Digital image scrambling based on elementary cellular automata

Image scrambling is the process of converting an image to an unintelligible format, mainly for security reasons. The scrambling is considered as a pre-process or a post-process of security related applications such as watermarking, information hiding, fingerprinting, and encryption. Cellular automata are parallel models of computation that prove an interesting concept where a simple configuration can lead to a complex behavior. Since there are a lot of parameters to configure, cellular automata have many types and these types differ in terms of complexity and behavior. Cellular automata were previously used in scrambling different types of multimedia, but only complex two-dimensional automata were explored. We propose a scheme where the simplest type of cellular automata is used that is the elementary type. We test the scrambling degree for different cellular automata rules that belong to classes three and four of Wolfram’s classification which correspond to complex and chaotic behavior; we also check the effect of other parameters such as the number of generations and the boundary condition. Experimental results show that our proposed scheme outperforms other schemes based on cellular automata in terms of scrambling degree.     

Characterization of the topography and thickness of gallium thin films by scanning tunneling microscopy

Scanning tunneling microscopy (STM) was employed to characterize the topography of 32 and 4 µm thick gallium films; thicknesses that have not yet been addressed. The STM images revealed submicron grains on both surfaces although a reduced grain density was observed on the thinner film. The granular structure may be explained by a thin gallium oxide layer that acted as an elastic membrane against liquid gallium underneath that expanded during freezing of the sample. We also believe that the same gallium oxide layer is also responsible for an intriguing effect that appears as soon as the tungsten tip lands on the gallium film: the onset of continuous regular z-oscillations of the tip even at rest. This is an effect that we believe has not been previously reported in the literature. We have also demonstrated, for the first time, a new thickness determination method for the gallium film based on an STM image obtained during the solid-to-liquid phase transition.     

The variants of the harmony search algorithm: an overview

The harmony search (HS) algorithm is a relatively new population-based metaheuristic optimization algorithm. It imitates the music improvisation process where musicians improvise their instruments’ pitch by searching for a perfect state of harmony. Since the emergence of this algorithm in 2001, it attracted many researchers from various fields especially those working on solving optimization problems. Consequently, this algorithm guided researchers to improve on its performance to be in line with the requirements of the applications being developed. These improvements primarily cover two aspects: (1) improvements in terms of parameters setting, and (2) improvements in terms of hybridizing HS components with other metaheuristic algorithms. This paper presents an overview of these aspects, with a goal of providing useful references to fundamental concepts accessible to the broad community of optimization practitioners.     

α-Bisabolol Attenuates Doxorubicin Induced Renal Toxicity by Modulating NF-κB/MAPK Signaling and Caspase-Dependent Apoptosis in Rats

Doxorubicin (DOX) is a well-known and effective antineoplastic agent of the anthracycline family. But, multiple organ toxicities compromise its invaluable therapeutic usage. Among many toxicity types, nephrotoxicity is one of the major concerns. In recent years many approaches, including bioactive agents of natural origin, have been explored to provide protective effects against chemotherapy-related complications. α-Bisabolol is a naturally occurring monocyclic sesquiterpene alcohol identified in the essential oils of various aromatic plants and possesses a wide range of pharmacological properties such as antioxidant, anti-inflammatory, analgesic, cardioprotective, antibiotic, anti-irritant, and anticancer activities. The present study aimed to evaluate the effects of α-Bisabolol on DOX-induced nephrotoxicity in Wistar male albino rats. Nephrotoxicity was induced in rats by injecting a single dose of DOX (12.5 mg/kg, i.p.), and the test compound, α-Bisabolol (25 mg/kg) was administered intraperitoneally along with DOX as a co-treatment daily for 5 days. DOX-injected rats showed reduction in body weight along with a concomitant fall in antioxidants and increased lipid peroxidation in the kidney. DOX-injection also increased levels/expressions of proinflammatory cytokines namely tumor necrosis factor-α (TNF-α), interleukin-6 (IL-6), and interleukin-1β (IL-1β) and inflammatory mediators like inducible nitric oxide synthase (iNOS) and cyclooxygenase-2 (COX-2) and activated nuclear factor kappa-B (NF-κB)/mitogen-activated protein kinases (MAPK) signaling in the kidney tissues. DOX also triggered apoptotic cell death, evidenced by the increased expression of pro-apoptotic markers like BCL2-Associated X Protein (Bax), cleaved caspase-3, caspase- 9, and cytochrome-C) and a decrease in the expressions of anti-apoptotic markers namely B-cell lymphoma 2 (Bcl2) and B-cell lymphoma-extra large (Bcl-xL) in the kidney. These biochemical alterations were additionally supported by light microscopic findings, which revealed structural alterations in the kidney. However, treatment with α-Bisabolol prevented body weight loss, restored antioxidants, mitigated lipid peroxidation, and inhibited the rise in proinflammatory cytokines, as well as favorably modulated the expressions of NF-κB/MAPK signaling and apoptosis markers in DOX-induced nephrotoxicity. Based on the results observed, it can be concluded that α-Bisabolol has potential to attenuate DOX-induced nephrotoxicity by inhibiting oxidative stress and inflammation mediated activation of NF-κB/MAPK signaling alongwith intrinsic pathway of apoptosis in rats. The study findings are suggestive of protective potential of α-Bisabolol in DOX associated nephrotoxicity and this could be potentially useful in minimizing the adverse effects of DOX and may be a potential agent or adjuvant for renal protection.     

