Barreiro-Iglesias R, Alvarez-Lorenzo C, Concheiro A
Departamento de Farmacia y Tecnología Farmacéutica, Facultad de Farmacia, Universidad de Santiago de Compostela, 15782, Santiago de Compostela, Spain.
Int J Pharm. 2003 Jun 4;258(1-2):179-91. doi: 10.1016/s0378-5173(03)00182-0.
The interaction of sodium dodecylsulfate (SDS) or benzalkonium chloride (BkCl) with carbopol microgels (0.25% (w/w)) in water was studied through pH, trasmittance, viscosity, surface tension, conductivity, fluorescence, oil solubilization, and microcalorimetry measurements. In the case of the anionic surfactant, enthalpy-driven hydrophobic absorption of SDS into carbopol microgels began when SDS concentration reached 0.05-0.08% and ended around 0.6%. These concentrations were estimated as the critical aggregation (cac) and saturation binding concentration, respectively. The hydrophobic absorption of the surfactant accompanied by its counter-ion caused carbopol microgels to swell and promoted the occurrence of bridges among several carbopol microgels. As a consequence, the consistency of the dispersions increased significantly. Above binding saturation, further addition of SDS produced a shielding effect among the anionic charges of carbopol and its dehydration, which was shown as a decrease in the viscosity of the dispersions. At low shear rates, the dispersions behaved as pseudoplastic owing to orientation of carbopol/SDS aggregates in the flow direction. Increasing shear rates caused the inter-microgel bridges to break, the water layer surrounding them to diminish, and the system to show a shear-thickening behavior. In contrast, carbopol/BkCl aggregates showed shear-thickening flow in the whole range of shear rates analyzed. Electrostatic interactions between BkCl and carbopol carboxylic groups release protons to the medium and decrease the internal osmotic pressure of the microgels. This may favor the establishment of hydrophobic interactions among surfactant tails, and induces carbopol microgels to collapse. The cac was approximately 0.01% BkCl. Saturation binding occurred at 0.3-0.5%, indicating that only 25-40mol% carboxylic groups were neutralized with BkCl. The shrinking of carbopol microgels as BkCl is absorbed prevents additional surfactant molecules from interacting with the remaining carboxylic groups. Microcalorimetry assays revealed that the aggregation process occurred with a strong gain in enthalpy.
通过pH值、透光率、粘度、表面张力、电导率、荧光、油增溶和微量量热法测量,研究了十二烷基硫酸钠(SDS)或苯扎氯铵(BkCl)与水中卡波姆微凝胶(0.25%(w/w))的相互作用。对于阴离子表面活性剂,当SDS浓度达到0.05 - 0.08%时,焓驱动的SDS向卡波姆微凝胶的疏水吸收开始,并在约0.6%时结束。这些浓度分别被估计为临界聚集浓度(cac)和饱和结合浓度。表面活性剂的疏水吸收及其抗衡离子导致卡波姆微凝胶膨胀,并促进了几个卡波姆微凝胶之间桥连的发生。结果,分散体的稠度显著增加。在结合饱和以上,进一步添加SDS会在卡波姆的阴离子电荷之间产生屏蔽效应并使其脱水,这表现为分散体粘度的降低。在低剪切速率下,由于卡波姆/SDS聚集体在流动方向上的取向,分散体表现为假塑性。增加剪切速率会导致微凝胶间的桥连断裂,其周围的水层减少,系统表现出剪切增稠行为。相比之下,卡波姆/BkCl聚集体在分析的整个剪切速率范围内均表现出剪切增稠流动。BkCl与卡波姆羧基之间的静电相互作用将质子释放到介质中,并降低微凝胶的内部渗透压。这可能有利于表面活性剂尾部之间疏水相互作用的建立,并诱导卡波姆微凝胶塌陷。cac约为0.01% BkCl。饱和结合发生在0.3 - 0.5%,表明只有25 - 40mol%的羧基被BkCl中和。随着BkCl被吸收,卡波姆微凝胶的收缩阻止了额外的表面活性剂分子与剩余的羧基相互作用。微量量热法测定表明,聚集过程伴随着焓的强烈增加而发生。