΠΌΠΎΠΌ логичСском ΠΊΠΎΠ½Ρ‚Ρ€ΠΎΠ»Π»Π΅Ρ€Π΅. Π’ процСссС исслСдования ΠΏΡ€ΠΎΠ²ΠΎΠ΄ΠΈΠ»ΠΈΡΡŒ исслСдования ΠΌΠ΅Ρ‚ΠΎΠ΄ΠΎΠ² Ρ€Π΅Π°Π»ΠΈΠ·Π°Ρ†ΠΈΠΈ Π°Π»Π³ΠΎΡ€ΠΈΡ‚ΠΌΠΎΠ² управлСния вСнтиляционной систСмы Π½Π° ΠΏΡ€ΠΎΠ³Ρ€Π°ΠΌΠΌΠΈΡ€ΡƒΠ΅ΠΌΠΎΠΌ логичСском ΠΊΠΎΠ½Ρ‚Ρ€ΠΎΠ»Π»Π΅Ρ€Π΅. Π Π°Π·Ρ€Π°Π±Π°Ρ‚Ρ‹Π²Π°Π»ΠΈΡΡŒ Π°Π»Π³ΠΎΡ€ΠΈΡ‚ΠΌΡ‹ управлСния ΠΈ ΠΌΠ΅Ρ‚ΠΎΠ΄Ρ‹ ΠΏΠΎΠ΄ΠΊΠ»ΡŽΡ‡Π΅Π½ΠΈΡ ΠΈ настройки ΠΈΡΠΏΠΎΠ»Π½ΠΈΡ‚Π΅Π»ΡŒΠ½ΠΎΠ³ΠΎ ΠΈ ΠΈΠ·ΠΌΠ΅Ρ€ΠΈΡ‚Π΅Π»ΡŒΠ½ΠΎΠ³ΠΎ оборудования, Π° Ρ‚Π°ΠΊΠΆΠ΅ панСль управлСния ΠΈ настройки систСмы вСнтиляции.The object of the study is: the control system of the fan system. The purpose of work is research of methods of realization of control algorithms of the ventilation system on a programmable logic controller. In the research process the research was conducted the methods of realization of control algorithms of the ventilation system on a programmable logic controller. Developed control algorithms and connectivity methods and configuration Executive and instrumentation and control panel and settings of the ventilation system

    The Evolving Landscape of Immunotherapy-Based Combinations for Frontline Treatment of Advanced Renal Cell Carcinoma

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    Insights into the biology of advanced renal cell carcinoma (aRCC) and the development of agents targeting the vascular endothelial growth factor (VEGF) pathway have positively impacted the outcomes for patients with aRCC. With the recent approval of the dual immune checkpoint inhibitors (ICIs), nivolumab and ipilimumab, by the U.S. Food and Drug Administration (USFDA), and the European Medicines Agency (EMA), the era of VEGF monotherapy for untreated aRCC appears to be coming to an end for patients with access to the combination therapy. The frontline treatment options for renal cell carcinoma are evolving rapidly and will lead to the approval of other combination immunotherapiesβ€”especially those with VEGF inhibitors. Here we review the clinical data for dual immune checkpoint inhibition with nivolumab plus ipilimumab as well as the emerging data for ICI plus VEGF inhibitor combinations and discuss the challenges these will pose for the clinical practitioner

    ИсслСдованиС поля Ρ‚ΠΎΡ€ΠΌΠΎΠ·Π½ΠΎΠ³ΠΎ рСнтгСновского излучСния ΠΊΠΎΠ½Π²Π΅Ρ€Ρ‚ΠΎΡ€Π° ΠΈΠΌΠΏΡƒΠ»ΡŒΡΠ½ΠΎΠ³ΠΎ элСктронного ускоритСля

