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Stability Analysis and Optimal Control of a Vector-Borne Disease with Nonlinear Incidence
Ozair, Muhammad,Lashari, Abid Ali,Jung, Il Hyo,Okosun, Kazeem Oare Hindawi Limited 2012 Discrete dynamics in nature and society Vol.2012 No.-
<P>The paper considers a model for the transmission dynamics of a vector-borne disease with nonlinear incidence rate. It is proved that the global dynamics of the disease are completely determined by the basic reproduction number. In order to assess the effectiveness of disease control measures, the sensitivity analysis of the basic reproductive number<SUB>R0</SUB>and the endemic proportions with respect to epidemiological and demographic parameters are provided. From the results of the sensitivity analysis, the model is modified to assess the impact of three control measures; the preventive control to minimize vector human contacts, the treatment control to the infected human, and the insecticide control to the vector. Analytically the existence of the optimal control is established by the use of an optimal control technique and numerically it is solved by an iterative method. Numerical simulations and optimal analysis of the model show that restricted and proper use of control measures might considerably decrease the number of infected humans in a viable way.</P>
Robust extraction of P300 using constrained ICA for BCI applications.
Khan, Ozair Idris,Farooq, Faisal,Akram, Faraz,Choi, Mun-Taek,Han, Seung Moo,Kim, Tae-Seong P. Peregrinus Ltd.] 2012 Medical & biological engineering & computing Vol.50 No.3
<P>P300 is a positive event-related potential used by P300-brain computer interfaces (BCIs) as a means of communication with external devices. One of the main requirements of any P300-based BCI is accuracy and time efficiency for P300 extraction and detection. Among many attempted techniques, independent component analysis (ICA) is currently the most popular P300 extraction technique. However, since ICA extracts multiple independent components (ICs), its use requires careful selection of ICs containing P300 responses, which limits the number of channels available for computational efficiency. Here, we propose a novel procedure for P300 extraction and detection using constrained independent component analysis (cICA) through which we can directly extract only P300-relevant ICs. We tested our procedure on two standard datasets collected from healthy and disabled subjects. We tested our procedure on these datasets and compared their respective performances with a conventional ICA-based procedure. Our results demonstrate that the cICA-based method was more reliable and less computationally expensive, and was able to achieve 97 and 91.6% accuracy in P300 detection from healthy and disabled subjects, respectively. In recognizing target characters and images, our approach achieved 95 and 90.25% success in healthy and disabled individuals, whereas use of ICA only achieved 83 and 72.25%, respectively. In terms of information transfer rate, our results indicate that the ICA-based procedure optimally performs with a limited number of channels (typically three), but with a higher number of available channels (>3), its performance deteriorates and the cICA-based one performs better.</P>
Shiv Kumar,S. A. Khan,Ozair Alam,Rizwan Azim,Atul Khurana,M. Shaquiquzzaman,Nadeem Siddiqui,Waquar Ahsan 대한화학회 2011 Bulletin of the Korean Chemical Society Vol.32 No.7
4-Chlorotetrazolo[1,5-a]quinoxaline (III) was synthesized by azide (2+3) cycloaddition of 2,3-dichloroquinoxaline (II). Compound (III) on further refluxing with hydrazine hydrate furnished 4-hydrazinotetrazolo[1,5-a]quinoxaline (IV). Further refluxing of (IV) with different aromatic aldehydes in methanol yielded corresponding Schiff’s bases V(a-j). Various 4-aminotetrazolo[1,5-a]quinoxaline based azetidinones VII(a-j) were synthesized by stirring the compounds V(a-j), at low temperature, with equimolar mixture of chloroacetylchloride & triethylamine in dry benzene, while 4-aminotetrazolo[1,5-a]quinoxaline based thiazolidinones VIII(a-j) were synthesized by refluxing Schiff’s bases V(a-j) with thioglycolic acid in oil-bath. The structures of all the compounds were confirmed on the basis of ^1H-NMR & FT-IR spectral data. All the newly synthesized compounds were screened for in-vitro antimicrobial activity against E. coli, S. aureus, K. pneumoniae & P. aeruginosa & antifungal activity against C. albicans. Few of them have exhibited the promising activity.
