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991.
Kuznetsova T. F. Ivanets A. I. Savka Yu. D. Kul’bitskaya L. V. 《Protection of Metals and Physical Chemistry of Surfaces》2020,56(1):30-37
Protection of Metals and Physical Chemistry of Surfaces - Mesoporous titanosilicate structures synthesized by the sol–gel method using the cetylpyridinium template at different Ti/Si ratios... 相似文献
992.
Russian Engineering Research - On the profilograms obtained for real surfaces machined by different methods, the microprojections resemble elements of sinusoids and cosinusoids. Accordingly, it is... 相似文献
993.
Rahul Sasidharan Pillai Matteo Frasnelli Vincenzo M. Sglavo 《Ceramics International》2018,44(2):1328-1333
The present work focuses on the fabrication of βTCP (β-tricalcium phosphate) and HA/βTCP (hydroxyapatite/β-tricalcium phosphate) composite coatings by plasma spraying. The starting powders were produced via solid-state method using 2 wt% MgO to stabilize βTCP phase. The synthesized powders were preliminarily granulated to be used by the plasma spray process. Coatings obtained on titanium substrates are uniform and well adherent but due to the high temperature and cooling rate typical for plasma spraying process, βTCP phase is almost totally transformed into the α allotrope. Thermal treatment at 800 °C allows the reconversion of the phase αTCP→ βTCP. It is therefore possible to produce coatings with tuneable dissolution properties by selecting the proper initial powder mixture and the specific thermal treatment. 相似文献
994.
Crossover designs are an extremely useful tool to investigators, and group sequential methods have proven highly proficient at improving the efficiency of parallel group trials. Yet, group sequential methods and crossover designs have rarely been paired together. One possible explanation for this could be the absence of a formal proof of how to strongly control the familywise error rate in the case when multiple comparisons will be made. Here, we provide this proof, valid for any number of initial experimental treatments and any number of stages, when results are analyzed using a linear mixed model. We then establish formulae for the expected sample size and expected number of observations of such a trial, given any choice of stopping boundaries. Finally, utilizing the four-treatment, four-period TOMADO trial as an example, we demonstrate that group sequential methods in this setting could have reduced the trials expected number of observations under the global null hypothesis by over 33%. 相似文献
995.
996.
Carbohydrates and their conjugates play important roles in many biological processes including fertilization, differentiation, development, immune response, and infection. Their activities are largely dependent on the properties of terminal mono‐ or disaccharides. Galactose, mannose, fucose, glucose, sialic acid, etc., are commonly used as powerful scaffolds installed on drug molecules for targeting specific tissues including brain, liver, and cancers, and as epitopes for enhancing the targeting of various vaccines. This review focuses on the influence of their structural variations, including changes in sugar type, substituent groups and their positions, as well as length of linker portion, on the targeting of drugs or their efficacy. Particular attention is paid to the targeting properties of mono‐ and disaccharides applied in drug design and discovery. 相似文献
997.
998.
Prof. Michael Murray Dr. Ariane Roseblade Dr. Yongjuan Chen Kirsi Bourget Dr. Tristan Rawling 《ChemMedChem》2020,15(2):247-255
Targeting the tumor cell mitochondrion could produce novel anticancer agents. We designed an aryl−urea fatty acid ( 1 g ; 16({[4-chloro-3-(trifluoromethyl)phenyl]carbamoyl}amino)hexadecanoic acid) that disrupted the mitochondrion and decreased MDA-MB-231 breast cancer cell viability. To optimize the aryl−ureas the present study evaluated mitochondrial targeting by 1 g analogues containing alkyl chains between 10–17 carbons. Using the dye JC-1, the C12−C17 analogues efficiently disrupted the mitochondrial membrane potential (IC50s 3.5±1.2 to 7.6±1.1 μM) and impaired ATP production; shorter analogues were less active. 7-Aminoactinomycin D/annexin V staining and flow cytometry showed that these agents activated the killing mechanisms of necrosis and apoptosis to varying extents (7-aminoactinomycin D/annexin V staining ratios 4.3–6.0). Indeed, 1 g and its C17 analogue preferentially activated necrosis and apoptosis, respectively (ratios 2.1 and 16). Taken together, alkyl chain length is a determinant of mitochondrial targeting by aryl−ureas and can be varied to develop analogues that activate apoptosis or necrosis in a regulated fashion. 相似文献
999.
Chalykh A. E. Petrova T. F. Antipov Yu. V. Aliev A. D. Matveev V. V. Telitsyna M. Yu. 《Protection of Metals and Physical Chemistry of Surfaces》2020,56(1):20-29
Protection of Metals and Physical Chemistry of Surfaces - The degree of crystallinity of carbon fibers (CFs) of different manufacturers has been determined by means of the Raman scattering method.... 相似文献
1000.
El Aoufir Y. Sebhaoui J. Lgaz H. El Bakri Y. Guenbour A. Bentiss F. Zarrouk A. Essassi E.M. Oudda H. 《Protection of Metals and Physical Chemistry of Surfaces》2020,56(5):1027-1038
Protection of Metals and Physical Chemistry of Surfaces - The inhibiting effect of benzimidazole derivate (DBI) on corrosion of carbon steel (CS) at temperature range of 303–333 K was... 相似文献