Comparative evaluation of FUNGITEST and broth microdilution methods for antifungal drug susceptibility testing of Candida species and Cryptococcus neoformans

The FUNGITEST method (Sanofi Diagnostics Pasteur, Paris, France) is a microplate-based procedure for the breakpoint testing of six antifungal agents (amphotericin B, flucytosine, fluconazole, itraconazole, ketoconazole, and miconazole). We compared the FUNGITEST method with a broth microdilution test, performed according to National Committee for Clinical Laboratory Standards document M27-A guidelines, for determining the in vitro susceptibilities of 180 isolates of Candida spp. (50 C. albicans, 50 C. glabrata, 10 C. kefyr, 20 C. krusei, 10 C. lusitaniae, 20 C. parapsilosis, and 20 C. tropicalis isolates) and 20 isolates of Cryptococcus neoformans. Overall, there was 100% agreement between the methods for amphotericin B, 95% agreement for flucytosine, 84% agreement for miconazole, 83% agreement for itraconazole, 77% agreement for ketoconazole, and 76% agreement for fluconazole. The overall agreement between the methods exceeded 80% for all species tested with the exception of C. glabrata (71% agreement). The poorest agreement between the results for individual agents was seen with C. glabrata (38% for fluconazole, 44% for ketoconazole, and 56% for itraconazole) and C. tropicalis (50% for miconazole). The FUNGITEST method misclassified as susceptible 2 of 12 (16.6%) fluconazole-resistant isolates, 2 of 10 (20%) itraconazole-resistant isolates, and 4 of 8 (50%) ketoconazole-resistant isolates of several Candida spp. Further development of the FUNGITEST procedure will be required before it can be recommended as an alternative method for the susceptibility testing of Candida spp. or C. neoformans.     

High power and low cross‐polarization microstrip patch array antenna at S‐band

This article reports the design and development of high power, low cross‐polarization, and high efficiency circularly polarized microstrip patch array antenna at S‐band, proposed for Indian Regional Navigation Satellite System payload. A novel feeding mechanism for truncated corner square patch based on square coaxial line for broadband impedance matching is discussed. Sequential rotation scheme for axial ratio improvement in an array is implemented. High power handling margins in critical regions of square coaxial line for multipaction breakdown is brought out. Measured 19 dB return loss bandwidth of array antenna is 15.6%. Axial ratio of 0.78 dB over global coverage is achieved in the desired frequency band of operation. © 2011 Wiley Periodicals, Inc. Int J RF and Microwave CAE, 2012.     

The Synthesis and Antitumor Activity of the Sodium Salt and Copper (II) Complex of N-[(Trimethylamineboryl)-Carbonyl]-L-Phenylalanine Methyl Ester

Sodium N-[(trimethylamineboryl)-carbonyl]-L-phenylalanine 2 and {N-[(trimethylamineboryl)-carbonyl]-L-phenylalanyl- carbxylato}-bis-{N-[(trimethylaminebryl)-carbonyl]-L-phenylalanine} dicopper (II) 3 were successfully synthesized. The agents blocked L(1210) leukemic cell DNA and RNA syntheses by inhibiting multiple enzyme activities for nucleic acid synthesis, e.g. PRPP amido transferase, IMP dehydrogenase, DNA polymerase alpha, thymidine kinase, and TMP kinase. The copper (II) complex 3 demonstrated improved ability to inhibit L(1210) partially purified DNA topoisomerase II compared to the parent compound while the sodium salt was inactive at 100 muM.     

A kinetic and surface study of the thermal decomposition of cellulose powder in inert and oxidizing atmospheres

The thermal decomposition of fibrous cellulose powder from 275° to 340°C has been studied by thermogravimetry, scanning electron microscopy, krypton adsorption, and gas-chromatographic analysis of the gaseous products arising from pyrolysis in various oxidizing and inert atmospheres. The reaction kinetics fit a phase boundary model where the rate is controlled by the movement of an interface through a cylindrical particle and the principal kinetic parameters fit a compensation curve described previously for the decomposition of wood products. An explanation of the physical mechanism of pyrolysis is proposed which is consistent with the observed rate data and the structural changes observed by scanning electron microscopy.     

Dependence of coal liquefaction behaviour on coal characteristics. 6. Product distributions from coals treated in a continuous-flow reactor

Further experimentation with coals in a continuous-flow reactor system at 440 and 455°C confirms the significance of the previous classification of a set of coals by cluster analysis. The greatest yields of distillable products tend to be given by coals of high sulphur content in the middle of the range of the high-volatile bituminous rank classes. Yet the lowest yields of preasphaltene (toluene-insoluble material) tend to be given by coals of high rank and medium sulphur content. The group of low sulphur, low-rank coals (mostly Rocky Mountain province), in a solvent different from that used for the other groups, showed poor conversion and poor distillate yield at the higher temperature. It is concluded that this coal/solvent combination is particularly prone to retrogressive reactions, including coking.     

The determination of the enthalpy of formation and the enthalpy increment of Cd0.5Te0.5 by Calvet calorimetry

The enthalpy of formation of Cd_0.5Te_0.5(s) has been determined using a Calvet calorimeter at 785 K by direct reaction calorimetry. The heat changes were measured for the additions of Cd(s) or Te(s) from 298 K to a reaction crucible containing the other liquid metal at 785 K. Measurements were also carried out to determine the enthalpy changes due to the direct reaction of the Te(l) and Cd(l) at 785 K. The enthalpies of formation of Cd_0.5Te_0.5 calculated from the two sets of experiments were in agreement. The H_T°---H₂₉₈° values of the Cd_0.5Te_0.5 compound have also been determined in the temperature range 406–826 K by the drop method. Using ΔH_fm° at 785 K and H_T---H₂₉₈° values of Cd_0.5Te_0.5, ΔH_fm° at 298 K was determined to be −(50.349±0.510) kJ mol⁻¹.     

