Theranostic Interpolation of Genomic Instability in Breast Cancer

Breast cancer is a diverse disease caused by mutations in multiple genes accompanying epigenetic aberrations of hazardous genes and protein pathways, which distress tumor-suppressor genes and the expression of oncogenes. Alteration in any of the several physiological mechanisms such as cell cycle checkpoints, DNA repair machinery, mitotic checkpoints, and telomere maintenance results in genomic instability. Theranostic has the potential to foretell and estimate therapy response, contributing a valuable opportunity to modify the ongoing treatments and has developed new treatment strategies in a personalized manner. “Omics” technologies play a key role while studying genomic instability in breast cancer, and broadly include various aspects of proteomics, genomics, metabolomics, and tumor grading. Certain computational techniques have been designed to facilitate the early diagnosis of cancer and predict disease-specific therapies, which can produce many effective results. Several diverse tools are used to investigate genomic instability and underlying mechanisms. The current review aimed to explore the genomic landscape, tumor heterogeneity, and possible mechanisms of genomic instability involved in initiating breast cancer. We also discuss the implications of computational biology regarding mutational and pathway analyses, identification of prognostic markers, and the development of strategies for precision medicine. We also review different technologies required for the investigation of genomic instability in breast cancer cells, including recent therapeutic and preventive advances in breast cancer.     

Influence of different viscosity grade cellulose-based polymers on the development of valsartan controlled release tablets

This work is based on formulating and optimizing controlled release (CR) valsartan (160 mg) tablets using different viscosity grades of the cellulosic polymer. The objective was to develop an effective once-daily drug delivery system of this cardiovascular agent. Central composite design was used for designing the formulations. Polymers used were Methocel® K4M, K15M and K100M. Compatibility of excipients with active was studied through FT-IR. Micromeritic properties were determined and formulations exhibiting appropriate flow characteristics were compressed. Swelling behavior and in vitro buoyancy effect were studied and response surface curves were constructed to optimize the formulation. Multi-point dissolution profiles of valsartan CR tablets at pH 1.2, 4.5 and 6.8 were obtained. Model-dependent and model-independent methods were performed including f2, stability test as per ICH guidelines and ANOVA. FT-IR studies revealed the compatibility of valsartan with all excipients. Formulation K4T9 (containing 25% K4M polymer) was selected to be the best optimized trial, based on physical properties and controlled release profile (23% at 4 h, 82% at 16 h and 100% at 24 h). Results of buoyancy and swelling behavior indicated that HPMC-K4M polymer exhibited excellent floating lag time and swelling indexes. In vitro drug release kinetics showed that formulation K4T9 displayed Korsmeyer–Peppas drug release pattern with r value > 0.99. The manufacturing process of K4T9 was also found to be reproducible with a shelf life period of 41 and 36 months at room temperature and accelerated conditions, respectively. Valsartan CR matrix-based formulation was successfully prepared with Methocel K4M retardant.     

A Reliable Stochastic Numerical Analysis for Typhoid Fever Incorporating With Protection Against Infection

In this paper, a reliable stochastic numerical analysis for typhoid fever incorporating with protection against infection has been considered. We have compared the solutions of stochastic and deterministic typhoid fever model. It has been shown that the stochastic typhoid fever model is more realistic as compared to the deterministic typhoid fever model. The effect of threshold number T* hold in stochastic typhoid fever model. The proposed framework of the stochastic non-standard finite difference scheme (SNSFD) preserves all dynamical properties like positivity, bounded-ness and dynamical consistency defined by Mickens, R. E. The stochastic numerical simulation of the model showed that increase in protection leads to low disease prevalence in a population.     

Numerical simulation of the MHD equations by a kinetic-type method

We introduce a flux-splitting formula for the approximation of the ideal MHD equations in conservative form. The Faraday equation is considered as the average of an abstract kinetic equation, giving a flux-splitting formula. For the other part of the equations, we generalize formally the classical half-Maxwellian flux-splitting of the Euler equations. Numerical results on MHD shock tube problems are displayed.     

