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1.
Springerplus ; 5(1): 2111, 2016.
Article in English | MEDLINE | ID: mdl-28074171

ABSTRACT

INTRODUCTION: The comprehension of legacy codes is difficult to understand. Various commercial reengineering tools are available that have unique working styles, and are equipped with their inherent capabilities and shortcomings. The focus of the available tools is in visualizing static behavior not the dynamic one. Therefore, it is difficult for people who work in software product maintenance, code understanding reengineering/reverse engineering. Consequently, the need for a comprehensive reengineering/reverse engineering tool arises. We found the usage of Imagix 4D to be good as it generates the maximum pictorial representations in the form of flow charts, flow graphs, class diagrams, metrics and, to a partial extent, dynamic visualizations. CASE DESCRIPTION AND EVOLUTION: We evaluated Imagix 4D with the help of a case study involving a few samples of source code. The behavior of the tool was analyzed on multiple small codes and a large code gcc C parser. Large code evaluation was performed to uncover dead code, unstructured code, and the effect of not including required files at preprocessing level. The utility of Imagix 4D to prepare decision density and complexity metrics for a large code was found to be useful in getting to know how much reengineering is required. At the outset, Imagix 4D offered limitations in dynamic visualizations, flow chart separation (large code) and parsing loops. CONCLUSION: The outcome of evaluation will eventually help in upgrading Imagix 4D and posed a need of full featured tools in the area of software reengineering/reverse engineering. It will also help the research community, especially those who are interested in the realm of software reengineering tool building.

2.
ScientificWorldJournal ; 2013: 267691, 2013.
Article in English | MEDLINE | ID: mdl-24311972

ABSTRACT

Region duplication forgery detection is a special type of forgery detection approach and widely used research topic under digital image forensics. In copy move forgery, a specific area is copied and then pasted into any other region of the image. Due to the availability of sophisticated image processing tools, it becomes very hard to detect forgery with naked eyes. From the forged region of an image no visual clues are often detected. For making the tampering more robust, various transformations like scaling, rotation, illumination changes, JPEG compression, noise addition, gamma correction, and blurring are applied. So there is a need for a method which performs efficiently in the presence of all such attacks. This paper presents a detection method based on speeded up robust features (SURF) and hierarchical agglomerative clustering (HAC). SURF detects the keypoints and their corresponding features. From these sets of keypoints, grouping is performed on the matched keypoints by HAC that shows copied and pasted regions.

3.
Med Oncol ; 30(4): 744, 2013 Dec.
Article in English | MEDLINE | ID: mdl-24135867

ABSTRACT

Current salvage regimens achieve complete remission (CR) in about a third of adults with relapsed/refractory acute lymphoblastic leukemia (ALL), and this represents a major barrier for performing allogeneic hematopoietic stem cell transplant (HSCT), the only potentially curative treatment. We conducted in adults with first relapse of ALL, a prospective clinical trial with intensive regimen derived from the pediatric Berlin-Frankfurt-Muenster-85 protocol, with addition of a continuous infusional multi-agent chemotherapy in phase II induction followed by consolidation with alternating monthly cycles. Objectives of this study included CR rate, leukemia-free survival (LFS) and toxicity of the regimen in adults. We report the outcome of 19 patients (19-51 years of age) treated prospectively on the study, as well as a subsequent cohort of 31 patients (18-53 years of age) treated off the study. Thirteen of 19 (68%) patients from the initial prospective study achieved CR, and the median overall survival (OS) of these 13 CR patients was 10.3 months. The median OS and LFS of all 19 patients were 5.6 and 4.3 months, respectively. The regimen was well tolerated, and no grade 4 non-hematological toxicity was observed. Of the 31 patients treated off the study and analyzed retrospectively, 16 (52%) achieved CR. After including all 50 patients, the CR rate was 58%. The regimen used in this trial appears to be feasible and effective salvage therapy option for adult patients younger than age 55 with relapsed ALL, produced a high CR rate and could facilitate subsequent allogeneic HSCT.


Subject(s)
Neoplasm Recurrence, Local/drug therapy , Neoplasm Recurrence, Local/therapy , Precursor Cell Lymphoblastic Leukemia-Lymphoma/drug therapy , Precursor Cell Lymphoblastic Leukemia-Lymphoma/therapy , Adolescent , Adult , Disease-Free Survival , Hematopoietic Stem Cell Transplantation/methods , Humans , Middle Aged , Neoplasm Recurrence, Local/mortality , Precursor Cell Lymphoblastic Leukemia-Lymphoma/mortality , Prospective Studies , Remission Induction , Retrospective Studies , Salvage Therapy/methods , Treatment Outcome , Young Adult
4.
Indian J Pharmacol ; 44(6): 672-7, 2012.
Article in English | MEDLINE | ID: mdl-23248392

