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Thermal gelation of aqueous hydroxypropylmethylcellulose solutions with SDS and hydrophobic drug particles

机译:羟丙基甲基纤维素水溶液与SDS和疏水性药物颗粒的热凝胶化

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The thermal gelation of hydroxypropylmethylcellulose (HPMC) solutions has been studied as a function of sodium dodecyl sulfate (SDS) concentration with and without griseofulvin, a model particulate BCS Class II drug by Theological measurements of gelation temperature (T_(gel)), steady-state viscosity (η) at 25 °C, and ξ-potential. Polymer adsorption on the drug was demonstrated by a decrease in η and potential in the absence of SDS. Griseofulvin had a synergistic effect on gelation which was attributed to an effective spanning of associated hydrophobic polymeric regions through interactions with the adsorbed polymer. Adding SDS offsets this effect on T_(gel) shielding hydrophobic interactions. Higher SDS concentrations had no effect on the particles surface as evidenced by constant ξ-potential and T_(gel). Yet, polymeric chains are saturated and larger surfactant aggregates account for the increase in viscosity. Understanding the gelation mechanism and complex interactions of HPMC with surfactants and drugs is necessary for the design of pharmaceutical products and optimization of their performance properties.
机译:通过胶凝温度(T_(gel))的神学测量,研究了在有和没有灰黄霉素的情况下,羟丙基甲基纤维素(HPMC)溶液的热凝胶化与十二烷基硫酸钠(SDS)浓度的函数关系。 25°C时的状态粘度(η)和ξ电位。在不存在SDS的情况下,η和电位的降低证明了聚合物在药物上的吸附。灰黄霉素对凝胶化具有协同作用,这归因于通过与吸附的聚合物的相互作用有效地扩展了相关的疏水性聚合物区域。添加SDS抵消了对T_(gel)屏蔽疏水相互作用的影响。恒定的ξ电位和T_(gel)证明较高的SDS浓度对颗粒表面无影响。然而,聚合物链是饱和的,并且较大的表面活性剂聚集体导致粘度增加。了解HPMC与表面活性剂和药物的胶凝机理以及复杂的相互作用对于设计药物产品和优化其性能非常必要。

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