CSIRO Materials Science & Engineering (CMSE), Bag 10, Clayton South, VIC 3169, Australia.
Langmuir. 2011 Mar 15;27(6):2317-26. doi: 10.1021/la104736u. Epub 2011 Feb 4.
The neat and lyotropic phase behavior of eight new ethylene oxide amphiphiles (EO = 1-8) with a hexahydrofarnesyl chain (3,7,11-trimethyldodecyl) and narrow polydispersity (>98.5% purity) is reported. Below five EO units the behavior of the neat surfactants show only a glass transition, Tg ∼ -90 °C. Above four EO units, crystallization (Tcrys) and crystal-isotropic liquid (Tm) transitions are also observed that increase with degree of ethoxylation of the surfactant headgroup. The lyotropic liquid crystalline phase behavior spans a complex spectrum of surfactant-water interfacial curvatures. Specifically, inverse phases are present below ambient temperatures for EO < 4, with HFarn(EO)2 exhibiting an inverse hexagonal (H(II)) phase stable to dilution. The phase diagram of HFarn(EO)3 displays both the gyroid (Ia3d) and double diamond (Pn3m) inverse bicontinuous cubic phases, with the latter being thermodynamically stable in excess water within the physiological regime. There is a strong preference for planar bilayer structures at intermediate headgroup ethoxylation, with the crossover to normal phases occurring at HFarn(EO)(7-8) which exhibits normal hexagonal (H(I)) and cubic (Q(I)) phases at ambient temperatures. The toxicity of colloidal dispersions of these EO amphiphiles was assayed against normal breast epithelial (HMEpiC) and breast cancer (MCF7) cell lines. The IC50 of the EO amphiphiles was similar in both cell lines with moderate toxicity ranging from ca. <5 to 140 μM in an in vitro cell viability assay. Observations are qualitatively rationalized in terms of the molecular geometry of the surfactant. The physicochemical behavior of the HFarnesyl ethylene oxide amphiphiles is compared to other ethylene oxide surfactants.
报告了具有六氢法呢基链(3,7,11-三甲基十二烷基)和窄分散性(>98.5%纯度)的 8 种新型乙氧基化物两亲物(EO=1-8)的整洁和溶致相行为。在低于 5 个 EO 单元的情况下,纯表面活性剂的行为仅表现出玻璃化转变,Tg∼-90°C。在 4 个 EO 单元以上,还观察到结晶(Tcrys)和晶-各向同性液体(Tm)转变,这些转变随表面活性剂头基乙氧基化程度的增加而增加。溶致液晶相行为跨越了表面活性剂-水界面曲率的复杂光谱。具体来说,在环境温度以下,EO<4 的情况下存在反相,HFarn(EO)2 表现出稳定的反六方(H(II))相,可稀释。HFarn(EO)3 的相图显示了双网格(Ia3d)和双金刚石(Pn3m)反连续立方相,在后一种情况下,在生理范围内的过量水中,热力学上是稳定的。在中间头基乙氧基化程度下,强烈倾向于平面双层结构,在 HFarn(EO)(7-8)中发生向正常相的转变,在环境温度下表现出正常六方(H(I))和立方(Q(I))相。这些乙氧基化物两亲物的胶体分散体的毒性针对正常乳腺上皮(HMEpiC)和乳腺癌(MCF7)细胞系进行了测定。在体外细胞活力测定中,EO 两亲物在两种细胞系中的 IC50 相似,毒性适中,范围约为 ca. <5 至 140μM。根据表面活性剂的分子几何形状,对观察结果进行了定性合理化。将六氢法呢基乙氧基化物的物理化学行为与其他乙氧基化物表面活性剂进行了比较。