507 research outputs found

    Evaluation of anticonvulsant activity of amlodipine in albino rats

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    Background: The objective of the study was to evaluate the anticonvulsant activity of amlodipine in albino rats.Methods: Anticonvulsant activity of amlodipine was done in three graded doses (1 mg/kg, 2 mg/kg, 4 mg/kg), and combination group with low dose of amlodipine (1 mg/kg) and standard drug (phenytoin) in maximal electroshock seizures (MES) experimental animal model.Results: Amlodipine in dose of 2, 4 mg/kg showed dose dependent significant anticonvulsant effect and combination of low dose amlodipine and low dose of standard drug also showed significant anticonvulsant effect in MES model.Conclusions: Amlodipine is having anticonvulsant activity and also potentiated the anticonvulsant effect of phenytoin in MES model.

    Faster Acquisition Technique for Software-defined GPS Receivers

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    Acquisition is a most important process and a challenge task for identifying visible satellites, coarse values of carrier frequency, and code phase of the satellite signals in designing software defined Global positioning system (GPS) receiver. This paper presents a new, simple, efficient and faster GPS acquisition via sub-sampled fast Fourier transform (ssFFT). The proposed algorithm exploits the recently developed sparse FFT (or sparse IFFT) that computes in sub-linear time. Further it uses the property of fourier transforms (FT): Aliasing a signal in the time domain corresponds to sub-sampling it in the frequency domain, and vice versa. The ssFFT is an FFT algorithm that computes sub-sampled version of the data by an integer factor ‘d’, and hence, the computational complexity is proportionately reduced by a factor of ‘d log d’ compared to conventional FFT-based algorithms for any length of the input GPS signal. The simulation results show that the proposed ssFFT based GPS acquisition computation is 8.5571 times faster than the conventional FFT-based acquisition computation time. The implementation of this method in an FPGA provides very fast processing of incoming GPS samples that satisfies real-time positioning requirements.Defence Science Journal, Vol. 65, No. 1, January 2015, pp.5-11, DOI:http://dx.doi.org/10.14429/dsj.65.557

    POLARIZATION-COUPLED FERROELECTRIC UNPOLARUNCTION MEMORY AND ENERGY STORAGE DEVICE

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    A memory device is provided. The memory device includes a plurality of memory cells and a controller to write data to and read data from the memory cells. Each memory cell includes a first semiconductor material having a spontaneous polarization, a resistive ferroelectric material having a switchable spontaneous polarization, and a second semiconductor material having a spontaneous polarization, the resistive ferroelectric material being positioned between and in contact with the first and second semiconductor materials. The memory device can be configured to store energy that can be released by applying a voltage pulse to the memory device

    A Novel Classifier for Digital Angle Modulated Signals

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    The identification of the modulation type of an arbitrary noisy signal is necessary in various applications including signal confirmation, interference identification, spectrum management, electronic support systems in warfare, electronic counter-counter measures etc. In this paper a novel classification scheme based on the variance of instantaneous frequency is proposed to discriminate between noisy M-ary Phase Shift Keyed (MPSK) and M-ary Frequency Shift Keyed (MFSK) signals. In the proposed method, the received signal is passed through a pair of band pass filters and the ratio of variances of instantaneous frequency of the filter outputs is used as a decision statistic. Analytic expressions are developed for the decision statistic. These expressions show that a high degree of discrimination is possible between PSK and FSK signals even at a carrier-to-noise ratio (CNR) of 0 dB. Simulation studies have been carried out and the theoretical predictions are validated

    The minimum mean monopoly energy of a graph

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    The motivation for the study of the graph energy comes from chemistry, where the research on the so-called total pi - electron energy can be traced back until the 1930s. This graph invariant is very closely connected to a chemical quantity known as the total pi - electron energy of conjugated hydro carbon molecules. In recent times analogous energies are being considered, based on Eigen values of a variety of other graph matrices. In 1978, I.Gutman [1] defined energy mathematically for all graphs. Energy of graphs has many mathematical properties which are being investigated. The ordinary energy of an undirected simple finite graph G is defined as the sum of the absolute values of the Eigen values of its associated matrix. i.e. if mu(1), mu(2), ..., mu(n) are the Eigen values of adjacency matrix A(G), then energy of graph is Sigma(G) = Sigma(n)(i=1) vertical bar mu(i)vertical bar Laura Buggy, Amalia Culiuc, Katelyn Mccall and Duyguyen [9] introduced the more general M-energy or Mean Energy of G is then defined as E-M (G) = Sigma(n)(i=1)vertical bar mu(i) - (mu) over bar vertical bar, where (mu) over bar vertical bar is the average of mu(1), mu(2), ..., mu(n). A subset M subset of V (G), in a graph G (V, E), is called a monopoly set of G if every vertex v is an element of (V - M) has at least d(v)/2 neighbors in M. The minimum cardinality of a monopoly set among all monopoly sets in G is called the monopoly size of G, denoted by mo(G) Ahmed Mohammed Naji and N.D.Soner [7] introduced minimum monopoly energy E-MM [G] of a graph G. In this paper we are introducing the minimum mean monopoly energy, denoted by E-MM(M) (G), of a graph G and computed minimum monopoly energies of some standard graphs. Upper and lower bounds for E-MM(M) (G)are also established.Publisher's Versio

    Development Of Antirigging Voting System Using Biometrics Based On Adharcard Numbering