Kumar, Shiv,Khan, S.A.,Alam, Ozair,Azim, Rizwan,Khurana, Atul,Shaquiquzzaman, M.,Siddiqui, Nadeem,Ahsan, Waquar Korean Chemical Society 2011 Bulletin of the Korean Chemical Society Vol.32 No.7
4-Chlorotetrazolo[1,5-a]quinoxaline (III) was synthesized by azide (2+3) cycloaddition of 2,3-dichloroquinoxaline (II). Compound (III) on further refluxing with hydrazine hydrate furnished 4-hydrazinotetrazolo[1,5-a]quinoxaline (IV). Further refluxing of (IV) with different aromatic aldehydes in methanol yielded corresponding Schiff's bases V(a-j). Various 4-aminotetrazolo[1,5-a]quinoxaline based azetidinones VII(a-j) were synthesized by stirring the compounds V(a-j), at low temperature, with equimolar mixture of chloroacetylchloride & triethylamine in dry benzene, while 4-aminotetrazolo[1,5-a]quinoxaline based thiazolidinones VIII(a-j) were synthesized by refluxing Schiff's bases V(a-j) with thioglycolic acid in oil-bath. The structures of all the compounds were confirmed on the basis of $^1H$-NMR & FT-IR spectral data. All the newly synthesized compounds were screened for in-vitro antimicrobial activity against E. coli, S. aureus, K. pneumoniae & P. aeruginosa & antifungal activity against C. albicans. Few of them have exhibited the promising activity.
Synthesis, Characterization and Antimicrobial Activity of New Thiadiazole Derivatives
Pooja Mullick,Suroor A. Khan,Surajpal Verma,Ozair Alam 대한화학회 2010 Bulletin of the Korean Chemical Society Vol.31 No.8
A series of thiadiazole derivatives were synthesized with differently substituted benzoic acids which were cyclized to give differently substituted thiazolidin-4-one. Elemental analysis, IR, 1H NMR, 13C NMR and mass spectral data confirmed the structure of the newly synthesized compounds. The derivatives of these moieties were evaluated for antimicrobial activity. Most of the synthesized compounds showed good antimicrobial activity at 200 and 100 μg/mL. Compounds showed most significant antibacterial activity against gram negative test organism Escherichia coli and most significant antifungal activity against test organisms Aspergillus niger and Candida albicans. It was observed that compounds with OCH3 at 3, 4 position of phenyl ring [5(a-l)] were more potent against microbes as compared to compounds having unsubstituted phenyl ring [4(a-l)].
Novel concepts of soft sets with applications
Muhammad Riaz,Khalid Naeem,M. Ozair. Ahmad 원광대학교 기초자연과학연구소 2017 ANNALS OF FUZZY MATHEMATICS AND INFORMATICS Vol.13 No.2
We introduce different concepts of soft sets, including soft $\sigma$-ring, soft algebra, and soft $\sigma$-algebra. We present different types of set functions, including soft finitely sub-additive, soft countably sub-additive, soft finitely additive, soft countably additive and soft monotone. We study the concept of soft outer measure and soft Lebesgue outer measure. We also describe interesting applications of soft mappings to decision-making.
Synthesis, Characterization and Antimicrobial Activity of New Thiadiazole Derivatives
Mullick, Pooja,Khan, Suroor A.,Verma, Surajpal,Alam, Ozair Korean Chemical Society 2010 Bulletin of the Korean Chemical Society Vol.31 No.8
A series of thiadiazole derivatives were synthesized with differently substituted benzoic acids which were cyclized to give differently substituted thiazolidin-4-one. Elemental analysis, IR, $^1H$ NMR, $^{13}C$ NMR and mass spectral data confirmed the structure of the newly synthesized compounds. The derivatives of these moieties were evaluated for antimicrobial activity. Most of the synthesized compounds showed good antimicrobial activity at 200 and $100\;{\mu}g/mL$. Compounds showed most significant antibacterial activity against gram negative test organism Escherichia coli and most significant antifungal activity against test organisms Aspergillus niger and Candida albicans. It was observed that compounds with $OCH_3$ at 3, 4 position of phenyl ring [5(a-l)] were more potent against microbes as compared to compounds having unsubstituted phenyl ring [4(a-l)].
Thiadiazole Derivatives as Potential Anticonvulsant Agents
Mullick, Pooja,Khan, Suroor A.,Verma, Surajpal,Alam, Ozair Korean Chemical Society 2011 Bulletin of the Korean Chemical Society Vol.32 No.3
A series of thiadiazole derivatives were synthesized with differently substituted benzoic acids which were cyclized to give differently substituted thiazolidin-4-one. Elemental analysis, IR, $^1H$ NMR, $^{13}C$ NMR and mass spectral data confirmed the structure of the synthesized compounds. The derivatives of these moieties were evaluated for anticonvulsant activity by MES model and neurotoxicity by rotarod method. The synthesized compounds showed good potential for anticonvulsant activity besides this, the compounds also showed neurotoxic effect. It was observed that compounds with $OCH_3$ at 3, 4 position of phenyl ring [5(a-l)] showed less protection against convulsions as compared to compounds having unsubstituted phenyl ring [4(a-l)].