首页> 外文期刊>International Journal of Pharmaceutics >Chitosan-magnesium aluminum silicate nanocomposite films: physicochemical characterization and drug permeability.
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Chitosan-magnesium aluminum silicate nanocomposite films: physicochemical characterization and drug permeability.

机译:壳聚糖-镁铝硅酸盐纳米复合膜:物理化学特征和药物渗透性。

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摘要

Chitosan-magnesium aluminum silicate (CS-MAS) films were prepared and the effects of MAS content and heat treatment of the CS-MAS dispersion before film casting on the physicochemical and drug permeability properties of the films were investigated. CS could interact with MAS via electrostatic interaction and intermolecular hydrogen bonding mechanisms, resulting in nanocomposite formation, for which it was not necessary to apply the heat treatment on the composite dispersions. The nature of the exfoliated and intercalated nanocomposite films formed was depended on the MAS content added. The heat treatment on the composite dispersions caused an increase in tensile strength, but reduced %elongation of the CS-MAS nanocomposite films. The exfoliated nanocomposite films showed higher flexibility, water uptake, and drug permeability compared to the CS and intercalated CS-MAS nanocomposite films. At higher MAS content, the CS-MAS films prepared using heat treatment had a lower water uptake, resulting in lower drug permeability when compared with those prepared using non-heated dispersions. The permeation mechanism of non-electrolyte and negatively charged drugs across the CS-MAS nanocomposite films was predominantly controlled by diffusion in water-filled microchannels, whereas both adsorption onto MAS and diffusion processes occurred concurrently for the film permeation of positively charged drugs. The findings of this study suggest that CS-MAS nanocomposite films can be formed without heating of the composite dispersion before casting. CS-MAS nanocomposites showed strong potential to be used as a film former for coated tablets intended for modulating drug release.
机译:制备了壳聚糖镁铝硅酸盐(CS-MAS)薄膜,研究了流延前的MAS含量和CS-MAS分散体的热处理对薄膜的理化性质和药物渗透性的影响。 CS可以通过静电相互作用和分子间氢键作用机理与MAS相互作用,从而形成纳米复合材料,因此无需对复合分散体进行热处理。形成的剥落和嵌入的纳米复合薄膜的性质取决于所添加的MAS含量。对复合分散体进行热处理可提高拉伸强度,但降低CS-MAS纳米复合膜的伸长率。与CS和插层CS-MAS纳米复合材料薄膜相比,脱落的纳米复合材料薄膜显示出更高的柔韧性,吸水性和药物渗透性。在较高的MAS含量下,与使用非加热的分散体制备的CS-MAS膜相比,通过吸水处理获得的CS-MAS膜的吸水率更低,从而导致较低的药物渗透性。非电解质和带负电荷的药物在CS-MAS纳米复合膜上的渗透机理主要受充水微通道中的扩散控制,而带正电荷的药物膜的渗透同时发生在MAS上的吸附和扩散过程。这项研究的发现表明,在浇铸前无需加热复合材料分散体即可形成CS-MAS纳米复合膜。 CS-MAS纳米复合材料显示出强大的潜力,可以用作旨在调节药物释放的包衣片剂的成膜剂。

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