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Relationships Between the Properties of Self-Emulsifying Pellets and of the Emulsions Used as Massing Liquids for Their Preparation

机译:自乳化微丸的性质与用作制备体液的乳液之间的关系

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摘要

Self-emulsifying pellets were prepared using microcrystalline cellulose, emulsions of caprylic/capric triglyceride, and three Cremophors (ELP, RH40, and RH60) at 1.5 and 2.3 weight ratios, and two drugs (furosemide and propranolol) of different lipophilicity. Droplet size, zeta potential (ζ) and viscosity of emulsions, and pellet size, shape, friability, tensile strength, disintegration, and drug migration in pellets were determined. Evaluation of reconstituted emulsions was based on droplet size and ζ. Factorial design and 3-way ANOVA was applied to estimate the significance of the effects of the drug, surfactant and oil/surfactant ratio. It was found that droplet size, viscosity and ζ of emulsions, and size, shape, and friability of pellets were affected by the studied factors and were significant interactions between their effects on pellet size and friability. Migration of drug towards the pellet surface was higher for the less lipophilic furosemide and higher oil content. Linear relationships were found between the emulsion viscosity and the shape parameters of the pellets (for the aspect ratio R2 = 0.796 for furosemide and R2 = 0.885 for propranolol and for the shape factor, eRR2 = 0.740 and R2 = 0.960, respectively). For all the formulations examined, an exponential relationship was found between migration (M%) and the product of viscosity (η) and solubility of drug in oil/surfactant mixture (S) (M% = 98.1e-0.016 [η•S], R2 = 0.856), which may be useful in formulation work.
机译:使用微晶纤维素,辛酸/癸酸甘油三酸酯和三种重量比为1.5和2.3的Cremophors(ELP,RH40和RH60)以及两种亲脂性不同的药物(速尿和普萘洛尔)制备自乳化微丸。测定液滴的大小,zeta电位(ζ)和乳液粘度,以及丸粒的大小,形状,脆性,拉伸强度,崩解和丸粒中的药物迁移。重构乳液的评估基于液滴大小和ζ。应用因子设计和三效方差分析来评估药物,表面活性剂和油/表面活性剂比率的影响的显着性。发现所研究的因素影响乳液的液滴尺寸,乳状液的粘度和ζ,以及颗粒的尺寸,形状和易碎性,并且它们对颗粒尺寸和易碎性的影响之间存在显着的相互作用。亲脂性速尿较少且油含量较高时,药物向沉淀表面的迁移较高。乳液粘度与颗粒形状参数之间存在线性关系(速尿的纵横比R 2 = 0.796,普萘洛尔的R 2 = 0.885,形状因子eRR 2 = 0.740和R 2 = 0.960)。对于所有检查的制剂,在迁移率(M%)与粘度(η)和药物在油/表面活性剂混合物中的溶解度(S)的乘积之间发现了指数关系(M%= 98.1e-0.016 [η•S] ,R 2 = 0.856),这可能对配制工作有用。

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