195 research outputs found
An Econometric Analysis of Bombay Stock Exchange: Annual Returns Analysis, Day-of-the-Week Effect and Volatility of Returns
This paper investigates the presence of day-of-the-week effect, returns volatility and analyzes the annual returns of Bombay Stock Exchange. A set of parametric and nonparametric tests is used to test equality of mean returns and standard deviations of the returns across the-days-of-the-week. To supplement this analysis, graphical representation of the index annual percentage changes was explored. The results contradict the presence of the-day-of-the- week but indicate insignificant daily returns volatility in most of these Markets. The stock exchanges experienced enormous growth between 2001 and 2010. The result of the Levenes test value for Bombay Stock Exchange was 0.847 which concludes that the daily return seasonalities are not accompanied by any volatility seasonality and investing on low (high) return weekday does not necessarily mean that risk is also low or high and Index that has marginally significant Levenes statistic. Key words: Volatility of Returns, Bombay Stock Exchange, Day-of-week effec
Performance evaluation of botnet detection using machine learning techniques
Cybersecurity is seriously threatened by Botnets, which are controlled networks of compromised computers. The evolving techniques used by botnet operators make it difficult for traditional methods of botnet identification to stay up. Machine learning has become increasingly effective in recent years as a means of identifying and reducing these hazards. The CTU-13 dataset, a frequently used dataset in the field of cybersecurity, is used in this study to offer a machine learning-based method for botnet detection. The suggested methodology makes use of the CTU-13, which is made up of actual network traffic data that was recorded in a network environment that had been attacked by a botnet. The dataset is used to train a variety of machine learning algorithms to categorize network traffic as botnet-related/benign, including decision tree, regression model, naïve Bayes, and neural network model. We employ a number of criteria, such as accuracy, precision, and sensitivity, to measure how well each model performs in categorizing both known and unidentified botnet traffic patterns. Results from experiments show how well the machine learning based approach detects botnet with accuracy. It is potential for use in actual world is demonstrated by the suggested system’s high detection rates and low false positive rates
An Efficient Image Fusion of Visible and Infrared Band Images using Integration of Anisotropic Diffusion and Discrete Wavelet Transform
Image fusion is a technique that combines two source images to generate more informative target image. It plays a vital role in medical image investigation, military, navigation, etc. visible images offer efficient texture detail with high spatial resolution. In contrast, based on the radiation difference infrared images are able to differentiate target from their background. There are many algorithms that helps in preserving the edges of image like Bilateral filter, anisotropic diffusion (ADF). This paper integrates Anisotropic Diffusion and Karhunen-Loeve (KL)Transformation with discrete wavelet transform (DWT). In proposed Method, DWT decomposes into four sub-bands. ADF is applied on approximation sub-band and absolute maximum selection is applied on other three sub-bands. ADF decomposes the image into detailed layer and base layer. Base layer and Detailed layer are calculated using Kl- Transformation and linear combination respectively. Once fusion is done, inverse DWT is applied on all sub-bands. The experimental outcomes depict that the offered approach result with sharp edges of the image. The proposed algorithm is evaluated on standard dataset Like Duine_Sequence, Tree_sequence, Street dataset. Standard metrics like Average Gradients and Spatial Frequency metrics are used to evaluate the performance of the image
PULSATILE RELEASE OF KETOPROFEN FROM COMPRESSION COATED TABLETS USING EUDRAGIT® POLYMERS
Objective: The objective of the present research work is to develop compression coated tablet of ketoprofen as a pulsatile release system for treatment of rheumatoid arthritis.Methods: Core tablets of ketoprofen were prepared using the wet granulation method and evaluated for appearance, hardness, friability, weight variation, thickness, disintegration time and % drug release. Core tablets were coated with Eudragit S100 and Eudragit L100 by compression coating method to achieve desired lag time. The blends of core and coating materials were evaluated for bulk density, tapped density, Hausner's ratio, % Compressibility index and angle of repose. Compression coated tablets were evaluated for appearance, hardness, friability, weight variation, thickness and % drug release.Results: Core tablets, as well as compression coated tablets, showed acceptable Pharmaco technical properties. Optimized core tablets were disintegrated within 15s due to the effectiveness of super disintegrant, sodium starch glycolate. Dissolution studies of compression coated tablets in media with different pH (1.2, 6.8, and 7.4) showed that drug release could be modulated by changing the concentration of EudragitL100 and Eudragit S100. The optimized batch exhibited 80% drug release up to 6 h with a 4 h lag time. Stability study of the optimized formulation indicated no significant change in appearance, physical parameters, drug content and drug release profile at accelerated conditions for two months.Conclusion: compression coated tablet of ketoprofen was successfully developed to achieve burst drug release after specific lag time.Keywords: Chronomodulated drug delivery, Pulsatile release, Compression coated tablets, Lag tim
