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Drug-loaded SLNs were prepared by the modified solvent emulsification diffusion technique 19, 23, 24, 25.
The objectives of the current study were to evaluate HP-SLNs prepared by the modified solvent emulsification diffusion technique, study the stability of the optimized formulation, and the pharmacokinetics of optimized HP-SLNs after intranasal administration.
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The drug-loaded NPs were prepared by a modified solvent extraction/evaporation method and then characterized for their MMT content, size and size distribution, surface charge and morphology, physical status and encapsulation efficiency of the drug in the NPs, and in vitro drug release profile.
The docetaxel-loaded PLGA-TPGS nanoparticles were prepared by a modified solvent extraction/evaporation method [17].
The docetaxel-loaded PLGA-TPGS nanoparticles were prepared by a modified solvent extraction/evaporation method.
The values at room temperature obtained for nanocomposites compounded by a modified solvent evaporation method via attrition milling in acetone were similar to those from samples compounded by twin screw extrusion.
The docetaxel-loaded PCL-PLA-TPGS nanoparticles were prepared by a modified solvent extraction/evaporation technique and characterized in terms of size and size distribution, morphology, surface charge and physical state of encapsulated docetaxel.
The docetaxel-loaded nanoparticles made of PLGA-TPGS copolymer were prepared by a modified solvent extraction/evaporation method.
Drug-loaded PLGA poloxamer nanoparticles were prepared by a modified solvent diffusion technique.
The porous poly(lactic acid) (PLA) foams potential for tissue engineering usage are prepared by a modified solvent casting/particulate leaching method with different crystallinity.
Based on the optimized results of single-factor and orthogonal design, actarit-loaded SLNs were prepared by a modified solvent diffusion evaporation method.
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