This paper presents the effect of modified halloysite nanotubes on the sustained drug release mechanisms of sodium salicylate. Acid treatment and composite polymer-halloysite modification techniques were adopted in this study. After each modification, sodium salicylate drug was loaded, and in vitro release properties were evaluated and compared with the raw unmodified halloysite nanotubes. The results obtained from SEM, TEM and FTIR analyses indicate that both acid treatment and composite formation have no effect on the tubular structure and morphology of halloysite. However, modification of the halloysite nanotubes did influence the drug release rate. In the acid treatment modification, there was an improved loading of sodium salicylate drug which resulted in the sustain release of large amount of the sodium salicylate. In the polymer/halloysite composite formation, a consistent layer of polymer was formed around the halloysite during the composite formation and thus delayed release providing sustained release of sodium salicylate drug over a longer period of time as compared to the acid treated and unmodified halloysite. The results from the invitro release were best fitted with the Higuchi and the Koresymer-Peppas models.
In this work, zeolite (Z) and Z-Fe3O4 nanocomposite (Z-Fe3O4 NC) have been synthesized. The Fe3O4 nanoparticles were synthesized using the extract from maize leaves and ferric and ferrous chloride salts and encapsulated into the zeolite framework. The nanocomposite (Z-Fe3O4 NC) was characterized using X-ray diffractometer (XRD), Fourier-transform infrared (FT-IR) spectroscopy, energy-dispersive X-ray (EDX) spectroscopy, and scanning electron microscopy (SEM). The potential of Z-Fe3O4 NC as an adsorbent for removing methylene blue molecules (MB) from solution was examined using UV-Vis and kinetic and equilibrium isotherm models. The adsorption data fitted best with the pseudo-second-order model and Weber and Morris model, indicating that the adsorption process was chemisorption, while the Weber and Morris described the rate-controlling steps. The intraparticle diffusion model suggests that the adsorption processes were pore and surface diffusion controlled. The Langmuir isotherm model best describes the adsorption process indicating homogeneous monolayer coverage of MB molecules onto the surface of the Z-Fe3O4 NC. The maximum Langmuir adsorption capacity was 2.57 mg/g at 25°C. The maximum adsorption efficiency was 97.5%. After regeneration, the maximum adsorption efficiency achieved at a pH of 7 was 82.6%.
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