scholarly journals VLSI Implementation of a High-Performance Nonlinear Image Scaling Algorithm

2021 ◽  
Vol 2021 ◽  
pp. 1-10
Author(s):  
Osamah Ibrahim Khalaf ◽  
Carlos Andrés Tavera Romero ◽  
A. Azhagu Jaisudhan Pazhani ◽  
G. Vinuja

This study implements the VLSI architecture for nonlinear-based picture scaling that is minimal in complexity and memory efficient. Image scaling is used to increase or decrease the size of an image in order to map the resolution of different devices, particularly cameras and printers. Larger memory and greater power are also necessary to produce high-resolution photographs. As a result, the goal of this project is to create a memory-efficient low-power image scaling methodology based on the effective weighted median interpolation methodology. Prefiltering is employed in linear interpolation scaling methods to improve the visual quality of the scaled image in noisy environments. By decreasing the blurring effect, the prefilter performs smoothing and sharpening processes to produce high-quality scaled images. Despite the fact that prefiltering requires more processing resources, the suggested solution scales via effective weighted median interpolation, which reduces noise intrinsically. As a result, a low-cost VLSI architecture can be created. The results of simulations reveal that the effective weighted median interpolation outperforms other existing approaches.




1995 ◽  
Author(s):  
John A. Neff ◽  
Charles Stirk




2020 ◽  
Vol 16 (3) ◽  
pp. 246-253
Author(s):  
Marcin Gackowski ◽  
Marcin Koba ◽  
Stefan Kruszewski

Background: Spectrophotometry and thin layer chromatography have been commonly applied in pharmaceutical analysis for many years due to low cost, simplicity and short time of execution. Moreover, the latest modifications including automation of those methods have made them very effective and easy to perform, therefore, the new UV- and derivative spectrophotometry as well as high performance thin layer chromatography UV-densitometric (HPTLC) methods for the routine estimation of amrinone and milrinone in pharmaceutical formulation have been developed and compared in this work since European Pharmacopoeia 9.0 has yet incorporated in an analytical monograph a method for quantification of those compounds. Methods: For the first method the best conditions for quantification were achieved by measuring the lengths between two extrema (peak-to-peak amplitudes) 252 and 277 nm in UV spectra of standard solutions of amrinone and a signal at 288 nm of the first derivative spectra of standard solutions of milrinone. The linearity between D252-277 signal and concentration of amironone and 1D288 signal of milrinone in the same range of 5.0-25.0 μg ml/ml in DMSO:methanol (1:3 v/v) solutions presents the square correlation coefficient (r2) of 0,9997 and 0.9991, respectively. The second method was founded on HPTLC on silica plates, 1,4-dioxane:hexane (100:1.5) as a mobile phase and densitometric scanning at 252 nm for amrinone and at 271 nm for milrinone. Results: The assays were linear over the concentration range of 0,25-5.0 μg per spot (r2=0,9959) and 0,25-10.0 μg per spot (r2=0,9970) for amrinone and milrinone, respectively. The mean recoveries percentage were 99.81 and 100,34 for amrinone as well as 99,58 and 99.46 for milrinone, obtained with spectrophotometry and HPTLC, respectively. Conclusion: The comparison between two elaborated methods leads to the conclusion that UV and derivative spectrophotometry is more precise and gives better recovery, and that is why it should be applied for routine estimation of amrinone and milrinone in bulk drug, pharmaceutical forms and for therapeutic monitoring of the drug.



Sign in / Sign up

Export Citation Format

Share Document