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Crystallinity of the formulation was analyzed by DSC and powder X-ray diffraction (PXRD).
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Both degradation of drug delivery devices and drug release profile are influenced by factors as morphology, crystallinity of the polymer, formulation, drug molecular size, and water solubility [ 35].
Also, X-ray diffraction (XRD) analysis revealed a significant loss of crystallinity of the drug in the optimized formulation and existence of both crystalline and amorphous form.
The free radicals were identified and their concentrations were related to both formulation and crystallinity of the polymer.
The drug loaded nanoparticles depicted no distinctive peak of the felodipine in the DSC profiles owing to the decreased crystallinity in the formulations and/or drug solvation in the amorphous carrier as well as solid state interaction induced by heating.
Crystallinity of the sericin hydrogel was analyzed using X-ray diffraction.
The crystallinity of the structure is defined by the intensity ratio (ID/IG) of these bands38.
Further, we characterized the crystallinity of the HA thus formed.
This occurs without perturbing the crystallinity of the lattice, which heats with a 2-ps time constant.
The magnified view confirms the crystallinity of the Si nanodots.
The sharp peaks confirm the high crystallinity of the material.
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