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    ΠœΠΎΡ‰Π½Ρ‹Π΅ ΠΈΠΌΠΏΡƒΠ»ΡŒΡΡ‹ ΠΊΠΎΡ€ΠΎΡ‚ΠΊΠΎΠΉ Π΄Π»ΠΈΡ‚Π΅Π»ΡŒΠ½ΠΎΡΡ‚ΠΈ (80 нс) Ρ‚ΠΎΡ€ΠΌΠΎΠ·Π½ΠΎΠ³ΠΎ рСнтгСновского излучСния ΡΠ²Π»ΡΡŽΡ‚ΡΡ соврСмСнным инструмСнтом для ΠΏΡ€ΠΎΠ²Π΅Π΄Π΅Π½ΠΈΠΈ исслСдований ΠΏΠΎ Ρ‚Π΅ΠΌΠ°Ρ‚ΠΈΠΊΠ°ΠΌ "ΠΌΠ°Ρ‚Π΅Ρ€ΠΈΠ°Π»Ρ‹ для ΡΠΊΡΡ‚Ρ€Π΅ΠΌΠ°Π»ΡŒΠ½Ρ‹Ρ… состояний", ΠΏΡ€ΠΈ ΠΌΠΎΠ΄Π΅Π»ΠΈΡ€ΠΎΠ²Π°Π½ΠΈΠΈ космичСских условий, для Ρ€Π°Π·Ρ€Π°Π±ΠΎΡ‚ΠΊΠΈ Ρ‚Π΅Ρ…Π½ΠΎΠ»ΠΎΠ³ΠΈΠΉ Ρ€Π°Π΄ΠΈΠ°Ρ†ΠΈΠΎΠ½Π½ΠΎΠΉ ΠΎΠ±Ρ€Π°Π±ΠΎΡ‚ΠΊΠΈ биологичСских ΠΌΠ°Ρ‚Π΅Ρ€ΠΈΠ°Π»ΠΎΠ². НСобходимым условиСм примСнСния Π΄Π°Π½Π½ΠΎΠ³ΠΎ инструмСнта являСтся информация ΠΎ гСомСтричСских ΠΈ Π΄ΠΎΠ·ΠΎΠ²Ρ‹Ρ… характСристиках поля Ρ‚ΠΎΡ€ΠΌΠΎΠ·Π½ΠΎΠ³ΠΎ рСнтгСновского излучСния Π² области Π³Π΅Π½Π΅Ρ€Π°Ρ†ΠΈΠΈ. ΠšΡ€ΠΎΠΌΠ΅ Ρ‚ΠΎΠ³ΠΎ, ΠΏΠΎΠ»ΡƒΡ‡Π΅Π½Π½Ρ‹Π΅ Π΄Π°Π½Π½Ρ‹Π΅ позволят ΠΎΠΏΡ‚ΠΈΠΌΠΈΠ·ΠΈΡ€ΠΎΠ²Π°Ρ‚ΡŒ настройки ускоритСля ΠΈ ΠΊΠΎΠ½ΡΡ‚Ρ€ΡƒΠΊΡ†ΠΈΡŽ ΠΊΠΎΠ½Π²Π΅Ρ€Ρ‚ΠΎΡ€Π° для достиТСния максимальной эффСктивности Π³Π΅Π½Π΅Ρ€Π°Ρ†ΠΈΠΈ.Powerful pulses of short duration (80 NS) braking x-ray radiation are the modern tool for conducting research on the topics "materials for extreme conditions", in the simulation of space conditions for the development of radiation processing of biological materials. A precondition for the application of this tool is the information on the geometrical characteristics of the dose and the field of the braking x-ray radiation to generate. In addition, the data obtained will allow to optimize the settings of the accelerator and the design of the Converter to achieve maximum lasing efficiency

    Frequency-dependent selection on female morphs driven by premating interactions with males

