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Gel formation of colloidal lipid dispersions

机译:胶体脂质分散体的凝胶形成

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Colloidla lipid suspensions are considered to be a promising drug delivery system, e.g., for parenteral, peroral and dermal applications. Aqueous suspensions of solid lipid nano-particles can be obtained by high pressure homogenization of melted lipids with adequate stabilizers followed by crystallization of the dispersed lipids. Triglyceride dispersions stabilized exclusively with phospholipids may, howeve,r form semi-solid gels during the cooling process after homogenization. This is an undesirable effect at least in formulations for parenteral administration, that can be avoided by adding co-surfactacnts (e.g., bile salts or poloxamers). Optimized gel compositions might, however, be considered as interesting warterrich semi-solid formulations for drug delviery purposes. It was supposed that the gel formation can be attributed to the recrystallization of the melt-homogenized triglycerides (1), but the mechanism of gel formation has not yet been investigated in detail. The temperature dependence of gel formation and the influence of different phospholipid qualities on gelation are the subject of the present study.
机译:胶体脂质悬浮液被认为是有前途的药物递送系统,例如,用于肠胃外,运动和皮肤应用。固体脂质纳米颗粒的含水悬浮液可以通过用足够的稳定剂的熔融脂质的高压均化而获得,然后通过分散的脂质结晶。在均质化后,在冷却过程中,在冷却过程中,甘油三酯分散体专门稳定在磷脂中,Howeve,R形成半固体凝胶。这是至少在肠胃外给药的制剂中的不希望的效果,可以通过添加共腐植物(例如胆汁盐或泊洛克马酯)来避免。然而,优化的凝胶组合物可以被认为是有趣的术治疗潜水的半固体制剂。假设凝胶形成可以归因于熔融均化甘油三酯(1)的重结晶,但尚未详细研究凝胶形成的机理。凝胶形成的温度依赖性以及不同磷脂质量对凝胶化的影响是本研究的主题。

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