Tangso Kristian J, Patel Hetika, Lindberg Seth, Hartley Patrick G, Knott Robert, Spicer Patrick T, Boyd Ben J
Drug Delivery, Disposition and Dynamics and ARC Centre of Excellence in Convergent Bio-Nano Science and Technology, Monash Institute of Pharmaceutical Sciences, Monash University (Parkville Campus) , 381 Royal Parade, Parkville, Victoria 3052, Australia.
School of Pharmacy, University College London , 29-39 Brunswick Square, London WC1N 1AX, United Kingdom.
ACS Appl Mater Interfaces. 2015 Nov 11;7(44):24501-9. doi: 10.1021/acsami.5b05821. Epub 2015 Oct 27.
The self-assembly of ordered structures in mixtures of oppositely charged surfactant and polymer systems has been exploited in various cleaning and pharmaceutical applications and continue to attract much interest since their discovery in the late twentieth century. The ability to control the electrostatic and hydrophobic interactions that dictate the formation of liquid crystalline phases in these systems is advantageous in manipulation of structure and rendering them responsive to external stimuli. Nanostructured capsules comprised of the cationic surfactant, cetyltrimethylammonium bromide (CTAB), and the diblock copolymer poly(acrylamide-acrylic acid) (PAAm-AA) were prepared to assess their potential as pH responsive nanomaterials. Crossed-polarizing light microscopy (CPLM) and small-angle X-ray scattering (SAXS) identified coexisting Pm3n cubic and hexagonal phases at the surfactant-polymer interface. The hydrophobic and electrostatic interactions between the oppositely charged components were studied by varying temperature and solution pH, respectively, and were found to influence the liquid crystalline nanostructure formed. The lattice parameter of the mesophases and the fraction of cubic phase in the system decreased upon heating. Acidic conditions resulted in the loss of the highly ordered structures due to protonation of the carboxylic acid group, and subsequent reduction of attractive forces previously present between the oppositely charged molecules. The rate of release of the model hydrophilic drug, Rhodamine B (RhB), from nanostructured macro-sized capsules significantly increased when the pH of the solution was adjusted from pH 7 to pH 2. This allowed for immediate release of the compound of interest "on demand", opening new options for structured materials with increased functionality over typical layer-by-layer capsules.
带相反电荷的表面活性剂与聚合物体系混合物中有序结构的自组装已被应用于各种清洁和制药领域,自20世纪末被发现以来一直备受关注。能够控制决定这些体系中液晶相形成的静电和疏水相互作用,有利于结构的操纵并使其对外部刺激做出响应。制备了由阳离子表面活性剂十六烷基三甲基溴化铵(CTAB)和二嵌段共聚物聚(丙烯酰胺 - 丙烯酸)(PAAm - AA)组成的纳米结构胶囊,以评估其作为pH响应性纳米材料的潜力。交叉偏振光显微镜(CPLM)和小角X射线散射(SAXS)确定了在表面活性剂 - 聚合物界面处共存的Pm3n立方相和六方相。分别通过改变温度和溶液pH值研究了带相反电荷组分之间的疏水和静电相互作用,发现它们会影响形成的液晶纳米结构。加热时,中间相的晶格参数和体系中立方相的比例降低。酸性条件下,由于羧酸基团的质子化以及随后带相反电荷分子之间先前存在的吸引力的降低,导致高度有序结构的丧失。当溶液的pH值从pH 7调节到pH 2时,模型亲水性药物罗丹明B(RhB)从纳米结构宏观胶囊中的释放速率显著增加。这使得目标化合物能够“按需”立即释放,为具有比典型的逐层胶囊更高功能的结构化材料开辟了新的选择。