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    Species showing color polymorphisms-the presence of two or more genetically determined color morphs within a single population-are excellent systems for studying the selective forces driving the maintenance of genetic diversity. Despite a shortage of empirical evidence, it is often suggested that negative frequency-dependent mate preference by males (or diet choice by predators) results in fitness benefits for the rare female morph (or prey type). Moreover, most studies have focused on the male (or predator) behavior in these systems and largely overlooked the importance of female (or prey) resistance behavior. Here, we provide the first explicit test of the role of frequency-dependent and frequency-independent intersexual interactions in female polymorphic damselflies. We identify the stage of the mating sequence when frequency-dependent selection is likely to act by comparing indexes of male mate preference when the female has little (females presented on sticks), moderate (females in cages), and high (females free to fly in the field) ability to avoid male mating attempts. Frequency-dependent male preferences were found only in those experiments where females had little ability to resist male harassment, indicating that premating interactions most likely drive negative frequency-dependent selection in this system. In addition, by separating frequency-dependent male mating preference from the baseline frequency-independent component, we reconcile the seemingly contradictory results of previous studies and highlight the roles of both forms of selection in maintaining the polymorphism at a given equilibrium. We conclude that considering interactions among all players-here, males and females-is crucial to fully understanding the mechanisms underlying the maintenance of genetic polymorphisms in the wild

    ОбоснованиС составлСния ΠΎΡ‚Ρ‡Π΅Ρ‚Π° GRI (General reporting initiative) Π½Π° прСдприятиях, Ρ€Π΅Π°Π»ΠΈΠ·ΡƒΡŽΡ‰ΠΈΡ… ΠΊΠΎΡ€ΠΏΠΎΡ€Π°Ρ‚ΠΈΠ²Π½ΡƒΡŽ ΡΠΎΡ†ΠΈΠ°Π»ΡŒΠ½ΡƒΡŽ ΠΎΡ‚Π²Π΅Ρ‚ΡΡ‚Π²Π΅Π½Π½ΠΎΡΡ‚ΡŒ

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    ΠžΠ±ΡŠΠ΅ΠΊΡ‚ΠΎΠΌ исслСдования являСтся: БистСма отчСтности GRI ПАО "Π‘ΠΈΠ±ΡƒΡ€ Π₯ΠΎΠ»Π΄ΠΈΠ½Π³" ЦСль Ρ€Π°Π±ΠΎΡ‚Ρ‹ – ОбоснованиС составлСния ΠΎΡ‚Ρ‡Π΅Ρ‚Π° GRI (General reporting initiative) Π½Π° прСдприятиях, Ρ€Π΅Π°Π»ΠΈΠ·ΡƒΡŽΡ‰ΠΈΡ… ΠΊΠΎΡ€ΠΏΠΎΡ€Π°Ρ‚ΠΈΠ²Π½ΡƒΡŽ ΡΠΎΡ†ΠΈΠ°Π»ΡŒΠ½ΡƒΡŽ ΠΎΡ‚Π²Π΅Ρ‚ΡΡ‚Π²Π΅Π½Π½ΠΎΡΡ‚ΡŒ. Π’ Ρ€Π΅Π·ΡƒΠ»ΡŒΡ‚Π°Ρ‚Π΅ исслСдования: ΠΏΡ€Π΅Π΄Π»ΠΎΠΆΠ΅Π½Ρ‹ Ρ€Π΅ΠΊΠΎΠΌΠ΅Π½Π΄Π°Ρ†ΠΈΠΈ ΠΏΠΎ ΡΠΎΠ²Π΅Ρ€ΡˆΠ΅Π½ΡΡ‚Π²ΠΎΠ²Π°Π½ΠΈΡŽ ΠΊΠΎΡ€ΠΏΠΎΡ€Π°Ρ‚ΠΈΠ²Π½ΠΎΠΉ ΡΠΎΡ†ΠΈΠ°Π»ΡŒΠ½ΠΎΠΉ отвСтствСнности ПАО "Π‘ΠΈΠ±ΡƒΡ€ Π₯ΠΎΠ»Π΄ΠΈΠ½Π³". ЭкономичСская ΡΡ„Ρ„Π΅ΠΊΡ‚ΠΈΠ²Π½ΠΎΡΡ‚ΡŒ состоит Π² Ρ‚ΠΎΠΌ, Ρ‡Ρ‚ΠΎ ΡΠΎΠ²Π΅Ρ€ΡˆΠ΅Π½ΡΡ‚Π²ΠΎΠ²Π°Π½ΠΈΠ΅ систСмы ΠΊΠΎΡ€ΠΏΠΎΡ€Π°Ρ‚ΠΈΠ²Π½ΠΎΠΉ ΡΠΎΡ†ΠΈΠ°Π»ΡŒΠ½ΠΎΠΉ отвСтствСнности ΠΏΠΎΠ·Π²ΠΎΠ»ΠΈΡ‚ ΠΏΠΎΠ²Ρ‹ΡΠΈΡ‚ΡŒ всС ΠΏΠΎΠΊΠ°Π·Π°Ρ‚Π΅Π»ΠΈ ПАО "Π‘ΠΈΠ±ΡƒΡ€ Π₯ΠΎΠ»Π΄ΠΈΠ½Π³" ΠΈ ΡΠΎΠ·Π΄Π°Ρ‚ΡŒ Π΅ΠΌΡƒ ΠΏΠΎΠ»ΠΎΠΆΠΈΡ‚Π΅Π»ΡŒΠ½Ρ‹ΠΉ ΠΈΠΌΠΈΠ΄ΠΆ Π² отрасли.The object of research is: GRI reporting system of PJSC Sibur Holding Purpose of work - Justification of the compilation of the GRI report (General reporting initiative) at enterprises implementing corporate social responsibility. As a result of the study: recommendations are proposed for improving corporate social responsibility of Sibur Holding PJSC. Economic efficiency consists in the fact that improving the corporate social responsibility system will increase all the performance of Sibur Holding PJSC and create a positive image for it in the industry

