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A.O. introduced K-8794 in the experimental design and characterized its pharmacology.
Vesicle size and entrapment efficiency were optimized using 24 full factorial design and characterized by DSC, PXRD and TEM.
Spiro-pyrazolidinedione derivatives without quaternary chiral center were discovered by structure-based drug design and characterized as potent acetyl-CoA carboxylase (ACC) inhibitors.
Sustained release nanoparticulate formulations of Rivastigmine tartrate (RT) were prepared, optimized (using factorial design) and characterized using the biodegradable polymers, PLGA and PBCA as carriers.
Bicalutamide (BCL -loaded nanoparticles were prepared using the nanoprecipitation method under a BCL -loaded-RSM designanoparticleserized through MPS, PDI, ZP, SEM, PXRD, DSC, in vitro release, in vitro cytotoxicity, protein adsorption, hemolysis and stability studies.
A new supramolecular compound (C10H8N2 3.2·H3PW12O40·25.6H2O (Bipy–Pwas) wasynthesizeded by self-assembly design, and characterized by elemental analysis, Fourier-transform infrared spectra (FTIR), and 31P NMR spectra.
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The purpose of this study was to design and characterize a novel cationic thiolated polymer.
The operator can design and characterize through molecular dynamics simulation the behavior of bionanorobotic components and structures through 3D visualization.
Rather, each approach is optimal for evaluations at a different stage of design and characterizes different usability aspect.
The aim of the work to report here was to design and characterize Diazepam-loaded PLGA nanoparticles in order to obtain a controlled release system.
The commercially available FEM based on state-of-the-art COMSOL v.5.0 has been used to design and characterize of the proposed porous-core square lattice PCF.
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