The Influence of Excitation Frequency on Magnetic Levitation Systems with a High-T c Superconductor

In this paper we present a numerical analysis of dynamic features of the levitation system generated by an interaction between a levitated permanent magnet (PM) and a high-T _c superconductor (HTSC) excited by an oscillatory external source. The obtained results show that the value of the frequency (f _free) of the PM displacement in the case of the levitation system generated by an interaction between a levitated PM and a fixed HTSC is equal at the resonance frequency (f _re) of the levitation system generated by an interaction between a levitated PM and HTS excited by an oscillatory external source and the resonance frequency (f _re) is mainly dependent upon the cooling position (Z ₀) and the mass of the PM. The numerical problem in this paper is solved by using the control volume method (CVM).     

Toxicity and cellular uptake of gold nanorods in vascular endothelium and smooth muscles of isolated rat blood vessel: importance of surface modification

Gold nanorods (GNRs) have promising applications in drug delivery and cancer treatment and are generally administered via direct injection into the circulation. Thus it is necessary to evaluate their potential adverse effects on blood vessels. Herein, GNRs with various surface modifications are used to evaluate the toxicity and cellular uptake of GNRs into vascular endothelial and smooth muscle cells of isolated rat aortic rings. Surfactant-capped GNRs are synthesized and either coated with polyelectrolyte (PE) to prepare PE-GNRs, or modified with thiolated polyethylene glycol (PEG) to prepare PEG-GNRs. Using toxicity assays, small-vessel myography, fluorescence microscopy, and electron microscopy, it is shown that therapeutic concentrations of PE-GNRs but not PEG-GNRs are toxic to the vascular endothelium, which leads to an impaired relaxation function of aortic rings. However, no toxicity to smooth muscles is observed. Moreover, electron microscopy analysis confirms the cellular uptake of PE-GNRs but not PEG-GNRs into the endothelium of exposed aortic rings. The difference in toxicity and cellular uptake of PE-GNRs versus PEG-GNRs is explained and linked to free surfactant molecules and protein adsorption, respectively. The results indicate that toxicity and cellular uptake in the vascular endothelium in blood vessels are potential adverse effects of systemically administered GNR solutions, which can be prevented by appropriate surface functionalization.     

Stereometric Analysis of Effects of Heat Stressing on Micromorphology of Si Single Crystals

Silicon - The purpose of this work is study of silicon single crystal wafer thermal stability in correlation with three-dimensional (3D) surface characterization using atomic force microscopy...     

MUC1 aptamer-conjugated mesoporous silica nanoparticles effectively target breast cancer cells

In the present study, we developed aptamer (Apt) conjugated mesoporous silica nanoparticles (MSNs) for specific delivery of epirubicin (EPI) to breast cancer cells. MSNs were synthesized and functionalized with 3-mercaptopropyltrimethoxysilane (3-MPTMS), followed by MUC1 aptamer conjugation through disulfide bonds. The nanoparticles were analyzed by transmission electron microscopy (TEM), particle size analyzer, zeta potential, elemental analysis (CHNS), aptamer conjugation efficiency, drug loading efficiency, and drug release profile. Cell uptake and in vitro cytotoxicity of different formulations were performed. The results of MSNs characterization confirmed spherical nanoparticles with thiol functional groups. Particle size of obtained nanoparticles was 163?nm in deionized water. After conjugation of MUC1 aptamer and EPI loading (MSN-MUC1-EPI), particle size increased to 258?nm. The aptamer conjugation to MSNs with disulfide bonds were confirmed using gel retardation assay. Cellular uptake studies revealed better cell uptake of MSN-MUC1-EPI compared to MSN-EPI. Moreover, cytotoxicity study results in MCF7 cell lines showed improved cytotoxicity of MSN-MUC1-EPI in comparison with MSN-EPI or EPI at the same concentration of drug. These results exhibited that MSN-MUC1-EPI has the potential for targeted drug delivery into MUC1 positive breast cancer cells to improve drug efficacy and alleviate side effects.