    Phase II study of nivolumab and salvage nivolumab/ipilimumab in treatment-naΓ―ve patients with advanced non-clear cell renal cell carcinoma (HCRN GU16-260-Cohort B)

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    Background To determine the efficacy and toxicity of nivolumab monotherapy in treatment-naive patients with non-clear cell renal cell carcinoma (nccRCC) and the efficacy of nivolumab/ipilimumab salvage therapy in patients with tumors unresponsive to initial nivolumab monotherapy.Methods Eligible patients with treatment-naive nccRCC received nivolumab until progressive disease (PD), toxicity, or completion of 96 weeks of treatment (Part A). Patients with PD prior to, or stable disease (SD) at 48 weeks (prolonged SD) were potentially eligible to receive salvage nivolumab/ipilimumab (Part B). Patients were required to submit tissue from a metastatic lesion obtained within 12 months prior to study entry and prior to Part B for correlative studies.Results 35 patients with nccRCC were enrolled: 19 (54%) had papillary, 6 (17%) had chromophobe and 10 (29%) had unclassified histology. At median follow-up of 22.9 months, RECIST-defined objective response rate (ORR) was 5 of 35 (14.3% 95% CI 4.8% to 30.3%) (complete response (CR) 2 (5.7%) and partial response (PR) 3 (8.6%)). ORR by histology was: papillary-1/19 (5%); chromophobe-1/6 (17%); and unclassified-3/10 (30%). Nine patients (26%) had tumors with sarcomatoid features with 3 (33%) (2 unclassified and 1 papillary) responding. ORR was 0/18, 3/11 (27%) and 2/6 (33%) for patients with tumor progammed death ligand 1 (PD-L1) expression of = 5% or not measured, respectively. Median progression-free survival was 4.0 (2.7-4.3) months. Two of five responders have progressed. Thirty-two patients had PD or prolonged SD and therefore, were potentially eligible for salvage nivolumab/ipilimumab (Part B), but 15 patients did not enroll due to grade 2-3 toxicity (6) on nivolumab, symptomatic disease progression (5), or other reasons including no biopsy tissue (4). In the 17 Part B patients, there was one PR (6%) (unclassified/non-sarcomatoid). Grade >3 treatment-related adverse events were seen in 7/35 (20%) on nivolumab and 7/17 (41%) on salvage nivolumab/ipilimumab with one patient experiencing sudden death.Conclusions Nivolumab monotherapy has limited activity in treatment-naive nccRCC with most responses (4 of 5) seen in patients with sarcomatoid and/or unclassified tumors. Toxicity is consistent with prior nivolumab studies. Salvage treatment with nivolumab/ipilimumab was provided in half of these patients with minimal activity

