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Effect of nonionic surfactant on transport of surface-active and non-surface-active model drugs and emulsion stability in triphasic systems

机译:非离子表面活性剂对三相体系表面活性和非表面活性模型药物转运及乳液稳定性的影响

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摘要

The effect of surfactant concentration on transport kinetics in emulsions using surface-active (phenobarbital, barbital) and non- surface-active is determined. Mineral oil was chosen as the oil phase and the nonionic surfactant polyoxyethylene-10-oleyl-ether (Brij 97) was chosen as the emulsifier. Model drug transport in the triphasic systems was investigated using side-by-side diffusion cells mounted with hydrophilic dialysis membranes (molecular weight cutoffs 1 kd and 50 kd) and a novel bulk equilibrium reverse dialysis bag technique. Emulsion stability was determined by droplet size analysis as a function of time, temperature, and the presence of model drugs, using photon correlation spectroscopy. Mineral oil/water (O/W) partition coefficients and aqueous solubilities were determined in the presence of surfactant. The transport rates of model drugs in emulsions increased with an increase in Brij 97 micellar concentrations up to 1.0% wt/vol and then decreased at higher surfactant concentrations. The transport profiles of the model drugs appeared to be governed by model drug O/W partition coefficient values and by micellar shape changes at higher surfactant concentrations.
机译:确定了表面活性剂浓度对使用表面活性剂(苯巴比妥,巴比妥和非表面活性剂)的乳剂运输动力学的影响。选择矿物油作为油相,选择非离子表面活性剂聚氧乙烯-10-油基醚(Brij 97)作为乳化剂。使用装有亲水性渗析膜(分子量截留值1 kd和50 kd)的并排扩散池和新颖的容积平衡反向渗析袋技术,研究了三相系统中的模型药物运输。使用光子相关光谱,通过液滴大小分析确定乳液稳定性,该液滴大小是时间,温度和模型药物存在的函数。在表面活性剂存在下测定矿物油/水(O / W)分配系数和水溶解度。模型药物在乳剂中的传输速率随Brij 97胶束浓度的增加而增加,最高至1.0%wt / vol,然后在较高的表面活性剂浓度时降低。模型药物的转运曲线似乎受模型药物O / W分配系数值和较高表面活性剂浓度下胶束形状变化的控制。

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