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    Now a days voting process is exercised by using EVM(Electronic voting machine). In this paper we present  and use implementation is to implement the development of anti rigging voting system using finger print .The purpose of the project and implementation is to provide a secured and reliable environment to the customers is to electing the candidates by using the intelligent electronic voting machine by providing a unique identity to every user using the FINGER PRINT identification technology. Here in this project and implementation we are going provide the at most security since it is taking the FINGER PRINTS as the authentication for EVM. Intelligent EVM is an Embedded based project and implementation. It involves microcontroller and interfaces. Intelligent EVM has been specially designed to collect, record, store, count and display cent percent accurately. It has got two units control unit and ballot unit. It has “DISPLAY” section that will display the number of votes to respective candidate at the end of the poll

    Efficient removal of methyl orange using magnesium oxide nanoparticles loaded onto activated carbon

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    ABSTRACT. In this work, an activated carbon composite made with magnesium oxide nanoparticles (MgONP-AC) was effectively utilized for methyl orange (MO) adsorption. The effect of pH (6-10), mass of MgONP-AC (0.1-0.3 g/L), initial MO concentration (10-30 mg/L), and temperature (283-323 K) on MO removal was investigated using a central rotatable composite experimental design based on the response surface technique (RSM) at an equilibrium agitation period of 60 min. The studies predicted the optimal MO removal of 98.99% at pH 7.68, MgONP-AC dosage of 0.24 g/L, and starting MO concentration of 15 mg/L, and temperature of 313 K. Furthermore, an artificial neural network (ANN) was utilized to simulate MO adsorption, and it properly predicted MO removal using mean squared error (MSE) and R2 for the testing data. The ANN predicts a maximum removal of 99.63% with ANN with R2 = 0.9926. The kinetic results suited the pseudo-second order kinetic equation, and the data from the equilibrium investigations corresponded well with the Langmuir isotherm (maximum uptake capacity qmax = 346 mg/g). Endothermic, spontaneous, and physical adsorption were discovered during the thermodynamic investigations.   KEY WORDS: Adsorption, Artificial neural network, Experimental design, isotherms, Kinetics, Methyl orange, MgONP-AC   Bull. Chem. Soc. Ethiop. 2022, 36(3), 531-544.                                                                DOI: https://dx.doi.org/10.4314/bcse.v36i3.

    MASS TRANSFER IN PACKED BEDS IN ANNULI ELECTROLYTIC REDOX REACTIONS

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    Development, implementation, and analysis of adverse drug reaction monitoring system in a rural tertiary care teaching hospital in Narketpally, Telangana

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    Background: Adverse drug reactions (ADR) are the fourth leading cause of mortality and a great concern in therapeutics. Pharmacovigilance is more important in India as the health care system is inadequate with poor doctor-patient ratio, high incidence of self-medication, and presence of counterfeit drugs. The present study was conducted with the aim of analyzing the pattern of ADR occurring in a rural tertiary care hospital with a newly established pharmacovigilance center and to identify the most frequent ADRs, common drugs implicated and severity of reactions.Methods: A non-interventional observational prospective study was conducted over a year. The red boxes for dropping the filled yellow ADR forms were installed in all the wards and outpatient departments. Additional information and missing data were obtained personally by either consulting the physician or through case sheets.Results: The most common class of drugs implicated in the causation of ADRs was antimicrobials (52%), followed by drugs acting on the central nervous system. The most commonly observed ADRs were dermatological Type B reactions. The majority of the reactions belonged to possible or probable category, but no reaction was categorized as definite.Conclusion: Dermatological reactions are the most common ADR occurring in our hospital and antimicrobials are the most common causative drugs. The reporting rate was adequate, and there is still a need for increasing the awareness and knowledge about ADR reporting system and pharmacovigilance for promoting the safe use of drugs

    UPLC SEPARATION ANALYSIS OF EMTRICITABINE, TENOFOVIR, COBICISTAT AND ELVITEGRAVIR FROM THEIR DEGRADATION PRODUCTS

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    Objective: A simple, rapid, accurate and precise stability-indicating UPLC analytical method has been developed and validated for the quantitative analysis of Emtricitabine, Tenofovir, Cobicistat and Elvitegravir in bulk drugs and combined dosage forms.Methods: ACE C18 (50 mm x 3 mm, 2µ). The column temperature was maintained at 30oC and run time 8 min. The mobile phase was a mixture of Mobile Phase: A–0.1% TFA in Acetonitrile, B–0.1% TFA in Milli-Q-water. The injection volume of samples was 20μl. UV detection was carried out using a UV-PDA detector at 240 nm. The validation of this method was done as per ICH guidelines.Results: The retention times were observed as 1.46, 3.59, 4.13, 4.64 min for Emtricitabine, Tenofovir disoproxyl fumarate, Cobicistat, and Elvitegravir respectively. Linearity ranges were observed 150-275 µg/ml Emtricitabine, 250-375 µg/ml Tenofovir, 100-225 µg/ml Cobicistat and 100-225 µg/ml Elvitegravir. Relative Standard Deviation did not exceed 2.Conclusion: The newly developed UPLC method for separation of different degradation products along with the pure drugs were found to be capable of giving faster retention times while still maintaining good resolution than that achieved with conventional HPLC. The decreased flow rate 0.4 ml/min, in UPLC indicate more economical. This method exhibited an excellent performance in terms of sensitivity and speed. The results of stress testing undertaken according to the ICH guidelines reveal that the method is specific and stability-indicating. The proposed method has the ability to separate these drugs from their degradation products in tablet dosage forms and hence can be applied to the analysis of routine quality control samples and samples obtained from stability studies.Keywords: Stability indicating assay, RP-UPLC, Emtricitabine, Tenofovir, Cobicistat, Elvitegravir, Forced degradation studie
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