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The preparation, loading efficiencies, release kinetics, cytotoxicity and in vivo behaviour of these systems is discussed in detail.
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The particles were characterized for morphology, size, aerodynamic diameter, entrapment efficiency, release patterns, and metabolic stability.
Furthermore, entrapment efficiency, release rate, and stability of transfersomes were evaluated as dependent variables.
Based on these considerations, it's necessary to modify the structure of PLGA/PLA in order to improve its hydrophilicity, the gene loading efficiency, release behavior, and stability both in vitro and in vivo.
In order to better characterize the microbiological behavior of the coatings more discriminating methods derived from the literature were tested to assess the performances of these CVD coatings in terms of efficiency, release of antibacterial agent and accelerated aging.
The influences of the pH, tripolyphosphate (TPP) concentration, and ionic strength of the gelling medium on the entrapment efficiency, release, and activity of lipase in chitosan hydrogel beads were studied.
PLGA nanobubbles show good stability, high-efficiency coating, stable loading, small size, and controlled and efficiency release.
The prepared nanoformulation was characterized for size, charge, loading efficiency, release kinetics, stability, cytotoxicity, and gene silencing assay.
Careful selection of a suitable method for microsphere preparation is required as the different techniques affect the final outcome on encapsulation efficiency, release kinetics, and preservation of bioactivity of the growth factors [ 100].
The effects of glucantime, chitosan and TiO2 NPs amounts were studied on the particle size, zeta potential, loading efficiency, and release efficiency of drug from nanoassemblies.
Nanoparticles were prepared by an ionic cross-linking method of P MVEMA) [ 42] to obtain optimized nanoparticles with suitable particle size, zeta potential, drug loading efficiency, drug release efficiency, and mucoadhesive properties.
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