An investigation of 2'-deoxyribonucleoside cyanoboranes in mice for therapeutic safety

A standard acute toxicity study was undertaken to assess 2'-deoxyribonucleoside cyanoboranes for therapeutic safety. 2'-Deoxyribonucleoside cyanoboranes and related derivatives were nontoxic at doses required for anti-neoplastic and hypolipidemic activities. At higher doses (50 and 100 mg/kg/day IP for 7 days), all treated animals survived with slight reductions in total body weight and small decrements in daily food consumption. No clinical chemistry value was elevated to a magnitude suggesting onset of organ specific toxicity. However, agents appeared to modulate subpopulations of white blood cells, i.e., more lymphocytes than PMNs were present in blood from treated animals as determined by differential cell counts. This modulation is correlated with increases in granulomatous foci in the spleen and mesentery of treated animals after 7 days. The kidney was damaged only by Compound 5 at 50 and 100 mg/kg/day; Compound 5 had the most potent anti-neoplastic activity. The compounds demonstrated no in vitro toxicity against human HCT-8 ileum cells. LD(50) values were greater than 1000 mg/kg, IP, for all compounds.     

The anti-inflammatory activity of boron derivatives in rodents

Acyclic amine-carboxyboranes were effective anti-inflammatory agents in mice at 8 mg/kg x 2. These amine-carboxyboranes were more effective than the standard indomethacin at 8 mg/kg x 2, pentoxifylline at 50 mg/kg x 2, and phenylbutazone at 50 mg/kg x 2. The heterocyclic amine derivatives as well as amine-carbamoylboranes, carboalkoxyboranes, and cyanoboranes were generally less active. However, selected aminomethyl-phosphonate-N-cyanoboranes demonstrated greater than 60% reduction of induced inflammation. The boron compounds were also active in the rat induced edema, chronic arthritis, and pleurisy screens, demonstrating activity similar to the standard indomethacin. The compounds were effecive in reducing local pain and decreased the tail flick reflex to pain. The derivatives which demonstrated good anti-inflammatory activity were effective inhibitors of hydrolytic lysosomal, and proteolytic enzyme activities with IC(50) 50 values equal to (-6)M in mouse macrophages, human leukocytes, and Be Sal osteofibrolytic cells. In these same cell lines, the agents blocked prostaglandin cyclooxygenase activity with IC(50) values of (-6)M. In mouse macrophage and human leukocytes, 5' lipoxygenase activity was also inhibited by the boron derivatives with IC(50) values of 10(-6)M. These IC(50) values for inhibition of these enzyme activities are consistent with published values of known anti-inflammatory agents which target these enzymes.     

Intrusion Detection System in Wireless Sensor Network Using Conditional Generative Adversarial Network

Wireless communication networks have much data to sense, process, and transmit. It tends to develop a security mechanism to care for these needs for such modern-day systems. An intrusion detection system (IDS) is a solution that has recently gained the researcher’s attention with the application of deep learning techniques in IDS. In this paper, we propose an IDS model that uses a deep learning algorithm, conditional generative adversarial network (CGAN), enabling unsupervised learning in the model and adding an eXtreme gradient boosting (XGBoost) classifier for faster comparison and visualization of results. The proposed method can reduce the need to deploy extra sensors to generate fake data to fool the intruder 1.2–2.6%, as the proposed system generates this fake data. The parameters were selected to give optimal results to our model without significant alterations and complications. The model learns from its dataset samples with the multiple-layer network for a refined training process. We aimed that the proposed model could improve the accuracy and thus, decrease the false detection rate and obtain good precision in the cases of both the datasets, NSL-KDD and the CICIDS2017, which can be used as a detector for cyber intrusions. The false alarm rate of the proposed model decreases by about 1.827%.

     

Inhibition of neuronal calcium channels by a novel peptide spider toxin, DW13.3

Peptide toxins have proved to be useful agents, both in discriminating between different components of native calcium channel currents and in the molecular isolation and designation of their cloned channel counterparts. Here, we describe the isolation and characterization of the biochemical and physiological properties of a novel 74-amino acid peptide toxin (DW13.3) extracted from the venom of the spider Filistata hibernalis. The subtype specificity of DW13.3 was investigated using calcium channel currents recorded from two separate expression systems and several different cultured mammalian cell preparations. Overall, DW13.3 potently blocked all native calcium channel currents studied, with the exception of T-type currents recorded from GH3 cells. Examination of transiently expressed calcium channels in oocytes showed that DW13.3 had the highest affinity for alpha1A, followed by alpha1B > alpha1C > alpha1E. The affinity of DW13.3 for alpha1B N-type currents varied by 10-fold between expressed channels and native currents. Although block occurred in a similar 1:1 manner for all subtypes, DW13.3 produced a partial block of both alpha1A currents and P-type currents in cerebellar Purkinje cells. Selective occlusion of the P/Q-type channel ligand omega-conotoxin MVIIC (but not omega-agatoxin IVA) from its binding site in Purkinje neurons suggests that DW13.3 binds to a site close to the pore of the channel. The inhibition of different subtypes of calcium channels by DW13.3 reflects a common "macro" binding site present on all calcium channels except T-type.