Prezotti Fabíola Garavello, Boni Fernanda Isadora, Ferreira Natália Noronha, Silva Daniella De Souza E, Campana-Filho Sérgio Paulo, Almeida Andreia, Vasconcelos Teófilo, Gremião Maria Palmira Daflon, Cury Beatriz Stringhetti Ferreira, Sarmento Bruno
Faculdade de Ciências Farmacêuticas, Universidade Estadual Paulista (UNESP), Araraquara, Rodovia Araraquara⁻Jaú, Km 1, Araraquara 14801-902, Brazil.
Instituto de Química de São Carlos, Universidade de São Paulo (USP), Avenida Trabalhador São-Carlense, 400, São Carlos 13560-970, Brazil.
Polymers (Basel). 2018 Jan 8;10(1):50. doi: 10.3390/polym10010050.
This work addresses the establishment and characterization of gellan gum:pectin (GG:P) biodegradable mucoadhesive beads intended for the colon-targeted delivery of resveratrol (RES). The impact of the polymer carrier system on the cytotoxicity and permeability of RES was evaluated. Beads of circular shape (circularity index of 0.81) with an average diameter of 914 μm, Span index of 0.29, and RES entrapment efficiency of 76% were developed. In vitro drug release demonstrated that beads were able to reduce release rates in gastric media and control release for up to 48 h at an intestinal pH of 6.8. Weibull's model correlated better with release data and parameter (0.79) indicated that the release process was driven by a combination of Fickian diffusion and Case II transport, indicating that both diffusion and swelling/polymer chains relaxation are processes that contribute equally to control drug release rates. Beads and isolated polymers were observed to be safe for Caco-2 and HT29-MTX intestinal cell lines. RES encapsulation into the beads allowed for an expressive reduction of drug permeation in an in vitro triple intestinal model. This feature, associated with low RES release rates in acidic media, can favor targeted drug delivery from the beads in the colon, a promising behavior to improve the local activity of RES.
本研究旨在制备用于结肠靶向递送白藜芦醇(RES)的结冷胶:果胶(GG:P)可生物降解粘膜粘附微球,并对其进行表征。评估了聚合物载体系统对RES细胞毒性和渗透性的影响。制备出的微球呈圆形(圆形度指数为0.81),平均直径为914μm,跨度指数为0.29,RES包封率为76%。体外药物释放实验表明,微球能够降低在胃介质中的释放速率,并在肠道pH值为6.8时控制释放长达48小时。威布尔模型与释放数据相关性更好,参数(0.79)表明释放过程是由菲克扩散和第二类转运共同驱动的,这表明扩散和溶胀/聚合物链松弛对控制药物释放速率的贡献相同。观察到微球和分离出的聚合物对Caco-2和HT29-MTX肠道细胞系是安全的。在体外三重肠道模型中,将RES包封到微球中可显著降低药物渗透。这一特性与酸性介质中RES的低释放速率相结合,有利于微球在结肠中的靶向药物递送,这是改善RES局部活性的一种有前景的行为。