A branch-and-bound algorithm to minimize total weighted completion time on identical parallel machines with job release dates

In this paper, we consider an identical parallel machine scheduling problem with release dates. The objective is to minimize the total weighted completion time. This problem is known to be strongly NP-hard. We propose some dominance properties and two lower bounds. We also present an efficient heuristic. A branch-and-bound algorithm, in which the heuristic, the lower bounds and the dominance properties are incorporated, is proposed and tested on a large set of randomly generated instances.     

Abiotic stress of ZnO‐PEG,ZnO‐PVP,CuO‐PEG and CuO‐PVP nanoparticles enhance growth,sweetener compounds and antioxidant activities in shoots of Stevia rebaudiana Bertoni

Nanoparticles are known to play remarkable role as abiotic stress elicitors in plants. This study reports the comparative analysis of effects produced by capped [zinc oxide (ZnO)‐polyethylene glycol (PEG), ZnO‐polyvinyl pyrrolidone (PVP), copper oxide (CuO)‐PEG, CuO‐PVP] and uncapped (ZnO and CuO) nanoparticles on the medicinal plant, Stevia rebaudiana raised in vitro for the production of commercially important sweetener compounds. In context of shoot organogenesis, ZnO‐PEG, ZnO‐PVP, CuO‐PEG, CuO‐PVP were employed to the growth medium that resulted in increased growth parameters, and larger content of steviol glycosides as compared to the shoots raised in medium containing ZnO and CuO, revealed by high‐performance liquid chromatography. In the meanwhile, non‐enzymatic antioxidant activities including total phenolic content, total flavonoid content, total antioxidant capacity, total reducing power and 2,2‐diphenyl‐1‐picryl hydrazyl‐free radical scavenging activity were calculated and showed comparatively greater amounts in shoots grown in medium containing capped ZnO or CuO nanoparticles. Furthermore, the ZnO and its derivatives revealed to be more reactive at 1 mg/l of concentration. Whereas, the CuO and its derivatives produced greater response on Stevia at 10 mg/l concentration of nanoparticles. This study paves the way for more such studies encompassing capped and uncapped nanoparticles and their ultimate effect on in‐vitro grown plant tissues for the production of active metabolites on industrial scale.Inspec keywords: nanoparticles, chromatography, resins, polymers, zinc compounds, copper compounds, food technology, agricultureOther keywords: nanoparticles, sweetener compounds, antioxidant activities, Stevia rebaudiana Bertoni, abiotic stress elicitors, zinc oxide‐polyethylene glycol, zinc oxide‐polyvinyl pyrrolidone, copper oxide‐polyethylene glycol, medicinal plant, shoot organogenesis, steviol glycosides, high‐performance liquid chromatography, nonenzymatic antioxidant activities, total phenolic content, total flavonoid content, total antioxidant capacity, total reducing power, 2,2‐diphenyl‐1‐picryl hydrazylfree radical scavenging activity, derivatives, active metabolite production, copper oxide‐polyvinyl pyrrolidone     

A New Active Micro-Mixing Strategy

An active micro-mixing strategy through forcing the flow by synthetic wall jets is proposed. It is based on the interaction of induced streamwise vortices in a specific way. There is a spanwise shift between two quasi-streamwise vortices in such a way that one of them compresses the wall normal vorticity layer created by the other, leading to the generation of new wall normal vortical structures. The latter are subsequently tilted by the shear to give birth to new small-scale longitudinal active structures that are efficient in mixing. The feasibility of this strategy is shown through direct numerical simulations of high spatial and temporal resolution.     

Forced migration of soluble and suspended materials by freezing front in aqueous systems

Migration of soluble and suspended materials by directional freezing of aqueous systems has been studied qualitatively. Slow freezing was employed vertically as well as horizontally through solutions and suspensions. In all cases, the impurities (soluble salts as well as suspended materials) were appreciably forced out by dynamic freezing front. The phenomenon worked for concentrating/separating inorganic ions, soluble organic compounds and dyes in synthetic solutions as well as in natural streams. Various analytical techniques were employed to monitor the migrating species through the freezing media. It was found that separation efficiency depends on different factors like rate of cooling, pH and concentration. Model experiments were designed and exercised successfully to employ the technique for treatment of dye-polluted water.