Raffin Pohlmann Adriana, Weiss Valeria, Mertins Omar, Pesce da Silveira Nádya, Stanisçuaski Guterres Sílvia
Instituto de Qui;mica, Universidade Federal do Rio Grande do Sul, Av. Bento Gonçalves 9500, CP 15003, 91501-970, RS, Porto Alegre, Brazil.
Eur J Pharm Sci. 2002 Sep;16(4-5):305-12. doi: 10.1016/s0928-0987(02)00127-6.
The industrial development of polymeric nanoparticle suspensions, as drug delivery systems, is limited due to the problems in maintaining stability of suspensions. In this work, a spray-drying technique was applied to dry nanocapsule and nanosphere suspensions prepared by nanoprecipitation of polyesters using SiO(2) as adjuvant. Powders obtained from nanocapsules presented stable drug recoveries and morphological characteristics after 5 months. For nanocapsules, nanostructures around 200 nm were observed by scanning electron microscopy (SEM) on the surface of microparticles of SiO(2), whereas for the nanosphere formulation, nanostructures with a reduced diameter (60-90 nm) were observed, despite the particle sizes of each original suspension being similar, when measured by photon correlation spectroscopy (PCS). In order to investigate the morphological aspects of nanocapsule and nanosphere powders, several nanosphere formulations were spray-dried using different concentrations of SiO(2) and a comparative study of the different colloidal systems (nanocapsules, nanospheres, nanoemulsion or nanodispersion) was carried out by PCS. SEM analyses showed that nanostructures with reduced diameter are formed independently of the adjuvant concentration. The dynamic properties of these systems allowed to suggest that the structure of the nanosphere particle (polymer, sorbitan monostearate and polysorbate 80) was a polymeric matrix dispersing the sorbitan monostearate which, when submitted to the spray-drying process in the presence of SiO(2), gave nanostructures presenting diameters around 80 nm covering the microparticles due to the release of lipophilic surfactant from the polymeric matrix.
作为药物递送系统,聚合物纳米颗粒悬浮液的工业发展因维持悬浮液稳定性方面的问题而受到限制。在这项工作中,采用喷雾干燥技术干燥通过以SiO₂为助剂对聚酯进行纳米沉淀制备的纳米胶囊和纳米球悬浮液。从纳米胶囊获得的粉末在5个月后呈现出稳定的药物回收率和形态特征。对于纳米胶囊,通过扫描电子显微镜(SEM)在SiO₂微粒表面观察到约200nm的纳米结构,而对于纳米球制剂,尽管通过光子相关光谱法(PCS)测量时每个原始悬浮液的粒径相似,但观察到直径减小(60 - 90nm)的纳米结构。为了研究纳米胶囊和纳米球粉末的形态方面,使用不同浓度的SiO₂对几种纳米球制剂进行喷雾干燥,并通过PCS对不同的胶体系统(纳米胶囊、纳米球、纳米乳液或纳米分散体)进行比较研究。SEM分析表明,直径减小的纳米结构的形成与助剂浓度无关。这些系统的动态特性表明,纳米球颗粒(聚合物、单硬脂酸山梨坦和聚山梨酯80)的结构是一种分散单硬脂酸山梨坦的聚合物基质,当在SiO₂存在下进行喷雾干燥过程时,由于亲脂性表面活性剂从聚合物基质中释放,产生直径约80nm的纳米结构覆盖微粒。