Statistical Study of Plasmoids associated with post-CME Current Sheet
We investigate the properties of plasmoids observed in the current sheet
formed after an X-8.3 flare followed by a fast CME eruption on September 10,
2017 using Extreme Ultraviolet (EUV) and white-light coronagraph images. The
main aim is to understand the evolution of plasmoids at different
spatio-temporal scales using existing ground- and space-based instruments. We
identified the plasmoids in current sheet observed in the successive images of
{\it Atmospheric Imaging Assembly} (AIA) and white-light coronagraphs, K-Cor
and LASCO/C2. We found that the current sheet is accompanied by several
plasmoids moving upwards and downwards. Our analysis showed that the downward
and upward moving plasmoids have average width of 5.92 Mm and 5.65 Mm,
respectively in the AIA field of view (FOV). However, upward moving plasmoids
have average width of 64 Mm in the K-Cor which evolves to a mean width of 510
Mm in the LASCO/C2 FOV. Upon tracking the plasmoids in successive images, we
observe that downward and upward moving plasmoids have average speeds of
272 km s and 191 km s respectively in the EUV
passbands. We note that the plasmoids become super-Alfv\'enic when they reach
at LASCO FOV. Furthermore, we estimate that the null-point of the current sheet
at 1.15 R where bidirectional plasmoid motion is observed. We
study the width distribution of plasmoids formed and notice that it is governed
by a power law with a power index of -1.12. Unlike previous studies there is no
difference in trend for small and large scale plasmoids. The presence of
accelerating plasmoids near the neutral point indicates a longer diffusion
region as predicted by MHD models.Comment: Accepted for the publication in Astronomy & Astrophysics (A&A). 10
pages, 11 figures. Animations can be found at
https://www.dropbox.com/sh/g0wjq2awxai1hy4/AAClkTHPFkTa5JU-Zulf9a75a?dl=
Development and validation of dissolution method for carvedilol compression-coated tablets
The present study describes the development and validation of a dissolution method for carvedilol compression-coated tablets. Dissolution test was performed using a TDT-06T dissolution apparatus. Based on the physiological conditions of the body, 0.1N hydrochloric acid was used as dissolution medium and release was monitored for 2 hours to verify the immediate release pattern of the drug in acidic pH, followed by pH 6.8 in citric-phosphate buffer for 22 hours, to simulate a sustained release pattern in the intestine. Influences of rotation speed and surfactant concentration in medium were evaluated. Samples were analysed by validated UV visible spectrophotometric method at 286 nm. 1% sodium lauryl sulphate (SLS) was found to be optimum for improving carvedilol solubility in pH 6.8 citric-phosphate buffer. Analysis of variance showed no significant difference between the results obtained at 50 and 100 rpm. The discriminating dissolution method was successfully developed for carvedilol compression-coated tablets. The conditions that allowed dissolution determination were USP type I apparatus at 100 rpm, containing 1000 ml of 0.1N HCl for 2 hours, followed by pH 6.8 citric-phosphate buffer with 1% SLS for 22 hours at 37.0 ± 0.5 ºC. Samples were analysed by UV spectrophotometric method and validated as per ICH guidelines.O presente estudo descreve o desenvolvimento e a validação de método de dissolução para comprimidos revestidos de carvedilol. O teste de dissolução foi efetuado utilizando-se o aparelho para dissolução TDT-06T. Com base nas condições fisiológicas do organismo, utilizou-se ácido clorídrico 0,1 N como meio de dissolução e a liberação foi monitorada por 2 horas para se verificar o padrão de liberação imediata do fármaco em condições de pH baixo, seguidas por pH 6,8 em tampão cítrico-fosfato por 22 horas, para simular o padrão de liberação controlada no intestino. Avaliou-se a influência da velocidade de rotação e a concentração de tensoativo no meio. As amostras foram analisadas por método espectrofotométrico UV-visível validado, em 286 nm. O laurilsulfato sódico a 1% (SLS) mostrou-se ótimo para aumentar a solubilidade do carvedilol em pH 6,8 em tampão cítrico-fosfato. A análise da variância não mostrou diferença significativa entre os resultados obtidos a 50 e a 100 rpm. O método da dissolução discriminante foi desenvolvido com sucesso para os comprimidos revestidos de carvedilol. As condições que permitiram a determinação da dissolução foram: aparelho USP tipo I a 100 rpm, contendo 1000 mL de HCL 0,1 N por 2 horas, seguido de pH 6,8 com tampão cítrico-fosfato, com 1% de SLS por 22 horas a 37,0 ± 0,5 ºC. Amostras foram analisadas por método espectrofotométrico e validadas pelas normas ICH
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