    Pentastatin-1, a collagen IV derived 20-mer peptide, suppresses tumor growth in a small cell lung cancer xenograft model

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    <p>Abstract</p> <p>Background</p> <p>Angiogenesis is the formation of neovasculature from a pre-existing vascular network. Progression of solid tumors including lung cancer is angiogenesis-dependent. We previously introduced a bioinformatics-based methodology to identify endogenous anti-angiogenic peptide sequences, and validated these predictions <it>in vitro </it>in human umbilical vein endothelial cell (HUVEC) proliferation and migration assays.</p> <p>Methods</p> <p>One family of peptides with high activity is derived from the Ξ±-fibrils of type IV collagen. Based on the results from the <it>in vitro </it>screening, we have evaluated the ability of a 20 amino acid peptide derived from the Ξ±5 fibril of type IV collagen, pentastatin-1, to suppress vessel growth in an angioreactor-based directed <it>in vivo </it>angiogenesis assay (DIVAA). In addition, pentastatin-1 suppressed tumor growth with intraperitoneal peptide administration in a small cell lung cancer (SCLC) xenograft model in nude mice using the NCI-H82 human cancer cell line.</p> <p>Results</p> <p>Pentastatin-1 decreased the invasion of vessels into angioreactors <it>in vivo </it>in a dose dependent manner. The peptide also decreased the rate of tumor growth and microvascular density <it>in vivo </it>in a small cell lung cancer xenograft model.</p> <p>Conclusions</p> <p>The peptide treatment significantly decreased the invasion of microvessels in angioreactors and the rate of tumor growth in the xenograft model, indicating potential treatment for angiogenesis-dependent disease, and for translational development as a therapeutic agent for lung cancer.</p

    Role of Neuroimaging in the Presurgical Evaluation of Epilepsy

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    A significant minority of patients with focal epilepsy are candidates for resective epilepsy surgery. Structural and functional neuroimaging plays an important role in the presurgical evaluation of theses patients. The most frequent etiologies of pharmacoresistant epilepsy in the adult population are mesial temporal sclerosis, malformations of cortical development, cavernous angiomas, and low-grade neoplasms. High-resolution multiplanar magnetic resonance imaging (MRI) with sequences providing T1 and T2 contrast is the initial imaging study of choice to detect these epileptogenic lesions. The epilepsy MRI protocol can be individually tailored when considering the patient's clinical and electrophysiological data. Metabolic imaging techniques such as positron emission tomography (PET) and single photon emission tomography (SPECT) visualize metabolic alterations of the brain in the ictal and interictal states. These techniques may have localizing value in patients with a normal MRI scan. Functional MRI is helpful in non-invasively identifying areas of eloquent cortex

    Nivolumab versus Everolimus in Advanced Renal-Cell Carcinoma

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    This randomised phase III trial compared standard of care Everolimus with the anti-PD1 monoclonal antibody Nivolumab in previously treated patients with locally advanced inoperable or metastatic clear cell renal cancer. 810 patients were randomised to receive either Everolimus 10 mg orally daily or 3 mg/kg of Nivolumab intravenously every two weeks. Patients were treated until unacceptable toxicity or disease progression. Patients could be treated beyond progression if the investigator believed that the patient was gaining clinical benefit. The primary endpoint was overall survival. The median survival was 25 months for Nivolumab and 19.8 months for Everolimus (p=0.002). The objective response rate was higher for Nivolumab (25 versus 5%; p=&#60;0.001).The median progression free survivals were 4.6 & 4.4 months (p=0.11). Grade 3 & 4 treatment related toxicities were observed in 19 & 37% of patients on Nivolumab or Everolimus respectively. In patients with previously treated renal cell carcinoma Nivolumab produced superior survival and more tolerable treatment than Everolimus
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