ABSTRACT

OBJECTIVE: The objective was to investigate the antiurolithiatic and antioxidant activity of ethanolic extract of Hordeum vulgare seeds (EHV) on ethylene glycol-induced urolithiasis in Wistar albino rats. MATERIALS AND METHODS: Urolithiasis was produced in Wistar albino rats by adding 0.75% v/v ethylene glycol (EG) to drinking water for 28 days. The ethanolic extract of Hordeum vulgare seeds (EHV) was assessed for its curative and preventive action in urolithiasis. In preventive treatment, the EHV given from 1st day to 28th day, while in the curative regimen, the EHV was given from 15th day to 28th day. Various renal functional and injury markers such as urine volume, calcium, phosphate, uric acid, magnesium, urea, and oxalate were evaluated using urine, serum, and kidney homogenate. Antioxidant parameters such as lipid peroxidation, superoxide dismutase, and catalase were also determined. RESULTS: The EHV treatment (both preventive and curative) increased the urine output significantly compared to the control. The EHV treatment significantly reduced the urinary excretion of the calcium, phosphate, uric acid, magnesium, urea, and oxalate and increased the excretion of citrate compared to EG control. The increased deposition of stone forming constituents in the kidneys of calculogenic rats were significantly lowered by curative and preventive treatment with EHV. It was also observed that the treatment with EHV produced significant decrease in lipid peroxidation, and increased levels of superoxide dismutase and catalase. CONCLUSION: These results suggest the usefulness of ethanolic extract of Hordeum vulgare seeds as an antiurolithiatic and antioxidant agent.


Subject(s)
Antioxidants/therapeutic use , Hordeum , Phytotherapy , Plant Extracts/therapeutic use , Urolithiasis/therapy , Animals , Antioxidants/pharmacology , Catalase/metabolism , Ethylene Glycol , Female , Male , Malondialdehyde/metabolism , Medicine, Ayurvedic , Mice , Plant Extracts/pharmacology , Rats , Rats, Wistar , Seeds , Superoxide Dismutase/metabolism , Urolithiasis/chemically induced , Urolithiasis/metabolism , Urolithiasis/pathology
5.
Article in English | MEDLINE | ID: mdl-22525033

ABSTRACT

A simple, rapid, cost effective and extractive UV spectrophotometric method was developed for the determination of Gemcitabine HCl (GMCT) in bulk drug and pharmaceutical formulation. It was based on UV spectrophotometric measurements in which the drug reacts with gold nanoparticles (AuNP) and changes the original colour of AuNP and forms a dark blue coloured solution which exhibits absorption maximum at 688nm. The apparent molar absorptivity and Sandell's sensitivity coefficient were found to be 3.95×10(-5)lmol(-1)cm(-1) and 0.060µgcm(-2) respectively. Beer's law was obeyed in the concentration range of 2.0-40µgml(-1). This method was tested and validated for various parameters according to ICH guidelines. The proposed method was successfully applied for the determination of GMCT in pharmaceutical formulation (parental formulation). The results demonstrated that the procedure is accurate, precise and reproducible (relative standard deviation <2%). As it is simple, cheap and less time consuming, it can be suitably applied for the estimation of GMCT in dosage forms.


Subject(s)
Antineoplastic Agents/analysis , Chemistry Techniques, Analytical/methods , Deoxycytidine/analogs & derivatives , Gold/chemistry , Metal Nanoparticles/chemistry , Nanotechnology/methods , Antineoplastic Agents/chemistry , Deoxycytidine/analysis , Deoxycytidine/chemistry , Injections , Light , Limit of Detection , Metal Nanoparticles/ultrastructure , Particle Size , Pharmaceutical Preparations , Reproducibility of Results , Scattering, Radiation , Solutions , Spectrophotometry, Ultraviolet , Spectroscopy, Fourier Transform Infrared , Gemcitabine
6.
Biomed Chromatogr ; 25(4): 524-30, 2011 Apr.
Article in English | MEDLINE | ID: mdl-20648686

ABSTRACT

A simple, rapid and sensitive method has been developed and validated for the determination of pramipexole in rat plasma by using gas chromatography mass spectrometry. The lower limit of quantification (LLOQ) is superior to the other reported LC-MS/MS methods. After being made alkaline with NaOH, plasma samples (0.1 mL) were subjected to liquid-liquid extraction using methyl-t-butyl ether. Analytes were determined using electron impact ionization in a single quadrupole mass spectrometer. GC/MS was performed in the selected ion monitoring mode using target ions at m/z 211, 212 and 152 for pramipexole and m/z 194 and 165 for caffeine as internal standard. A linear calibration curve was plotted over the range of 20-1000 pg/mL for pramipexole (r(2) > 0.996). The LLOQ was 20.0 pg/mL, respectively, which offered high sensitivity and selectivity enough for bioanalytical investigation. Inter- and intraday precisions ranged from 0.3 to 8.8% and from 0.9 to 11.33%, respectively. The recovery of pramipexole from plasma ranged from 82.4 ± 7.1 to 87.8 ± 5.7%. The method fulfills all standards required for bioanalytical methods and can be successfully applied to a pharmacokinetic study of pramipexole in rats.


Subject(s)
Benzothiazoles/blood , Gas Chromatography-Mass Spectrometry/methods , Animals , Benzothiazoles/pharmacokinetics , Caffeine/analysis , Dopamine Agonists/blood , Dopamine Agonists/pharmacokinetics , Drug Stability , Linear Models , Pramipexole , Rats , Rats, Wistar , Reproducibility of Results , Sensitivity and Specificity
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