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Sodium alginate-magnesium aluminum silicate composite gels: Characterization of flow behavior, microviscosity, and drug diffusivity

机译:海藻酸钠-镁铝硅酸盐复合凝胶:流动行为,微粘度和药物扩散性的表征

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摘要

The aims of the present study were to characterize the flow behavior and thixotropic properties of sodium alginate-magnesium aluminum silicate (SA-MAS) composite gels with various ratios of SA and MAS, and to investigate the drug diffusivity and microviscosity of the composite gels. Moreover, interaction of SA and MAS in the form of dry composite was examined by using Fourier Transform Infrared (FTIR), and a possible structure model of SA-MAS composite gel was illustrated. Incorporating MAS into the SA gels provided higher viscosity and changed the flow behavior from Newtonian to pseudoplastic with thixotropy. This was due to the formation of electrostatic force and inter-molecular hydrogen bonding between SA and MAS, leading to a denser matrix structure of the composite gels. Increasing the content of MAS decreased the drug diffusivity but increased the microviscosity of the composite gels. The denser matrix structure of the composite gels had a higher tortuosity, resulting in slower drug diffusion through water-filled channels in the gels. This finding suggested that incorporating MAS into the SA gels could improve the flow behavior and sustain drug release from the gels because of the formation of a matrix structure between SA and MAS in the gels.
机译:本研究的目的是表征不同比例的SA和MAS的藻酸钠-硅酸铝镁(SA-MAS)复合凝胶的流动行为和触变性,并研究复合凝胶的药物扩散性和微粘度。此外,通过使用傅立叶变换红外光谱(FTIR)研究了干燥复合材料形式的SA和MAS的相互作用,并阐明了SA-MAS复合材料凝胶的可能结构模型。将MAS掺入SA凝胶中可提供更高的粘度,并将流动性从牛顿型变为具有触变性的假塑性。这是由于在SA和MAS之间形成静电力和分子间氢键,导致复合凝胶的基质结构更致密。增加MAS的含量降低了药物扩散性,但增加了复合凝胶的微粘度。复合凝胶的致密基质结构具有较高的曲折度,导致药物通过凝胶中充水通道的扩散较慢。这一发现表明,由于在凝胶中SA和MAS之间形成了基质结构,因此将MAS掺入SA凝胶中可以改善流动性并维持药物从凝胶中的释放。

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