Abstract

The trans-resveratrol (RSV)-loaded silica aerogel (RLSA) was prepared by the sol-gel method, adding the drug during the aging process, solvent replacement and freeze drying. A series of characterizations showed that RSV stays in the silica aerogel in two ways. First, RSV precipitates due to minimal solubility in water during the solvent replacement process. After freeze drying, the solvent evaporates and the RSV recrystallizes. It can be seen from scanning electron microscope (SEM) and transmission electron microscope (TEM) images that the recrystallized RSV with micron-sized long rod-shaped is integrated with the dense silica network skeleton. Second, from small-angle X-ray scattering (SAXS) results, a portion of the RSV molecules is not crystallized and the size is extremely small. This can be attached to the primary and secondary particles of silica to enhance its network structure and inhibit shrinkage, which is why the volume and pore size of RLSA is larger. In addition, the diffusion of RSV in silica alcogel was studied by a one-dimensional model. The apparent diffusion coefficients of inward diffusion, outward diffusion and internal diffusion were calculated by fitting the time- and position-dependent concentration data. It was found that the outward diffusion coefficient (5.25 × 10−10 m2/s) is larger than the inward (2.93 × 10−10 m2/s), which is probably due to the interface effect. The diffusion coefficients obtained for different concentrations in the same process (inward diffusion) are found to be different. This suggests that the apparent diffusion coefficient obtained is affected by molecular adsorption.

Highlights

  • Drug-delivery systems are difficult to design as there exist various mechanisms that are involved in the release processes of drug [1,2]

  • We can see that the volume of the RSV-loaded silica aerogel (RLSA) is larger than silica aerogel, and the color becomes more opaque

  • A transmission electron microscope (TEM) image of silica aerogel shows that it is a dense structure formed by the accumulation of spherical particles, which is consistent with a scanning electron microscope (SEM) image

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Summary

Introduction

Drug-delivery systems are difficult to design as there exist various mechanisms that are involved in the release processes of drug [1,2]. The use of porous silica materials in drug delivery has attracted a lot of interest due to its potential for the development of systems that are site-specific and that offer time-dependent controlled delivery [3,4,5]. Given in particular their non-toxic properties, silica aerogels are a special kind of porous silica materials consisting of highly mesoporous nanostructures.

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