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Achromatopsia (ACHM) is a genetically heterogeneous visual disorder, also known as rod monochromatism, in which human get affected due to cone cells. Mutation in five genes viz. CNGA3, CNGB3, GNAT2, PDE6C, and PDE6H have been reported in ACHM. These genes encode essential constitutes of the cone-specific photo transduction cascade. Present study was focused on CNGB3 gene that accounts 40%-50% mutations of all ACHM cases. A new approach for analyzing drug-drug interactions based on modularity was adopted. This approach depends on the behavioral relationship of drugs against CNGB3 for ACHM, particularly the ADME and toxicity between drugs. Data of 2475 compounds were retrieved, out of which 185 were selected on the basis of Lipinski rule of five. In total, eight clusters were made for which the strongly interacted DDI networks were build based on their modularity values. Strong DDI and minimum toxic values indicates that 5 drugs are effective, but on the basis of docking only 2 drugs indicated no bumps, which shows that they are most appropriate for treating ACHM. Our findings revealed that drug-drug interactions disclose the intervention of drug nature and can also successfully diagnose new indications and more convincing drugs for other diseases as well. Keywords: Achromatopsia, CNGB3, In silico, Integrated drugs

Nanocomposites consisting of polyvinyl alcohol embedded with nanoparticles of Zn0.80Co0.1Ni0.1Fe2O4 and ZnFe2O4 were successfully synthesized by employing a facile two-steps process. The nanoparticles of Zn0.80Co0.1Ni0.1Fe2O4 and ZnFe2O4 were synthesized via a micro emulsion procedure and then embedded into a polyvinyl alcohol matrix by an ultrasound-assisted in-situ emulsion. The result showed that the prepared nanoparticles of Zn0.80Co0.1Ni0.1Fe2O4 & ZnFe2O4 diffuse homogeneously in a polyvinyl alcohol matrix, maintaining the particle shape and size of the Zn0.80Co0.1Ni0.1Fe2O4 nanoparticles. Transmission electron microscope images revealed that polyvinyl alcohol chains have encircled the Zn0.80Co0.1Ni0.1Fe2O4 & ZnFe2O4 nanoparticles. The interaction between the polyvinyl alcohol and the nanoparticles in the prepared nanocomposites was confirmed by Fourier-transform infrared spectroscopy via the shifting of bands revealed from the Fourier-transform infrared spectra. Dielectric studies explained the decreasing trend by varying concentrations of nanoparticles with a constant polymer concentration. The dielectric constant and dielectric loss both revealed a decreasing trend by varying the concentration of the nanoparticles with a constant polymer concentration. This occurred due to the grain boundary effect which becomes dominant at low frequencies. The Transmission electron microscope images result shows that polycrystalline Zn0.80Co0.1Ni0.1Fe2O4 & ZnFe2O4 nanoparticles with an average size of 10–15 nm were incorporated with PVA to form nanocomposites. Keywords: Nanocomposites, Polyvinyl alcohol (PVA), Ultrasound-assisted, In-situ emulsions

RNA silencing is a novel gene regulatory mechanism that confines the transcript level by either preventing translation or by the initiation of particular RNA degradation. Small interfering RNAs are regularly represented as the exogenously made or viral inducers of RNAi. Such small RNAs have been used in biomedical research for particular repression of genes. A small hairpin RNA is an artificially synthesized RNA molecule with a hairpin or loop like structure, that is inserted into the designed siRNA to induce interference. In this research work, computational techniques are used to design the siRNA and shRNA against the P53 gene. Approximately four target sites are identified in the p53 gene to which the siRNA and shRNA can bind, for each target site the siRNAs and shRNAs are designed as complementary sequence of the target site. Furthermore, a small hairpin RNA is inserted as a loop in the designed siRNA molecules for better results. This computational analysis of siRNA and shRNA can be further used with the help of in-vitro exploratory techniques to check efficacy and adequacy. Keywords: Gene silencing, Interference, Motifs, P53, siRNA, shRNA