Oshiro Joao Augusto, Lusuardi Angelo, Beamud Elena M, Chiavacci Leila Aparecida, Cuberes M Teresa
Department of Applied Mechanics and Project Engineering, University of Castilla-La Mancha, Plaza Manuel Meca 1, 13400 Almadén, Spain.
Laboratory of Development and Characterization of Pharmaceutical Products, Department of Pharmacy, Center for Biological and Health Sciences, State University of Paraíba (UEPB), Campina Grande, Paraíba 58429-600, Brazil.
Nanomaterials (Basel). 2021 May 21;11(6):1362. doi: 10.3390/nano11061362.
Ureasil-Poly(ethylene oxide) (ureasil-PEO500) and ureasil-Poly(propylene oxide) (u-PPO400) films, unloaded and loaded with dexamethasone acetate (DMA), have been investigated by carrying out atomic force microscopy (AFM), ultrasonic force microscopy (UFM), contact-angle, and drug release experiments. In addition, X-ray diffraction, small angle X-ray scattering, and infrared spectroscopy have provided essential information to understand the films' structural organization. Our results reveal that while in u-PEO500 DMA occupies sites near the ether oxygen and remains absent from the film surface, in u-PPO400 new crystalline phases are formed when DMA is loaded, which show up as ~30-100 nm in diameter rounded clusters aligned along a well-defined direction, presumably related to the one defined by the characteristic polymer ropes distinguished on the surface of the unloaded u-POP film; occasionally, larger needle-shaped DMA crystals are also observed. UFM reveals that in the unloaded u-PPO matrix the polymer ropes are made up of strands, which in turn consist of aligned ~180 nm in diameter stiffer rounded clusters possibly formed by siloxane-node aggregates; the new crystalline phases may grow in-between the strands when the drug is loaded. The results illustrate the potential of AFM-based procedures, in combination with additional physico-chemical techniques, to picture the nanostructural arrangements in polymer matrices intended for drug delivery.
通过进行原子力显微镜(AFM)、超声力显微镜(UFM)、接触角和药物释放实验,对未负载和负载醋酸地塞米松(DMA)的脲硅-聚环氧乙烷(脲硅-PEO500)和脲硅-聚环氧丙烷(u-PPO400)薄膜进行了研究。此外,X射线衍射、小角X射线散射和红外光谱提供了重要信息,以了解薄膜的结构组织。我们的结果表明,在u-PEO500中,DMA占据靠近醚氧的位置,并且在薄膜表面不存在,而在u-PPO400中,当负载DMA时会形成新的晶相,这些晶相表现为直径约30-100nm的圆形簇,沿明确的方向排列,大概与未负载的u-POP薄膜表面上区分出的特征聚合物绳所定义的方向有关;偶尔也会观察到更大的针状DMA晶体。UFM显示,在未负载的u-PPO基质中,聚合物绳由股线组成,而股线又由直径约180nm的排列更紧密的圆形簇组成,这些簇可能由硅氧烷节点聚集体形成;当负载药物时,新的晶相可能在股线之间生长。结果说明了基于AFM的程序与其他物理化学技术相结合,用于描绘用于药物递送的聚合物基质中的纳米结构排列的潜力。