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In contrast, commercially available formulations achieved a maximum enhancement of 1.9-fold.
end{aligned} (13)This model, with various anisotropy formulations, achieved a broad approval in the phase-field community.
Patients continuing with once weekly dosing maintained HbA1c improvements through 52 weeks, and those who were switched from short-acting to ER formulations achieved further HbA1c reductions.
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Notably, the polymeric nanoparticle formulation achieved greater tumour retention, resulting in prolonged exposure of cancer cells to the active drug.
Furthermore, the ER formulation achieved a lower Cmax central value and a higher Cmin mean than the corresponding values for the DR formulation.
Such a NP formulation achieved more than 10 times higher oral bioavailability than Taxol®, which resulted 9.74-fold higher therapeutic effect and 12.56-fold 12.56-foldtainablongerrapeutic time than Taxol®.
The prepared nano-complex formulation achieved high gene transfection efficiency.
This formulation achieved an encapsulation efficiency of ~50%.
The sentence-based formulation achieved better precision in comparison with the dictionary-based methods.
Overall, the results indicated that the 200 units/mL IDeg formulation achieved glucose control similar to that of IGlar without higher rates of hypoglycemia.
The polydispersity index (PDI) of these extruded liposomes was less than 0.5 of the scale of 1 and liposomal formulation achieved an encapsulation efficacy of 55.1 ± 3.4% (0.15 μg decitabine/mg of lipid).
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