AI Article Synopsis

  • The study focused on creating a dioscin nanosuspension (Dio-NS) that improves its solubility and effectiveness for oral administration, as well as evaluating its effects on liver protection.
  • Researchers optimized manufacturing parameters and ingredient concentrations using specific experimental methods to achieve a nanosuspension with favorable particle size and stability.
  • Findings showed that Dio-NS had better dissolution compared to other forms, and it effectively protected against liver damage in mice, similar to an established medication, suggesting potential for further research on how it is absorbed in the body.

Article Abstract

The purpose of this study was to prepare a dioscin nanosuspension (Dio-NS) that has a better distance and high solubility for oral administration and to evaluate its hepatoprotective effects. Optimal primary manufacture parameters, including shear time, shear speed, emulation temperature, pressure, and cycles of homogenization, were determined by single-factor experiments. The concentrations of dioscin, SDS, and soybean lecithin were optimized using the central composite design-response surface method, and their effects on the mean particle size (MPS) and particle size distribution of Dio-NS were investigated. Characterization of the Dio-NS formulations included examinations of the surface morphology and physical status of dioscin in Dio-NS, the stability of Dio-NS at different temperatures, solubility, and liver protective effect . Under optimal conditions, Dio-NS had an MPS of 106.72 nm, polydispersity index of 0.221, and zeta potential of -34.27 mV. Furthermore, the proportion of dioscin in Dio-NS was approximately 21.26%. The observation of particles with a spherical shape and the disappearance of crystalline peaks indicated that the physical and chemical properties of Dio-NS were altered. Furthermore, we observed that the dissolution of Dio-NS was superior to that of a physical mixture and Dio-GZF. Moreover, Dio-NS was demonstrated to have a protective effect against CCl-induced acute liver damage in mice that was equivalent to that of silymarin (a positive control drug) at the same dose. The good hepatoprotective effect of our Dio-NS preparation can provide a theoretical basis for investigating its absorption mechanisms in the body.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6878791PMC
http://dx.doi.org/10.1155/2019/3907915DOI Listing

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