Department of Medicinal Chemistry, Uppsala University, P.O. Box 547, 751 23 Uppsala, Sweden.
Department of Chemistry─Ångström, P.O. Box 573, Uppsala University, 751 23 Uppsala, Sweden.
Langmuir. 2023 Aug 15;39(32):11337-11344. doi: 10.1021/acs.langmuir.3c01023. Epub 2023 Aug 2.
We have observed ultrasmall unilamellar vesicles, with diameters of less than 20 nm, in mixtures of the tricyclic antidepressant drug amitriptyline hydrochloride (AMT) and the unsaturated zwitterionic phospholipid 1,2-dioleoyl-sn-glycero-3-phosphocholine (DOPC) in physiological saline solution. The size and shape of spontaneously formed self-assembled aggregates have been characterized using complementary techniques, i.e., small-angle neutron and X-ray scattering (SANS and SAXS) and cryo-transmission electron microscopy (cryo-TEM). We observe rodlike mixed micelles in more concentrated samples that grow considerably in length upon dilution, and a transition from micelles to vesicles is observed as the concentration approaches the critical micelle concentration of AMT. Unlike the micelles, the spontaneously formed vesicles decrease in size with each step of dilution, and ultrasmall unilamellar vesicles, with diameters as small as about 15 nm, were observed at the lowest concentrations. The spontaneously formed ultrasmall unilamellar vesicles maintain their size for as long we have investigated them (i.e., several months). To the best of our knowledge, such small vesicles have never before been reported to form spontaneously in a biocompatible phospholipid-based system. Most interestingly, the size of the vesicles was observed to be strongly dependent on the chemical structure of the phospholipid, and in mixtures of AMT and the phospholipid 1,2-dimyristoyl-sn-glycero-3-phosphocholine (DMPC), the vesicles were observed to be considerably larger in size. The self-assembly behavior in the phospholipid-drug surfactant system in many ways resembles the formation of equilibrium micelles and vesicles in mixed anionic/cationic surfactant systems.
我们在三环抗抑郁药盐酸阿米替林(AMT)和不饱和两性离子磷脂 1,2-二油酰基-sn-甘油-3-磷酸胆碱(DOPC)在生理盐水中的混合物中观察到直径小于 20nm 的超小单层囊泡。使用互补技术,即小角中子和 X 射线散射(SANS 和 SAXS)和冷冻传输电子显微镜(cryo-TEM),对自发形成的自组装聚集体的大小和形状进行了表征。在浓度较高的样品中,我们观察到棒状混合胶束,其长度在稀释后大大增加,并且当浓度接近 AMT 的临界胶束浓度时,观察到从胶束到囊泡的转变。与胶束不同,自发形成的囊泡随着稀释的每一步而减小,并且在最低浓度下观察到直径小至约 15nm 的超小单层囊泡。自形成的超小单层囊泡在我们研究的时间内(即几个月)保持其大小。据我们所知,在生物相容性磷脂基系统中,从未有报道过如此小的囊泡自发形成。最有趣的是,观察到囊泡的大小强烈依赖于磷脂的化学结构,并且在 AMT 和 1,2-二肉豆蔻酰基-sn-甘油-3-磷酸胆碱(DMPC)的磷脂混合物中,囊泡的尺寸观察到明显更大。在磷脂-药物表面活性剂系统中的自组装行为在许多方面类似于混合阴离子/阳离子表面活性剂系统中平衡胶束和囊泡的形成。